UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM ~~10-Q/A~~10-Q

~~(Amendment No. 1)~~

x	Quarterly Report Under Section 13 or 15(d) of the Securities Exchange Act of 1934 for the quarterly period ended June 30, ~~2015~~2016

¨	Transition Report Under Section 13 or 15(d) of the Securities Exchange Act of 1934 for the transition period from to .

Commission File Number: 000-27239

TAPIMMUNE INC.

(Name of registrant in its charter)


NEVADA		~~88-0277072~~45-4497941
(State or other jurisdiction of incorporation or organization)		(I.R.S. Employer Identification No.)

50 N. Laura Street, Suite 2500 Jacksonville, FL ~~32202~~		~~98102~~32202
(Address of principal executive offices)		(Zip Code)

904-516-5436
(Issuer’s telephone number)

~~(206) 504 7267~~

~~(Issuer’s telephone number)~~

Indicate by check mark whether the registrant (1) filed all reports required to be filed by Section 13 or 15(d) of the Exchange Act during the past 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes x No ¨

Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files). Yes x No ¨

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, non-accelerated filer or a smaller reporting company. See definition of “accelerated filer”, “large accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act (check one):

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ¨ No x

As of August ~~14, 2015,~~15, 2016, the Company had ~~46,140,771~~98,481,757 shares of common stock issued and outstanding.

~~EXPLANATORY NOTE~~

This Amendment No. 1 on Form 10-Q/A (the “Form 10-Q/A”) to the Quarterly Report on Form 10-Q for TapImmune Inc. (“we” or the “Company”) for the quarterly period ended June 30, 2015, initially filed with the Securities and Exchange Commission (the “SEC”) on August 14, 2015 (the “Original Filing”), is being filed to restate accounting for the share purchase warrants and recording the fair value of the warrants under “Derivative liability- warrants” on its balance sheet with changes in the fair value over time reflected in the statements of operations as “Changes in fair value of derivative liabilities”. The restatement of the Company’s accounting for the share purchase warrants arose after a review by the Company’s management.

As a result, the Board of Directors of the Company has determined that the Company’s previously issued consolidated unaudited financial statements and reports filed with the SEC for the quarterly period ended June 30, 2015 should not be relied upon. For a more detailed description of the effects of the restatement, see further discussion in Note 1A, “Amendment to Previously Reported Quarterly Financial Statements” to our consolidated financial statements included in Part I, Item 1 of this report.

For the convenience of the reader, this Form 10-Q/A sets forth the Original Filings in their entirety. However, this Form 10-Q/A only amends and restates Items 1 and 2 of Part I of the Original Filing, in each case, solely as a result of, and to reflect, the restatement, and no other information in the Original Filing is amended hereby. The foregoing items have not been updated to reflect other events occurring after the Original Filings or to modify or update those disclosures affected by subsequent events. In addition, pursuant to the rules of the SEC, Item 6 of Part II of the Original Filings has been amended to contain currently dated certifications from the Company’s Chief Executive Officer and Chief Financial Officer, as required by Sections 302 and 906 of the Sarbanes-Oxley Act of 2002, and are attached as Exhibits 31.1 and 32.1 to this report. We have also updated our financial statements formatted in Extensible Business Reporting Language (XBRL) in Exhibits 101.

Except for the foregoing amended information, this Form 10-Q/A continues to speak as of the dates of the Original Filings, and the Company has not updated the disclosures contained herein to reflect events that occurred at a later date. Other events occurring after the filings of the Original Filings or other disclosures necessary to reflect subsequent events will be addressed in any reports filed with the SEC subsequent to the date of this filing.

~~PART I – FINANCIAL INFORMATION~~

~~Item 1.~~

~~Financial Statements~~


~~Description~~			Page
PART I – FINANCIAL INFORMATION				1

~~Condensed Interim Financial Statements~~Item 1.	Financial Statements (Unaudited)			1


Condensed Consolidated Balance Sheets as of June 30, ~~2015 (Unaudited)~~2016 and December 31, ~~2014~~2015		41

	Condensed Consolidated Statements of Operations ~~and Comprehensive Loss~~ for the Three and Six Months Ended June 30, ~~2015~~2016 and ~~2014 (Unaudited)~~2015			52

	Condensed Consolidated Statement of Stockholders’ Equity (Deficit) for the Six Months Ended June 30, 2016			3

	Condensed Consolidated Statements of Cash Flows for the Six Months Ended June 30, 2016 and 2015 ~~(Unaudited)~~			4

	Notes to Condensed Consolidated Financial Statements			6

Item 2.	~~Condensed Consolidated Statements~~Management’s Discussion and Analysis of ~~Cash Flows for the Three~~Financial Condition and ~~Six Months Ended June 30, 2015 and 2014 (Unaudited)~~Results of Operations.			712

Item 3.	Quantitative and Qualitative Disclosures About Market Risk.			20

Item 4.	Controls and Procedures.			20

~~Unaudited Notes to Condensed Consolidated Financial Statements~~PART II – OTHER INFORMATION				920

Item 1.	Legal Proceedings.			20

Item 1A.	Risk Factors.			20

Item 2.	Unregistered Sales of Equity Securities and Use of Proceeds.			20

Item 3.	Defaults Upon Senior Securities.			20

Item 4.	Mine Safety Disclosures.			21

Item 5.	Other Information.			21

Item 6.	Exhibits.			22

Signatures				24

PART I.

FINANCIAL INFORMATION

Item 1.

Financial Statements (unaudited)

TAPIMMUNE INC.

CONDENSED CONSOLIDATED BALANCE SHEETS

(UNAUDITED)


	June 30, 2016			December 31, 2015
ASSETS
Current Assets
Cash	$	3,767,656		$	6,576,564
Prepaid expenses and deposits		21,394			68,803

	$	3,789,050		$	6,645,367

LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)
Current Liabilities
Accounts payable and accrued liabilities	$	1,346,391		$	967,358
Research agreement obligations		492,365			492,365
Derivative liability – warrants		21,252,000			26,493,000
Promissory note		5,000			30,000
Promissory note, related party		23,000			23,000

		23,118,756			28,005,723

Stockholders’ Equity (Deficit)
Convertible preferred stock, $0.001 par value — 5,000,000 shares authorized:
Series A, $0.001 par value, 1,250,000 shares designated, -0- shares issued and outstanding		—			—
Series B, $0.001 par value, 1,500,000 shares designated, -0- shares issued and outstanding		—			—
Common stock, $0.001 par value, 500,000,000 shares authorized 71,416,268 shares issued and outstanding (2015 – 70,550,763)		71,416			70,551
Additional paid-in capital		112,882,904			112,077,520
Accumulated deficit		(132,284,026	)		(133,508,427	)

		(19,329,706	)		(21,360,356	)

	$	3,789,050		$	6,645,367

The accompanying notes are an integral part of these condensed consolidated financial statements.

TAPIMMUNE INC.

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(UNAUDITED)


	Three Months Ended June 30,						Six Months Ended June 30,
	2016			2015			2016			2015
Operating expenses:
Research and development	$	1,248,165		$	201,157		$	2,233,916		$	810,535
General and administrative		1,177,408			936,887			1,945,396			1,355,673

Loss from Operations		(2,425,573	)		(1,138,044	)		(4,179,312	)		(2,166,208	)
Other Income (Expense)
Changes in fair value of derivative liabilities		8,237,000			(59,079,025	)		5,241,000			(58,751,585	)
Foreign exchange		—			775			—			775
Grant income		231,200			—			231,200			—
Shares issued in debt settlement agreements		(70,315	)		—			(70,315	)		—
Other income		1,828			—			1,828			—

Net Income (Loss) for the Period	$	5,974,140		$	(60,216,294	)	$	1,224,401		$	(60,917,018	)

Basic Net Income (Loss) per Share	$	0.08		$	(1.80	)	$	0.02		$	(1.99	)
Diluted Net Income (Loss) per Share	$	0.03		$	(1.80	)	$	(0.02	)	$	(1.99	)

Weighted Average Number of Common Shares Outstanding, Basic		71,220,000			33,525,656			70,907,000			30,584,794
Weighted Average Number of Common Shares Outstanding, diluted		78,297,000			33,525,656			79,829,000			30,584,794

The accompanying notes are an integral part of these condensed consolidated financial statements.

TAPIMMUNE INC.

CONDENSED CONSOLIDATED STATEMENT OF STOCKHOLDERS’ EQUITY (DEFICIT)

(UNAUDITED)


					Additional Paid In Capital $
	Common Stock						Accumulated Deficit $			Total $
	Number of		Amount
	shares		$
Balance, December 31, 2015		70,550,763		70,551		112,077,520		(133,508,427	)		(21,360,356	)
Shares issued in debt settlement agreements		122,287		122		70,193		—			70,315
Stock- based compensation		743,218		743		735,191		—			735,934
Net income		—		—		—		1,224,401			1,224,401

Balance, June 30, 2016		71,416,268		71,416		112,882,904		(132,284,026	)		(19,329,706	)

The accompanying notes are an integral part of these condensed consolidated financial statements.

TAPIMMUNE INC.

CONDENSED CONSOLIDATED ~~BALANCE SHEETS~~STATEMENTS OF CASH FLOWS

(UNAUDITED)

   June 30,
2015
As Restated December 31,
2014
   (Unaudited)
ASSETS
Current Assets

Cash
   $ 3,105,320    $ 141,944
Prepaid expenses and deposits
   142,590    82,504


   $ 3,247,910    $ 224,448


LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)
Current Liabilities

Accounts payable and accrued liabilities
   $ 842,682    $ 693,362
Research agreement obligations
   492,365    492,365
Derivative liability – warrants
   69,962,000    9,415
Promissory notes
   52,942    52,942


   71,349,989    1,248,084


COMMITMENTS AND CONTINGENCIES

Stockholders’ Equity (Deficit)

Convertible preferred stock, $0.001 par value — 10,000,000 shares authorized:

Series A, $0.001 par value, 1,250,000 shares designated, -0- shares issued and outstanding as of June 30, 2015 and December 31, 2014
   —      —
Series B, $0.001 par value, 1,500,000 shares designated, -0- shares issued and outstanding as of June 30, 2015 and December 31, 2014
   —      —
Common stock, $0.001 par value, 500,000,000 shares authorized 38,038,921 shares issued and outstanding (2014 – 20,318,815)
   38,039    20,319
Additional paid-in capital
   92,218,937    85,265,776
Accumulated deficit
   (160,359,055 ) (86,309,731 )


   (68,102,079 ) (1,023,636 )


   $ 3,247,910    $ 224,448


	Six Months Ended June 30, 2016			Six Months Ended June 30, 2015
CASH FLOWS FROM OPERATING ACTIVITIES
Net income (loss)	$	1,224,401		$	(60,917,018	)
Adjustments to reconcile net income (loss) to net cash from operating activities:
Changes in fair value of derivative liabilities		(5,241,000	)		58,751,585
Shares issued in debt settlement agreements		70,315			—
Stock based compensation		544,934			248,561
Changes in operating assets and liabilities:
Prepaid expenses		47,409			(60,086	)
Accounts payable and accrued liabilities		570,033			149,320

NET CASH USED IN OPERATING ACTIVITIES		(2,783,908	)		(1,827,638	)

CASH FLOWS FROM FINANCING ACTIVITIES
Issuance of shares, net of finders’ fee		—			2,326,014
Repayment of promissory note		(25,000	)		—
Proceeds from exercise of warrants		—			2,500,000
Finders’ fee on exercise of warrants		—			(35,000	)

NET CASH (USED IN) PROVIDED BY FINANCING ACTIVITIES		(25,000	)		4,791,014

INCREASE (DECREASE) IN CASH		(2,808,908	)		2,963,376
CASH, BEGINNING OF PERIOD		6,576,564			141,944

CASH, END OF PERIOD	$	3,767,656		$	3,105,320

The accompanying notes are an integral part of these condensed consolidated financial statements.

TAPIMMUNE INC.

CONDENSED CONSOLIDATED STATEMENTS OF ~~OPERATIONS AND COMPREHENSIVE LOSS~~CASH FLOWS

(UNAUDITED)

Three Months Ended
June 30,

Six Months Ended
June 30,

   2015
As Restated 2015
As Restated
   2014 2014
Operating expenses:

General and administrative
   $ 936,887    $ 488,427    $ 1,355,673    $ 1,687,794
Research and development
   201,157    22,500    810,535    45,000


Loss from Operations
   (1,138,044 ) (510,927 ) (2,166,208 ) (1,732,794 )
Other Income (Expense)

Accretion of interest on convertible debt
   —      (8,660 ) —      (492,296 )
Changes in fair value of derivative liabilities
   (59,079,025 ) 352,834    (58,751,585 ) 14,537
Foreign exchange
   775    —      775    —
Gain (loss) on settlement of debt
   —      920,233    —      (26,743,197 )


Net Income (Loss) for the Period
   $ (60,216,294 ) $ 753,480    $ (60,917,018 ) $ (28,953,750 )


Other comprehensive income (loss)

Foreign exchange translation adjustment
   —      1,042    —      (207 )


TOTAL COMPREHENSIVE INCOME (LOSS)
   $ (60,216,294 ) $ 754,522    $ (60,917,018 ) $ (28,953,957 )


Basic and Diluted Net Income (Loss) per Share
   $ (1.80 ) $ 0.05    $ (1.99 ) $ (2.57 )


Weighted Average Number of Common Shares Outstanding
   33,525,656    15,523,016    30,584,794    11,250,240


	Six Months Ended June 30, 2016		Six Months Ended June 30, 2015
SUPPLEMENTAL SCHEDULE OF NON-CASH ACTIVITIES
Reclassification of accrued liability upon issuance of common shares relating to Dr. Glynn Wilson’s compensation	$	191,000	$	—
Accounts payable settled in common stock		—		231,000
Fair value of issuance of warrants in January and March 2015 financing		—		9,313,000
Issuance of additional warrants in May 28, 2015 transaction		—		6,133,000
Reclassification of Derivative Warrant Liabilities to Equity at Exercise Date		—		4,245,000

The accompanying notes are an integral part of these condensed consolidated financial statements.

TAPIMMUNE INC.

~~CONDENSED CONSOLIDATED STATEMENT OF STOCKHOLDERS’ EQUITY (DEFICIT)~~

~~AS RESTATED~~

      Additional
   Common Stock    Paid In Accumulated
   Number of
shares    Amount
$    Capital
$ Deficit
$ Total
$
Balance, December 31, 2014
   20,318,816       20,319       85,265,776    (86,309,731 ) (1,023,636 )
Private placement (net of finders’ fee of $140,000)
   12,319,995       12,320       2,313,694    —      2,326,014
Fair value of warrants recognized as derivative liabilities in January and March 2015 Financing
   —         —         (2,313,694 ) (6,999,306 ) (9,313,000 )
Fair value of warrants issued on May 28, 2015
   —         —         —      (6,133,000 ) (6,133,000 )
Exercise of warrants
   5,000,000       5,000       2,495,000    —      2,500,000
Reclassification of derivative warrant liabilities to equity at exercise date
   —         —         4,245,000    —      4,245,000
Finders’ fee on exercise of warrants
   —         —         (35,000 ) —      (35,000 )
Stock- based compensation
   400,110       400       248,161    —      248,561
Net loss
   —         —         —      (60,917,018 ) (60,917,018 )






Balance, June 30, 2015
   38,038,921       38,039       92,218,937    (160,359,055 ) (68,102,079 )

~~The accompanying notes are an integral part of these condensed consolidated financial statements.~~

~~TAPIMMUNE INC.~~

~~CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS~~

~~(UNAUDITED)~~

   Six Months Ended
June 30,
2015
As Restated Six Months Ended
June 30,
2014
CASH FLOWS FROM OPERATING ACTIVITIES

Net loss
   $ (60,917,018 ) $ (28,953,750 )
Adjustments to reconcile net loss to net cash from operating activities:

Changes in fair value of derivative liabilities
   58,751,585    (14,537 )
Loss on extinguishment of debt
   —      26,743,197
Non-cash interest and finance charges
   —      492,296
Stock based compensation
   248,561    799,075
Changes in operating assets and liabilities:

Prepaid expenses
   (60,086 ) —
Accounts payable and accrued liabilities
   149,320    322,277


NET CASH USED IN OPERATING ACTIVITIES
   (1,827,638 ) (611,442 )


CASH FLOWS FROM FINANCING ACTIVITIES

Issuance of shares, net of issuance costs of $173,000
   2,326,014    583,000
Proceeds from loans payable
   —      500
Proceeds from exercise of warrants
   2,500,000    —
Finders’ fee on exercise of warrants
   (35,000 ) —


NET CASH PROVIDED BY FINANCING ACTIVITIES
   4,791,014    583,500


INCREASE (DECREASE) IN CASH
   2,963,376    (27,942 )
CASH, BEGINNING OF PERIOD
   141,944    48,589


CASH, END OF PERIOD
   $ 3,105,320    $ 20,647

~~The accompanying notes are an integral part of these condensed consolidated financial statements.~~

~~TAPIMMUNE INC.~~

~~CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS~~

   Six Months Ended
June 30,
2015
As Restated    Six Months Ended
June 30,
2014
SUPPLEMENTAL SCHEDULE OF NON-CASH ACTIVITIES

Accounts payable settled in common stock
   $ 231,000       $ 683,000
Fair value of issuance of warrants in January and March 2015 financing
   9,313,000       —
Issuance of additional warrants in May 28, 2015 transaction
   6,133,000       —
Reclassification of derivative warrant liabilities to equity at exercise date
   4,245,000       —
Conversion of debt obligations into common stock:

Accrued interest
   —         476,000
Convertible notes payable
   —         3,797,000
Loans payable, related party
   —         42,000
Promissory notes, related party
   —         210,000
Due to related parties
   —         369,000
Fair value derivative liability – conversion option at conversion
   —         708,000

~~The accompanying notes are an integral part of these condensed consolidated financial statements.~~

~~TAPIMMUNE INC.~~

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

June 30, ~~2015~~2016

(Unaudited)

~~NOTE 1: NATURE OF OPERATIONS~~

NOTE 1:

NATURE OF OPERATIONS

TapImmune Inc. (the “Company”), a Nevada corporation incorporated in 1992, is a biotechnology Company focusing on immunotherapy specializing in the development of innovative peptide and gene-based immunotherapeutics and vaccines for the treatment of oncology and infectious disease. Unlike other vaccine technologies that narrowly address the initiation of an immune response, TapImmune’s approach broadly stimulates the cellular immune system by enhancing the function of killer T-cells and T-helper cells and by restoring antigen presentation in tumor cells allowing their recognition and killing by the immune system.

~~NOTE 1A: AMENDMENT TO PREVIOUSLY REPORTED QUARTERLY FINANCIAL STATEMENTS~~

The Company’s previously issued consolidated financial statements for the three and six months ended June 30, 2015 have been restated related to the Company’s accounting for share purchase warrants issued as part of two registered transactions in January 2015 and March 2015. Previously, the fair value of certain series of the share purchase warrants (Series B, B-1, C, C-1, D, D-1, E and E-1) was concluded by management to be classified within stockholders’ equity (deficit). The Company has reviewed the terms and conditions underlying its outstanding share purchase warrants and determined that the accounting for certain series of the warrants should be amended.

~~Management reviewed ASC 480-10~~ ~~Distinguishing liabilities from equity~~ ~~and ASC 815-40~~ ~~Contracts in an Entity’s Own Equity~~ to arrive at this conclusion that the common stock purchase warrants should be classified as a liability, not equity, as the Company cannot control their ability to gross settle the financial instruments with registered securities.

The Company has restated its accounting for certain series of the share purchase warrants and recorded the fair value of the warrants under “Derivative liability- warrants” on its balance sheet with changes in the fair value over time reflected in the statements of operations as “Changes in fair value of derivative liabilities”.

As a result of these adjustments, net loss for the three and six months ended June 30, 2015 was increased by $41,771,000 and $41,490,000, respectively. The Company has reported an amended net loss of $60,216,000 versus the previously reported net loss of approximately $18,446,000 for the three months ended June 30, 2015 and an amended net loss of $60,917,000 versus the previously reported net loss of approximately $19,427,000 for the six months ended June 30, 2015.

~~The following table summarizes the effect of the restatement on the consolidated statement of operations for the three and six months ended June 30, 2015:~~

~~TAPIMMUNE INC.~~

~~CONDENSED CONSOLIDATED BALANCE SHEETS~~

   June 30, 2015 (Unaudited)
   As
Previously
Reported Adjustments As Restated
ASSETS
Current Assets

Cash
   3,105,320    —      3,105,320
Prepaid expenses and deposits
   142,590    —      142,590


   3,247,910    —      3,247,910



LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)
Current Liabilities

Accounts payable and accrued liabilities
   842,682    —      842,682
Research agreement obligations
   492,365    —      492,365
Derivative liability – warrants
   11,673,347    58,288,653    69,962,000
Promissory notes
   52,942    —      52,942


   13,061,336    58,288,653    71,349,989


COMMITMENTS AND CONTINGENCIES

Stockholders’ Equity (Deficit)

Convertible preferred stock, $0.001 par value — 10,000,000 shares authorized:

Series A, $0.001 par value, 1,250,000 shares designated, -0- shares issued and outstanding as of March 31, 2015 and December 31, 2014
   —      —      —
Series B, $0.001 par value, 1,500,000 shares designated, -0- shares issued and outstanding as of March 31, 2015 and December 31, 2014
   —      —      —
Common stock, $0.001 par value, 500,000,000 shares authorized 32,638,811 shares issued and outstanding (2014 – 20,318,815)
   38,039    —      38,039
Additional paid-in capital
   95,885,631    (3,666,694 ) 92,218,937
Accumulated deficit
   (105,737,096 ) (54,621,959 ) (160,359,055 )


   (9,813,426 ) (58,288,653 ) (68,102,079 )


   3,247,910    —      3,247,910

~~TAPIMMUNE INC.~~

~~CONDENSED CONSOLIDATED STATEMENTS OF~~

~~OPERATIONS AND COMPREHENSIVE LOSS~~

~~(UNAUDITED)~~

   Three Months Ended June 30, 2015
   As Previously
Reported Adjustments As Restated
Operating expenses:

General and administrative
   936,887    —      936,887
Research and development
   201,157    —      201,157


Loss from Operations
   (1,138,044 ) —      (1,138,044 )
Other Income (Expense)

Changes in fair value of derivative liabilities
   (9,052,372 ) (50,026,653 ) (59,079,025 )
Foreign exchange
   775    —      775
Inducement expense
   (8,256,000 ) 8,256,000    -


Net Loss for the Period
   (18,445,641 ) (41,770,653 ) (60,216,294 )


Other comprehensive income

Foreign exchange translation adjustment
   —      —      —


TOTAL COMPREHENSIVE LOSS
   (18,445,641 ) (41,770,653 ) (60,216,294 )


Basic and Diluted Net Lossper Share
   (0.55 ) (1.25 ) (1.80 )


Weighted Average Number ofCommon Shares Outstanding
   33,525,656    33,525,656    33,525,656

~~TAPIMMUNE INC.~~

~~CONDENSED CONSOLIDATED STATEMENTS OF~~

~~OPERATIONS AND COMPREHENSIVE LOSS~~

~~(UNAUDITED)~~

   Six Months Ended June 30, 2015
   As Previously
Reported Adjustments As Restated
Operating expenses:

General and administrative
   1,355,673    —      1,355,673
Research and development
   810,535    —      810,535


Loss from Operations
   (2,166,208 ) —      (2,166,208 )
Other Income (Expense)

Changes in fair value of derivative liabilities
   (9,005,932 ) (49,745,653 ) (58,751,585 )
Foreign exchange
   775    —      775
Inducement expense
   (8,256,000 ) 8,256,000    —


Net Loss for the Period
   (19,427,365 ) (41,489,653 ) (60,917,018 )
Other comprehensive income

Foreign exchange translation adjustment
   —      —      —


TOTAL COMPREHENSIVE LOSS
   (19,427,365 ) (41,489,653 ) (60,917,018 )


Basic and Diluted Net Lossper Share
   (0.64 ) (1.36 ) (1.99 )


Weighted Average Number ofCommon Shares Outstanding
   30,584,794    30,584,794    30,584,794

~~TAPIMMUNE INC.~~

~~CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS~~

~~(UNAUDITED)~~

Six Months Ended June 30, 2015

   As
Previously
Reported Adjustments As Restated
CASH FLOWS FROM OPERATING ACTIVITIES

Net loss
   (19,427,365 ) (41,489,653 ) (60,917,018 )
Adjustments to reconcile net loss to net cash from operating activities:

Changes in fair value of derivative liabilities
   9,005,932    49,745,653    58,751,585
Inducement expense
   8,256,000    (8,256,000 ) —
Non-cash interest and finance charges
   —      —      —
Stock based compensation
   248,561    —      248,561
Changes in operating assets and liabilities:

Prepaid expenses
   (60,086 ) —      (60,086 )
Accounts payable and accrued liabilities
   149,320    —      149,320


NET CASH USED IN OPERATING ACTIVITIES
   (1,827,638 ) —      (1,827,638 )


CASH FLOWS FROM FINANCING ACTIVITIES

Issuance of shares, net of issuance costs of $173,000
   2,291,014    35,000    2,326,014
Proceeds from exercise of warrants
   2,500,000    2,500,000
Finders’ fee on exercise of warrants
   —      (35,000 ) (35,000 )


NET CASH PROVIDED BY FINANCING ACTIVITIES
   4,791,014    —      4,791,014


INCREASE IN CASH
   2,963,376    —      2,963,376
CASH, BEGINNING OF PERIOD
   141,944    —      141,944


CASH, END OF PERIOD
   3,105,320    —      3,105,320

~~NOTE 2: BASIS OF PRESENTATION~~

NOTE 2:

BASIS OF PRESENTATION

The accompanying unaudited condensed financial statements have been prepared in accordance with the accounting principles generally accepted in the United States of America (“U.S. GAAP”) for interim financial information and pursuant to the instructions to Form 10-Q and Article 8 of Regulation S-X of the Securities and Exchange Commission (“SEC”) and on the same basis as the Company prepares its annual audited consolidated financial statements. The condensed consolidated balance sheet as of June 30, ~~2015,~~2016, condensed consolidated statements of interim financials include all adjustments, consisting only of normal recurring adjustments, which the Company considers necessary for a fair presentation of the financial position, operating results and cash flows for the periods presented.

The results for the statement of operations are not necessarily indicative of results to be expected for the year ending December 31, ~~2015~~2016 or for any future interim period. The condensed consolidated balance sheet at December 31, ~~2014~~2015 has been derived from audited financial statements; however, it does not include all of the information and notes required by U.S. GAAP for complete financial statements. The accompanying condensed consolidated financial statements should be read in conjunction with the consolidated financial statements for the year ended December 31, ~~2014,~~2015, and notes thereto included in the Company’s annual report on Form 10-K.

~~NOTE 3: LIQUIDITY AND FINANCIAL CONDITION~~

NOTE 3:

LIQUIDITY AND FINANCIAL CONDITION

The Company’s activities since inception have consisted principally of acquiring product and technology rights, raising capital, and performing research and development. Successful completion of the Company’s development programs and, ultimately, the attainment of profitable operations are dependent on future events, including, among other things, its ability to access potential markets; secure financing, develop a customer base; attract, retain and motivate qualified personnel; and develop strategic alliances. From inception, the Company has been funded by a combination of equity and debt financings.

The Company expects to continue to incur substantial losses over the next several years during its development phase. To fully execute its business plan, the Company will need to complete certain research and development activities and clinical studies. Further, the Company’s product candidates will require regulatory approval prior to commercialization. These activities may span many years and require substantial expenditures to complete and may ultimately be unsuccessful. Any delays in completing these activities could adversely impact the Company. The Company plans to meet its capital requirements primarily through issuances of debt and equity securities and, in the longer term, revenue from product sales.

As of June 30, ~~2015,~~2016, the Company had cash and cash equivalents of approximately ~~$3,105,000.~~$3,768,000. Historically, the Company has net losses and negative cash flows from operations. The Company believes its current capital resources are not sufficient to support its operations. Management intends to continue its research efforts and to finance operations of the Company through debt and/or equity financings. Management plans to seek additional debt and/or equity financing through private or public offerings or through a business combination or strategic partnership. There can be no assurance that the Company will be successful in obtaining additional financing on favorable terms, or at all. These matters raise substantial doubt about the Company’s ability to continue as a going concern. The financial statements do not include any adjustments that might result from the outcome of these uncertainties.

146

~~NOTE 4: SIGNIFICANT ACCOUNTING POLICIES~~

NOTE 4:

SIGNIFICANT ACCOUNTING POLICIES

There have been no material changes in the Company’s significant accounting policies to those previously disclosed in the Company’s annual report on Form 10-K, which was filed with the SEC on April ~~15, 2015.~~14, 2016 other than the one disclosed below:

~~Prior Period Reclassifications~~Grant Income

The ~~expense categories~~Company recognizes grant income in accordance with the terms stipulated under the grant awarded to the Company’s collaborators at the Mayo Foundation from the U. S. Department of Defense. In various situations, the Company receives certain payments from the U. S. Department of Defense for reimbursement of clinical supplies. These payments are non-refundable, and are not dependent on the Company’s ongoing future performance. The Company has adopted a policy of recognizing these payments as grant income when received.

Recent accounting pronouncement

Accounting Standards Update (“ASU”), No. 2016-09 - In March 2016, the Financial Accounting Standards Board (the “FASB”) issued ASU No. 2016-09, Compensation-Stock Compensation. The new guidance simplifies several aspects of the ~~comparable prior~~accounting for share-based payment transactions, including the income tax consequences, classification of awards as either equity or liabilities, and classification on the statement of cash flows. The amendments in this standard are effective for the Company’s annual year and first fiscal quarter beginning on January 1, 2017 with early adoption permitted. The Company is currently evaluating the impact of the application of this accounting standard update on its financial statements and related disclosures.

NOTE 5:

EARNINGS PER SHARE APPLICABLE TO COMMON STOCKHOLDERS

Basic income (loss) per common share is computed by dividing net income by the weighted average number of common shares outstanding during the reporting period. Diluted income per common share is computed similar to basic income per common share except that it reflects the potential dilution that could occur if dilutive securities or other obligations to issue common stock were exercised or converted into common stock.

Potential dilutive common shares also include the dilutive effect of the common stock underlying in-the-money stock options and warrants that were calculated based on the average share price for each period ~~have been reclassified~~using the treasury stock method. Under the treasury stock method, the proceeds from the exercise of an option or warrant is assumed to be used to repurchase shares in the current period. In addition, the average amount of compensation cost for ~~comparability with~~in-the-money options, if any, for future service that the ~~June 30, 2015 presentation. These reclassifications had no effect on previously reported net loss.~~Company has not yet recognized when the option is exercised, is also assumed to repurchase shares in the current period.

~~NOTE 5: POTENTIALLY DILUTIVE SECURITIES~~A reconciliation of the numerator and denominator used in the calculation is as follows:


	For the Three Months Ended June 30,					For the Six Months Ended June 30,
	2016		2015			2016			2015
Numerator:
Net income (loss)	$	5,974,000	$	(60,216,294	)	$	1,224,000		$	(60,917,018	)
Less: noncash income from change in fair value of common stock warrants		3,697,000		—			2,492,000			—

Net income (loss) – diluted		2,277,000		(60,216,294	)		(1,268,000	)		(60,917,018	)


Denominator:
Weighted average shares outstanding – basic		71,220,000		33,525,656			70,907,000			30,584,794
Dilutive effect of warrants, net		6,785,000		—			8,922,000			—
Dilutive effect of stock options, net		292,000		—			—			—

Weighted average shares outstanding – diluted		78,297,000		33,525,656			79,829,000			30,584,794


Net income (loss) per share data: Basic	$	0.08	$	(1.80	)	$	0.02		$	(1.99	)
Diluted	$	0.03	$	(1.80	)	$	(0.02	)	$	(1.99	)

~~Options, warrants, and convertible debt outstanding were all considered anti-dilutive for the six months ended June 30, 2015 and 2014, due to net losses.~~7

The following securities were not included in the diluted net ~~loss~~income (loss) per share calculation because their effect was anti-dilutive as offor the periods presented:

   June 30,
   2015    2014
Common stock options
   465,000       65,000
Common stock warrants - equity treatment
   2,556,000       185,000
Common stock warrants - liability treatment
   81,834,000       49,000
Convertible notes
   —         7,000




Potentially dilutive securities
   84,855,000       306,000

~~NOTE 6: DERIVATIVE LIABILITY - WARRANTS AND DERIVATIVE LIABILITY – CONVERSION OPTION, AS RESTATED~~


	For the Three Months Ended June 30,				For the Six Months Ended June 30,
	2016		2015		2016		2015
Common stock options		3,014,000		465,000		3,564,000		465,000
Common stock warrants - equity treatment		2,556,000		2,556,000		2,556,000		2,556,000
Common stock warrants - liability treatment		27,390,000		81,834,000		24,817,000		81,834,000

Potentially dilutive securities		32,960,000		84,855,000		30,937,000		84,855,000

NOTE 6:

DERIVATIVE LIABILITY - WARRANTS

A summary of quantitative information with respect to valuation methodology and significant unobservable inputs used for the Company’s common stock purchase warrants that are categorized within Level 3 of the fair value hierarchy for the six months ended ~~2015~~2016 and ~~2014~~2015 is as follows:


Share Purchase Warrants	Weighted Average Inputs for the Period						Weighted Average Inputs for the Period
Date of valuation	For the Six Months Ending June 30, 2015			For the Six Months Ending June 30, 2014			For the Six Months Ending June 30, 2016			For the Six Months Ending June 30, 2015
Fair market value of stock	$	0.96		$	0.02		$	0.51		$	0.96
Strike price	$	0.50		$	5.84		$	0.70		$	0.50
Contractual term (years)								3.7			3.2
Volatility (annual)		148.00	%		159.00	%		150.00	%		148.00	%
Risk-free rate		1.1	%		1.08	%		0.9	%		1.1	%
Contractual term (years)		3.2			3.58
Dividend yield (per share)		0	%		0	%		0	%		0	%

The foregoing assumptions are reviewed quarterly and are subject to change based primarily on management’s assessment of the probability of the events described occurring. Accordingly, changes to these assessments could materially affect the valuations.

Financial Assets and Liabilities Measured at Fair Value on a Recurring Basis

Financial assets and liabilities measured at fair value on a recurring basis are summarized below and disclosed on the balance sheet under Derivative liability – warrants:


	As of June 30, 2015										As of June 30, 2016
	Fair Value Measurements										Fair Value Measurements
	Fair Value		Level 1		Level 2		Level 3		Total		Fair Value		Level 1		Level 2		Level 3		Total
Derivative liability - warrants	$	69,962,000		—		—	$	69,962,000	$	69,962,000	$	21,252,000		—		—	$	21,252,000	$	21,252,000

Total	$	69,962,000		—		—	$	69,962,000	$	69,962,000	$	21,252,000		—		—	$	21,252,000	$	21,252,000


	As of December 31, 2014										As of December 31, 2015
	Fair Value Measurements										Fair Value Measurements
	Fair Value		Level 1		Level 2		Level 3		Total		Fair Value		Level 1		Level 2		Level 3		Total
Derivative liability - warrants	$	9,000		—		—	$	9,000	$	9,000	$	26,493,000		—		—	$	26,493,000	$	26,493,000

Total	$	9,000		—		—	$	9,000	$	9,000	$	26,493,000		—		—	$	26,493,000	$	26,493,000

There were no transfers between Level 1, 2 or 3 during the ~~three~~six months ended June 30, ~~2015.~~2016.

The following table presents changes in Level 3 liabilities measured at fair value for the six months ended June 30, ~~2015:~~2016:

   Derivative liability – warrants
Balance – December 31, 2014
   $ 9,000
Additions during the period
   15,446,000
Exercise of warrants
   (4,245,000 )
Change in fair value of warrant liability
   58,752,000


Balance – June 30, 2015
   $ 69,962,000


	Derivative liability – warrants
Balance – January 1, 2016	$	26,493,000
Change in fair value of warrant liability		(5,241,000	)

Balance – June 30, 2016	$	21,252,000

The valuation of warrants is subjective and is affected by changes in inputs to the valuation model including the price per share of common stock, the historical volatility of the stock price, risk-free rates based on U.S. Treasury security yields, the expected term of the warrants and dividend yield. Changes in these assumptions can materially affect the fair value estimate. The Company could ultimately incur amounts to settle the warrant at a cash settlement value that is significantly different than the carrying value of the liability on the financial statements. The Company will continue to classify the fair value of the warrants as a liability until the warrants are exercised, expire, or are amended in a way that would no longer require these warrants to be classified as a liability. Changes in the fair value of the common stock warrants liability are recognized as a component of other income (expense) in the ~~Statements~~condensed and consolidated statements of ~~Operations.~~

operations.

During 2014 the Company entered into numerous extinguishment agreements with various holders. As a result the derivative liability associated with the bifurcated conversion options were extinguished at the date of conversion and recorded in the loss on extinguishment in the Statement of Operations. The inputs utilized in the final mark to market were as follows:

Conversion Option
   Weighted Average Inputs for the Period
Date of valuation
   For the Quarter
Ending June 30,
2015 For the Quarter
Ending June 30,
2014
Strike price
   $ —      $ 1.03
Volatility (annual)
   —   % 199.00 %
Risk-free rate
   —   % 0.05 %
Contractual term (years)
   —      0.24
Dividend yield (per share)
   —   % —   %


��

Fair value of Conversion Option at extinguishment
   $ —      $ 708,000

~~NOTE 7: PROMISSORY NOTES, RELATED PARTY~~

NOTE 7:

PROMISSORY NOTE

The Company has outstanding promissory ~~notes~~note in the amount of ~~$52,942~~$5,000 (December 31, ~~2014~~2015 - ~~$52,942),~~$30,000). The promissory note bears 10% annual interest.

NOTE 8:

PROMISSORY NOTE, RELATED PARTY

The Company has an outstanding promissory note in the amount of ~~which~~ $23,000 ~~of promissory notes are from~~(December 31, 2015 - $23,000) owed to an officer ~~and a director~~ of the Company. The promissory ~~notes bear~~note bears no interest charges and ~~have~~has no fixed repayment terms.

~~NOTE 8: CAPITAL STOCK, AS RESTATED~~

~~2015~~9

NOTE 9:

CAPITAL STOCK

2016 Share Transactions

~~Private placements~~Management Compensation

In ~~January,~~November 2015, the Company entered into ~~a Securities Purchase Agreement~~an employment agreement with ~~certain investors for~~Dr. Glynn Wilson, the ~~sale of 7,320,000 units at a purchase price of $0.20 per unit, for a total purchase price of approximately $1,250,000, net of finders’ fee~~Company’s Chief Executive Officer, President and ~~offering expenses of approximately $214,000. Each unit consisting of (i) one share~~Chairman of the ~~Company’s Common Stock, (ii) one Series A warrant to purchase one share~~Company. As part of common stock, (iii) one Series B warrant to purchase one share of common stock (iv) one Series C warrant to purchase one share of common stock, (v) one Series D warrant to purchase one share of common stock, and (vi) one Series E warrant to purchase one share of common stock (the Series A, B, C, D and E warrants are hereby collectively referred to as the “January 2015 Warrants”). Series A warrants are exercisable at $1.50 per share, with a five year term. Series B warrants are exercisable at $0.40 per share, with a six month term. Series C warrants are exercisable at $1.00 per share, with a five year term. Series D warrants are exercisable at $0.75 per share only if and to the extent that the Series B warrants are exercised, with a five year term from the date that the Series B warrants are exercised. Series E warrants are exercisable at $1.25 per share, only if and to the extent that the Series C warrants are exercised, with a five year term from the date that the Series C warrants are exercised.

~~Pursuant to a placement agent~~ agreement, ~~the Company agreed to issue warrants to purchase 366,000~~Dr. Wilson was awarded 0.3 million fully vested common shares ~~with substantially the same terms as the January 2015 Warrants.~~

~~In March, 2015, the Company entered into a Securities Purchase Agreement with certain accredited investors for the sale of 5,000,000 units~~ at ~~a purchase price of $0.20 per unit, for a total purchase price of approximately $950,000, net of finders’ fee and offering expenses of approximately $50,000. Each unit consisting of (i) one share~~consummation of the ~~Company’s Common Stock, (ii) one Series A warrant~~agreement. The Company recorded an obligation to ~~purchase one share~~deliver the shares of common stock, (iii) one Series B warrant to purchase one share of common stock (iv) one Series C warrant to purchase one share of common stock, (v) one Series D warrant to purchase one share of common stock, and (vi) one Series E warrant to purchase one share of common stock (the Series A, B, C, D and E warrants are hereby collectively referred to as$0.3 million based on the ~~“March 2015 Warrants”). The March 2015 Warrants have substantially the same terms as the January 2015 Warrants.~~

~~Pursuant to a placement agent agreement, the Company agreed to issue warrants to purchase 125,000 common shares with substantially the same terms as the March 2015 Warrants.~~

~~Initial Fair Value of Warrants Issued~~

Pursuant to ASC 480-10 Distinguishing liabilities from equity and ASC 815-40 Contracts in an Entity’s Own Equity, the common stock purchase warrants are classified as a derivative liability as the Company cannot control their ability to gross settle the financial instruments with registered securities. The fair value of the ~~warrants~~Common stock at December 31, 2015. The Company issued ~~pursuant~~the shares in March 2016 and reclassified the accrued liability to stockholders’ equity (deficit). In the quarter ended June 30, 2016, to adjust for the withholding tax liability, which is payable in cash, Dr. Wilson returned the 0.3 million fully vested common shares to the ~~January~~treasury and ~~March 2015 stock purchase agreement~~ was ~~$9,313,000.~~issued 0.2 million fully vested common shares. The ~~weighted average inputs include contractual term of 5.0 years, volatility of 158% and risk free rate of 1.2%.~~

~~May 2015 Restructuring agreement~~

~~In May 2015,~~recorded obligation was reduced to $0.1 million based on the ~~Company entered into a restructuring agreement with the investors of the January 2015 and March 2015 private placements, where:~~

~~The exercise price of the Series A warrants was changed from $1.50 per warrant to $0.10 per warrant,~~

~~The exercise price of Series B warrants was changed from $0.40 per warrant to $0.20 per warrant,~~

~~Each warrant of Series B existing prior to the restructuring agreement was replaced with two warrants of such series,~~

~~The exercise price of the Series C warrants was changed from $1.00 per warrant to $0.50 per warrant, and~~

~~Each warrant of Series C existing prior to the restructuring agreement was replaced with two warrants of such series.~~

~~As a result of the restructuring agreement, the Company issued an additional 12,320,000 Series B warrants and 12,320,000 Series C Warrants. The~~ fair value of the ~~warrants issued pursuant to the~~common stock at May ~~2015 restructuring agreement was $6,133,000.~~1, 2016.

~~The weighted average inputs include contractual term of 2.46 years, volatility of 141% and risk free rate of 1.5%.~~

~~Share Purchase Warrants~~Consulting arrangements

During the six months ended June 30, ~~2015, a warrant holder exercised 5,000,000 of Series C warrants at $0.50 per warrant for a total of $2,500,000.~~

~~A summary of the Company’s share purchase warrants as of June 30, 2015 and changes during the period is presented below:~~

   Number of
Warrants    Weighted Average
Exercise Price    Weighted Average
Remaining Life
Balance, December 31, 2014
   2,659,417       1.83       4.15
Issued
   86,730,975       0.54       3.25
Exercised
   (5,000,000 )    0.50       —
Extinguished or expired
   (7,500 )    50.00       —






Balance, June 30, 2015
   84,382,892       $ 0.54       3.26

~~Stock Compensation Plan~~

~~On October 14, 2009,~~2016, the Company ~~adopted the 2009 Stock Incentive Plan (the “2009 Plan”) which supersedes and replaces the 2007 Stock Plan. The 2009 Plan allows for the issuance~~issued 0.5 million common shares as part of ~~up to 10,000,000 common shares. Options granted under the Plan shall be at prices and for terms as determined by the Board of Directors.~~

On February 10, 2015, the Company granted 250,000 stock options at an exercise price of $0.145 per share, of which, 33,333 vested on May 31, 2015 and the remaining vesting monthly over a nine month period, to a consultant of the Company. The term of the options is five years.consulting agreements. The fair value of the ~~new grant~~common stock of approximately $0.3 million was ~~estimated at $33,000, or $0.133 per option, using~~recognized as stock-based compensation in general and administrative expense.

Debt Settlement

In May 2016, the ~~Black-Scholes Option Pricing Model with a risk free interest rate~~Company issued 0.1 million common shares as part of ~~1.52%, a dividend yield of 0%, volatility of 154.6%, and life of 5 years.~~debt conversion agreements from 2014. The ~~expensed portion~~fair value of the ~~value~~common stock of ~~these options during~~approximately $0.1 million was recognized as shares issued in debt settlement agreements in other income (expense).

NOTE 10:

GRANT INCOME

During the six months ended June 30, ~~2015 was $7,635, which was recorded as stock based consultant compensation.~~

~~On March 6, 2015,~~2016, the Company ~~granted 150,000~~received $0.2 million of grant awarded to Mayo Foundation from the US Department of Defense for the Phase II Clinical Trial of TPIV 200. The grant paid for the clinical supplies purchased by the Company.

NOTE 11:

SUBSEQUENT EVENT

On August 10 2016, the Company completed a private placement of units with certain accredited investors The units (“Units”) consisted of (i) one share of the Company’s common stock, ~~options~~par value $0.001 per share and (ii) one warrant to purchase one share of Company common stock for $0.50 (the “PIPE Warrants”). The Company issued and sold an aggregate of 6,065,489 Units at a purchase price per Unit of $0.40 for an aggregate of approximately$2.5 million.

In addition, the Company issued warrants to the placement agent in the offering providing for the purchase of up to 606,549 shares of Company common stock for $0.40 per share.

In connection with the closing of the offering, holders of an aggregate of 7 million outstanding Series C Warrants and 5 million Series C-1 Warrants, each providing for the purchase of one share of Company common stock for $0.50 per share, entered into binding commitments to exercise their warrants for an aggregate exercise price of $6,000,000 and such warrants were exercised on August 11, 2016.

In connection with this warrant exercise, the Company and the holders of the warrants entered into a Warrant Amendment Agreement amending the terms of other outstanding warrants to remove provisions that had previously caused them to be classified as a derivative liability as opposed to equity on the Company’s balance sheet. In consideration for such amendment and the exercise of the 12 million warrants, the Company issued an aggregate of 9,000,000 additional shares of common stock to such warrant holders and new five-year warrants to purchase 12 million shares of Company common stock at an exercise price of ~~$0.20~~$0.60 per ~~share, vesting monthly over~~share. On a twenty four month period, to a director of the Company. The term of the options is five years. The fair value of the new grant was estimated at $29,000, or $0.194 per option, using the Black-Scholes Option Pricing Model with a risk free interest rate of 1.70%, a dividend yield of 0%, volatility of 155.2%, and life of 5 years. The expensed portion of the value of these options during the six months ended June 30, 2015 was $4,850, which was recorded as stock based management compensation.

~~Share purchase options~~

~~A summary of the Company’s stock options~~pro forma basis, as of June 30, ~~2015~~2016, the exercise of the 12 million warrants and ~~changes during~~ the ~~period is presented below:~~amendment of the other warrants will reduce the derivative liability relating to warrants reflected on the Company’s June 30 balance sheet by $21,092,000, from $21,252,000 to $160,000.

The Company incurred approximately $925,000 in expenses relating to the offering, the exercise of the outstanding Series C Warrant and Series C-1 Warrants and the amendment of the Outstanding Series Warrants, including agency fees resulting in net proceeds to the Company of approximately $7.5 million.

   Number of
Options    Weighted Average
Exercise Price    Weighted Average
Remaining Life
Balance, December 31, 2013
   65,430       18.00       5.04
Issued
   —         —         —
Cancelled/Forfeited
   —         —         —






Balance, December 31, 2014
   65,430       18.00       4.04

1810

   Number of
Options    Weighted Average
Exercise Price    Weighted Average
Remaining Life
Issued
   400,000       0.17       4.64






Balance, June 30, 2015
   465,430       $ 2.62       4.49

~~At June 30, 2015, the intrinsic value of the vested options was equal to $66,000 (2014 - $nil).~~

~~A summary of the status of the Company’s unvested options~~Below is a Pro Forma Balance Sheet as of June 30, ~~2015 is presented below:~~2016 which shows the retroactive effect of the financing and warrant exercise and amendment, net of closing costs and fees.

TapImmune Inc. and Subsidiaries

Condensed Consolidated Pro Forma Balance Sheets

(Unaudited)

   Number of
Shares    Weighted Average
Grant-Date
Fair Value
Unvested, December 31, 2014
   278       $ 18.00
Granted
   400,000       0.16
Vested
   (82,685 )    0.21
Cancelled
   —         —




Unvested, June 30, 2015
   317,593       $ 0.16


	June 30, 2016 (As Stated)			Adjustment			June 30, 2016 (Adjusted)
Total assets	$	3,789,050			7,509,194		$	11,298,244

Other current liabilities		1,866,756						1,866,756
Derivative liability - warrants		21,252,260			(21,092,000	)		160,260
Total liabilities		23,119,016			(21,092,000	)		2,027,016

Total stockholders’ equity		(19,329,966	)		28,601,194			9,271,228

Total liabilities and stockholders’ equity	$	3,789,050			7,509,194		$	11,298,244

~~NOTE 9: SUBSEQUENT EVENTS~~

Below is a Pro Forma table of common shares outstanding as of June 30, 2016.

Between July 16, 2015 and August 13, 2015, holders of the Series B warrant exercised 7,890,000 of the Series B Warrants registered under our recent registration statements on Form S-1 resulting in proceeds of $1,578,000 to the Company.

Common stock outstanding at June 30, 2016

On July 21, 2015, the Company entered into a License and Assignment Agreement with the Mayo Foundation for Medical Education and Research (“Mayo Foundation”) pursuant to which we acquired certain intellectual property rights from the Mayo Foundation for the development and commercialization of certain products, methods and processes property relating to a folate receptor alpha immunotherapeutic vaccine comprised of a set of unique peptide epitopes targeting breast, lung and ovarian cancer. The Mayo Foundation granted us a license (with a right to sublicense) on a worldwide basis to make, sell and use products for therapeutic use against breast, ovarian, lung and other cancers that express folate receptor alpha. This license is an exclusive license for products that are based on the intellectual property and non-exclusive for products that are based on Mayo Foundation know–how and materials. The intellectual property that is being licensed includes (i) U.S. patent application numbers 12/303,054 and 13/202,236, (ii) U.S. patent number 8,486,412 and 8,858,952 and provisionals, (iii) divisionals including 13/917,410 and (iv) continuations including 14/484,057.71,416,268

Warrants Exercised

	3.	~~On July 31, 2015, the Company~~12,000,000
Common stock issued to ~~its counsel 118,450 shares~~warrant holders as part of ~~common stock for legal services rendered through January 21, 2015. Such shares were authorized to be issued on January 23, 2015, but were not issued until July 31, 2015.~~financing

	4.	~~On August 10, 2015, the Company issued 50,000 shares~~9,000,000
Common stock sold as part of ~~common~~Private Placement			6,065,489

Pro Forma Common stock ~~as full settlement of a dispute with a marketing consultant that provided services to the Company in 2014 and 2015.~~outstanding at June 30, 2016			98,481,757

1911

Item 2.

Management’s Discussion and Analysis of Financial Condition and Results of Operations

This quarterly report on Form 10-Q contains forward-looking statements within the meaning of Section 21E of the Securities and Exchange Act of 1934, as amended, that involve risks and uncertainties. All statements other than statements relating to historical matters including statements to the effect that we “believe”, “expect”, “anticipate”, “plan”, “target”, “intend” and similar expressions should be considered forward-looking statements. Our actual results could differ materially from those discussed in the forward-looking statements as a result of a number of important factors, including factors discussed in this section and elsewhere in this quarterly report on Form 10-Q, and the risks discussed in our other filings with the Securities and Exchange Commission. Readers are cautioned not to place undue reliance on these forward-looking statements, which reflect management’s analysis, judgment, belief or expectation only as the date hereof. We assume no obligation to update these forward-looking statements to reflect events or circumstance that arise after the date hereof.

As used in this quarterly report: (i) the terms “we”, “us”, “our”, “TapImmune” and the “Company” mean TapImmune Inc. and its wholly owned subsidiary, GeneMax Pharmaceuticals Inc. which wholly owns GeneMax Pharmaceuticals Canada Inc., unless the context otherwise requires; (ii) “SEC” refers to the Securities and Exchange Commission; (iii) “Securities Act” refers to the Securities Act of 1933, as amended; (iv) “Exchange Act” refers to the Securities Exchange Act of 1934, as amended; and (v) all dollar amounts refer to United States dollars unless otherwise indicated.

The following should be read in conjunction with our unaudited consolidated interim financial statements and related notes for the three and six months ended June 30, ~~2015~~2016 included in this quarterly report, as well as our Annual Report on Form 10-K for the year ended December 31, ~~2014.~~2015.

Company Overview

Our Cancer Vaccines

~~TapImmune is a biotechnology~~We are an immune-oncology company ~~focusing on immunotherapy~~ specializing in the development of innovative peptide and gene-based immunotherapeutics and vaccines for the treatment of cancer and ~~infectious~~metastatic disease. ~~The Company combines~~We combine a set of proprietary technologies to improve the ability of the cellular immune system to recognize and destroy diseased cells. These are peptide antigen technologies and DNA expression technologies, Polystart and TAP.

To enhance shareholder value and taking into account development timelines, ~~the Company plans~~we plan to focus on advancing ~~its~~our clinical programs including ~~our HER2/neu peptide antigen program and~~ our Folate Receptor Alpha program for breast and ovarian ~~trials~~and our HER2/neu peptide antigen program into Phase ~~II.~~II clinical trials. In parallel, we plan to complete the preclinical development of our Polystart technology and to continue to develop the TAP-based franchise as an integral component of our prime-and-boost vaccine methodology.

The Immunotherapy Industry for Cancer

~~Immunotherapy~~Immuno-oncology has become the most rapidly growing sector in the pharmaceutical and biotech industry. The approval and success of checkpoint inhibitors Yervoy and Opdivo (Bristol Myers Squibb) and Keytruda (Merck) together with the development of CAR T-cell therapies (Juno, Kite) has provided much momentum in this sector. In addition, new evidence points to the increasing use of combination immunotherapies for the treatment of cancer. This has provided greater opportunities for the successful development of T-cell vaccines in combination with other approaches.

Products and Technology in ~~Development~~

~~Clinical~~Development-Clinical

Phase I Human Clinical Trials –Folate Alpha Breast and Ovarian Cancer – Mayo Clinic

Folate Receptor Alpha is expressed in over 80% of triple negative breast cancers and in addition, over 90% of ovarian cancers, for which the only treatment options are surgery and chemotherapy, leaving a very important and urgent clinical need for a new therapeutic. Time to recurrence is relatively short for these types of cancer and survival prognosis is extremely poor after recurrence. In the United States alone, there are approximately 30,000 ovarian cancer patients and 40,000 triple negative breast cancer patients newly diagnosed every year.

A 24 patient Phase I clinical trial has been completed. The vaccine is well tolerated and safe and 20 out of 21 evaluable patients showed positive immune responses providing a strong rationale rational for progressing to phase II trials. GMP manufacturing for Phase II trials is progressing well towards a commercial formulation and final analyses of clinical plans are near completion. On July 27, 2015, TapImmune exercised its option agreement with Mayo Clinic with the signing of a worldwide exclusive license agreement to commercialize a proprietary folate receptor alpha vaccine technology for all cancer indications. As part of this Agreement, the IND from for the folate receptor alpha Phase I trial was transferred from Mayo to TapImmune for amendment for the Company’s Phase II Clinical Trials on our lead product.

On September 15, 2015, we announced that our collaborators at the Mayo Clinic had been awarded a grant of $13.3 million from the U.S. Department of Defense. This grant, commencing September 15, 2015, will cover the costs for a 280 patient Phase II Clinical Trial of Folate Receptor Alpha Vaccine in patients with Triple Negative Breast Cancer. TapImmune will

work closely with Mayo Clinic on this clinical trial by providing clinical and manufacturing expertise as well as providing GMP vaccine formulations. These vaccine formulations are being developed for multiple Phase II clinical programs in triple negative breast and ovarian cancer in combination with other immunotherapeutics.

On December 9, 2015, we announced that we received Orphan Drug Designation from the U. S. Food & Drug Administration’s Office of Orphan Products Development (OOPD) for our cancer vaccine TPIV 200 in the treatment of ovarian cancer. The TPIV 200 ovarian cancer clinical program will now receive benefits including tax credits on clinical research and 7-year market exclusivity upon receiving marketing approval. TPIV 200 is a multi-epitope peptide vaccine that targets Folate Receptor Alpha which is overexpressed in multiple cancers.

On February 3, 2016 we announced that the U.S. Food & Drug Administration (FDA) has designated the investigation of multiple-epitope Folate Receptor Alpha Peptide Vaccine (TPIV 200) with GM-CSF adjuvant for maintenance therapy in subjects with platinum-sensitive advanced ovarian cancer who achieved stable disease or partial response following completion of standard of care chemotherapy, as a Fast Track Development Program.

Phase I Human Clinical Trials – HER2/neu+ Breast Cancer – Mayo Clinic

Patient dosing has been completed. Final safety analysis on all the patients treated is complete and shown to be safe. In addition, 19 out of 20 evaluable patients showed robust T-cell immune responses to the antigens in the vaccine composition providing a solid case for advancement to Phase II in 2015. An additional secondary endpoint incorporated into this Phase I Trial will be a two year follow on recording time to disease recurrence in the participating breast cancer patients.

For Phase I(b)/II studies, we plan to add a Class I peptide, licensed from the Mayo Clinic (April 16, 2012), to the four Class II peptides. Management believes that the combination of Class I and Class II HER2/neu antigens, gives us the leading HER2/neu vaccine platform. ~~Therefore a key goal in 2015~~As the folate receptor alpha vaccine is our lead product our plans are now initiating formulation studies to progress the HER2/neu vaccine towards ~~the above mentioned~~a Phase ~~1(b)/~~II Clinical ~~Trial.~~

Trial in 2016.

~~Phase I Human Clinical Trials –~~~~Folate Alpha Breast~~Products and ~~Ovarian Cancer – Mayo Clinic~~

Folate Receptor Alpha is expressed in over 80% of triple negative breast cancers, and in addition, over 90% of ovarian cancers, for which the only treatment options are surgery and chemotherapy, leaving a very important and urgent clinical need for a new therapeutic. Time to recurrence is relatively short for these types of cancer and survival prognosis is extremely poor after recurrence. In the United States alone, there are approximately 30,000 ovarian cancer patients and 40,000 triple negative breast cancer patients newly diagnosed every year.

~~Preclinical~~Polystart

~~Polystart~~

~~The Company has~~We converted the previously filed U.S. Provisional Patent Application on Polystart into a full Patent Application, and ~~will extend technology constructs~~in February 2016 we received a Notice of Allowance from the U.S. Patent and Trademark Office (USPTO) for a patent application entitled, “A chimeric nucleic acid molecule with non-AUG initiation sequences.” The term of this patent extends to March 17, 2034. Additional patent filings are in progress. We plan to develop PolyStart as ~~boost strategies~~both a stand-alone therapy and as a ‘boost strategy’ to be used synergistically with our peptide-based vaccines for ~~the current clinical programs in~~ breast and ovarian cancer.

Current State of the Company

~~TapImmune is~~We are a clinical-stage immunotherapy company specializing in the development of innovative peptide and gene-based immunotherapeutics and vaccines for the treatment of cancer. ~~The Company~~We now ~~has~~plan to conduct multiple Phase II clinical trials ~~underway~~on our vaccines. The largest of these studies in triple-negative breast cancer is expected to be totally funded by a $13.3 million grant from the US Department of Defense to our collaborators at the Mayo Clinic in ~~Rochester, MN. In addition to~~Jacksonville, FL. A Company sponsored trial in triple negative breast cancer started in Q2 with recruitment at multiple sites and treatment of first patients. We believe that our own sponsored clinical trials, a new grant-funded breast and ovarian cancer trial was started by Mayo using the same Folate Alpha Receptor peptides to which we have the exclusive commercial rights. Our development pipeline is ~~extremely~~ strong and provides us the opportunity to continue to expand on collaborations with leading institutions and corporations.

~~In Q1 and Q2 2015, we strengthened our cash position by raising additional $4.8 M in working capital giving us confidence in our ability to continue developing our products on~~We believe, the ~~path to commercialization. The structure of this financing gives us additional opportunities to raise additional capital through the exercise of short-term and long-term warrants. The~~ strength of our science and development approaches is becoming more widely appreciated, particularly as our clinical program has now generated positive interim data on both clinical programs in Breast and Ovarian Cancer. ~~Also, we are pleased to report that our clinical programs are seeing positive outcomes and we expect to present more detailed findings at major symposia toward the end of the year.~~

We continue to be focused on our entry into Phase II Triple Negative Cancer Trials including application for Fast Track & Orphan Drug Status as well as planning for Phase II HER2/neu Breast Cancer Trials.

We ~~will also produce~~expect to continue to prosecute our PolyStart patent filings and develop new ~~PolyStart~~ constructs ~~in-house,~~ to facilitate collaborative efforts in our current clinical indications and those where others have already indicated interest in combination therapies.

~~In addition, we will continue to work on deficit reduction and capital improvement in order to make the required benchmarks for an uplisting to the NASDAQ or another major US exchange. To~~We believe that ~~end we are also anticipating the result of grant applications submitted early this year.~~

~~Together,~~ these fundamental programs and corporate activities have positioned TapImmune ~~extremely well~~ to capitalize on the acceptance of immunotherapy as a leading therapeutic strategy in cancer and infectious ~~disease resulting in exploding valuations in the market.~~disease.

TapImmune’s Pipeline

~~The Company has~~We have a ~~deep~~ pipeline of potential ~~blockbuster~~ immunotherapies under development. ~~Two of the~~Phase I clinical programs ~~are completing Phase I studies~~on HER2/neu and ~~are expected~~breast and ovarian cancer have been completed and strong immune responses in over 90% of patients treated has provided the rationale and catalyst to advance these programs to Phase II in 2015. These are major inflection and valuation events, and we believe that, in light of these assets, the Company is significantly undervalued. Over the past year a number of highly visible transactions and billion dollar acquisitions have taken place that validate the work we are doing. We believe that, if our treatment successfully reaches commercialization, our treatment is applicable to 50% of the HER2/neu Breast Cancer market, which is a $21 billion annual market. We further believe that if our Ovarian Cancer treatment reaches commercialization, it will be applicable to 95% of the market which Decision Resources, one of the world’s leading research firms for pharmaceuticals and healthcare, believes will triple in the next 10 years to at least $1.5 billion annually.clinical trials.

In addition to the exciting clinical developments, our peptide vaccine technology may be coupled with our recently developed in-house Polystart nucleic acid-based technology designed to make vaccines significantly more effective by producing four times the required peptides for the immune systems to recognize and act on. Our nucleic acid-based systems can also incorporate “TAP” which stands for Transporter associated with Antigen Presentation. ~~Our technologies are also widely applicable to the treatment of emerging viral threats and pandemics. In particular, our highly versatile PolyStart technology~~

has application in these areas. With respect to validation of our technologies, it is important to note that the majority of our technologies have been published in leading peer-reviewed journals. The timing of such publications is consistent with the filing of patents.

~~A list of publications on our TAP technology can be found on our website (www.tapimmune.com). Publication of our data on PolyStart will occur after current patent filings have been completed.~~

A key component to success is having a comprehensive patent strategy that continually updates and extends patent coverage for key products. It is highly unlikely that early patents will extend through ultimate product marketing, so extending patent life is an important strategy for ensuring product protection.

We have three active patent families that we are supporting:

1. Filed patents on PolyStart expression vector (owned by TapImmune ~~has four patent estates, details of which can be found~~and filed in 2014: this IP covers the use with TAP)

2. Filed patents on ~~our website:www.tapimmune.com~~HER2/neu Class II and Class I antigens: exclusive license from Mayo Foundation; and

3. Filed patents on Folate Receptor Alpha antigens: exclusive license from Mayo Foundation

While the pathway to successful product development takes time, we believe we have put in place significant ~~resources in technical and corporate fundamentals~~ for success. The strength of our product pipeline and access to leading scientists and institutions gives us a unique opportunity to make a major contribution to global health care.

A number of early stage billion dollar pharma acquisitions and recent IPOs have highlighted the growing interest in investment in immunotherapy space. Looking at our current valuation and those of our peers and considering our pipeline of clinical programs with very near-term advancements and the value inflections those represent, we believe this is an excellent opportunity and presents exceptional entry point for those that have not yet become a shareholder.

With respect to the broader market, a major driver and positive influence on our activities has been the emergence and general acceptance of the potential of a new generation of immunotherapies that promise to change the standard of care for cancer. The immunotherapy sector has been greatly stimulated by the approval of Provenge^® for prostate cancer and Yervoy™ for metastatic melanoma, progression of the areas of checkpoint inhibitors and adoptive T-cell therapy and multiple approaches reaching Phase II and Phase III status.

We believe that through our combination of technologies, we are well positioned to be a leading player in this emerging market. It is important to note that many of the late stage immunotherapies currently in development do not represent competition to our programs, but instead offer synergistic opportunities to partner our antigen based immunotherapeutics, and Polystart ~~and/or TAP~~ expression ~~systems.~~system. Thus, the use of naturally processed T-cell antigens discovered using samples derived from cancer patients plus our Polystart expression technology to improve antigen presentation to T-cells could not only produce an effective cancer vaccines in its own right but also to enhance the efficacy of other immunotherapy approaches such as CAR-T and PD1 inhibitors for example.

~~Consistent~~Recent Developments and Highlights

August 2016 Private Placement Transaction. On August 10, 2016, we completed a private placement of units with certain accredited investors. The units (“Units”) consisted of (i) one share of our ~~corporate development~~common stock, par value $0.001 per share and ~~advancement~~(ii) one five-year warrant to purchase one share of ~~clinical trials~~our common stock for $0.50 (the “PIPE Warrants”). We issued and sold an aggregate of 6.06 million Units at a purchase price per Unit of $0.40 for an aggregate of approximately $2.5 million.

August 2016 Warrant Exercises. On August 11, 2016, holders of an aggregate of 7 million outstanding Series C Warrants and 5 million Series C-1 Warrants, each providing for the purchase of one share of our common stock for $0.50 per share, exercised their warrants for an aggregate exercise price of $6,000,000.

August 2016 Warrant Amendments.Simultaneous with the exercise of the warrants, we ~~have made significant additions~~and holders of an aggregate of 37,159,975 outstanding Series A Warrants, Series A-1 Warrants, Series C Warrants, Series C-1 Warrants, Series D Warrants, Series D-1 Warrants, Series E Warrants and Series E-1 Warrants (the “Outstanding Series Warrants”) entered into Warrant Amendment Agreements (the “Amendment Agreement”), in which they agreed to amend the terms of the Outstanding Series Warrants to remove provisions from the Outstanding Series Warrants that had previously caused them to be classified as a derivative liability as opposed to equity on our ~~personnel through appointments~~balance sheet. In consideration for such amendment and the exercise of ~~a Consultant Medical Director (Patrick Yeramian, M.D.)~~the Series C Warrants and ~~a Consultant Regulatory Director (Dr. Stacy Suber)~~Series C-1 Warrants, we issued an aggregate of 9 million additional shares of common stock to such warrant holders and new five-year warrants to purchase 12 million shares of our common stock at an exercise price of $0.60 per share (the “Series F and F-1Warrants”).

The following table reflects the status of the outstanding warrants from the January and March 2015, and August 2016 private placement financings (including placement agent warrants) following the Amendment Agreement and private placement:


Series	Outstanding Warrants		Exercise Price		Expiration
A		2,573,195	$	0.10	01/13/2020
C		5,019,990	$	0.50	01/13/2020
D		7,319,995	$	0.75	Between 07/16/2020 and 08/13/2020 and 08/19/2020 and 09/09/2020
E		7,393,195	$	1.25	Between 10/01/2020 and 11/12/2020 and 11/30/2020 and 12/09/2020
A-1		5,025,000	$	0.10	03/09/2020
D-1		5,000,000	$	0.75	Between 08/19/2020 and 09/09/2020
E-1		5,025,000	$	1.25	06/16/2020
F		7,000,000	$	0.60	8/11/2021
F-1		5,000,000	$	0.60	8/11/2021
PIPE Warrants		6,065,489	$	0.50	8/11/2021
Broker Warrants		606,549	$	0.40	8/11/2021

Addition of Executive Officer. ~~In addition,~~On July 18, 2016 we ~~have appointed~~announced that Dr. John Bonfiglio, as a ~~Corporate Strategic Advisor~~consultant and ~~also to~~a member of our Board of Directors was appointed as our President and ~~have appointed David Laskow-Pooley~~Chief Operating Officer and entered into an employment agreement with us. Concurrent with such appointment we amended the employment agreement of Dr. Wilson for Dr. Wilson to ~~our Board~~relinquish the office of ~~Directors~~President.

Her2neu License Agreement.On June 7, 2016 the Company announced that it exercised its option agreement with Mayo Clinic and signed a worldwide license agreement to a proprietary HER2neu vaccine technology. The license gives TapImmune the right to develop and commercialize the technology ~~and product pipeline side, management believes that~~in any cancer indication in which the ~~company~~Her2neu antigen is ~~fundamentally strong and poised~~overexpressed.

Phase II Trials Started. On April 26, 2016 the Company announced plans to ~~be a leading company~~participate in a ~~highly attractive, multi-billion dollar~~Phase 2 trial of its cancer vaccine, TPIV 200, a multi-epitope anti-folate receptor vaccine (FRa), in combination with durvalumab (MEDI4736), an anti-PD-L1 antibody, in patients with platinum-resistant ovarian cancer. The study started with the enrollment and ~~expanding market,~~treatment of patients in the second quarter of 2016 at Memorial Sloan Kettering Cancer Center in New York and is being led by Jason Konner, M.D. as Principal Investigator. On June 21, 2016, we announced the treatment of the first patient in a ~~position reinforced by our recruitment~~company-sponsored Phase II trial in triple negative breast cancer as part of ~~top-class managers, advisors~~a multi-center study.

Manufacturing. On April 7, 2016, the Company announced that it has successfully completed formulation development, scale-up, GMP (Good Manufacturing Practice) manufacturing, and ~~investors who all share our vision.~~the release of TPIV 200, its multi-epitope folate receptor peptide vaccine for breast and ovarian cancer. The manufactured product contains five peptide antigens freeze dried in a single vial, ready for injection after reconstitution and addition of granulocyte-macrophage colony-stimulating factor (GM-CSF). TPIV 200 doses are now available for the upcoming Phase II clinical trials in both triple negative breast cancer and ovarian cancer.

Results of Operations

In this discussion of the Company’s results of operations and financial condition, amounts, other than per-share amounts, have been rounded to the nearest thousand dollars.

Three Months Ended June 30, ~~2015~~2016 Compared to Three Months Ended June 30, ~~2014~~2015

We recorded a net ~~loss~~income of ~~$60,216,000~~$5,974,000 or $0.08 basic and ($~~1.80)~~0.03) diluted per share during the three months ended June 30, ~~2015~~2016 compared to a net ~~income~~loss of ~~$753,000~~$60,216,000 or ~~$0.05~~($1.80) basic and diluted per share for the three months ended June 30, ~~2014.~~2015 due primarily to the changes in the fair value of our derivative liability.

Operating costs increased to ~~$1,138,000~~$2,426,000 during the three months ended June 30, ~~2015~~2016 compared to ~~$511,000~~$1,138,000 in the prior period. Significant changes in operating expenses are outlined as follows:

General and administrative expenses increased to $937,000 during the three months ended June 30, 2015 from $488,000 during the prior period. The increase was primarily due to increased investor relations activities and higher legal fee during the three months ended June 30, 2015 compared to the prior period. The decrease in non-cash consulting fees from the prior year was due to the Company curtailing its business development activities in the current year.

Research and development costs during the three months ended June 30, ~~2015~~2016 were ~~$201,000~~$1,248,000 compared to ~~$23,000~~$201,000 during the prior period. The increase was primarily due to the Company expensing the Mayo Foundation license fee payments in the current period and higher expenses relating to research.

General and administrative expenses increased to $1,177,000 during the three months ended June 30, 2016 from $937,000 during the prior period. This was due to generally increased expenses relating to consulting, general and administrative and professional fees during the ~~Company’s plan~~three months ended June 30, 2016 due to ~~exercise its option to acquire Mayo Clinic technology as part of an agreement entered into in March 2014 and~~ increased ~~in in-house research~~ activity in ~~the current period.~~operations.

The ~~weighted average number~~changes in fair value of ~~shares outstanding was 33,525,656~~derivative liabilities for the three months ended June 30, ~~2015~~2016 was $8,237,000 as compared to ~~15,523,016~~($59,079,000) for the ~~prior year.~~

three months ended June 30, 2015. The variance is due to the revaluation of the Series A, Series C, Series D and Series E warrants issued by us in January and March 2015. We revalue the derivative liabilities at each balance sheet date to fair value. The fair value is determined using Black-Scholes valuation model using various assumptions. The two most significant changes in the assumptions was the difference in the strike price used at June 30, 2016 of $0.51 compared to $0.96 at June 30, 2015 and the number of warrants with derivative liabilities. Due to these significant changes, the fair value of the derivative liabilities decreased by $8,237,000 with a corresponding gain in the condensed and consolidated statement of operations.

Six Months Ended June 30, ~~2015~~2016 Compared to Six Months Ended June 30, ~~2014~~2015

We recorded a net income of $1,224,000 or $0.02 basic and loss of ~~$60,917,000 or~~ ($~~1.99)~~0.02) diluted per share during the six months ended June 30, ~~2015~~2016 compared to ~~$28,954,000~~a net loss of $60,917,000 or ($~~2.57)~~1.99) basic and diluted per share for the six months ended June 30, ~~2014.~~2015.

Operating costs increased to ~~$2,166,000~~$4,179,000 during the six months ended June 30, ~~2015~~2016 compared to ~~$1,733,000~~$2,166,000 in the prior period. Significant changes in operating expenses are outlined as follows:

General and administrative expenses decreased to $1,356,000 during the six months ended June 30, 2015 from $1,688,000 during the prior period. The decrease was primarily due to decrease in non-cash consulting fees paid as stock-based compensation during the six months ended June 30, 2015 compared to the prior period. The decrease in non-cash consulting fees from the prior year was due to the Company curtailing its business development activities in the current year.

Research and development costs during the six months ended June 30, ~~2015~~2016 were ~~$811,000~~$2,234,000 compared to ~~$45,000~~$811,000 during the prior period. This was due to the Company exercising its option to acquire Mayo Clinic technology as part of an agreement entered into in March 2014 and increased in in-house research activity in the current period.

~~The weighted average number of shares outstanding was 30,584,794 for~~

General and administrative expenses increased to $1,945,000 during the ~~three~~six months ended June 30, ~~2015~~2016 from $1,356,000 during the prior period. This was due to generally increased expenses relating to consulting, general and administrative and professional fees during the six months ended June 30, 2016 as the Company’s operating activities increased substantially.

The changes in fair value of derivative liabilities for the six months ended June 30, 2016 was $5,241,000 as compared to ~~11,250,240~~$(58,752,000) for the ~~prior year.~~six months ended June 30, 2015. The variance in the current period is due to the revaluation of the Series A, Series C, Series D and Series E warrants issued by us in January and March 2015. We revalue the derivative liabilities at each balance sheet date to fair value. The two most significant changes in the assumptions was the difference in the strike price used at June 30, 2016 of $0.51 compared to $0.96 at June 30, 2015 and the number of warrants with derivative liabilities. Due to these significant changes, the fair value of the derivative liabilities decreased by $5,241,000 with a corresponding gain in the condensed and consolidated statement of operations.

During the six months ended June 30, 2016, the Company received $231,000 of a grant awarded to Mayo Foundation from the US Department of Defense for the Phase II Clinical Trial of TPIV 200. The grant paid for the clinical supplies purchased by the Company.

Liquidity and Capital Resources

We have not generated any revenues since inception, we have financed our operations primarily through public and private offerings of our stock and debt including warrants and the exercise thereof. The following table sets forth our cash and working capital as of June 30, 2016 and December 31, 2015:


	June 30, 2016			December 31, 2015
Cash reserves	$	3,768,000		$	6,577,000
Working capital (deficit)	$	(19,330,000	)	$	(21,360,000	)

Net Cash Used in Operating Activities

Net cash used in operating activities during the six months ended June 30, 2016 was $2,784,000 compared to $1,828,000 during the prior period. We had no revenues during the current or prior periods. Operating expenditures, excluding non-cash interest and stock-based charges during the current period primarily consisted of consulting and management fees, office and general expenditures, and professional fees.

Net Cash Used in / Provided by Financing Activities

Net cash used in financing activities during the six months ended June 30, 2016 was $25,000 compared to net cash provided by financing activities of $4,791,000 during the prior period. In the current period we repaid a promissory note while prior period financing relates to proceeds from private placement.

Financings

Our current available funding has come from financings that we conducted in January and March of 2015 and from warrants issued in connection with our January and March, 2015 financings as well as our recent August 2016 private placement.

January 2015 Financing

In January, 2015, we entered into a Securities Purchase Agreement with certain investors for the sale of 7,320,000 units at a purchase price of $0.20 per unit, for a total purchase price of approximately $1,250,000, net of finders’ fee and offering expenses of approximately $214,000. Each unit consisting of (i) one share of the Company’s Common Stock, (ii) one Series A warrant to purchase one share of common stock, (iii) one Series B warrant to purchase one share of common stock (iv) one Series C warrant to purchase one share of common stock, (v) one Series D warrant to purchase one share of common stock, and (vi) one Series E warrant to purchase one share of common stock (the Series A, B, C, D and E warrants are hereby collectively referred to as the “January 2015 Warrants”). Series A warrants are exercisable at $1.50 per share, with a five year term. Series B warrants are exercisable at $0.40 per share, with a six month term. Series C warrants are exercisable at $1.00 per share, with a five year term. Series D warrants are exercisable at $0.75 per share only if and to the extent that the Series B warrants are exercised, with a five year term from the date that the Series B warrants are exercised. Series E warrants are exercisable at $1.25 per share, only if and to the extent that the Series C warrants are exercised, with a five year term from the date that the Series C warrants are exercised. Pursuant to a placement agent agreement, we agreed to issue warrants to purchase 366,000 common shares with substantially the same terms as the January 2015 Warrants.

March 2015 Financing

In March, 2015, we entered into a Securities Purchase Agreement with certain accredited investors for the sale of 5,000,000 units at a purchase price of $0.20 per unit, for a total purchase price of approximately $950,000, net of finders’ fee and offering expenses of approximately $50,000. Each unit consisting of (i) one share of the Company’s Common Stock, (ii) one Series A-1 warrant to purchase one share of common stock, (iii) one Series B-1 warrant to purchase one share of common stock (iv) one Series C-1 warrant to purchase one share of common stock, (v) one Series D-1 warrant to purchase one share of common stock, and (vi) one Series E-1 warrant to purchase one share of common stock (the Series A-1, B-1, C-1, D-1 and E-1 warrants are hereby collectively referred to as the “March 2015 Warrants”). The March 2015 Warrants have substantially the same terms as the January 2015 Warrants. Pursuant to a placement agent agreement, we agreed to issue warrants to purchase 125,000 common shares with substantially the same terms as the March 2015 Warrants.

Restructuring of January and March 2015 Financings

In May 2015, we entered into a restructuring agreement with the investors of the January 2015 and March 2015 financings, where:

The exercise price of the Series A and Series A-1 warrants was changed from $1.50 per warrant to $0.10 per warrant,

The exercise price of Series B and Series B-1 warrants was changed from $0.40 per warrant to $0.20 per warrant,

Each warrant of Series B and Series B-1 existing prior to the restructuring agreement was replaced with two warrants of such series,

The exercise price of the Series C and Series C-1 warrants was changed from $1.00 per warrant to $0.50 per warrant, and

Each warrant of Series C and Series C-1 existing prior to the restructuring agreement was replaced with two warrants of such series.

As a result of the restructuring agreement, we issued an additional 12,320,000 Series B warrants and 12,320,000 Series C Warrants.

2016 Financing

August 2016 Private Placement Transaction. On August 10, 2016, we completed a private placement of units with certain accredited investors. The units (“Units”) consisted of (i) one share of our common stock, par value $0.001 per share and (ii) one five-year warrant to purchase one share of our common stock for $0.50 (the “PIPE Warrants”). We issued and sold an aggregate of 6.25 million Units at a purchase price per Unit of $0.40 for an aggregate of $2.5 million, pursuant to Subscription Agreements, in which we and investors made customary representations to each other.

Warrant Exercises

Between June 16, 2015 and December ~~31, 2014:~~9, 2015, 37,080,000 shares were issued upon exercise of certain warrants we issued in connection with our 2015 financings, providing $9.22 million in proceeds. On August 12, 2016, holders of an aggregate of 7 million outstanding Series C Warrants and 5 million Series C-1 Warrants, each providing for the purchase of one share of our common stock for $0.50 per share exercised their warrants for an aggregate exercise price of $6,000,000.

Future Capital Requirements

   June 30, 2015    December 31, 2014
Cash reserves
   $ 3,105,000       $ 142,000
Working capital (deficit)
   $ (68,102,000 )    $ (1,024,000 )

Our capital requirements for 2016 will depend on numerous factors, including the success of our research and development, the resources we devote to develop and support our technologies and our success in pursuing strategic licensing and funded product development relationships with external partners. Subject to ~~the availability of~~our ability to raise additional ~~financing,~~capital including through possible joint ventures and/or partnerships, we expect to incur substantial expenditures to further develop our technologies including continued increases in costs related to research, nonclinical testing and clinical studies, as well as costs associated with our capital raising efforts and being a public company. We intend to spend approximately $7,500,000 over the next twelve months in carrying out our plan of operations . We will require substantial funds to conduct research and development and nonclinical and Phase II clinical testing of our licensed, patented technologies and to develop sublicensing relationships for the Phase II and III clinical testing. Our plans include seeking both equity and debt financing, alliances or other partnership agreements with entities interested in our technologies, or other business transactions that would generate sufficient resources to ensure continuation of our operations and research and development programs.

Our current available cash and cash equivalents (inclusion of our recent August 2016 private placement financing and proceeds of the exercise of outstanding warrants) are sufficient to satisfy our liquidity requirements. We believe our existing cash and cash equivalents will allow us to fund our operating plan through the end of 2017. We expect to continue to seek additional funding for our operations. ~~At June 30, 2015,~~Any such required additional capital may not be available on reasonable terms, if at all. If we ~~had $3,105,000~~were unable to obtain additional financing, we may be required to reduce the scope of, ~~cash on hand~~delay or eliminate some or all of our planned clinical testing and aresearch and development activities, which could harm our business. The sale of additional equity or debt securities may result in additional dilution to our shareholders. If we raise additional funds through the issuance of debt securities or preferred stock, these securities could have rights senior to those of our common stock and could contain covenants that would restrict our operations. We also will require additional capital beyond our currently forecasted amounts.

Because of the numerous risks and uncertainties associated with research, development and commercialization of our product candidates, we are unable to estimate the exact amounts of our working capital ~~deficit~~requirements. Our future funding requirements will depend on many factors, including, but not limited to:

the number and characteristics of ~~$68,102,000. In January~~the product candidates we pursue;

the scope, progress, results and ~~March 2015,~~costs of researching and developing our product candidates, and conducting nonclinical and clinical trials including the research and development expenditures we ~~raised approximately $2.33 million~~expect to make in connection with our license agreements with Mayo Foundation;

the timing of, and the costs involved in, obtaining regulatory approvals for our product candidates;

our ability to maintain current research and development licensing agreements and to establish new strategic partnerships, licensing or other arrangements and the financial terms of such agreements;

our ability to achieve our milestones under our licensing arrangements and the payment obligations we may have;

the costs involved in preparing, filing, prosecuting, maintaining, defending and enforcing patent claims, including litigation costs and the outcome of such litigation; and

the timing, receipt and amount of sales of, or royalties on, our future products, if any.

We have based our estimates on assumptions that may prove to be wrong. We may need to obtain additional funds sooner or in greater amounts than we currently anticipate. Potential sources of financing include strategic relationships, public or private sales of our shares or debt and ~~brokered placements~~other sources. We may seek to access the public or private equity markets when conditions are favorable due to our long-term capital requirements. We do not have any committed sources of financing at this time, and ~~another $2,500,000 in warrants exercised in May 2015.~~it is uncertain whether additional funding will be available when we need it on terms that will be acceptable to us, or at all. If we raise funds by selling additional shares of common stock or other securities convertible into common stock, the ownership interest of our existing stockholders will be diluted. If we are not able to obtain financing when needed, we may be unable to carry out our business plan. As a result, we may have to significantly limit our operations and our business, financial condition and results of operations would be materially harmed.

Various conditions outside of our control may detract from our ability to raise additional capital needed to execute our plan of operations, including overall market conditions in the international and local economies. We recognize that the United States economy has suffered through a period of uncertainty during which the capital markets have been ~~depressed,~~impacted, and that there is no certainty that these levels will stabilize or reverse despite the optics of an improving economy. Any of these factors could have a material impact upon our ability to raise financing and, as a result, upon our short-term or long-term liquidity.

~~Net Cash Used in Operating Activities~~

Net cash used in operating activities during the six months ended June 30, 2015 was $1,828,000 compared to $611,000 during the prior period. We had no revenues during the current or prior periods. Operating expenditures, excluding non-cash interest and stock-based charges during the current period primarily consisted of consulting and management fees, office and general expenditures, and professional fees.

~~Net Cash Provided by Financing Activities~~

Net cash provided by financing activities during the six months ended June 30, 2015 was $4,791,000 compared to $584,000 during the prior period. Current period financing consisted of proceeds from private placements and warrant exercises while prior period financing relates to proceeds from convertible notes.

As of June 30, 2015, we anticipate that we will need significant financing to enable us to meet our anticipated expenditures for the next twelve months, which are expected to be in the range of $7,500,000 assuming a single Phase 2 clinical trial.

Going Concern

We have no sources of revenue to provide incoming cash flows to sustain our future operations. As outlined above, our ability to pursue our planned business activities is dependent upon our successful efforts to raise additional ~~financing. These~~capital.

While these factors raise substantial doubt regarding our ability to continue as a going concern. Our condensed consolidated financial statements have been prepared on a going concern basis, which implies that we will continue to realize our assets and discharge our liabilities in the normal course of business. ~~As at June 30, 2015, we had accumulated losses of $160,359,000 since inception.~~ Our financial statements do not include any adjustments to the recoverability and classification of recorded asset amounts and classification of liabilities that might be necessary should we be unable to continue as a going concern.

Off-Balance Sheet Arrangements

We have not entered into any off-balance sheet arrangements that have or are reasonably likely to have a current or future effect on our financial condition, changes of financial condition, revenues, expenses, results of operations, liquidity, capital expenditures or capital resources that is material to investors.

Tax Loss and Credit Carryforwards

As of December 31, 2015 and 2014, we have approximately $24,123,000 of federal and $4,336,000 of state NOLs that may be available to offset future taxable income, if any. The federal net operating loss carryforwards, if not utilized, will expire between 2029 and 2035. The state net operating loss carryforwards, if not utilized, will expire in 2035. Any greater than 50% change in ownership under Section 382 of the Internal Revenue Code, or the Code, places significant annual limitations on the use of such net operating loss carryforwards.

At December 31, 2015 and 2014, we recorded a 100% valuation allowance against our deferred tax assets of approximately $10,826,000 and $12,471,000, respectively, as our management believes it is uncertain that they will be fully realized. If we determine in the future that we will be able to realize all or a portion of our net operating loss carryforwards, an adjustment to our net operating loss carryforwards would increase net income in the period in which we make such a determination.

Inflation

Inflation affects the cost of raw materials, goods and services that we use. In recent years, inflation has been modest. However, fluctuations in energy costs and commodity prices can affect the cost of all raw materials and components. The competitive environment somewhat limits our ability to recover higher costs resulting from inflation by raising prices. Although we cannot precisely determine the effects of inflation on our business, it is management’s belief that the effects on revenues and operating results will not be significant. We do not believe that inflation has had a material impact on our results of operations for the periods presented, except with respect to payroll-related costs and other costs arising from or related to government imposed regulations.

Item 3.

Quantitative and Qualitative Disclosures About Market Risk

We are a smaller reporting company as defined by Rule 12b-2 of the Exchange Act and are not required to provide the information required under this item.

~~Item 4. Controls and Procedures~~

Item 4.

Controls and Procedures

Evaluation of Disclosure Controls and Procedures

Our management, with the participation of our Principal Executive Officer and Principal Financial Officer, has evaluated the effectiveness of our disclosure controls and procedures (as such term is defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act, as of the end of the period covered by this report. Disclosure controls and procedures include, without limitation, controls and procedures designed to ensure that information required to be disclosed in the reports we file or submit under the Exchange Act is accumulated and communicated to management, including our Principal Executive Officer and Principal Financial Officer, as appropriate, to allow timely decisions regarding required disclosure. Based on such evaluation, our ~~Chief~~Principal Executive Officer and ~~Chief~~Principal Financial Officer has concluded that, as of the end of the period covered by this report, our disclosure controls and procedures are not effective in recording, processing, summarizing and reporting, on a timely basis, information required to be disclosed by us in the reports that we file or submit under the Exchange Act.

It should be noted that any system of controls is based in part upon certain assumptions designed to obtain reasonable (and not absolute) assurance as to its effectiveness, and there can be no assurance that any design will succeed in achieving its stated goals.

Changes in Internal Control Over Financial Reporting

There have been no changes in our internal control over financial reporting during the six months ended June 30, ~~2015~~2016 that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

PART II – OTHER INFORMATION

Item 1.

Legal Proceedings

~~Consultant Litigation~~

~~In May 2012, we issued what~~Management is ~~now equal to 112,000 shares~~not aware of ~~our common stock to two consultants. We contested~~any material legal proceedings and there are no pending material procedures that would affect the ~~validity~~property of the ~~issuances~~Company. Management is not aware of any legal proceedings and contemplated by any government authority or any other party involving the Company. As of the date of this ~~common stock based on our belief that the consultants did~~Quarterly Report, no director, officer or affiliate is (i) a party adverse to us in any legal proceeding, or (ii) has an adverse interest to us in any legal proceeding. Management is not ~~perform the services agreed to under their respective consulting agreements. While we initially were able to delay the sale~~aware of the contested shares, we were not successful in clawing back the contested shares. A claim for perceived damages from Michael Gardner (one of the consultants) suffered as a result of our contesting the issuance under the consulting agreements has been filed in the Supreme Court of New York. He has based his claim for damages on the difference between market price at the time we were able to delay the sale of his shares and the market price at the time of the sale of all of his shares. As the result of a judicial decision in New York he received a bond payment of ($100,000) that the Company had used to secure a temporary restraining orderany other legal proceedings pending or threatened against the ~~issuance of stock to him.~~

On July 18, 2014, the International Center for Dispute Resolution International Arbitration Tribunal issued a Final Award in the matter of TapImmune Inc. vs. Michael Gardner awarding TapImmune $196,204 plus post-award interest at a rate of 9% per year. This award stemmed from the dispute discussed above with Mr. Gardner regarding the May 2012 consulting agreement. The arbitrator found that we were fraudulently induced into entering said agreement through “1) misrepresentations as to what he would or could do for the Company, including raising funds, and 2) omissions about his reputation and ability to obtain or assist in obtaining financing for TapImmune” among other reasons. We are attempting to collect the award from Mr. Gardner.

~~Vendor Litigation~~

~~One of our suppliers, Fischer Scientific was awarded a judgment against us for $51,000 which is equal to the amount owed to them. We intend on settling that matter in the third quarter of 2015.~~Company.

Item 1A.

Risk Factors

Not required.

Item 2.

Unregistered Sales of Equity Securities and Use of Proceeds

(a)	We issued the following restricted securities during the period covered by this report to the named individual pursuant to exemptions under the Securities Act of 1933 including Section 4(2):

~~We have not~~On May 1, 2016 the Company returned the 315,000 shares of Glynn Wilson, Ph.D., to the treasury and issued ~~any unregistered equity securities that we have not previously reported in~~228,218 shares to Dr. Glynn Wilson, Ph.D., to adjust for the withholding tax liability for the shares awarded.

On May 3, 2016 the Company issued 40,000 shares to Gary Poelstra, pursuant to a ~~current or periodic report filed with~~financial consulting agreement.

On May 28, 2016 the ~~US Securities~~Company issued 41,037, 40,625 and ~~Exchange Commission.~~40,625 shares to Arsalan Farmanfarmai, Tona Family Trust and Frank Baughman, respectively, pursuant to debt conversion agreements of 2014.

On May 30, 2016 the Company issued 30,000 and 70,000 shares to Dennis S. Dobson and Dennis Dobson Jr., respectively, pursuant to an investor relations agreement.

On May 30, 2016 the Company issued 100,000 shares to Proactive Capital Resource Group, LLC, pursuant to an investor relations agreement.

Item 3.

Defaults Upon Senior Securities

None.

~~None.~~

Item 4.

Mine Safety Disclosure

Not Applicable.

Item 5.

Other Information

The disclosure set forth below is provided in lieu of a separate Form 8-K filing.

~~None.~~On August 10, 2016, holders of an aggregate of 7 million outstanding Series C Warrants and 5 million Series C-1 Warrants, each providing for the purchase of one share of Company common stock for $0.50 per share, entered into binding commitments to exercise those warrants for an aggregate exercise price of $6,000,000. The closing of the exercise of the warrants was conditioned on the closing of the Warrant Amendment Agreements entered into on August 10, 2016, between the Company and the holders of the Series C and Series C-1 Warrants, who also hold an aggregate of 37,159,975 outstanding Series A Warrants, Series A-1 Warrants, Series C Warrants, Series D Warrants, Series D-1 Warrants, Series E Warrants and Series E-1 Warrants (the “Outstanding Series Warrants”), in which they agreed to amend the terms of the Outstanding Series Warrants to remove provisions from the Outstanding Series Warrants that had previously caused them to be classified as a derivative liability as opposed to equity on the Company’s balance sheets.

The holders of the 7 million Series C Warrants and 5 million Series C-1 Warrants paid the $6 million exercise price for such warrants to the Company on August 11, 2016, and the Outstanding Series Warrants were amended on such date. In consideration for such amendment and the exercise of the Series C Warrants and Series C-1 Warrants, on August 11, 2016, the Company issued an aggregate of 9 million additional shares of restricted common stock to such warrant holders and new five-year Series F Warrants and Series F-1 Warrants to purchase an aggregate of 12 million shares of Company common stock at an exercise price of $0.60 per share. The form of the Series F and Series F-1 Warrants were filed as exhibits to the Prior Report.

2521

Item 6.

Exhibits

The following exhibits are included with this Quarterly Report on Form 10-Q:


		Incorporated by Reference
Exhibit number	Exhibit description	Form	File no.	Exhibit	Filing date	Filed herewith

3.1	Amended and Restated Bylaws of TapImmune Inc.	8-K	000-27239	3.1	7/15/16

4.1	Form of PIPE warrant	8-K	000-27239	4.1	8/11/16

4.2	Form of Amended Series A Warrant	8-K	000-27239	4.2	8/11/16

4.3	Form of Amended Series C Warrant	8-K	000-27239	4.3	8/11/16

4.4	Form of Amended Series D Warrant	8-K	000-27239	4.4	8/11/16

4.5	Form of Series E Warrant	8-K	000-27239	4.5	8/11/16

4.6	Form of Amended Series A-1 Warrant	8-K	000-27239	4.6	8/11/16

4.7	Form of Amended Series D-1 Warrant	8-K	000-27239	4.7	8/11/16

4.8	Form of Amended Series E-1 Warrant	8-K	000-27239	4.8	8/11/16

4.9	Form of Series F Warrant	8-K	000-27239	4.9	8/11/16

4.10	Form of Series F1 Warrant	8-K	000-27239	4.10	8/11/16

4.11	Form of Katalyst Warrant	8-K	000-27239	4.11	8/11/16

10.1	Amendment to Employment Agreement between TapImmune Inc. and Glynn Wilson, dated as of July 18, 2016	8-K	000-27239	10.1	7/19/16

10.2	Employment Agreement between TapImmune Inc. and John Bonfiglio dated as of July 18, 2016.	8-K	000-27239	10.2	7/19/16

10.3	Form of Subscription Agreement	8-K	000-27239	10.1	8/11/16

10.4	Registration Rights Agreement	8-K	000-27239	10.2	8/11/16

10.5	Form of Warrant Amendment Agreement	8-K	000-27239	10.3	8/11/16

10.6	Agency Agreement with Katalyst Securities LLC and GP Nurmenkari Inc., dated as of July 21, 2016	8-K	000-27239	10.4	8/11/16

10.7	License and Assignment Agreement with Mayo Foundation for Medical Education and Research dated May 19, 2016.**					X

31.1	Certification of Principal Executive Officer and Acting Principal Accounting Officer Pursuant to Rule 13a-14(a) or 15d-14(a) of the Securities Exchange Act of 1933, as amended.					X

32.1	Certification of Principal Executive Officer and Acting Principal Accounting Officer pursuant to 18 U.S.C. 1350 as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.					X

**
~~Exhibit Number~~		~~Description~~Confidential treatment has been requested for the redacted portions of ~~Exhibit~~

~~31.1~~		~~Certification of Principal Executive Officer and Acting Principal Accounting Officer Pursuant~~this exhibit pursuant to Rule ~~13a-14(a) or 15d-14(a)~~24b-2 of the Securities Exchange Act of ~~1933,~~1934, as amended.

~~32.1~~		~~Certification of Principal Executive Officer and Acting Principal Accounting Officer pursuant to 18 U.S.C. 1350 as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.~~

~~Exhibit 101~~

~~101.INS - XBRL Instance Document~~

~~101.SCH - XBRL Taxonomy Extension Schema Document~~

~~101.CAL - XBRL Taxonomy Extension Calculation Linkbase Document~~

~~101.DEF - XBRL Taxonomy Extension Definition Linkbase Document~~

~~101.LAB - XBRL Taxonomy Extension Label Linkbase Document~~

~~101.PRE - XBRL Taxonomy Extension Presentation Linkbase Document~~

2622

Exhibit 101

101.INS - XBRL Instance Document

101.SCH - XBRL Taxonomy Extension Schema Document

101.CAL - XBRL Taxonomy Extension Calculation Linkbase Document

101.DEF - XBRL Taxonomy Extension Definition Linkbase Document

101.LAB - XBRL Taxonomy Extension Label Linkbase Document

101.PRE - XBRL Taxonomy Extension Presentation Linkbase Document

SIGNATURES

In accordance with the requirements of the Exchange Act, the registrant caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

TAPIMMUNE INC.


		/s/ Glynn Wilson
		Glynn Wilson
		Chairman, Chief Executive Officer, Principal Executive Officer and Chief Financial Officer
		Date: ~~April 14,~~August 15, 2016


	June 30, 2015 As Restated			December 31, 2014
	(Unaudited)
ASSETS
Current Assets
Cash	$	3,105,320		$	141,944
Prepaid expenses and deposits		142,590			82,504

	$	3,247,910		$	224,448

LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)
Current Liabilities
Accounts payable and accrued liabilities	$	842,682		$	693,362
Research agreement obligations		492,365			492,365
Derivative liability – warrants		69,962,000			9,415
Promissory notes		52,942			52,942

		71,349,989			1,248,084

COMMITMENTS AND CONTINGENCIES
Stockholders’ Equity (Deficit)
Convertible preferred stock, $0.001 par value — 10,000,000 shares authorized:
Series A, $0.001 par value, 1,250,000 shares designated, -0- shares issued and outstanding as of June 30, 2015 and December 31, 2014		—			—
Series B, $0.001 par value, 1,500,000 shares designated, -0- shares issued and outstanding as of June 30, 2015 and December 31, 2014		—			—
Common stock, $0.001 par value, 500,000,000 shares authorized 38,038,921 shares issued and outstanding (2014 – 20,318,815)		38,039			20,319
Additional paid-in capital		92,218,937			85,265,776
Accumulated deficit		(160,359,055	)		(86,309,731	)

		(68,102,079	)		(1,023,636	)

	$	3,247,910		$	224,448


	Three Months Ended June 30,						Six Months Ended June 30,
	2015 As Restated						2015 As Restated
	2015 As Restated			2014			2015 As Restated			2014
Operating expenses:
General and administrative	$	936,887		$	488,427		$	1,355,673		$	1,687,794
Research and development		201,157			22,500			810,535			45,000

Loss from Operations		(1,138,044	)		(510,927	)		(2,166,208	)		(1,732,794	)
Other Income (Expense)
Accretion of interest on convertible debt		—			(8,660	)		—			(492,296	)
Changes in fair value of derivative liabilities		(59,079,025	)		352,834			(58,751,585	)		14,537
Foreign exchange		775			—			775			—
Gain (loss) on settlement of debt		—			920,233			—			(26,743,197	)

Net Income (Loss) for the Period	$	(60,216,294	)	$	753,480		$	(60,917,018	)	$	(28,953,750	)

Other comprehensive income (loss)
Foreign exchange translation adjustment		—			1,042			—			(207	)

TOTAL COMPREHENSIVE INCOME (LOSS)	$	(60,216,294	)	$	754,522		$	(60,917,018	)	$	(28,953,957	)

Basic and Diluted Net Income (Loss) per Share	$	(1.80	)	$	0.05		$	(1.99	)	$	(2.57	)

Weighted Average Number of Common Shares Outstanding		33,525,656			15,523,016			30,584,794			11,250,240


					Additional
	Common Stock				Paid In			Accumulated
	Number of shares		Amount $		Capital $			Deficit $			Total $
Balance, December 31, 2014		20,318,816		20,319		85,265,776			(86,309,731	)		(1,023,636	)
Private placement (net of finders’ fee of $140,000)		12,319,995		12,320		2,313,694			—			2,326,014
Fair value of warrants recognized as derivative liabilities in January and March 2015 Financing		—		—		(2,313,694	)		(6,999,306	)		(9,313,000	)
Fair value of warrants issued on May 28, 2015		—		—		—			(6,133,000	)		(6,133,000	)
Exercise of warrants		5,000,000		5,000		2,495,000			—			2,500,000
Reclassification of derivative warrant liabilities to equity at exercise date		—		—		4,245,000			—			4,245,000
Finders’ fee on exercise of warrants		—		—		(35,000	)		—			(35,000	)
Stock- based compensation		400,110		400		248,161			—			248,561
Net loss		—		—		—			(60,917,018	)		(60,917,018	)

Balance, June 30, 2015		38,038,921		38,039		92,218,937			(160,359,055	)		(68,102,079	)


	Six Months Ended June 30, 2015 As Restated			Six Months Ended June 30, 2014
CASH FLOWS FROM OPERATING ACTIVITIES
Net loss	$	(60,917,018	)	$	(28,953,750	)
Adjustments to reconcile net loss to net cash from operating activities:
Changes in fair value of derivative liabilities		58,751,585			(14,537	)
Loss on extinguishment of debt		—			26,743,197
Non-cash interest and finance charges		—			492,296
Stock based compensation		248,561			799,075
Changes in operating assets and liabilities:
Prepaid expenses		(60,086	)		—
Accounts payable and accrued liabilities		149,320			322,277

NET CASH USED IN OPERATING ACTIVITIES		(1,827,638	)		(611,442	)

CASH FLOWS FROM FINANCING ACTIVITIES
Issuance of shares, net of issuance costs of $173,000		2,326,014			583,000
Proceeds from loans payable		—			500
Proceeds from exercise of warrants		2,500,000			—
Finders’ fee on exercise of warrants		(35,000	)		—

NET CASH PROVIDED BY FINANCING ACTIVITIES		4,791,014			583,500

INCREASE (DECREASE) IN CASH		2,963,376			(27,942	)
CASH, BEGINNING OF PERIOD		141,944			48,589

CASH, END OF PERIOD	$	3,105,320		$	20,647


	June 30, 2015 (Unaudited)
	As Previously Reported			Adjustments			As Restated
ASSETS
Current Assets
Cash		3,105,320			—			3,105,320
Prepaid expenses and deposits		142,590			—			142,590

		3,247,910			—			3,247,910


LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)
Current Liabilities
Accounts payable and accrued liabilities		842,682			—			842,682
Research agreement obligations		492,365			—			492,365
Derivative liability – warrants		11,673,347			58,288,653			69,962,000
Promissory notes		52,942			—			52,942

		13,061,336			58,288,653			71,349,989

COMMITMENTS AND CONTINGENCIES
Stockholders’ Equity (Deficit)
Convertible preferred stock, $0.001 par value — 10,000,000 shares authorized:
Series A, $0.001 par value, 1,250,000 shares designated, -0- shares issued and outstanding as of March 31, 2015 and December 31, 2014		—			—			—
Series B, $0.001 par value, 1,500,000 shares designated, -0- shares issued and outstanding as of March 31, 2015 and December 31, 2014		—			—			—
Common stock, $0.001 par value, 500,000,000 shares authorized 32,638,811 shares issued and outstanding (2014 – 20,318,815)		38,039			—			38,039
Additional paid-in capital		95,885,631			(3,666,694	)		92,218,937
Accumulated deficit		(105,737,096	)		(54,621,959	)		(160,359,055	)

		(9,813,426	)		(58,288,653	)		(68,102,079	)

		3,247,910			—			3,247,910


	Three Months Ended June 30, 2015
	As Previously Reported			Adjustments			As Restated
Operating expenses:
General and administrative		936,887			—			936,887
Research and development		201,157			—			201,157

Loss from Operations		(1,138,044	)		—			(1,138,044	)
Other Income (Expense)
Changes in fair value of derivative liabilities		(9,052,372	)		(50,026,653	)		(59,079,025	)
Foreign exchange		775			—			775
Inducement expense		(8,256,000	)		8,256,000			-

Net Loss for the Period		(18,445,641	)		(41,770,653	)		(60,216,294	)

Other comprehensive income
Foreign exchange translation adjustment		—			—			—

TOTAL COMPREHENSIVE LOSS		(18,445,641	)		(41,770,653	)		(60,216,294	)

Basic and Diluted Net Lossper Share		(0.55	)		(1.25	)		(1.80	)

Weighted Average Number ofCommon Shares Outstanding		33,525,656			33,525,656			33,525,656


	Six Months Ended June 30, 2015
	As Previously Reported			Adjustments			As Restated
Operating expenses:
General and administrative		1,355,673			—			1,355,673
Research and development		810,535			—			810,535

Loss from Operations		(2,166,208	)		—			(2,166,208	)
Other Income (Expense)
Changes in fair value of derivative liabilities		(9,005,932	)		(49,745,653	)		(58,751,585	)
Foreign exchange		775			—			775
Inducement expense		(8,256,000	)		8,256,000			—

Net Loss for the Period		(19,427,365	)		(41,489,653	)		(60,917,018	)
Other comprehensive income
Foreign exchange translation adjustment		—			—			—

TOTAL COMPREHENSIVE LOSS		(19,427,365	)		(41,489,653	)		(60,917,018	)

Basic and Diluted Net Lossper Share		(0.64	)		(1.36	)		(1.99	)

Weighted Average Number ofCommon Shares Outstanding		30,584,794			30,584,794			30,584,794


	June 30,
	2015		2014
Common stock options		465,000		65,000
Common stock warrants - equity treatment		2,556,000		185,000
Common stock warrants - liability treatment		81,834,000		49,000
Convertible notes		—		7,000

Potentially dilutive securities		84,855,000		306,000


	Derivative liability – warrants
Balance – December 31, 2014	$	9,000
Additions during the period		15,446,000
Exercise of warrants		(4,245,000	)
Change in fair value of warrant liability		58,752,000

Balance – June 30, 2015	$	69,962,000


Conversion Option	Weighted Average Inputs for the Period
Date of valuation	For the Quarter Ending June 30, 2015			For the Quarter Ending June 30, 2014
Strike price	$	—		$	1.03
Volatility (annual)		—	%		199.00	%
Risk-free rate		—	%		0.05	%
Contractual term (years)		—			0.24
Dividend yield (per share)		—	%		—	%
				��
Fair value of Conversion Option at extinguishment	$	—		$	708,000


	Number of Warrants			Weighted Average Exercise Price		Weighted Average Remaining Life
Balance, December 31, 2014		2,659,417			1.83		4.15
Issued		86,730,975			0.54		3.25
Exercised		(5,000,000	)		0.50		—
Extinguished or expired		(7,500	)		50.00		—

Balance, June 30, 2015		84,382,892		$	0.54		3.26


	Number of Options		Weighted Average Exercise Price		Weighted Average Remaining Life
Balance, December 31, 2013		65,430		18.00		5.04
Issued		—		—		—
Cancelled/Forfeited		—		—		—

Balance, December 31, 2014		65,430		18.00		4.04


	Number of Shares			Weighted Average Grant-Date Fair Value
Unvested, December 31, 2014		278		$	18.00
Granted		400,000			0.16
Vested		(82,685	)		0.21
Cancelled		—			—

Unvested, June 30, 2015		317,593		$	0.16


	June 30, 2015			December 31, 2014
Cash reserves	$	3,105,000		$	142,000
Working capital (deficit)	$	(68,102,000	)	$	(1,024,000	)

Large accelerated filer

Accelerated filer

Non-accelerated filer

¨ (Do not check if smaller reporting company)

Smaller reporting company