U.S. SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 10-Q

 

☒     QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the quarterly period ended December 31, 20222023

 

OR

 

☐     TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

 

For the transition period from ______________ to ______________

 

Commission File Number: 000-55299

 

NASCENT BIOTECH INC

(Exact Name of Registrant as Specified in Its Charter)

 

Nevada

46-5001940

(State of Incorporation)

(IRS Employer Identification No.)

631 US Hwy 1, Suite 407, North Palm Beach, FL

3340833480

(Address of Principal Executive Offices)

(Zip Code)

 

(612) 961-5656

(Registrant’s Telephone Number)

 

Indicate by check mark whether the Registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the Registrant was required to file such reports), and (2) been subject to such filing requirements for the past 90 days. Yes ☒ 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 ☒ No ☐

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

 

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated file, non-accelerated filer, or a smaller reporting company.

 

Large accelerated filer

Accelerated filerfiled 

Non-accelerated filer

Smaller reporting company

 

Emerging Growth Company

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

 

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

 

As of February 14, 20232024 the Registrant had, 124,485,269169,729,565 shares of common stock and no shares of Series A convertible preferred issued and outstanding.

 

 

 

 

TABLE OF CONTENTS

 

PART I – FINANCIAL INFORMATION

 

Page

 

 

 

 

 

 

Item 1.

Financial Statement (Unaudited)

 

3

 

 

 

 

 

 

 

Unaudited Consolidated Balance Sheets as of December 31, 2022,2023, and audited March 31, 20222023

 

3

 

 

 

 

 

 

 

Unaudited Consolidated Statements of Operations for the Three and Nine Months Ended December 31, 20222023 and 20212022

 

4

 

 

 

 

 

 

 

Unaudited Consolidated Statements of Stockholders’ DeficitEquity (Deficit) for the Three and Nine Months Ended December 31, 20222023 and 20212022

 

5

 

 

 

 

 

 

 

Unaudited Consolidated Statements of Cash Flows for the Nine Months Ended December 31, 20222023 and 20212022

 

6

 

 

 

 

 

 

 

Notes to Unaudited Consolidated Financial Statements

 

7

 

 

 

 

 

 

Item 2.

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

 

15

 

 

 

 

 

 

Item 3.

Quantitative and Qualitative Disclosures About Market Risks

 

17

 

 

 

 

 

 

Item 4.

Controls and Procedures

 

17

 

 

 

 

 

 

PART II – OTHER INFORMATION

 

 

 

 

 

 

 

 

Item 1.

Legal Proceedings

 

18

 

 

 

 

 

 

Item 1A.

Risk Factors

 

18

 

 

 

 

 

 

Item 2.

Unregistered Sales of Equity and Use of Proceeds

 

18

 

 

 

 

 

 

Item 3.

Default upon Senior Securities

 

18

 

 

 

 

 

 

Item 4.

Mine Safety Information

 

18

 

 

 

 

 

 

Item 5.

Other Information

 

18

 

 

 

 

 

 

Item 6.

Exhibits

 

19

 

 

 

 

 

 

SIGNATURES

 

20

 

 

 
2

Table of Contents

 

PART I – FINANCIAL INFORMATION

ITEM: 1 FINANCIAL STATEMENT

  

NASCENT BIOTECH, INC.

CONSOLIDATED BALANCE SHEETS

 

 

December 31,

2022

 

 

March 31,

2022

 

 

December 31,

2023

 

 

March 31,

2023

 

 

(Unaudited)

 

 

(Audited)

 

 

(Unaudited)

 

 

(Audited)

 

ASSETS

 

 

 

 

 

ASSETS

 

Current assets:

 

 

 

 

 

 

 

 

 

 

Cash

 

$558,761

 

$94,414

 

 

$623,854

 

$172,186

 

Prepaid

 

 

7,083

 

 

 

11,000

 

 

 

17,442

 

 

 

82,816

 

Total current assets

 

 

565,844

 

 

 

105,414

 

 

641,696

 

255,002

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Total assets

 

$565,844

 

 

$105,414

 

 

$641,296

 

 

$255,002

 

 

 

 

 

 

 

 

 

 

 

LIABILITIES AND STOCKHOLDERS’ DEFICIT

 

 

 

 

 

LIABILITIES AND STOCKHOLDERS’ DEFICIT

Current liabilities:

 

 

 

 

 

 

 

 

 

 

Accounts payable and accrued liabilities

 

$387,253

 

$776,891

 

 

$483,751

 

$498,122

 

Convertible note- net of discount

 

470,171

 

-

 

 

125,000

 

428,719

 

Accrued liabilities- related party

 

2,179

 

-

 

Derivative liability

 

 

1,072,494

 

 

 

-

 

 

 

-

 

 

 

663,426

 

Total current liabilities

 

1,929,918

 

776,891

 

 

610,930

 

1,551,139

 

 

 

 

 

 

 

 

 

 

 

Total liabilities

 

 

1,929,918

 

 

 

776,891

 

 

 

610,930

 

 

 

1,551,139

 

 

 

 

 

 

 

 

 

 

 

Commitments and contingencies

 

-

 

-

 

 

 

 

-

 

 

 

 

 

 

 

 

 

 

 

Stockholders’ deficit:

 

 

 

 

 

Stockholders’ equity (deficit)

 

 

 

 

 

Preferred stock, $0.001 par value, 50,000,000 authorized, none issued and outstanding. respectively

 

-

 

-

 

 

-

 

-

 

Common stock, $0.001 par value; 500,000,000 authorized, 122,046,172 and 111,313,175 issued and outstanding, respectively

 

122,046

 

111,313

 

Common stock, $0.001 par value; 500,000,000 authorized, 168,729,565 and 131,764,348 issued and outstanding, respectively

 

168,729

 

131,764

 

Additional paid-in capital

 

19,618,596

 

18,039,016

 

 

23,609,519

 

20,194,874

 

Accumulated deficit

 

 

(21,104,716)

 

 

(18,821,806)

 

 

(23,747,881)

 

 

(21,622,775)

Total stockholders’ deficit

 

 

(1,364,074)

 

 

(671,476)

Total liabilities and stockholders’ deficit

 

$565,844

 

 

$105,414

 

Total stockholders’ equity (deficit)

 

 

30,367

 

 

 

(1,296,137)

Total liabilities and stockholders’ equity (deficit)

 

$641,296

 

 

$255,002

 

 

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

 

 
3

Table of Contents

  

NASCENT BIOTECH, INC.

CONSOLIDATED STATEMENTS OF OPERATIONS

AS OF DECEMBER 31,

(Unaudited)

 

 

Three Months Ended

December 31,

 

Nine Months Ended

December 31,

 

 

Three Months

 

Nine Months

 

 

2022

 

 

2021

 

 

2022

 

 

2021

 

License fee revenue

 

$-

 

$1,000,000

 

$-

 

$1,000,000

 

 

 

 

 

 

 

 

 

 

 

2023

 

 

2022

 

 

2023

 

 

2022

 

Operating expenses:

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Consulting

 

246,590

 

108,000

 

883,655

 

388,813

 

 

194,521

 

$246,590

 

$1,120,073

 

$883,655

 

General and administrative expense

 

132,934

 

70,538

 

324,623

 

313,536

 

 

101,941

 

132,934

 

271,727

 

324,623

 

Clinical trials

 

39,627

 

149,487

 

219,155

 

200,192

 

 

19,102

 

39,627

 

82,467

 

219,155

 

Product manufacturing and filling

 

1,688

 

-

 

138,195

 

-

 

Research and development

 

 

55,875

 

 

 

41,000

 

 

 

188,503

 

 

 

139,531

 

 

 

47,170

 

 

 

55,875

 

 

 

101,388

 

 

 

188,503

 

Operating expense

 

(475,026)

 

(369,025)

 

(1,615,936)

 

(1,042,072)

 

 

 

 

 

 

 

 

 

Income (loss) from operations

 

(475,026)

 

630,975

 

(1,615,936)

 

(42,072)

Loss from operations

 

 

(364,422)

 

 

(475,026)

 

 

(1,713,850)

 

 

(1,615,936)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Other income (expense):

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Interest income

 

144

 

-

 

160

 

10

 

 

3,920

 

144

 

4,312

 

160

 

Gain on debt settlement

 

28,000

 

-

 

28,000

 

5,000

 

Change in fair value of derivative

 

258,462

 

57,703

 

634,118

 

373,585

 

 

179,989

 

258,462

 

472,168

 

634,118

 

Financing costs

 

-

 

-

 

(5,124)

 

(101,150)

 

-

 

-

 

-

 

(5,124)

Gain on debt settlement

 

-

 

28,000

 

50,000

 

28,000

 

Loss on original issuance discount

 

-

 

(86,314)

 

(329,390)

 

(287,979

 

(25,000)

 

-

 

(25,000)

 

(329,390)

Interest expense

 

 

(648,900)

 

 

(5,041)

 

 

(994,738)

 

 

(11,177)

 

 

107

 

 

 

(648,900)

 

 

(362,736)

 

 

(994,738)

Total other income (expense)

 

(362,294)

 

(33,652)

 

(666,974)

 

(21,711)

 

159,016

 

(362,294)

 

138,744

 

(666,974)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net income (loss) before taxes

 

(837,320)

 

597,323

 

(2,282,910)

 

(63,783)

Net loss

 

$(205,406)

 

$(837,320)

 

$(1,575,106)

 

$(2,282,910)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Income tax

 

-

 

-

 

-

 

-

 

Net loss per share, basic and diluted

 

$(0.00)

 

$(0.01)

 

$(0.01)

 

$(0.02)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net income (loss)

 

$(837,320)

 

$597,323

 

 

$(2,282,910)

 

$(63,783)

 

 

 

 

 

 

 

 

 

Net income (loss) per share, basic

 

$(0.01)

 

$0.01

 

$(0.02)

 

$(0.00)

Net income (loss) per share - diluted

 

$(0.01)

 

$0.01

 

 

$(0.02)

 

$(0.00)

 

 

 

 

 

 

 

 

 

Weighted average number of shares outstanding, basic

 

119,500,985

 

107,728,175

 

115,398,628

 

107,471,003

 

Weighted average number of shares outstanding- diluted

 

 

119,500,985

 

 

 

112,358,175

 

 

 

115,398,628

 

 

 

107,471,003

 

Weighted average number of shares outstanding, basic and diluted

 

 

167,244,367

 

 

 

119,500,985

 

 

 

151,121,962

 

 

 

115,398,628

 

 

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

 

 
4

Table of Contents

 

NASCENT BIOTECH, INC.

CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ DEFICIT

THREE AND NINE MONTHS ENDED DECEMBER 31, 20222023 AND 20212022

(Unaudited)

 

 

 

 

 

Additional

 

 

Total

 

 

 

 

Additional

 

 

 

Total

 

 

Preferred Shares

 

Common Stock

 

Paid-In

 

Accumulated

 

 

Stockholders’

 

 

Common stock

 

Paid In

 

 

Accumulated

 

Stockholders'

 

 

Shares

 

 

Amount

 

 

Shares

 

 

Amount

 

 

Capital

 

 

Deficit

 

 

(Deficit)

 

 

Shares

 

 

Amount

 

 

Capital

 

 

Deficit

 

 

Equity (Deficit)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Balance at March 31, 2021

 

54,130

 

$54

 

104,834,083

 

$104,834

 

$17,774,023

 

$(18,351,416)

 

$(472,505)

Common stock issued to related parties

 

-

 

-

 

568,719

 

569

 

59,147

 

-

 

59,716

 

Common stock issued for service

 

-

 

-

 

50,000

 

50

 

5,200

 

-

 

5,250

 

Common stock issued for AP – related parties

 

-

 

-

 

307,010

 

307

 

23,025

 

-

 

23,332

 

Common stock issued for preferred shares

 

(54,130)

 

(54)

 

1,968,363

 

1,968

 

(1,914)

 

-

 

-

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net loss

 

-

 

-

 

-

 

-

 

-

 

(450,076)

 

(450,076)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Balance at June 30, 2021

 

-

 

-

 

107,728,175

 

107,728

 

17,859,481

 

(18,801,492)

 

(834,283)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net loss

 

-

 

 

 

-

 

-

 

-

 

(211,030)

 

(211,030)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Balance at September 30, 2021

 

-

 

-

 

107,728,175

 

107,728

 

17,859,481

 

(19,012,522)

 

(1,045,313)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net income

 

-

 

 

 

-

 

-

 

-

 

597,323

 

597,323

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Balance at December 31, 2021

 

 

-

 

 

$-

 

 

 

107,728,175

 

 

$107,728

 

 

$17,859,481

 

 

$(18,415,199)

 

$(447,990)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Balance at March 31, 2022

 

-

 

$-

 

111,313,175

 

$111,313

 

$18,039,016

 

$(18,821,806)

 

$(671,476)

 

111,313,175

 

$111,313

 

$18,039,016

 

$(18,821,806)

 

$(671,476)

Common stock issued to related parties

 

-

 

-

 

1,052,500

 

1,052

 

304,172

 

-

 

305,224

 

 

1,052,500

 

1,052

 

304,172

 

-

 

305,224

 

Common stock issued for warrant exercise

 

-

 

-

 

3,700,000

 

3,700

 

144,300

 

-

 

148,000

 

 

3,700,000

 

3,700

 

144,300

 

-

 

148,000

 

Common stock issued for service

 

-

 

-

 

1,000,000

 

1,000

 

59,000

 

-

 

60,000

 

 

1,000,000

 

1,000

 

59,000

 

-

 

60,000

 

Warrants issued with convertible notes

 

-

 

-

 

-

 

-

 

21,336

 

-

 

21,336

 

 

-

 

-

 

21,336

 

-

 

21,336

 

Net loss

 

-

 

-

 

-

 

-

 

-

 

(1,299,876)

 

(1,299,876)

 

-

 

-

 

-

 

(1,299,876)

 

(1,299,876)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Balance at June 30, 2022

 

-

 

-

 

117,065,675

 

117,065

 

18,567,825

 

(20,121,682)

 

(1,436,792)

 

117,065,675

 

117,065

 

18,567,825

 

(20,121,682)

 

(1,436,792)

Common stock issued to related parties

 

 

 

 

 

212,629

 

213

 

65,703

 

-

 

65,916

 

 

212,629

 

213

 

65,703

 

-

 

65,916

 

Common stock issued for warrant exercise

 

 

 

 

 

500,000

 

500

 

59,500

 

-

 

60,000

 

 

500,000

 

500

 

59,500

 

-

 

60,000

 

Common stock issued for convertible debt

 

 

 

 

 

379,080

 

379

 

101,594

 

-

 

101,973

 

 

379,080

 

379

 

101,594

 

-

 

101,973

 

Common stock issued for AP

 

 

 

 

 

37,700

 

38

 

9,237

 

-

 

9,275

 

 

37,700

 

38

 

9,237

 

-

 

9,275

 

Warrants issued with convertible notes

 

 

 

 

 

-

 

-

 

157,402

 

-

 

157,402

 

 

-

 

-

 

157,402

 

-

 

157,402

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net loss

 

 

 

 

 

-

 

-

 

-

 

(145,714)

 

(145,714)

 

-

 

-

 

-

 

(145,714)

 

(145,714)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Balance at September 30, 2022

 

-

 

-

 

118,195,084

 

118,195

 

19,961,261

 

(20,267,396)

 

(1,187,940)

 

118,195,084

 

118,195

 

19,961,261

 

(20,267,396)

 

(1,187,940)

Common stock issued to related parties

 

-

 

-

 

718,000

 

718

 

142,882

 

-

 

143,600

 

 

718,000

 

718

 

142,882

 

-

 

143,600

 

Common stock issued for convertible debt

 

-

 

-

 

3,133,088

 

3,133

 

451,461

 

-

 

454,594

 

 

3,133,088

 

3,133

 

451,461

 

-

 

454,594

 

Stock option expense

 

-

 

-

 

-

 

-

 

62,992

 

-

 

62,992

 

 

-

 

-

 

62,992

 

-

 

62,992

 

Net loss

 

 

-

 

 

 

-

 

 

 

-

 

 

 

(837,320)

 

 

(837,320)

 

 

 

 

 

 

 

 

 

 

 

Balance at December 31, 2022

 

 

122,046,172

 

 

$122,046

 

 

$19,618,596

 

 

$(21,104,716)

 

$(1,364,074)

 

 

 

 

 

 

 

 

 

 

 

Balance at March 31, 2023

 

131,764,348

 

$131,764

 

$20,194,874

 

$(21,622,775)

 

$(1,296,137)

Common stock issued to related parties

 

2,235,250

 

2,235

 

109,527

 

-

 

111,762

 

Common stock issued for convertible debt

 

9,537,180

 

9,537

 

358,259

 

-

 

367,796

 

Common stock issued for service

 

100,000

 

100

 

5,500

 

-

 

5,600

 

Change in derivative at conversion

 

 

 

-

 

191,258

 

-

 

191,258

 

Option expense

 

-

 

-

 

4,911

 

-

 

4,911

 

Net loss

 

-

 

-

 

-

 

(540,224)

 

(540,224)

 

 

 

 

 

 

 

 

 

 

 

Balance at June 30, 2023

 

143,636,778

 

143,636

 

20,864,329

 

(22,162,999)

 

(1,115,034)

Common stock issued to related parties

 

4,198,652

 

4,198

 

523,991

 

-

 

528,189

 

Common stock issued for cash

 

18,720,000

 

187,200

 

1,417,280

 

-

 

1,436,000

 

Common stock issued for service

 

180,000

 

180

 

8,820

 

-

 

9,000

 

Option expense

 

-

 

-

 

4,911

 

-

 

4,911

 

Deemed dividend from down round

 

 

 

-

 

550,000

 

(550,000)

 

-

 

Net loss

 

-

 

-

 

-

 

(829,476)

 

(829,476)

 

 

 

 

 

 

 

 

 

 

 

Balance at September 30, 2023

 

166,735,430

 

166,734

 

23,369,331

 

(23,542,475)

 

(6,410)

Common stock issued to related parties

 

387,885

 

388

 

65,634

 

-

 

66,022

 

Common stock for service

 

106,250

 

107

 

21,143

 

-

 

21,250

 

Common stock issued for cash

 

250,000

 

250

 

24,750

 

-

 

25,000

 

Common stock issued for convertible debt

 

1,250,000

 

1,250

 

123,750

 

-

 

125,000

 

Option expense

 

-

 

-

 

4,911

 

-

 

4,911

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Net loss

 

-

 

-

 

-

 

-

 

-

 

(837,320)

 

(837,320)

 

 

-

 

 

 

-

 

 

 

-

 

 

 

(205,406)

 

 

(205,406)

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Balance at December 31, 2022

 

 

-

 

 

$-

 

 

 

122,046,172

 

 

$122,046

 

 

$19,618,596

 

 

$(21,104,716)

 

$(1,364,074)

Balance at December 31, 2023

 

 

168,729,565

 

 

$168,729

 

 

$23,609,519

 

 

$(23,747,881)

 

$30,367

 

 

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

 

 
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NASCENT BIOTECH, INC.

CONSOLIDATED STATEMENTS OF CASH FLOWS

AS OF DECEMBER 31,

(Unaudited)

 

 

Nine Months Ended December 31,

 

 

Nine Months

 

 

2022

 

 

2021

 

 

2023

 

 

2022

 

 

 

 

 

 

 

 

 

 

 

Cash flows from operating activities:

 

 

 

 

 

 

 

 

 

 

Net loss

 

$(2,282,910)

 

$(63,783)

 

$(1,575,106)

 

$(2,282,910)

Adjustments to reconcile net loss to net cash used in operating activities:

 

 

 

 

 

 

 

 

 

 

Stock based compensation – related parties

 

514,740

 

59,716

 

 

705,974

 

514,740

 

Stock-based compensation

 

60,000

 

5,250

 

 

35,849

 

60,000

 

(Gain) loss in fair value of derivative liability

 

(634,118)

 

(373,585)

 

(472,168)

 

(64,118)

Debt discount amortization

 

962,257

 

287,979

 

 

380,409

 

(962,257

 

Loss on notes

 

286,265

 

-

 

 

(50,000)

 

286,265

 

Option expense

 

62,992

 

 

 

 

14,733

 

62,992

 

Changes in operating assets and liabilities:

 

 

 

 

 

 

 

 

 

 

Accounts payable and accrued expenses

 

(373,796)

 

154,891

 

 

58,425

 

(373,796)

Accrued liabilities- related parties

 

2,179

 

-

 

Prepaid

 

3,917

 

-

 

 

 

65,374

 

 

 

3,917

 

Due to related parties

 

 

-

 

 

 

50,335

 

Net cash provided by (used in) operating activities

 

 

(1,400,650)

 

 

120,803

 

 

 

(834,332)

 

 

(1,400,650)

 

 

 

 

 

 

 

 

 

 

Cash flows from financing activities:

 

 

 

 

 

 

 

 

 

 

Repayment of convertible notes

 

(275,000)

 

(320,500)

Proceeds from warrant exercise

 

208,000

 

-

 

Proceeds from the sale of common stock

 

1,461,000

 

-

 

Repayments of convertible notes

 

(400,000)

 

(275,000)

Proceeds from warrant conversion

 

-

 

208,000

 

Proceeds from convertible notes

 

 

1,932,000

 

 

 

200,000

 

 

 

225,000

 

 

 

1,932,000

 

Net cash provided (used) by financing activities

 

 

1,865,000

 

 

 

(120,500)

 

 

1,286,000

 

 

 

1,865,000

 

 

 

 

 

 

 

 

 

 

 

Net increase (decrease) in cash

 

464,350

 

303

 

 

451,668

 

464,350

 

Cash -beginning of year

 

 

94,414

 

 

 

1,434

 

 

 

172,186

 

 

 

94,414

 

Cash -end of period

 

$558,764

 

 

$1,737

 

 

$623,854

 

 

$558,764

 

 

 

 

 

 

 

 

 

 

 

SUPPLEMENT DISCLOSURES:

 

 

 

 

 

 

 

 

 

 

Interest paid

 

$11,135

 

$20,055

 

 

$-

 

$11,135

 

Income taxes paid

 

$-

 

$-

 

 

$-

 

$-

 

 

 

 

 

 

 

 

 

 

 

Non Cash Transactions

 

 

 

 

 

 

 

 

 

 

Common stock issued for conversion of preferred shares

 

$-

 

$1,968

 

Common stock issued for convertible debt

 

$556,567

 

$-

 

Common stock issued for accrued expenses- related party

 

$-

 

$23,332

 

Warrants issued with convertible notes

 

$-

 

$-

 

Initial discount from derivatives

 

$178,739

 

$-

 

 

$-

 

$178,739

 

Common stock issued for debt conversion

 

$492,796

 

$556,567

 

Retirement of derivative at conversion of debt

 

$191,258

 

$-

 

Common stock issued for AP

 

$9,275

 

$-

 

 

$-

 

$9,275

 

 

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

 

 
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NASCENT BIOTECH, INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS

(UNAUDITED)

 

NOTE 1 - ORGANIZATION AND NATURE OF OPERATIONS

 

Nascent Biotech, Inc. (“Nascent” or the “Company”) was incorporated on March 3, 2014 under the laws of the State of Nevada. The Company is actively developing Pritumumab for the treatment of brain cancer and pancreatic cancer. Nascent is also actively researching other cancers that have a high probability of benefiting from the therapeutic effects of Pritumumab because they share a common target. Pritumumab has shown to be very effective at low doses in previous clinical studies in Japan. Nascent is a phase 12 clinical trial biopharmaceutical company that focuses on biologic drug candidates that are preparing for initial clinical testing for the treatment of brain and pancreatic cancer.

 

On March 31, 2017, the Company filed its IND submission with the United States Food and Drug Administration (FDA) for clearance to begin Phase I clinical trials. On December 7, 2018, the Company received a letter from the FDA allowing it to use a specific lot of drug substance to begin phase 1 clinical trials. On March 15, 2021, the Company opened phase1 clinical trials. As of December 31, 2022,On August 10, 2023 the Company had completed dosing of patients inreceived clearance from the last cohort of the phase 1 clinical trials. The company is in the process of completing the required protocolUnited States Food and submitting the data to the FDA for approvalDrug Administration to commence phase 2 clinical trials.

On November 8, 2022 the Company was granted patient No. 11.492,394 from the Untied States Patient and Trademark Office for the patient entitled “Kits and Containers for Treating Vimentin Expressing Tumors.” This is the second patient issued in favortrials of the Company for Pritumumab.brain cancer.

 

NOTE 2 - BASIS OF PRESENTATION

 

The accompanying consolidated financial statements have been prepared in accordance with U.S. generally accepted accounting principles. The Company has elected a fiscal year ending on March 31.

 

The accompanying unaudited interim consolidated financial statements of the Company for the three and nine months ended December 31, 20222023 and 20212022 have been prepared in accordance with accounting principles generally accepted in the United States for interim financial information in accordance with Securities and Exchange Commission and should be read in conjunction with the audited financial statements and notes thereto contained in the Company’s annual report on Form 10-K for the year ended March 31, 2022.2023. In the opinion of management, the unaudited financial statements have been prepared on the same basis as the annual financial statements and reflect all adjustments, which include only normal recurring adjustments, necessary to present fairly the financial position and the results of operations for the interim periods presented herein. The results of operations for the interim periods are not necessarily indicative of the results to be expected for any subsequent quarters or for an entire year.

 

Basis of Presentation

 

The Company computes net loss per share in accordance with ASC 260, Earnings per Share, which requires presentation of both basic and diluted loss per share (“EPS”) on the face of the statement of operations. Basic EPS is computed by dividing net loss available to common shareholders (numerator) by the weighted average number of common shares outstanding (denominator) during the period. Diluted EPS gives effect to all dilutive potential common shares outstanding during the period including stock options and warrants, using the treasury stock method, convertible preferred stock, and convertible debt, using the if-converted method. In computing diluted EPS, the average stock price for the period is used in determining the number of shares assumed to be purchased from the exercise of stock options or warrants. Diluted EPS excludes all potentially dilutive common shares if their effect is antidilutive.

 

We have identified the conversion features of certain of our convertible notes payable as derivatives. We estimate the fair value of the derivatives using the Black-ScholesAmerican Option Binomial pricing model. We estimate the fair value of the derivative liabilities at the inception of the financial instruments, at the date of conversions to equity and at each reporting date, recording a derivative liability, debt discount, and a gain or loss on change in derivative liabilities as applicable. These estimates are based on multiple inputs, including the market price of our stock, interest rates, our stock price volatility and variable conversion prices based on market prices as defined in the respective agreements. These inputs are subject to significant changes from period to period and to management's judgment; therefore, the estimated fair value of the derivative liabilities will fluctuate from period to period, and the fluctuation may be material.

 

 
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Revenue recognition

 

In April 2016, the FASB issued ASU 2016–10 Revenue from Contracts with Customers (Topic 606): Identifying Performance Obligations and Licensing. The amendments in this Update do not change the core principle of the guidance in Topic 606. Rather, the amendments in this Update clarify the following two aspects of Topic 606: identifying performance obligations and the licensing implementation guidance, while retaining the related principles for those areas. Topic 606 includes implementation guidance on (a) contracts with customers to transfer goods and services in exchange for consideration and (b) determining whether an entity’s promise to grant a license provides a customer with either a right to use the entity’s intellectual property (which is satisfied at a point in time) or a right to access the entity’s intellectual property (which is satisfied over time). The amendments are intended to render more detailed implementation guidance with the expectation to reduce the degree of judgement necessary to comply with Topic 606.

 

ASC Topic 606 prescribes a new five-step model entities should follow in order to recognize revenue in accordance with the core principle. These five steps are:

 

1. Identify the contract(s) with a customer.

2. Identify the performance obligations in the contract.

3. Determine the transaction price.

4. Allocate the transaction price to the performance obligations in the contract.

5. Recognize revenue when (or as) the entity satisfied the performance obligations.

 

The Company implemented the transition using the modified retrospective method of transition. The funds are not earned on milestones that have not been reached per the contract. Based on the cut off treatment of the recognition of revenue per the milestones specific to the license agreements, the Company has determined that there are no adjustments in the value of the revenue recognized from these contracts.

 

The Company has one revenue stream, which are the milestone payments of the license agreement with BioRay Pharmaceutical which is not earned or billed until the milestone per the agreement is met. During the nine months period ended December 31, 2022, no revenue was received.

Accounts receivableDerivative debt

 

Accounts receivablesIn August 2020, the FASB issued ASU 2020-06, Debt – Debt with Conversion and Other Options (Subtopic 470-20) and Derivatives and Hedging – Contracts in Entity’s Own Equity (Subtopic 815-40). The new ASU eliminates the beneficial conversion and cash conversion accounting models for convertible instruments and supersedes the respective guidance within ASC 470-20 and ASC 740-10-55-51. With the elimination of the cash conversion and beneficial conversion feature models, more instruments will be accounted for as a single instrument rather than having their proceeds allocated between liability and equity accounting units.

The amendments in the ASU are carriedeffective for public business entities that meet the definition of an SEC filer, excluding entities eligible to be smaller reporting companies as defined by the SEC, for fiscal years beginning after December 15, 2021, including interim periods within those fiscal years. For all other entities, the amendments are effective for fiscal years beginning after December 15, 2023, including interim periods within those fiscal years. Early adoption is permitted at face value less any provisions for uncollectible amounts. Accounts receivable are receivables from a license agreement. No allowance for bad debt was considered necessary for the three and nine months endedbeginning of an entity’s annual fiscal year, but no earlier than fiscal years beginning after December 31, 2022 and 2021, respectively. As15, 2020. The Company is still evaluating the effects of December 31, 2022, the Company did not have any accounts receivable.adoption of the amendment.

 

NOTE 3 - GOING CONCERN

 

The Company’s consolidated financial statements are prepared using accounting principles generally accepted in the United States of America applicable to a going concern that contemplates the realization of assets and liquidation of liabilities in the normal course of business. The Company has aminimal working capital deficit and has incurred losses from operations. The Company has no revenue to cover its operating costs and the Company will incur additional expenses in the future developing their product. These factors raise substantial doubt about the company’s ability to continue as a going concern. The Company engages in research and development activities that must be satisfied in cash secured through outside funding. The Company may offer noncash consideration and seek equity lines as a means of financing its operations. If the Company is unable to obtain revenue producing contracts or financing or if the revenue or financing it does obtain is insufficient to cover any operating losses it may incur, it may substantially curtail or terminate its operations or seek other business opportunities through strategic alliances, acquisitions or other arrangements that may dilute the interests of existing stockholders. The financial statements do not include any adjustments that might result from the outcome of this uncertainty.

 

 
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NOTE 4 - RELATED PARTY TRANSACTIONS

 

On September 1, 2015, the Company entered five-year employment contracts with three of its officers and directors. One of the officers and director resigned as of September 30, 2020. Under the terms of the agreements the Company issued shares of common stock to the officers and directors equaling 11% of the outstanding shares of the Company as of the date of the contracts. As additional future shares are issued, the officers and directors are entitled to additional shares, so their aggregate ownership percentage initially remained at 11% (undated to 18% as noted below) of the outstanding shares of the Company. The agreements were amended on September 1, 2020, as noted below, and the table reflects the amendment to these agreements. The following table sets forth the shares earned under these contracts for the two active officers as of December 31, 2022:2023:

 

Officer and Director

 

Initial Share Awards Under the Contracts

 

 

Additional Shares Earned to Maintain Ownership Percentage

 

 

Total Shares Earned

 

 

Initial Share Awards Under the Contracts

 

 

Additional Shares Earned to Maintain Ownership Percentage

 

 

Total Shares Earned

 

President

 

1,028,910

 

8,890,269

 

9,919,179

 

 

1,028,910

 

14,487,669

 

15,516,579

 

Chief Financial Officer

 

 

617,346

 

 

 

4,677,723

 

 

 

5,295,069

 

 

 

617,346

 

 

 

7,476,173

 

 

 

8,093,519

 

Total

 

 

1,646,256

 

 

 

13,567,992

 

 

 

15,214,248

 

 

 

1,646,256

 

 

 

21,963,842

 

 

 

23,610,098

 

 

On September 1, 2020, the Company entered five-year compensation agreements with two of its officers and directors. Under the terms of the agreements the Company issued shares of common stock to the two senior officers equaling 18% of the outstanding shares of the Company as additional future shares are issued. The officers are entitled to additional future shares, so their aggregate ownership percentage remains at 18% of the future outstanding shares of the Company.

 

Officer and Director

 

Fiscal Year Annualized Compensation Being Paid

 

President

 

$250,000

 

Chief Financial Officer

 

$180,000

 

Total

 

$430,000

 

 

During the nine months ended December 31, 2022,2023, two officers and a director were issued 1,983,1296,821,785 shares of common stock with a value of $514,740$705,974 for service.

As of December 31, 2023, the Company owed a related party $2,179 in expenses.

 

NOTE 5 - EQUITY

 

Preferred

On April 1, 2021, 54,130 shares of preferred stock were converted into 1,968,363 shares of common stock. The conversion eliminated all outstanding convertible preferred shares.

Common

During the nine months ended December 31, 2021, three officers and directors were issued 568,719 shares of common stock with a value of $59,716 for service.

During the nine months period ended December 31, 2021 a director of the Company converted $23,332 of accrued compensation into 307,010 shares of common stock of the Company.

During the nine months period ended December 31, 2021, the Company issued 50,000 shares of common stock with a value of $5,250 for service.

During the nine months period ended December 31, 2021, 54,130 shares of preferred stock were converted into 1,968,363 shares of common stock. The conversion eliminated all outstanding convertible preferred shares.

 

During the nine months ended December 31, 2022, two officers and a director were issued 1,983,1291,983,363 shares of common stock with a value of $514,740 for service.

 

During the nine months ended December 31, 2022, four entities were issued 4,200,0003,700,000 shares of common stock with a value of $208,000 for the exercise of 3,700,0004,200,000 warrants.

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During the nine months ended December 31, 2022, the Company issued 37,700 shares of common stock with a value of $9,275 for accounts payable.

 

During the nine months ended December 31, 2022, the medical director was issued 1,000,000 shares of common stock with a value of $60,000 for service.

 

During the nine months period ended December 31, 2022, the Company issued 3,512,168issued3,512,168 shares of common stock with a value of $556,565 for the conversion of $550,000 of convertible notes and $6,565 in interest.

 

During the nine months ended December 31, 2023, two officers and a director were issued 6,821,785 shares of common stock with a value of $705,974 for service.

During the nine months ended December 31, 2023, the Company issued 10,787,180 shares of common stock with a value of $492,796 for the conversion of debt and accrued interest.

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During the nine months ended December 31, 2023, the Company issued 100,000 shares of common stock with a value of $5,600 for service.

During the nine months ended December 31, 2023, the Company issued 18,970,000 shares of common stock with a value of $1,461,000 for cash.

During the nine months ended December 31, 2023, the Company issued 386,250 shares of common stock with a value of $35,850 for service.

NOTE 6 - OPTIONS

 

On November 17, 2022During the nine months period ended December 31, 2023, the Company issued 500,000 options to one individual with an exercise pricerecognized $14,733 in option expense leaving a balance of $0.18 per share. The options have a 5 year life and vested 250,000 options at inception and 25,000 options per month thereafter until fully vested. The options were fair valued using a volatilityunrecognized option expense of 250%, discount rate of 4.35% at $114,531 to be amortized over the 5 year period.

As of December 31, 2022, the Company expensed $5,727 in options.$61,259.

 

The following sets forth the options granted and outstanding during the nine months ended December 31, 2022:2023:

 

 

Options

 

 

Weighted

Average

Exercise

Price

 

Weighted

Average

Remaining

Contract

Life

 

Number of

Options

Exercisable

 

Intrinsic

Value

 

 

 

 

 

 

Weighted

 

 

 

 

 

Outstanding at March 31, 2022

 

930,000

 

$0.34

 

3.80

 

930,000

 

$-

 

 

 

 

Weighted

 

Average

 

 

 

 

 

 

 

 

Average

 

Remaining

 

Number of

 

 

 

 

 

 

Exercise

 

Contract

 

Options

 

Intrinsic

 

 

Options

 

Price

 

Life

 

Exercisable

 

Value

 

Outstanding at March 31, 2023

 

1,430,000

 

$0.28

 

3.81

 

930,000

 

$--

 

Granted

 

500,000

 

0.18

 

5.0

 

250,000

 

-

 

 

 

 

--

 

--

 

--

 

--

 

Exercised

 

 

-

 

 

 

-

 

 

 

-

 

 

 

-

 

 

 

-

 

 

 

--

 

 

 

--

 

 

 

--

 

 

 

--

 

 

 

--

 

Outstanding at December 31, 2022

 

 

1,430,000

 

 

$0.28

 

 

 

4.06

 

 

 

1,180,000

 

 

$10,000

 

Outstanding at December 31, 2023

 

 

1,430,000

 

 

$0.28

 

 

 

3.06

 

 

 

1,230,000

 

 

$60,000

 

 

The weighted average remaining life and intrinsic value of the options as of December 31, 2022,2023, was 4.063.06 years and zero, respectively.

 

NOTE 7 - WARRANTS

 

During the year ended March 31, 2021 the Company issued 3,700,000 warrants and  used the Black ScholesBinomial Pricing model to estimate the fair value of the warrants as of grant date, using the following key inputs: market prices of the Company’s common stock at dates of grant between $0.08-0.11 per share, conversion price of $0.15, volatility of 312.5%-314.49% and discount rate of 0.14-0.16%. Based on the fair value of the common stock of $437,000 and  value of the warrants of $349,605 the fair value of the warrants was calculated to be 41% of the total value or $303,000. During the year ended March 31, 2021 the valuation resulted in a deemed dividend from the down round calculation of $555,000. As of December 31, 2022  3,700,000 warrants were converted into 3,700,000 shares of common stock for cash at a value for $148,000.

 

On April 7, 2022, the Company issued 500,000 warrants as part of a convertible note issued the same date. The Company used the Black ScholesBinomial  Pricing model to estimate the fair value of the warrants as of grant date using the following key inputs; market prices of the Company’s stock at date of grant  of $0.08 per share, conversion price of $0.12 per share, volatility of 132% and discount of 1.78%. The fair value of the warrants were calculated to be $ 26,000 and was used to allocate the proceeds to the two elements based on the relative fair value of the debt instruments without the warrants and of the warrants at the time of issuance. The portion of the proceeds were allocated to the warrants of $21,336 is accounted for as paid in capital. As of December 31,September 23, 2022 the 500,000 warrants were converted into 500,000 shares of common stock with a value of $60,000.

 

On August 31, 2022 the Company issued 750,000 warrants as part of a convertible note issued the same date. The Company used the Black ScholesBinomial  Pricing model to estimate the fair value of the warrants as of grant date using the following key inputs; market prices of the Company’s stock at date of grant  of $0.41 per share, conversion price of $0.60 per share, volatility of 137% and discount of 3.50%. The fair value of the warrants were calculated to be $ 188,760 and was used to allocate the proceeds to the two elements based on the relative fair value of the debt instruments without the warrants and of the warrants at the time of issuance. The portion of the proceeds that were allocated to the warrants of $9,902 is accounted for as paid in capital.

 

 
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On September 2, 2022 the Company issued 250,000 warrants as part of a convertible note issued the same date. The Company used the Black ScholesBinomial Pricing model to estimate the fair value of the warrants as of grant date using the following key inputs; market prices of the Company’s stock at date of grant  of $0.345 per share, conversion price of $0.60 per share, volatility of 137% and discount of 3.47%. The fair value of the warrants were calculated to be $50,273 and was used to allocate the proceeds to the two elements based on the relative fair value of the debt instruments without the warrants and of the warrants at the time of issuance. The portion of the proceeds were allocated to the warrants of $2,484 is accounted for as paid in capital.

 

The warrants contain an anti-dilution clause which become effective if any instrument is issued after the warrant  issuance is converted into common stock at a price lower than the warrant conversion price. During the nine months ended December 31, 2023 the valuation resulted in a deemed dividend from the down round calculation of $550,000 with a recalculated conversion price change to $0.05 per share.

The weighted average remaining life and intrinsic value of the warrants as of December 31, 20222023 was:

 

 

Warrants

 

 

Weighted

Average

Exercise

Price

 

Weighted

Average

Remaining

Contract Life

 

Intrinsic

Value

 

Outstanding at March 31, 2021

 

3,700,000

 

$0.15

 

2.00

 

$-

 

Granted

 

-

 

-

 

-

 

-

 

Exercised

 

-

 

-

 

-

 

-

 

Expired

 

-

 

-

 

-

 

-

 

Warrants

Outstanding at March 31, 2022

 

3,700,000

 

$0.15

 

1.35

 

$-

 

Granted

 

1,500,000

 

0.44

 

1.83

 

-

 

Exercised

 

(4,200,000)

 

-

 

��

 

-

 

-

 

Expired

 

-

 

-

 

-

 

-

 

Outstanding as of December 31, 2022

 

 

1,000,000

 

 

$0.60

 

 

 

1.75

 

 

$-

 

Outstanding as of March 31, 2023

Granted

Exercised

Expired

Balance at December 31, 2023

As of December 31, 2023 there were 1,000,000 warrants outstanding. The remaining life weighted average was 0.75 and intrinsic value of zero.

 

NOTE 8 - CONVERTIBLE DEBT

On October 28, 2020, the Company issued a $138,000 convertible note with an OID of $10,000. The note matured on October 28,2021 with interest at 10% per annum. After 180 days the note was convertible into common stock of the Company at $0.04 per share or a 30% discount to the VWAP during the 20 days prior to conversion. The initial derivative was calculated using risk free interest of .18%, volatility of 212% and expected life of .50 years. On April 20, 2021 note was paid with the principal of $138,000, accrued interest of $6,805 and financing costs of $41,400.

On November 11, 2020, the Company issued a $82,500 convertible note with an OID of $7,500. The note matured on October 28, 2021 with fixed interest of 10%. After 180 days the note was convertible into common stock of the Company at a 35% discount to the lowest trading price during the 20 days prior to conversion. On April 22, 2021, the note was paid consisting of principal of $82,500, accrued interest of $8,250 and finance costs of $24,750.

On February 16, 2021, the Company issued a $100,000 convertible note with an OID of $5,000. The note matured on February 16, 2022, with fixed interest of 10%. After 180 days the note was convertible into common stock of the Company at a 30% discount to the lowest trading price during the 15 days prior to conversion. The initial derivative was calculated using risk free interest of .18%, volatility of 213% and expected life of 1.00 years. On August 16, 2021, the note was paid consisting of principal of $100,000, accrued interest of $5,000 and financing costs of $35,000.

On August 10, 2021, the Company issued a $200,000 convertible note. The note matured on February 10, 2022, with fixed interest of 10%. Within 180 days of issuance the note may be repaid at an escalating premium up to 125% of the face value of the note. After 180 days the note was convertible into common stock of the Company at $0.06 per share or a 25% discount to the lowest trading price during the 10 days prior to conversion. The initial derivative was calculated using risk free interest of .05%, volatility of 132% and expected life of 0.50 years. On March 28, 2022, the Note was paid consisting of $200,000 in principal, accrued interest of $9,973 and financing costs of $50,000.

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On April 7, 2022, the Company issued a $275,000 convertible note with an OID of $25,000. The note matures on March 29, 2023, bears fixed interest of 8% plus contains a most favored nations statement. Within 180 days of issuance, the note may be repaid at a premium of 115% of the face value of the note and 150% of the unconverted balance of the note after 180 days and prior to maturity. After 180 days the note may be converted into common stock of the Company at $0.075 per share or a 20% discount to the lowest VWAP (Volume- Weighted Average Pricing) price during the 10 days prior to conversion. The initial derivative was calculated using risk free interest of .05%, volatility of 132% and expected life of 0.50 years. On September 9, 2022 the note was paid with the note principal of $275,000, interest of $9,162 and premium of $42,624 for a total of $326,786.

 

On August 31, 2022 the Company entered into an agreement with an unrelated third party for convertible debentures totaling $1,500,000. The first $500,000 was paid at closing with the second $500,000 paid on September 20, 2022, upon filing of an S-1 Registration, and the third $500,000 paid on September 27, 2022, upon the S-1 becoming effective. Each debenture matures one year from date of issuance. The interest rate for each debenture is six percent (6%) per annum and the Debenture may be converted at the lesser of $0.30 per share or eighty percent (80%) of the lowest VWAP of the Company’s common stock for ten consecutive trading days immediately prior to the conversion date and carried an original discount of 3% of the debenture face value. The Company also issued a warrant to purchase 750,000 shares of the Company’s common stock for a period of two years, expiring on August 30, 2024, at an exercise price of $0.60 per share. As part of the agreement the Company filed an S-1 registration statement registering the underlying common shares for the debenture conversion and the warrants.

 

The initial derivatives were calculated for each debenture as follows:

 

1. Debenture 1- risk free interest of 3.50%, volatility of 137% and expected life of 1.00 years

2. Debenture 2- risk free interest of 4.03%, volatility of 140% and expected life of 1.00 years

3. Debenture 3- risk free interest of 3.98%, volatility of 141% and expected life of 1.00 years

 

During the nine months period ended December 31, 2022,2023, the Company issued 2,524,629to the note holder 8,205,263 shares of common stock with a value of $406,566 for the conversion of $400,000$300,000 of the convertible notes plus $17,556 of accrued interest.

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On June 29, 2023 the Company signed a redemption agreement, amended on August 31, 2023, with the debentures owner pertaining to the outstanding principal balance of $400,000. Under the terms of the agreement the Company paid the debenture owner $50,000 on August 24, 2023. The terms of the agreement requires principal payments of $50,000, which was made before September 30, 2023, $50,000 to be paid on or before October 31, 2023 and the balance of $250,000 on or before December 31, 2023. The debenture owner has agreed not to convert any of the principal or interest to common stock through December 31, 2023 and if the terms of the agreement are met will forgive any interest on the outstanding amounts of the debentures. On October 30, 2023 ,the Company paid $50,000 against the note and $6,566 in interest,outstanding per the settlement agreement leaving a balance due on December 31, 2023 of $1,100,000$250,000. On December 15, 2023 the balance of convertible notes plus accrued interest.the note of $250,000 was paid in full.

 

On September 2, 2022 the Company entered into an agreement with an unrelated third party for convertible debentures totaling $500,000. The first $250,000 was paidadvanced to the Company at closing with the second $250,000 to be paid to the Company upon the S-1 becoming effective.effective (note next paragraph below). Each debenture matures one year from date of issuance. The interest rate for each debenture is six percent (6%) per annum and the Debenture may be converted at the lesser of $0.30 per share or eighty percent (80%) of the lowest VWAP of the Company’s common stock for ten consecutive trading days immediately prior to the conversion date and carried an original discount of 3% of the debenture face value. The Company also issued a warrant to purchase 250,000 shares of the Company’s common stock for a period of two years, expiring on August 30, 2024, at an exercise price of $0.60 per share. As part of the agreement the Company filed an S-1 registration statement registering the underlying common shares for the debenture conversion and the warrants. The initial derivative was calculated using risk free interest of 3.47%, volatility of 137% and expected life of 1 year. As of December 31, 2022 the funds for the second debenture had not been received. During the nine month periodmonths ended December 31, 20222023, the Company issued 987,539to the note holder 1,331,919 shares of common stock for the conversion of $150,000$45,000 of the convertible note plus $5,240 of accrued interest leaving a note balance of $5,000 plus accrued interest. On October 23, 2023, the Company paid $5,000 against the outstanding convertible notes payable and the interest was forgiven, leaving a balance due of $100,000zero.

On December 1, 2023 the Company issued an amended convertible debenture to an unrelated third party under the agreement dated September 2, 2022 (noted in the paragraph above), totaling $250,000 The debenture had an original discount of 10% with no accrued interest and matures on May 30, 2024. The note is convertible into common stock of the Company at the rate of $0.10 per share. On December 6, 2023, the note holder converted $125,000 of the note into 1,250,000 shares of common stock of the Company. As of December 31, 2023, the outstanding balance of the note was $125,000.

During the nine months ended December 31, 2023, the Company issued an aggregate of 10,787,180 shares of common stock with a value of $482,796 for the conversion of $470,000 of convertible note and $22,795 in interest. The conversion of the shares plus the principal payment noted above leaves a balance due of $125,000 in convertible notes plus accrued interest.

 

NOTE 9 - FAIR VALUE MEASUREMENTS AND DERIVATIVE LIABILITIES

 

As defined in (Financial Accounting Standards Board ASC 820), fair value is the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date (exit price). The Company utilized the market data of similar entities in its industry or assumptions that market participants would use in pricing the asset or liability, including assumptions about risk and the risks inherent in the inputs to the valuation technique. These inputs can be readily observable, market corroborated, or generally unobservable. The Company classifies fair value balances based on the observability of those inputs. FASB ASC 820 establishes a fair value hierarchy that prioritizes the inputs used to measure fair value. The hierarchy gives the highest priority to unadjusted quoted prices in active markets for identical assets or liabilities (level 1 measurement) and the lowest priority to unobservable inputs (level 3 measurement).

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The three levels of the fair value hierarchy are as follows:

 

Level 1 

Quoted prices are available in active markets for identical assets or liabilities as of the reporting date. Active markets are those in which transactions for the asset or liability occur in sufficient frequency and volume to provide pricing information on an ongoing basis. Level 1 primarily consists of financial instruments such as exchange-traded derivatives, marketable securities, and listed equities.

 

 

 

Level 2 

Pricing inputs are other than quoted prices in active markets included in level 1, which are either directly or indirectly observable as of the reported date and includes those financial instruments that are valued using models or other valuation methodologies. These models are primarily industry-standard models that consider various assumptions, including quoted forward prices for commodities, time value, volatility factors, and current market and contractual prices for the underlying instruments, as well as other relevant economic measures. Substantially all of these assumptions are observable in the marketplace throughout the full term of the instrument, can be derived from observable data or are supported by observable levels at which transactions are executed in the marketplace. Instruments in this category generally include non-exchange-traded derivatives such as commodity swaps, interest rate swaps, options, and collars.

 

 

 

Level 3 

– 

Pricing inputs include significant inputs that are generally less observable from objective sources. These inputs may be used with internally developed methodologies that result in management’s best estimate of fair value

 

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As December 31, 2022,2023, the Company believes the amounts reported for cash, payables, accrued liabilities and amounts due to related parties approximate their fair values, due to the nature or duration of these instruments. During the nine months ended December 31, 2023, the Convertible note holder entered into an agreement in which the Company will pay the principal note balance by December 31, 2023. The note holder will not convert any amount of the outstanding notes into common stock unless the principal has not been paid per the agreement. As of December 31, 2023 the note was paid in full.

 

The following table represents the change in the fair value of the derivative liabilities during the quarter ended December 31, 2022:2023:

 

 

 

Level 1

 

 

Level 2

 

 

Level 3

 

Fair value of derivative liability as of March 31, 2022

 

$-

 

 

$-

 

 

$-

 

Additions at fair value

 

 

-

 

 

 

-

 

 

 

1,706,612

 

Change in fair value of the derivative

 

 

-

 

 

 

-

 

 

 

(634,118)

Balance at December 31, 2022

 

$-

 

 

$-

 

 

$1,072,494

 

The estimated fair value of the derivative liabilities at December 31, 2022 was calculated using the Black Scholes pricing model with the following assumptions:

Risk-free interest rate

4.73%

Expected life in years

.67-.74

Dividend yield

0%

Expected volatility

135-163

 

 

Level 1

 

 

Level 2

 

 

Level 3

 

Fair value of derivative liability as of March 31, 2023

 

$-

 

 

$-

 

 

$663,426

 

Change at conversion

 

 

 

 

 

 

 

 

 

 

(191,258)

Change in fair value of the derivative

 

 

-

 

 

 

-

 

 

 

(472,168)

Balance at December 31, 2023

 

$-

 

 

$-

 

 

$-

 

 

NOTE 10 –COMMITMENTS- COMMITMENTS AND CONTINGENCIES

 

On September 30, 2016, the Company entered a cell line sales agreement with the product manufacturer. Under the terms of the agreement the Company is obligated to make future payments based on the milestones of its achievements. These future payments may be as followed;

 

1.

$100,000 upon the initiation (first dose/first patient) of the first Phase I clinical trial (or equivalent) of a Product;

2.

$225,000 upon the initiation (first dose/first patient) of the first Phase III clinical trial (or equivalent) of a Product

3.

$225,000 payable upon the first Biologics License Application approval (or equivalent) of a product.

4.

Annual maintenance fee upon completion of phase I manufacturing or the transfer of the cell line from Catalent’s control of $50,000;

5.

1. $225,000 upon the initiation (first dose/first patient) of the first Phase III clinical trial (or equivalent) of a Product

2. $225,000 payable upon the first Biologics License Application approval (or equivalent) of a product.

3. Annual maintenance fee upon completion of phase I manufacturing or the transfer of the cell line from Catalent’s control of $50,000;

4. A contingent sales fee upon first commercial sale of a product of 1% of sales or $150,000 whichever is greater payable quarterly.

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As of December 31, 2022, the Company paid2023 the outstanding net balance of $325,000 due the manufacture for the balance of the annuals fees due and initiation of the phase 1 clinical trials payment.was $50,090.

 

On March 9, 2020, the Board of Directors of the Company adapted an expense bonus program. Under the program, if an acquisition, merger or change in control is affected, 10% of the value of the transaction will be allocated to pay the expenses of the transaction including but not limited to legal, accounting, transfer fees and other miscellaneous expense. The balance of the fund after expenses will be allocated 20% to directors and 80% to officers and employees of the Company as allocated by the Chief Executive Officer and approved by the Board of Directors.

 

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NOTE 11 - LICENSE AGREEMENT

 

On March 31, 2021, the Company issued a license agreement for US $5,000,000 to BioRay Pharmaceutical Co, LTD, (Licensee) licensing Pritumumab internationally with the exclusion of North and Central America and the Caribbean Islands. Under the terms of the agreement the Company receivesreceived $250,000 upon signing of the agreement plus $750,000 with the start of the phase 1 clinical trials, which started in March 2021. In addition, the Company received $750,000 upon the enrollment of the 12thinitial patient orenrolled at the dosage level of 8.0 mg/kg, whichever was achieved first.kg. Further paymentpayments of $2,500,000 willwere to be received when the FDA approves the phase 2 clinical trials and $750,000 to receive when the phase 2 clinical trials begin. Upon commercialization by the Licensee, the Company willwas to receive a 9% royalty on net sales for 20 years. AsSince the inception of December 31, 2022the license agreement the Company had received the three initialreceive payments totaling $1,750,000.$1,750,000for the first 2 payments . On June 6, 2023 the Company and BioRay mutually agreed to terminate the license agreement, at no cost to either party, returning the worldwide rights to the Company. Under the terms of the agreement no further payments were to be received.

 

NOTE 12 - SUBSEQUENT EVENTS

 

On January 23, 202330, 2024 the Company issued 1,028,6971,000,000 shares of common stock for the conversionwith a value of $100,000 of convertible debt and $1,841 in interest for a total value of $101,841.cash.

 

On February 9, 2023January 30, 2024 the Company issued 1,410,400 shares250,000 two year warrants with a exercise price of common stock for the conversion of $100,000 of convertible debt and $279 of interest for a total of $100,279.$0.60 per share.

 

The Company has evaluated subsequent events to determine events occurring after December 31, 20222023 through the date of this filing that would have a material impact on the Company’s financial results or require disclosure and have determined none exist, other than those noted above in this footnote.

 

 
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ITEM 2: MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERTIONS

 

This report contains forward looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended and Section 21E of the Securities Exchange Act of 1934, as amended. The Company’s actual results could differ materially from those set forth on the forward-looking statements because of the risks set forth in our filings with the Securities and Exchange Commission, general economic conditions, and changes in the assumptions used in making such forward looking statements.

 

Nascent Biotech, Inc (“Nascent” or the “Company”) was incorporated on March 3, 2014 under the laws of the State of Nevada. The Company is actively developing Pritumumab for the treatment of brain cancer and pancreatic cancer. Nascent is also actively researching other cancers that have a high probability of benefiting from the therapeutic effects of Pritumumab because they share a common target.

 

Nascent is a phase 12 clinical stage biopharmaceutical company that develops monoclonal antibodies for the treatment of various forms of cancer. The Company focuses on biologic drug candidates that are undergoing or have already completed initial clinical testing for the treatment of cancer and then seek to further develop those drug candidates for commercial use. Nascent currently is developing for the treatment of brain cancer and pancreatic cancer both of which we hold orphan drug status granted by the FDA. Nascent has completed Cohort 4 and open cohort 5 on September 16, 2022 of the phase 1 clinical trials. As of December 31, 2022On August 10, 2023 the Company had completedreceived clearance from the infusion of final patients in Cohort 5 ending the addition of any new patients in theUnited States Food and Drug Administration to commence phase 12 clinical trials.trials for brain cancer.

 

In addition, Nascent, has begun, in collaboration with academic and corporate partners, to assesshas asserted the potential for pritumumab to be involved as both a treatment and a vaccine for the SARS-CoV-2 virus.virus (responsible for COVID-19).

 

Overview

 

The Company is focused on developing pritumumab for the treatment of patients with brain cancer malignancies such as gliomas and astrocytomas. Current therapeutic strategies for brain cancer include the use of the chemotherapy, surgical intervention or radiation therapy. Because these treatments have marginal outcomes there exists a need to develop safer, more effective drugs. Temodar-the most commonly used Chemotherapeutic drug used to treat brain cancer, is attributed to only median rates of survival and many brain tumors are eligible for surgery. Moreover, even when removed, most brain tumors come back within one year post-operation. Today, with current standards of care, less than 60% of all brain cancer patients will live past the first year after diagnosis, and less than 35% of patients will live to five years. Glioblastoma, a particularly aggressive form of brain cancer that constitutes 42% of ALL brain and other nervous system cancers, has survival rates of 36.5% at 1 year and 5% at 5 years. (SEER Registry Data, September 15th, 2016 (Central Brain Tumor Registry of the United States).

 

On March 31, 2017, the Company filed its IND submission with the United States Food and Drug Administration (FDA) for clearance to begin Phase I clinical trials. On December 7, 2018, the Company received a letter from the FDA allowing it to use a specific lot of drug substance to begin phase 1 clinical trials. The Company is incommenced human clinical trials with a major oncology hospital for brain cancer, both primary and metastatic As of December 31, 2022,metastatic. Phase 1 clinical trials has been completed. On August 10, 2023 the Company had completed dosing of patients inreceived clearance from the last cohort of the phase 1 clinical trials. The company is in the process of completing the required protocolUnited States Food and submitting the data to the FDA for approvalDrug Administration to commence phase 2 clinical trials.trials of brain cancer.

 

In May of 2020, Nascent announced a research collaboration to study, both in vitro and in vivo (mouse models), the ability of pritumumab to block the SARS-Cov-2 virus from infecting cells. This notion has been raised by a published article in the scientific literature (Yu et al. Journal of Biomedical Science (2016) 23:14 DOI 10.1186/s12929-016-0234-7), which specifically mentioned cell surface vimentin (the protein to which pritumumab binds selectively) as a potential target in the treatment of conditions related to coronaviruses. These preliminary studies are on-going. Further, in May of 2020, Nascent announced a joint collaboration with Manhattan BioSolutions, Inc (NY, NY) to employ Manhattan’s platform, based on the recombinant Mycobacterium bovis Bacillus Calmette-Guerin (BCG) vaccine, but engineered to target SARS-CoV-2. BCG is a live non-pathogenic bacterium that stimulates diverse innate and adaptive immune responses and is well-known for its long safety track record as a tuberculosis vaccine. Thus, with these collaborations, Nascent is investigating the potential utility of pritumumab as both a treatment for COVID-19 and a preventive vaccine for COVID-19.

 

 
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Results of Operations

 

The Company recorded zero revenue during the three and nine month periods ended December 31, 2023 and 2022, and $1,000,000 in license payments for the same periods in 2021.respectively.

 

Total operatingGeneral and administrative expenses for the three and nine month periods ended December 31, 20222023 was $475,026$101,941 and $1,615,936$271,727 compared to $369,025$132,934 and $1,042,072324,623 for the same periods ended December 31,  2021.2022. Consulting expense for the three and nine month periods ending December 31, 2022 were2023 was $194,521 and $1,120,073 compared to $246,590 and $883,655 compared to $108,000 and $388,813 for the same periods in 2021.2022. This increase in expenses for the three and nine month periods ended December 31, 20222023 over the same period in 20212022 was due primarily to increased consulting fee of $494,842, a result of$236,418 from the pricing of the shares issued to management for maintaining the percentage of ownership per their agreements. Expense was also increased by product filling cost of $138,195 for the nine months period ended December 31, 2023 verse none in the same period in 2022. This is the vialing of the bulk drug product for use in the clinical trials.

 

Research and development expenses for the three and nine month periods ended December 31, 20222023 was $47,170 and $101,388 compared to $55,875 and $188,503 compared to $41,000 and $139,531 in the same periods in 2021.2022. Clinical trials costs were $39,627was $19,102 and $219,155$82,467 for the three and nine month periods ended December 31, 20222023 compared to $149,48739,627 and $200,192 for$219,155 in the same periods in 2021.2022. Phase 1 clinical trials ended in March 2023. Until the commencing of  phase 2 clinical trials, the expenses for research and development plus clinical trial expenses will be minimal.

 

Total other income expense incurred induring the three and nine month periods ended December 31, 20222023 was other income of $159,016 and138,744, compared to other expense of $362,294 and $666,974 compared to other expenses of $33,652 and $21,711 forin the same periods in 2021.2022. Other expense during the nine months in three and nine month periods in 20222023 consisted of interest expense of $648,900 and $994,738, original discount interest of zero and $329,390 and finance costs of zero and 5,124$362,736, offset by a gain in debt settlement of $50,000 and a gain on the change of fair value of $258,462 and $634,118.$472,168. Other income/expenses in the nine months period ended December 31, 2022 consisted of gain in fair value of $634,118, offset by interest expense of $994,738 and original note discount of $329,390.

For the three monthsmonth and nine month periods ended December 31, 2021 consisted of income from the change in fair value of $57,703 and $375,585, interest expense of $5,041 and $11,177, original note discount expense of $86,314 and $287,979 and financing costs of zero and $101,150.

For the three and nine month periods ended December 31, 2022,2023, our net loss was $837,320$205,406 and $2,282,910$1,575,106 compared to a net income of $597,323 and net loss of $63,783$837,320 and $2,282,910 for the same periods in 2021.2022. The difference between the periods relateswas due primarily to higher consulting costs experiencedthe loss on original note discount in 2022 plus higher other expenses, during the nine months period in 2022 verses 2021 plus the license revenue earned in the nine month period endedending December 31, 2021 with no income in2022 over the same period in 2022.2023.

 

Liquidity and Capital Resources

 

The Company’s liquidity and capital is dependent on the capital it can raise to continue the Company’s testing and clinical trials of its product. The Company projects it must raise additional fundsapproximately $15-20 million to complete its Phase II clinical studies for both brain and pancreatic cancer.studies.

 

There are no agreements or understandings about future loans by or with the officers, directors, principals, affiliates, or shareholders of the Company. The Company will continue to raise outside capital through loans, equity sales and possible licensing agreements. These factors raise substantial doubt about the company’s ability to continue as a going concern.concern

 

At December 31, 2022,2023, the Company had negative working capital of $1,364,074.$30,367. Current assets consist of cash of $558,764623,854 and prepaid of $7,083$17,442 with current liabilities $1,929,918$610,930 consisting of accounts payable and accrued expensesexpense of $387,253,$483,751and convertible notes, net of discount of $470,171, plus derivative liability of $1,072,494. The decrease in accounts payable and accrued expense was due primarily to the payment of an outstanding payment payable with a manufacturer of $325,000.$125,000.

 

Net cash used in operating activities in the nine monthmonths period ended December 31, 20222023 was $1,400,650$834,332 compared to net cash providedused of $120,803$1,400,650 in the same period in 2021.2022. The variance between the same periods in 2023 and 2022 over 2021 relates mainly to a significantlower loss in 2022 of $2,282,910the nine months period ended December 31, 2023 over the same period in 2022.

Net cash provided by financing activities for the nine months period ended December 31, 2023 was $1,286,000 compared to $ 63,783 resultingnet cash provided by financing activities of $1,865,000 in the same period in 2022. Cash provided in the nine months period ended December 31, 2023 consisted of common stock sold for cash of $1,461,000 offset by repayment of convertible notes of $400,000, compared to proceeds from higher expense in 2022 against revenueconvertible notes of $1,000,000 in 2021 with none$1,932,000 and warrant conversion of $208,000, offset by payment of convertible notes of $275,000 during the same period in 2022.

 

 
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Net cash provided by financing activities for the nine month period ended December 31, 2022 was $1,865,000 compared to net cash used in financing activities of $120,500 in the same period in 2021. Cash provided in the period ended December 31, 2022 was due to warrant conversion of $208,000, net proceeds from convertible notes of $1,932,000, offset by repayment of convertible note of $275,000 compared to proceeds from convertible note of $200,000 offset by repayment of convertible notes of $320,500 for the same period in 2021.

As of December 31, 2022,2023, the Company had total assets of $565,844$641,296 and total liabilities of $1,929,918.$610,929. Stockholders’ deficitequity as of December 31, 20222023 was $1,364,074.$30,367. This compares to a stockholders’ deficit of $671,476$1,296,137 as of March 31, 2022.2023. Liabilities increaseddecreased in 20222023 mainly as a function of the issuance oflower convertible notes, net of discount of $470,171 and no derivative liability of $1.027,494 compared to zero for both as of March 31, 2021.liability.

 

NEED FOR ADDITIONAL FINANCING:

 

The Company is engaged in research and development activities that must be satisfied in cash secured through outside funding. The Company will offer noncash consideration and seek equity lines as a means of financing its operations. If the Company is unable to obtain revenue producing contracts or financing or if the revenue or financing it does obtain is insufficient to cover any operating losses it may incur, it may substantially curtail or terminate its operations or seek other business opportunities through strategic alliances, acquisitions or other arrangements that may dilute the interests of existing stockholders.

 

Our current capital needs are estimated to be approximately $15-18 million. This will take us through Phase III clinical trials which was completed as of December 31, 2022 and the FDA approval process for Phase 2. It is estimated Phase 2 trials will require an additional $20-25 million for completion of the brain and pancreatic cancer trials.scheduled to begin in in 2024.

 

Off-Balance Sheet Arrangements

 

We had no off-balance sheet arrangements or guarantees of third party obligations at December 31, 2022.2023

 

Inflation

 

We believe that inflation has not had a significant impact on our operations since inception.

 

ITEM 3: QUANTITATIVE AND QUALITATIVE DISCLOSURE ABOUT MARKET RISK

 

Not applicable.

 

ITEM 4: CONTROLS AND PROCEDURES

 

Under the supervision and the participation of our management, including our principal executive officer and principal financial officer, we conducted an evaluation as of September30, 2022,December 31, 2023, of the effectiveness of the design and operation of our disclosure controls and procedures, as such term is defined under Rule 13a-15(e) promulgated under the Securities Exchange Act of 1934, as amended. Based on this evaluation, our principal executive officer and our principal financial officer concluded that our disclosure controls and procedures were not effective as of December 31, 2022.2023. Such conclusion reflects the identification of material weakness as follows: (1) lack of accounting proficiency of our chief executive officer who is our sole officer and our principal accounting officer which has resulted in a reliance on part-time outside consultants to perform substantially all of our accounting functions, (2) a lack of adequate segregation of duties and necessary corporate accounting resources in our financial reporting process and accounting function, and (3) lack of control procedures that include multiple levels of review. Until we can remedy these material weaknesses, we have engaged third party consultants and accounting firm to assist with financial reporting.

 

Changes in Internal Control over Financial Reporting

 

There have been no changes in our internal control over financial reporting that occurred during the nine months ended December 31, 20222023 that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

 

 
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PART II – OTHER INFORMATION

 

ITEM 1: LEGAL PROCEEDINGS

 

None

 

ITEM 1A: RISK FACTORS

 

There have been no material changes to Nascent Biotech’s risk factors as previously disclosed in our most recent Form 10-K filing.

 

ITEM 2: UNREGISERED SALES OF EQUITY AND USE OF PROCEEDS.

 

During the nine months ended December 31, 2022,2023, two officers and a director were issued 1,983,1296,821,785 shares of common stock with a value of $514,740$705,974 for service.

 

During the nine months ended December 31, 2022, four entities were2023, the Company issued 4,200,00010,787,180 shares of common stock with a value of $208,000$492,796 for the exerciseconversion of 4,200,000 warrants.debt and accrued interest.

 

During the nine months ended December 31, 2022,2023, the Company issued 37,700100,000 shares of common stock with a value of $9,275$5,600 for accounts payable.service.

 

During the nine months ended December 31, 2022,2023, the medical director wasCompany issued 1,000,00018,970,000 shares of common stock with a value of $60,000$1,461,000 for service.cash.

 

During the nine months period ended December 31, 2022,2023, the Company issued 3,512,168386,250 shares of common stock with a value of $556,565$35,850 for the conversion of $550,000 of convertible notes and $6,565 in interest.service.

 

ITEM 3: DEFAULT ON SENIOR SECURITIES

 

None

 

ITEM 4: MINE SAFETY INFORMATION

 

None

 

ITEM 5: OTHER INFORMATION

 

None.

 

 
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Table of Contents

 

ITEM 6: EXHIBITS

 

Exhibit No.

 

Description

 

 

 

31

 

Certification of Principal Executive Officer and CFO pursuant to Section 302 of the Sarbanes-Oxley Act of 2002

32

 

Certification of Principal Executive Officer and CFO Pursuant to 18 U.S.C. Section 1350, as Adopted Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002

101.INS

 

Inline XBRL Instance Document (the instance document does not appear in the Interactive Data File because its XBRL tags are embedded within the Inline XBRL document).

101.SCH

 

Inline XBRL Taxonomy Extension Schema Document.

101.CAL

 

Inline XBRL Taxonomy Extension Calculation Linkbase DocumentDocument.

101.DEF

 

Inline XBRL Taxonomy Extension Definition Linkbase Document.

101.LAB

 

Inline XBRL Taxonomy Extension Labels Linkbase Document.

101.PRE

 

Inline XBRL Taxonomy Extension Presentation Linkbase Document.

104

 

Cover Page Interactive Data File (formatted as inline XBRL and contained in Exhibit 101).

 

 
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Table of Contents

 

SIGNATURE

 

Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the Company has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

 

NASCENT BIOTECH, INC.

    

Dated: February 14, 20232024

By:

/s/ Sean Carrick

 

 

Sean Carrick

 
  

Principal Executive Officer

 

 

 
20