UNITED STATES
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 September 30, 2017March 31, 2019
 
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: 000-25132
 
MYMETICS CORPORATION
(Exact name of registrant as specified in its charter)
 
DELAWARE
  25-1741849
State or Other jurisdiction of Incorporation or Organization 
 
 25-1741849
State or Other jurisdiction of
Incorporation or Organization 
I.R.S. Employer Identification No.

c/o Mymetics SA
Route de la Corniche 4
Epalinges, Switzerland 
 
CH-1066
Address of Principal Executive Offices
Zip Code
 
011 41 21 653 4535
Registrant’s Telephone Number, Including Area Code
 
 
Former Name, Former Address and Former Fiscal Year, if Changed Since Last Report
 
Securities registered pursuant to Section 12(b) of the Act:
Title of each classTrading Symbol(s)Name of each exchange on which registered
Common Stock, Par Value $0.01 per shareMYMXOTCQB venture stage marketplace

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) has 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 ☐
 
 Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.
 

 Large accelerated filer ☐   Accelerated filer ☐ 
 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 Act). Yes ☐         No ☒

APPLICABLE ONLY TO CORPORATE ISSUERS
 
Indicate theThe number of shares outstanding of each of the registrant's classes of common stock,Registrant’s Common Stock, $0.01 par value, was 303,757,622 as of the latest practicable date:
ClassOutstanding at November 13, 2017
Common Stock, usd0.01 par value303,757,622
May 15, 2019
    

 
 
 
PARTPART I.    FINANCIAL INFORMATION
 
ITEMITEM 1. FINANCIAL STATEMENTS
 
MYMETICS CORPORATION
CONSOLIDATED BALANCE SHEETS
 (UNAUDITED)
(In Thousands of Euros, Except Share and Per Share Amounts)
 
 
March 31,
 
 
December 31,
 
 
September 30,
 
 
December 31,
 
 
2019
 
 
2018
 
 
2017
 
 
2016
 
 
 
 
ASSETS
 
 
 
 
 
 
Current Assets
 
 
 
 
 
 
Cash
 E830 
 E1,391 
 E475 
 E479 
Receivables
  56 
  170 
  48 
  585 
Prepaid expenses
  41 
  44 
  37 
Total current assets
  927 
  1,602 
  567 
  1,101 
    
    
Property and equipment, net of accumulated depreciation of E363 at September 30, 2017 and E418 at December 31, 2016
  73 
  67 
Property and equipment, net of accumulated depreciation of E439 at March 31, 2019 and E434 at December 31, 2018
  31 
  36 
Goodwill
  6,671 
  6,671 
 E7,269 
 E7,808 
 E7,671 
 E8,340 
    
    
    
LIABILITIES AND SHAREHOLDERS' EQUITY (DEFICIT)
    
    
Current Liabilities
    
    
Accounts payable
 E96 
 E120 
 E36 
 E75 
Deferred revenue from grants
  733 
  1,165 
Non-convertible notes payable and related accrued interest to related parties
  1,167 
  -- 
  4,026 
  4,002 
Convertible notes payable and related accrued interest to related parties
  47,472 
  45,834 
  51,453 
  50,756 
Total liabilities
  49,468 
  47,119 
  55,515 
  54,833 
    
    
    
    
Shareholders' Equity (Deficit)
    
    
Common stock, U.S. $0.01 par value;1,000,000,000 shares authorized; issued 303,757,622 at September 30, 2017 and at December 31, 2016
  2,530 
Preferred stock, U.S. $0.01 par value; 5,000,000 shares authorized; none issued or Outstanding
  -- 
Common stock, U.S. $0.01 par value; 1,000,000,000 shares authorized; issued and outstanding 303,757,622 at March 31, 2019 and at December 31, 2018
  2,530 
Preferred stock, U.S. $0.01 par value; 5,000,000 shares authorized; none issued or outstanding
  -- 
Additional paid-in capital
  34,423 
  34,392 
  34,443 
  34,441 
Accumulated deficit
  (79,422)
  (76,391)
  (85,903)
  (84,675)
Accumulated other comprehensive income
  672 
  690 
  684 
  679 
  (41,797)
  (38,779)
  (48,246)
  (47,025)
 E7,671 
 E8,340 
 E7,269 
 E7,808 
 
The accompanying notes are an integral part of these consolidated financial statements.
 

 
MYMETICS CORPORATION
CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS
 (UNAUDITED)
(In Thousands of Euros, Except Per Share Data)
 
 
 
For The Three Months Ended
September 30,
 
 
For The Nine Months Ended
September 30,
 
 
 
2017
 
 
2016
 
 
2017
 
 
2016
 
Revenue
 
 
 
 
 
 
 
 
 
 
 
 
Research and development services
 E-- 
 E30 
 E202 
 E379 
Grants
  399 
  149 
  897 
  528 
 
  399 
  179 
  1,099 
  907 
Expenses
    
    
    
    
Research and development
  555 
  241 
  1,522 
  599 
General and administrative
  276 
  298 
  900 
  930 
Bank fee
  1 
  1 
  2 
  2 
Depreciation
  10 
  11 
  28 
  33 
Directors' fees
  5 
  5 
  15 
  15 
Foreign exchange and other
  (78)
  (20)
  (285)
  (62)
 
  769 
  536 
  2,182 
  1,517 
 
    
    
    
    
Operating loss
  (370)
  (357)
  (1,083)
  (610)
 
    
    
    
    
Interest expense
  647 
  642 
  1,942 
  1,926 
Loss before income tax (provision) benefit
  (1,017)
  (999)
  (3,025)
  (2,536)
 
    
    
    
    
Income tax (provision) benefit
  (3)
  (4)
  (6)
  16 
Net loss
  (1,020)
  (1,003)
  (3,031)
  (2,520)
 
    
    
    
    
Other comprehensive loss
    
    
    
    
Foreign currency translation adjustment
  (9)
  -- 
  (18)
  (4)
Comprehensive loss
 E(1,029)
 E(1,003)
 E(3,049)
 E(2,524)
 
    
    
    
    
 
    
    
    
    
Basic earnings per share
 E(0.00)
 E(0.00)
 E(0.01)
 E(0.01)
Diluted earnings per share
 E(0.00)
 E(0.00)
 E(0.01)
 E(0.01)
 
 
For The Three Months Ended
 
 
For The Three Months Ended
 
 
 
March 31,
2019
 
 
March 31,
2018
 
Revenue
 
 
 
 
 
 
Research and Development services
 E-- 
 E-- 
Grants revenue
  -- 
  297 
 
  -- 
  297 
Expenses
    
    
Research and development
  215 
  308 
General and administrative
  278 
  277 
Bank fees
  1 
  -- 
Depreciation
  5 
  8 
Directors' fees
  5 
  5 
Foreign exchange (gain) loss
  55 
  (65)
 
  559 
  533 
Operating Loss
  (559)
  (236)
 
    
    
Interest expense
  666 
  653 
Loss before income tax provision
  (1,225)
  (889)
 
    
    
  Income tax provision
  (3)
  (9)
Net Loss
  (1,228)
  (898)
 
    
    
Other comprehensive income (loss)
    
    
Foreign currency translation adjustment
  5 
  (1)
Comprehensive loss
 E(1,223)
 E(899)
 
    
    
Basic and diluted earnings per share
 E(0.00)
 E(0.00)
 
The accompanying notes are an integral part of these consolidated financial statements.


MYMETICS CORPORATION
CONSOLIDATED STATEMENTS OF CHANGES IN SHAREHOLDERS' EQUITY (DEFICIT)
 (UNAUDITED)
 (In Thousands of Euros)
 
 
Three-month Period Ended March 31, 2018
 
 
 
Common Stock
 
 
Additional Paid in Capital
 
 
Accumulated Deficit
 
 
Accumulated Other Comprehensive Income
 
 
Total
 
January 1, 2018
 E2,530 
 E34,428 
 E(80,503)
 E667 
 E(42,878)
Stock compensation expense
    
  6 
    
    
  6 
Net loss
    
    
  (898)
    
  (898)
Other comprehensive loss:
    
    
    
    
    
Translationadjustment
    
    
    
  (1)
  (1)
March 31, 2018
 E2,530 
 E34,434 
 E(81,401)
 E666 
 E(43,771)
 
 
Three-month Period Ended March 31, 2019
 
 
 
Common Stock
 
 
Additional Paid in Capital
 
 
Accumulated Deficit
 
 
Accumulated Other Comprehensive Income
 
 
Total
 
January 1, 2019
 E2,530 
 E34,441 
 E(84,675)
 E679 
 E(47,025)
Stock compensation expense
    
  2 
    
    
  2 
Net loss
    
    
  (1,228)
    
  (1,228)
Other comprehensive loss:
    
    
    
    
    
Translationadjustment
    
    
    
  5 
  5 
March 31, 2019
 E2,530 
 E34,443 
 E(85,903)
 E684 
 E(48,246)
The accompanying notes are an integral part of these consolidated financial statements.
 


MYMETICS CORPORATION
CONSOLIDATED STATEMENTS OF CASH FLOWS
(UNAUDITED)
(In Thousands of Euros)
 
 
For The Nine Months Ended
September 30,
 
 
For The Three Months Ended
 
 
2017
 
 
2016
 
 
March 31,
2019
 
 
March 31,
2018
 
Cash Flow from Operating Activities
 
 
 
 
 
 
Net loss
 E(3,031)
 E(2,520)
Net Loss
 E(1,228)
 E(898)
Adjustments to reconcile net loss to net cash used in operating activities
    
    
Depreciation
  28 
  33 
  5 
  8 
Stock compensation expense – options
  31 
  63 
  2 
  6 
Changes in operating assets and liabilities
    
    
Receivables
  114 
  163 
  537 
  33 
Accrued interests on notes payable
  1,655 
  1,863 
  721 
  586 
Accounts payable
  (24)
  (341)
  (39)
  (166)
Deferred revenue from grants
  (432)
  (528)
  -- 
  (189)
Other
  -- 
  (3)
  (7)
  (14)
Net cash used in operating activities
  (1,659)
  (1,270)
  (9)
  (634)
    
    
Cash Flows from Investing Activities
    
Purchase of property and equipment
  (34)
  (3)
Net cash used in investing activities
  (34)
  (3)
    
Cash Flows from Financing Activities
    
Increase in notes payable
  1,150 
  -- 
Net cash provided by financing activities
  1,150 
  -- 
    
Effect of foreign exchange rate on cash
  (18)
  (4)
Effect on foreign exchange rate on cash
  5 
  (1)
Net change in cash
  (561)
  (1,277)
  (4)
  (635)
    
    
Cash, beginning of period
  1,391 
  2,381 
  479 
  1,180 
Cash, end of period
 E830
 
 E1,104
 
 E475 
 E545 
 
The accompanying notes are an integral part of these consolidated financial statements. 
 

MYMETICS CORPORATION
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
SEPTEMBER 30, 2017MARCH 31, 2019
(UNAUDITED)
 
Note 1. The Company and Summary of Significant Accounting Policies
 
BASIS OF PRESENTATION AND GOING CONCERN
 
The amounts in the notes are shown in thousands of EURO, unless otherwise noted, and rounded to the nearest thousand except for share and per share amounts.

The accompanying interim period consolidated financial statements of Mymetics Corporation (the "Company") set forth herein have been prepared by the Company pursuant to the rules and regulations of the U.S. Securities and Exchange Commission (the "SEC"). Certain information and footnote disclosure normally included in financial statements prepared in accordance with accounting principles generally accepted in the United States have been condensed or omitted pursuant to such SEC rules and regulations. The interim period consolidated financial statements should be read together with the audited financial statements and the accompanying notes included in the Company's latest annual report on Form 10-K for the fiscal year ended December 31, 2016.2018.
 
The accompanying financial statements of the Company are unaudited. However, in the opinion of the Company, the unaudited consolidated financial statements contained herein contain all adjustments necessary to present a fair statement of the results of the interim periods presented. All adjustments made during the nine-monththree-month period ending September 30, 2017March 31, 2019 were of a normal and recurring nature.
 
  The Company was created for the purpose of engaging in vaccine research and development. Its main research efforts in the beginning have been concentrated in the prevention and treatment of the AIDS virus and malaria. The Company has established a network which enables it to work with education centers, research centers, pharmaceutical laboratories and biotechnology companies. Besides the HIV and malaria vaccine candidates under development, the Company additionally has the following vaccines in its pipeline.pipeline; (i) Herpes Simplex which is at the preclinicalpre-clinical stage and currently on hold, (ii) an intra nasal influenza vaccinefor elderly which has finished a clinical trial Phase I, (iii) Respiratory Syncytial Virus (RSV) which is at the preclinicalpre-clinical stage and currently on hold and (iv) Chikungunya virus at the discovery stage.stage and currently on hold.
 
  As of September 30, 2017,March 31, 2019, the Company iswas engaged in the preclinicalpre-clinical testing of some of its vaccine candidates and a commercially viable product is not expected for several more years. However, the Company generated some revenue as of the prior quarter through a small research project with Sanofi for influenza vaccines and fromlicense, collaboration and grant agreementsagreements. The Company is working on several research projects with commercial partners for R&D services.immunotherapy in the fields of allergy and oncology. The allergy project is in collaboration with Anergis SA, for which the Company prepared virosome based vaccines which include Anergis peptides for treating birch pollen allergy. These formulations were tested in preclinical studies and compared to the Anergis earlier formulations. The success criteria were met and Anergis has now a time limited exclusive option to enter into a License and Collaboration Agreement (“LCA”) with Mymetics for the use of virosomes in the field of allergies that will require it to raise funds from third parties to pay Mymetics the license fee under the terms of the LCA and the clinical development, and there is no certainty that Anergis will be able to do so. The Company also finished the grant funded project in the field of HIV from the EU Horizon 2020 and Switzerland SERI which focused on developing thermostable and cold chain independent virosome based vaccines (MACIVIVA project). This project ended on November 3, 2018. Management believes that the Company’s research and development activities will result in valuable intellectual property that can generate significant revenues in the future such as bythrough licensing. Vaccines are one of the fastest growing markets in the pharmaceutical industry.
 
These consolidated financial statements have been prepared assuming the Company will continue as a going concern. The Company has experienced negative cash flows from operations and significant losses since inception resulting in an accumulated deficit of E79,422E85,903 at September 30, 2017.March 31, 2019. Further, the Company’s current liabilities exceed its current assets by E48,541E54,948 as of September 30, 2017,March 31, 2019, and there is no assurance that cash will become available to pay current liabilities in the near term. Management is seeking additional financing but there can be no assurance that management will be successful in any of those efforts. These conditions raise substantial doubt about the Company’sour ability to continue as a going concern.concern within one year from the issuance of the financial statements.

 
PRINCIPLES OF CONSOLIDATION
 
The consolidated financial statements include the accounts of the Company and its subsidiaries. Significant intercompany accounts and transactions have been eliminated.
NEW ACCOUNTING PRONOUNCEMENT
  In February 2016, the Financial Accounting Standards Board (FASB) issued Accounting Standards Update No. 2016-02, Leases: Topic 842 (ASU 2016-02), which replaces existing lease guidance. The new standard is intended to provide enhanced transparency and comparability by requiring lessees to record right-of-use (ROU) assets and corresponding lease liabilities on the balance sheet. The new standard initially required application with a modified retrospective approach to each prior reporting period presented with various optional practical expedients. In July 2018, this requirement was amended with the issuance of Accounting Standards Update No. 2018-11, Leases: Topic 842: Targeted Improvements (ASU 2018-11), which permits an additional (and optional) transition method to adopt the new leases standard.
  The Company adopted ASU 2016-02 and related ASUs, collectively ASC 842, on January 1, 2019 using the optional transition method. Consequently, periods before January 1, 2019 will continue to be reported in accordance with the prior accounting guidance, ASC 840, Leases.
  The Company elected the package of practical expedients, which permits the Company to retain prior conclusions about lease identification, lease classification and initial direct costs for leases that commenced before January 1, 2019. The new standard also provides practical expedients for an entity’s ongoing accounting. The Company elected the short-term lease recognition exemption for all leases that qualify. The Company also elected the practical expedient to combine lease and non-lease components for all of its leases. Adoption of ASC 842 did not affect the Company’s consolidated financial statements’ at January 1, 2019, as one of its leases is considered short-term and the other is not material to the consolidated financial statements.
 
FOREIGN CURRENCY TRANSLATION
 
The Company translates non-Euro assets and liabilities of its subsidiaries at the rate of exchange at the balance sheet date. Revenues and expenses are translated at the average rate of exchange throughout the period. Unrealized gains or losses from these translations are reported as a separate component of comprehensive loss.income. Transaction gains or losses are included in operatinggeneral and administrative expenses in the consolidated statements of comprehensive loss. The translation adjustments do not recognize the effect of income tax because the Company expects to reinvest the amounts indefinitely in operations. The Company's reporting currency is the Euro because substantially all of the Company's activities are conducted in Europe.
 

CASH
 
We consider all highly liquid investments purchased with maturities of three months or less to be cash equivalents. Cash deposits are occasionally in excess of insured amounts.
 
REVENUE RECOGNITION
 
  Exclusive LicensesUnder Topic 606, an entity recognizes revenue when its customer obtains control of promised goods or services, in an amount that reflects the consideration which the entity expects to receive in exchange for those goods or services. To determine revenue recognition for arrangements that an entity determines are within the scope of Topic 606, the entity performs the following five steps: (i) identify the contract(s) with a customer; (ii) identify the performance obligations in the contract; (iii) determine the transaction price; (iv) allocate the transaction price to the performance obligations in the contract; and (v) recognize revenue when (or as) the entity satisfies a performance obligation. We only apply the five-step model to contracts when it is probable that the entity will collect the consideration it is entitled to in exchange for the goods or services it transfers to the customer. At contract inception, once the contract is determined to be within the scope of Topic 606, we assess the goods or services promised within each contract and determine those that are performance obligations, and assess whether each promised good or service is distinct. We then recognize as revenue the amount of the transaction price that is allocated to the respective performance obligation when (or as) the performance obligation is satisfied.
 
The deliverables under an exclusive license agreement generally includeCompany has concluded that government grants are not within the exclusive licensescope of Topic 606, as they do not meet the definition of a contract with a “customer”. We concluded the definition of a contract with a “customer” was not met as the counterparty to the Company’s technology,government grants has not contracted to obtain goods or services and may also include deliverablesthus the contracts are not considered to have commercial substance. Government grants provide the Company with payments for certain types of expenditures related to research and development activities to be performed on behalf ofover a contractually defined period. Revenue from government grants is recognized in the collaborative collaborator andperiod during which the manufacture of preclinical or clinical materials forrelated costs are incurred, provided that the collaborative collaborator.applicable conditions under the government contracts have been met.
 
  Generally, exclusive license and or collaboration agreements contain nonrefundable terms for payments and, depending on the terms of the agreement, provide that the Company will (i) provide research services which are reimbursed at a contractually determined rate which includes margin for the Company, (ii) participate in a joint steering committee to monitor the progress of the research and development which will be reimbursed at a contractually determined rate which includes margin for the Company, (iii) earn payments upon the achievement of certain milestones and (iv) earn royalty payments at the time of commercialization until the later of expiration of the last to expire valid patent rights expire or 10 years after the first commercial sale. The Company may provide technical assistance and share any technology improvements with its collaborators during the term of the collaboration agreements. The Company does not directly control when any collaborator will request research or manufacturing services, achieve milestones or become liable for royalty payments. As a result, the Company cannot predict when it will recognize revenues in connection with any of the foregoing.
 
  The Company follows the provisions of the Financial Accounting Standards Board (FASB) Accounting Standards Codification (ASC) Topic 605-25, "Revenue Recognition—Multiple Element Arrangements," and ASC Topic 605-28, "Revenue Recognition—Milestone Method," in accounting for these agreements. In order to account for these agreements, the Company must identify the deliverables included within the agreement and evaluate which deliverables represent separate units of accounting based on if certain criteria are met, including whether the delivered element has standalone value to the collaborator. The consideration received is allocated among the separate units of accounting, and the applicable revenue recognition criteria are applied to each of the separate units. Factors considered in this determination include the research and manufacturing capabilities of the collaborator and the availability of technology research expertise in the general marketplace.
Fixed price contracts and research and collaboration agreements
  When the performance under a fixed price contract can be reasonably estimated, revenue for such a contract is recognized under the proportional performance method and earned in proportion to the contract costs incurred in performance of the work as compared to total estimated contract costs. Costs incurred under fixed price contracts represent a reasonable measurement of proportional performance of the work. Direct costs incurred under collaborative research and development agreements are recorded as research and development expenses. If the performance under a fixed price contract cannot be reasonably estimated, the Company recognizes the revenue on a straight-line basis over the contract term.
Grant Revenue - HORIZON 2020
 
  In April 2015, the Company was selected to receive project grants with a total of E8.4 million. A total of E5.3 million iswould be funded as part of Horizon 2020, the European Union research and innovation framework program and up to E3.1 million of funding willwould be provided by the Swiss State “Secretariat for Education, Research and Innovation” (SERI) for the Swiss based consortium partners. The grant fundsfunded the evaluation, development and manufacturing scale-up of thermo-stable and cold-chain independent nano-pharmaceutical virosome-based vaccine candidates. Of the total amount, E3.4E3.8 million iswas directly attributable to Mymetics’ activities, with the remaining balance going to the consortium partners.partners and has not been part of Mymetics financial statements. The project duration is 42 months and started on May 4, 2015.2015 and officially ended on November 3, 2018, after which a final report had been prepared, presented and submitted to the EU for a total costs declared of E8,262 for the total project and E3,673 for Mymetics.
  The amounts mentioned in the following statements are purely related to Mymetics and not to the other partners in the project: The Company received a pre-payment from the two granting organizations for a total value of E1.5 millionE1,554 in May 2015, a second tranche of E917 from the EU was received in December 2016, and E614 from “SERI” was received in April 2017, which will bewas used to finance the next reporting covering the period of November 2016 to October 2017. ThereafterIn November 2017, the Company submitted the second report and a new funding request, which resulted in another tranche of funding from the EU will beof E77 received in February 2018. This brought the total funding received at December 31, 2018 to E3,162, which accumulated with earlier tranches, cannot exceed 90%represented 82% of the agreed budget.awarded grant contribution. On December 21, 2018, the final report was submitted to the EU with a total cost incurred by the Company of E3,673, which represented 96% of the maximum grant. The pre-payments havereport has been recorded asaudited and validated by the EU and SERI for a current liabilitytotal eligible cost of E3,368. As a result, the Company received a final amount of E164 by the EU in deferred revenueFebruary 2019 and E342 by SERI in March 2019.No revenue has been recognized as services are delivered.

SANOFI PASTEUR BIOLOGICS
  On December 1, 2016, Mymetics Corporation entered into a material definitive Research Agreement with Sanofi Pasteur Biologics, LLC,related to this grant during the vaccine division of Sanofi (SNY). The project will investigate the immunogenicity of influenza vaccines based on the Company’s proprietary virosome technology platform in preclinical settings. If this project is successful it could result in a further and more extensive collaboration between the two companies. The project duration is six to twelve months and started in January 2017. The revenue is recognized upon delivery of the contractual material.period ended March 31, 2019.
 
RECEIVABLES
 
Receivables are stated at their outstanding principal balances. Management reviews the collectability of receivables on a periodic basis and determines the appropriate amount of any allowance. There was no allowance necessary at September 30, 2017March 31, 2019 or December 31, 2016.2018. The Company chargeswrites off receivables to the allowance when management determines that a receivable is not collectible. The Company may retain a security interest in the products sold.
 
PROPERTY AND EQUIPMENT
 
Property and equipment is recorded at cost and is depreciated over its estimated useful life on straight-line basis from the date placed in service. Estimated useful lives are usually taken as three years.
 
IMPAIRMENT OF LONG LIVED ASSETS
 
Long-lived assets, which include property and equipment, are assessed for impairment whenever events or changes in circumstances indicate the carrying amount of the asset may not be recoverable. The impairment testing involves comparing the carrying amount to the forecasted undiscounted future cash flows generated by that asset. In the event the carrying value of the assets exceeds the undiscounted future cash flows generated by that asset and the carrying value is not considered recoverable, impairment exists. An impairment loss is measured as the excess of the asset’s carrying value over its fair value, calculated using a discounted future cash flow method. An impairment loss would be recognized in net income (loss) in the period that the impairment occurs.
 
GOODWILL
 
  Goodwill represents the excess of purchase price over the value assigned to the net tangible and identifiable intangible assets of a business acquired. The Company typically performs its annual goodwill impairment test effective as of April 1 of each year, unless events or circumstances indicate impairment may have occurred before that time. The Company assesses qualitative factors to determine whether it is more likely than not that the fair value of the reporting unit is less than its carrying amount. After assessing qualitative factors, the Company determined that no further testing was necessary. If further testing was necessary, the Company would determine the fair value of each reporting unit, and compare the fair value to the reporting unit'sunit’s carrying amount. An impairment loss would be recognized for the excess of aThe Company has one reporting unit's carrying amount over its fair value. As of September 30, 2017, management believes there are no indications of impairment.unit.
 
RESEARCH AND DEVELOPMENT
 
Research and development costs are expensed as incurred.

 
TAXES ON INCOME
 
The Company accounts for income taxes under an asset and liability approach that requires the recognition of deferred tax assets and liabilities for expected future tax consequences of events that have been recognized in the Company's financial statements or tax returns. In estimating future tax consequences, the Company generally considers all expected future events other than enactments of changes in the tax laws or rates.
 
The Company reports a liability, if any, for unrecognized tax benefits resulting from uncertain income tax positions taken or expected to be taken in an income tax return. Estimated interest and penalties, if any, are recorded as a component of interest expense and other expense, respectively.
 

The Company has not recorded any liabilities for uncertain tax positions or any related interest and penalties at September 30, 2017March 31, 2019 or December 31, 2016.2018. The Company’s United States tax returns are open to audit for the years ended December 31, 20142015 to 2016.2018. The returns for the Swiss subsidiary, Mymetics S.A., are open to audit for the yearsyear ended December 31, 2010 to 2016.2018. The returns for the Netherlands subsidiaries, Bestewil B.V. and Mymetics B.V., are open to audit for the year ended December 31, 2016.2018.
 
EARNINGS PER SHARE
 
  Basic earnings per share is computed by dividing net income or loss attributable to common shareholders by the weighted average number of common shares outstanding in the period. Diluted earnings per share takes into consideration common shares outstanding (computed under basic earnings per share) and potentially dilutive securities. For the periodsquarters ended September 30, 2017March 31, 2019 and 2016,2018, options and convertible debt were not included in the computation of diluted earnings per share because their effect would be anti-dilutive due to net losses incurred under the treasury stock method.
 
  For the three and nine months ended September 30, 2017, the basic weighted and diluted average number of shares was 303,757,622. The total potential number of shares issuable of 614,033,846 at September 30, 2017 includes 584,933,846 potential issuable shares related to convertible loans, and 29,100,000 potential issuable shares related to outstanding stock options granted to employees.
For the three months ended September 30, 2016,March 31, 2019, the basic weighted average number of shares was 303,757,622. The total potential number of shares issuable of 577,568,516668,933,362 at September 30, 2016March 31, 2019 includes 548,334,168639,833,362 potential issuable shares related to convertible loans and 29,234,34829,100,000 potential issuable shares related to outstanding stocknot expired options granted to employees.
 
For the ninethree months ended September 30, 2016,March 31, 2018, the basic weighted average number of shares was 303,757,622. The total potential number of shares issuable of 577,580,317632,333,684 at September 30, 2016March 31, 2018 includes 548,334,168603,233,684 potential issuable shares related to convertible loans and 29,246,14929,100,000 potential issuable shares related to outstanding stocknot expired options granted to employees.
 
PREFERRED STOCK
 
The Company has authorized 5,000,000 shares of preferred stock that may be issued in several series with varying dividend, conversion and voting rights. No preferred shares are issued or outstanding at September 30, 2017March 31, 2019 or December 31, 2016.2018.
 
STOCK-BASED COMPENSATION
 
  Compensation cost for all share-based payments is based on the estimated grant-date fair value. The Company amortizes stock compensation cost ratably over the requisite service period.
 
The issuance of common shares for services is recorded at the quoted price of the shares on the date the shares are issued. No shares were issued to individuals as fee for services rendered in the ninethree months ended September 30, 2017March 31, 2019 nor in the ninethree months ended September 30, 2016.March 31, 2018.
 
During the three month periods ended September 30, 2017 and 2016, stock compensation expense amounted to E13 and E18, respectively. Stock compensation expense amounted to E31E2 and E63E6 during the nine monththree months periods ended September 30, 2017March 31, 2019 and 2016,2018, respectively, and is included in the consolidated statements of comprehensive loss within general and administrative expenses.

 
ESTIMATES
 
The preparation of financial statements in conformity with United States generally accepted accounting principles requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates.
 
FAIR VALUE MEASUREMENTS
 
Fair value guidance establishes a three-tier fair value hierarchy, which prioritizes the inputs used in measuring fair value. These tiers include:
 
Level 1-
Quoted prices in active markets for identical assets or liabilities.
Level 2-
Inputs other than Level 1 that are observable, either directly or indirectly, such as quoted prices for similar assets or liabilities; quoted prices in markets that are not active; or other inputs that are observable or can be corroborated by observable market data for substantially the full term of the assets or liabilities.
Level 3-
Unobservable inputs that are supported by little or no market activity and that are significant to the fair value of the assets or liabilities.

 
FAIR VALUES OF FINANCIAL INSTRUMENTS
 
The Company generally has the following financial instruments: cash, receivables, accounts payable, and notes payable. The carrying value of cash, receivables and accounts payable, approximates their fair value based on the short-term nature of these financial instruments. Management believes that it is not practicable to estimate the fair value of the notes payable due to conversion features and the unique nature of these instruments.
 
CONCENTRATIONS
 
  The Company derived 100% and 83% of grant revenue from its relationship with one collaborative partner duringfor the three month periodsperiod ended September 30, 2017 and September 30, 2016, respectively, and 82% and 57% with the same collaborative partner during the nine month periods ended September 30, 2017 and September 30, 2016, respectively.March 31, 2018 from one partner.
 
RELATED PARTY TRANSACTIONS
 
Mr. Ernest M. Stern, the Company’s outside U.S. counsel, is both a director of the Company and wasis a partner in Akerman LLP,Culhane Meadows PLLC, the firm retained as legal counsel by the Company. Mr. Stern resigned from the firm Akerman LLP and became a partner in the law firm of Culhane Meadows PLLC as of March 1, 2017. Culhane Meadows PLLC is the Company’s legal counsel effective March 1, 2017. The Company incurred professional fees to the counsel's law firmsfirm totaling E31E8 and E51E6 for the ninethree months ended September 30, 2017March 31, 2019 and 2016,2018, respectively.
 
Two of the Company’s major shareholders have granted secured convertible notes and short term convertible notes and promissory notes, which have a total carrying amount of E48,276,E55,085, including interest due to date. Conversion prices on the Euro-denominated convertible debt have been fixed to a fixed Euro/US dollar exchange rate.
NEW ACCOUNTING PRONOUNCEMENTS
  On May 28, 2014, FASB issued ASU No. 2014-09, Revenue from Contracts with Customers, Topic 606, requiring an entity to recognize the amount of revenue to which it expects to be entitled for the transfer of promised goods or services to customers. The updated standard will replace most existing revenue recognition guidance in U.S. GAAP when it becomes effective and permits the use of either the retrospective or cumulative effect transition method. The updated standard becomes effective for us in the first quarter of fiscal 2018. The Company is in the process of analyzing the impact adoption will have on our annual and interim financial statements. The Company will also be required to make additional disclosures under the new guidance. We continue to assess the impact on all areas of our revenue recognition, disclosure requirements, and changes that may be necessary to our internal controls over financial reporting.
  In January 2017, the FASB issued ASU 2017-04, Intangibles, Goodwill and Other, to supersede the current guidance by replacing the current two-step impairment test with a one-step impairment test. The guidance is effective for annual and interim goodwill impairment tests in fiscal years beginning after December 15, 2019. Early adoption is permitted for goodwill impairment tests performed after January 1, 2017. The Company elected early adoption as of January 1, 2017. Adoption of this standard did not have an impact on Company's consolidated financial statements.
 
Note 2. Debt Financing
 
Certain principal shareholders have granted the Company secured convertible notes (in accordance with the Uniform Commercial Code in the State of Delaware), short term convertible notes and other short term notes, which have a total carrying value of E48,276E55,479 including interest due to date. Interest incurred on these notes since inception has been added to the principal amounts.
 

   
The details of the convertible notes and loans are as follows at September 30, 2017:March 31, 2019:
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Fixed
 
 
 
 
 
 
 
 
 
 
Fixed
 
 
 
 
 
 
 
 
 
 
 
Conversion
 
 
Rate
 
 
 
 
 
 
 
Conversion
 
 
Rate
 
Lender
 
1st-Issue
 
Principal
 
 
Duration
 
Interest
 
Price
 
 
EUR/USD
 
1st-Issue
 
Principal
 
 
Duration
 
Interest
 
Price
 
 
EUR/USD
 
Price
 
Date
 
Amount
 
 
(Note)
 
Rate
 
(stated)
 
 
Conversion
 
 
Date
 
 
Amount
 
 
(Note)
 
 
Rate
 
 
(stated)
 
 
Conversion
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Eardley Holding A.G. (1)
 
06/23/2006
  E 
  161 
  (2)
10% pa
 $0.10 
  N/A 
06/23/2006
 E169 
  (2)
10% pa
 $0.10 
  N/A 
Anglo Irish Bank S.A.(3)
 
10/21/2007
  E 
  500 
  (2)
10% pa
 $0.50 
  1.4090 
10/21/2007
 E500 
  (2)
10% pa
 $0.50 
  1.4090 
Round Enterprises Ltd.
 
12/10/2007
  E 
  1,500 
  (2)
10% pa
 $0.50 
  1.4429 
12/10/2007
 E1,500 
  (2)
10% pa
 $0.50 
  1.4429 
Round Enterprises Ltd.
 
01/22/2008
  E 
  1,500 
  (2)
10% pa
 $0.50 
  1.4629 
01/22/2008
 E1,500 
  (2)
10% pa
 $0.50 
  1.4629 
Round Enterprises Ltd.
 
04/25/2008
  E 
  2,000 
  (2)
10% pa
 $0.50 
  1.5889 
04/25/2008
 E2,000 
  (2)
10% pa
 $0.50 
  1.5889 
Round Enterprises Ltd.
 
06/30/2008
  E 
  1,500 
  (2)
10% pa
 $0.50 
  1.5380 
06/30/2008
 E1,500 
  (2)
10% pa
 $0.50 
  1.5380 
Round Enterprises Ltd.
 
11/18/2008
  E 
  1,200 
  (2)
10% pa
 $0.50 
  1.2650 
11/18/2008
 E1,200 
  (2)
10% pa
 $0.50 
  1.2650 
Round Enterprises Ltd.
 
02/09/2009
  E 
  1,500 
  (2)
10% pa
 $0.50 
  1.2940 
02/09/2009
 E1,500 
  (2)
10% pa
 $0.50 
  1.2940 
Round Enterprises Ltd.
 
06/15/2009
  E 
  5,500 
  (2,4)
10% pa
 $0.80 
  1.4045 
06/15/2009
 E5,500 
  (2,4)
10% pa
 $0.80 
  1.4045 
Eardley Holding A.G.
 
06/15/2009
  E 
  100 
  (2,4)
10% pa
 $0.80 
  1.4300 
06/15/2009
 E100 
  (2,4)
10% pa
 $0.80 
  1.4300 
Von Meyenburg
 
08/03/2009
  E 
  200 
  (2)
10% pa
 $0.80 
  1.4400 
08/03/2009
 E200 
  (2)
10% pa
 $0.80 
  1.4400 
Round Enterprises Ltd.
 
10/13/2009
  E 
  2,000 
  (2)
5% pa
 $0.25 
  1.4854 
10/13/2009
 E2,000 
  (2)
5% pa
 $0.25 
  1.4854 
Round Enterprises Ltd.
 
12/18/2009
  E 
  2,200 
  (2)
5% pa
 $0.25 
  1.4338 
12/18/2009
 E2,200 
  (2)
5% pa
 $0.25 
  1.4338 
Round Enterprises Ltd.
 
08/04/2011
  E 
  1,016 
  (5,6)
10% pa
 $0.034 
  N/A 
08/04/2011
 E1,070 
  (5,6)
10% pa
 $0.034 
  N/A 
Eardley Holding A.G.
 
08/04/2011
  E 
  254 
  (5,6)
10% pa
 $0.034 
  N/A 
08/04/2011
 E268 
  (5,6)
10% pa
 $0.034 
  N/A 
Round Enterprises Ltd.
 
11/08/2011
  E 
  400 
  (6)
10% pa
 $0.034 
  1.3787 
11/08/2011
 E400 
  (6)
10% pa
 $0.034 
  1.3787 
Eardley Holding A.G.
 
11/08/2011
  E 
  100 
  (6)
10% pa
 $0.034 
  1.3787 
11/08/2011
 E100 
  (6)
10% pa
 $0.034 
  1.3787 
Round Enterprises Ltd.
 
02/10/2012
  E 
  1,000 
  (6)
10% pa
 $0.034 
  1.3260 
02/10/2012
 E1,000 
  (6)
10% pa
 $0.034 
  1.3260 
Eardley Holding A.G.
 
02/14/2012
  E 
  200 
  (6)
10% pa
 $0.034 
  1.3260 
02/14/2012
 E200 
  (6)
10% pa
 $0.034 
  1.3260 
Round Enterprises Ltd.
 
04/19/2012
  E 
  322 
  (6)
10% pa
 $0.034 
  1.3100 
04/19/2012
 E322 
  (6)
10% pa
 $0.034 
  1.3100 
Eardley Holding A.G.
 
04/19/2012
  E 
  80 
  (6)
10% pa
 $0.034 
  1.3100 
04/19/2012
 E80 
  (6)
10% pa
 $0.034 
  1.3100 
Round Enterprises Ltd.
 
05/04/2012
  E 
  480 
  (6)
10% pa
 $0.034 
  1.3152 
05/04/2012
 E480 
  (6)
10% pa
 $0.034 
  1.3152 
Eardley Holding A.G.
 
05/04/2012
  E 
  120 
  (6)
10% pa
 $0.034 
  1.3152 
05/04/2012
 E120 
  (6)
10% pa
 $0.034 
  1.3152 
Round Enterprises Ltd.
 
09/03/2012
  E 
  200 
  (6)
10% pa
 $0.034 
  1.2576 
09/03/2012
 E200 
  (6)
10% pa
 $0.034 
  1.2576 
Eardley Holding A.G.
 
09/03/2012
  E 
  50 
  (6)
10% pa
 $0.034 
  1.2576 
09/03/2012
 E50 
  (6)
10% pa
 $0.034 
  1.2576 
Round Enterprises Ltd.
 
11/14/2012
  E 
  500 
  (6)
10% pa
 $0.034 
  1.2718 
11/14/2012
 E500 
  (6)
10% pa
 $0.034 
  1.2718 
Eardley Holding A.G.
 
12/06/2012
  E 
  125 
  (6)
10% pa
 $0.034 
  1.3070 
12/06/2012
 E125 
  (6)
10% pa
 $0.034 
  1.3070 
Round Enterprises Ltd.
 
01/16/2013
  E 
  240 
  (6)
10% pa
 $0.034 
  1.3318 
01/16/2013
 E240 
  (6)
10% pa
 $0.034 
  1.3318 
Eardley Holding A.G.
 
01/16/2013
  E 
  60 
  (6)
10% pa
 $0.034 
  1.3318 
01/16/2013
 E60 
  (6)
10% pa
 $0.034 
  1.3318 
Round Enterprises Ltd.
 
03/25/2013
  E 
  400 
  (6)
10% pa
 $0.037 
  1.2915 
03/25/2013
 E400 
  (6)
10% pa
 $0.037 
  1.2915 
Eardley Holding A.G.
 
04/14/2013
  E 
  150 
  (6)
10% pa
 $0.034 
  1.3056 
04/14/2013
 E150 
  (6)
10% pa
 $0.034 
  1.3056 
Round Enterprises Ltd.
 
04/14/2013
  E 
  600 
  (6)
10% pa
 $0.034 
  1.3056 
04/14/2013
 E600 
  (6)
10% pa
 $0.034 
  1.3056 
Eardley Holding A.G.
 
05/15/2013
  E 
  170 
  (6)
10% pa
 $0.037 
  1.2938 
05/15/2013
 E170 
  (6)
10% pa
 $0.037 
  1.2938 
Round Enterprises Ltd.
 
05/15/2013
  E 
  680 
  (6)
10% pa
 $0.037 
  1.2938 
05/15/2013
 E680 
  (6)
10% pa
 $0.037 
  1.2938 
Eardley Holding A.G.
 
06/24/2013
  E 
  60 
  (6)
10% pa
 $0.025 
  1.3340 
06/24/2013
 E60 
  (6)
10% pa
 $0.025 
  1.3340 
Round Enterprises Ltd.
 
06/24/2013
  E 
  240 
  (6)
10% pa
 $0.025 
  1.3340 
06/24/2013
 E240 
  (6)
10% pa
 $0.025 
  1.3340 
Eardley Holding A.G.
 
08/05/2013
  E 
  80 
  (6)
10% pa
 $0.018 
  1.3283 
08/05/2013
 E80 
  (6)
10% pa
 $0.018 
  1.3283 
Round Enterprises Ltd.
 
08/05/2013
  E 
  320 
  (6)
10% pa
 $0.018 
  1.3283 
08/05/2013
 E320 
  (6)
10% pa
 $0.018 
  1.3283 
Eardley Holding A.G.
 
03/01/2017
  E 
  230 
  (7)
2.5% pa
  N/A 
03/01/2017
 E230 
  (2)
2.5% pa
  N/A 
Round Enterprises Ltd.
 
03/01/2017
  E 
  920 
  (7)
2.5% pa
  N/A 
03/01/2017
 E920 
  (2)
2.5% pa
  N/A 
Eardley Holding A.G.10/18/2017
 E230 
  (2)
2.5% pa
  N/A 
Round Enterprises Ltd.10/18/2017
 E920 
  (2)
2.5% pa
  N/A 
Eardley Holding A.G.06/01/2018
 E160 
  (7)
2.5% pa
  N/A 
Round Enterprises Ltd.06/01/2018
 E640 
  (7)
2.5% pa
  N/A 
Eardley Holding A.G.11/10/2018
 E160 
  (7)
2.5% pa
  N/A 
Round Enterprises Ltd.11/10/2018
 E640 
  (7)
2.5% pa
  N/A 
Total Short Term Principal Amounts
 
 
  E 
  28,858 
    
 
    
 
 E31,684 
    
 
    
Accrued Interest
 
 
  E 
  19,781 
    
 
    
 
 E23,795 
    
 
    
 
    
    
    
 
    
    
 
    
TOTAL LOANS AND NOTES
 
 
  E 
  48,639 
    
 
    
 
 E55,479 
    
 
    

 
(1) Private investment company of Dr. Thomas Staehelin, member of the Board of Directors and of the Audit Committee of the Company. Face value is stated in U.S. dollars at $190.
 
(2) This maturity date is automatically prolonged for periods of three months, unless called for repayment.
 
(3) Renamed Hyposwiss Private Bank Genève S.A. and acting on behalf of Round Enterprises Ltd. which is a major shareholder.
 

(4) The loan is secured against 2/3rds of the IP assets of Bestewil Holding BV and against all property of the Company.
 
(5) The face values of the loans are stated in U.S. dollars at $1,200 and $300, respectively.
 
(6) This maturity date is automatically prolonged for periods of three months, unless called for repayment. The conversion price per
   share is determined by the lower of (i) reducing by 10% the price per share of the Company’s common stock paid by the investors
   in connection with an investment in the Company of not less than US$20,000, or (ii) at the stated conversion price using a fixed
   exchange rate which are noted in the table above.
 
(7) On MarchJune 1, 2017,2018, Round Enterprises Ltd. and Eardley Holding AG each provided two promissory Notes for a total of E1,840E1,280 and E460,E320 in two tranches, respectively, with a 2.5% interest per annum and a maturity date of February 28, 2018.annum. The first 50%tranche of the promissory Notesof E920E640 and E230,E160, respectively, were provided immediately.The second 50%tranche of the promissory notes of E920E640 and E230,E160, respectively, were provided on October 18, 2017.November 10, 2018 with a 2.5% interest per annum. The maturity date of these promissory notes to follow the same principle of other convertible loans and is the later of (i) June 30, 2019, or (ii) the end of a subsequent calendar quarter in which the Company receives a written request from the lender for repayment of the unpaid principal and accrued interest due under the Notes.
 
Note 3. Subsequent Events
 
On October 18, 2017, Eardley Holding AGApril 29, 2019, Mymetics announced that the National Institutes of Health (NIH) has awarded Mymetics and Round Enterprises Ltd. executedTexas Biomedical Research Institute (Texas Biomed) a five-year grant for the second set of promissory notesproject called “Cold Chain-independent, Needle-free Mucosal Virosomal Vaccine to Prevent HIV-1 Acquisition at Mucosal Levels”.
The project starts on May 1, 2019 and is planned for a total of E1,150. These notes havefive years. The overall budget related to the same terms and conditions asproject is USD 8.67 million, with USD 1.9 million approved for the first setyear. The overall portion of promissory notes issued on March 1, 2017,the grant allocated to the Company is USD 6.76 million, with an interestUSD 1.2 million approved for the first year. It is co-led by Dr. Ruprecht of 2.5% per annumthe Texas Biomedical Research Institute and a maturity dateDr. Fleury, Mymetics CSO, and includes sub-awards to Dr. François Villinger of October 18, 2018.the University of Louisiana at Lafayette, and Dr. Sarah Ratcliffe of the University of Virginia. First results are expected to be reported in 2020.
 
  On October 20, 2017,The project has the Company entered into an Amendmentobjective to prepare Mymetics’ promising HIV-1 vaccine candidate for clinical trials. The vaccine is created to induce protective mucosal antibodies acting as a frontline defense against sexual HIV transmission. This newly awarded grant from the NIH can continue some of the Research Agreement dated December 1, 2016 with Sanofi Pasteur Biologics, LLC, the vaccine division of Sanofi SA, (“Sanofi”), to extend the date of the Research Agreement for an additional year. Under the terms of the Research Agreement Sanofi wanted to compare the immunogenicity of Mymetics’ influenza virosomes compared to Sanofi Pasteur’s egg-based split vaccine. The interest of Sanofi in a collaboration with Mymetics was based on the results of preclinical and clinical studies a few years ago with Solvay Pharmaceuticals that was acquired by Abbott in 2013. The initial results of the recent study did not achieve the expected benefits of Mymetics’ influenza virosomes and were contrary to earlier results Mymetics obtained with Solvay in multiple studies. Mymetics believes that there was an issue with the influenza virosome formulationsdevelopments that were produced. Mymetics has agreed to payachieved during the European Horizon 2020 project.
Note 4. Leases
The facility lease agreement for Epalinges, Switzerland, is automatically renewed month by month with a redesigned study, which Mymetics believes will be approximately US$125,000.-. Following the new studynotice period of three months. The related rent is paid monthly in the coming months, Mymetics will reviewamount of E4 and is considered a short-term lease. The facility lease agreement for Leiden, The Netherlands, runs until March 31, 2020 and can be terminated with a six months' notice period. The related rent is paid monthly in the outcomes with Sanofiamount of E9. This lease is not considered short-term, however, the effect of recording the right to use asset and determine next steps.related liability are not material to the consolidated financial statements. The Company doesn't have any other operating lease for its research and development facilities, corporate headquarter, offices and equipment.
 

 
ITEM 2.
MANAGEMENT'S DISCUSSION AND ANALYSIS OF FINANCIAL CONDITION AND RESULTS OF OPERATIONS
 
GENERAL
 
The following discussion and analysis of the results of operations and financial condition of Mymetics Corporation for the periods ended September 30, 2017March 31, 2019 and 20162018 should be read in conjunction with the Company's audited consolidated financial statements for the year ended December 31, 20162018 and related notes and the description of the Company's business and properties included elsewhere herein.
 
This report contains forward-looking statements that involve risks and uncertainties. The statements contained in this report are not purely historical but are forward-looking statements within the meaning of Section 21E of the Securities Exchange Act of 1934, as amended, and Section 27A of the Securities Act of 1933, as amended. These forward looking statements concern matters that involve risks and uncertainties that could cause actual results to differ materially from those projected in the forward-looking statements. Words such as "may," "will," "should," "could," "expect," "plan," "anticipate," "believe," "estimate," "predict," "potential," "continue", "probably" or similar words are intended to identify forward looking statements, although not all forward looking statements contain these words.
 
Although we believe that the expectations reflected in the forward-looking statements are reasonable, we cannot guarantee future results, levels of activity performance or achievements. Moreover, neither we nor any other person assumes responsibility for the accuracy and completeness of the forward-looking statements. We are under no duty to update any of the forward-looking statements after the date hereof to conform such statements to actual results or to changes in our expectations.
 
Readers are urged to carefully review and consider the various disclosures made by us which attempt to advise interested parties of the factors which affect our business, including without limitation disclosures made under the captions "Management Discussion and Analysis of Financial Condition and Results of Operations," "Risk Factors," "Consolidated Financial Statements" and "Notes to Consolidated Financial Statements" included in our annual report on Form 10-K for the year ended December 31, 20162018 and, to the extent included therein, our quarterly reports on Form 10-Q filed during fiscal year 2017.2018.
 
THREE MONTHS ENDED SEPTEMBER 30, 2017MARCH 31, 2019 AND 20162018
 
For the three months ended March 31, 2019, no revenue was earned. Revenue was E399 and E179E297 for the three months ended September 30, 2017 and 2016, respectively,March 31, 2018, mainly related to the revenue recognized for the work performed under the Horizon 2020 grants.
 
Costs and expenses increased to E769E559 for the three months ended September 30, 2017March 31, 2019 from E536 (43.5%E533 (+4.8%) for the three months ended September 30, 2016,March 31, 2018. While R&D expenses were lower as the Maciviva project ended, there was an increase mainly due to the subcontracting services related toforeign exchange loss from the Horizon 2020 project with acronym “Maciviva” (Manufacturing process for Cold-chain Independent Virosome-based Vaccines) incurred during the three months ended September 30, 2017.revaluation of shareholders’ loans based in US$.
 
Research and development expenses increaseddecreased to E555E215 in the current period from E241 (130.3%E308 (-30.2%) in the comparative period of 2016,2018, mainly due to theE85 of subcontracting services related to the project with acronym “Maciviva”paid during the three month period ending September 30, 2017.March 2018 in relation with the Horizon 2020 Maciviva project. During the three months ended March 31, 2019, no R&D expenses have been incurred related to the Horizon 2020 Maciviva project as the projected ended in November 2018.
 
General and administrative expenses decreased to E276of E278 in the three months ended September 30, 2017 from E298 (-7.4%)March 31, 2019 are comparable with E277 incurred in the comparative period of 2016.2018.
Foreign exchange (gain) loss increased to E55 for the three months ended March 31, 2019 from (E65) (+184.6%) for the three months ended March 31, 2018, mainly due to the foreign exchange revaluation impact of shareholders’ loans based in US$.
Interest expense increased to E666 for the three months ended March 31, 2019 from E653 for the three months ended March 31, 2018 related to existing loans from third party investors.
 
The Company reported a net loss of (E1,020)(E1,228), or (E0.00) per share, for the three months ended September 30, 2017,March 31, 2019, compared to a net loss of (E1,003)(E898), or (E0.00) per share, for the three months ended September 30, 2016.
NINE MONTHS ENDED SEPTEMBER 30, 2017 AND 2016
Revenue was E1,099 and E907 for the nine months ended September 30, 2017 and 2016, respectively. The increase was mainly related to the revenue recognition of the GMP production related to the Maciviva project.
Costs and expenses increased to E2,182 for the nine months ended September 30, 2017 from E1,517 (43.8%) for the nine months ended September 30, 2016, mainly due to the reversal of aged R&D cost accrual of E154 during the nine months ended September 30, 2016 and to the subcontracting services related to the project with acronym “Maciviva” during the nine month period ending September 30, 2017.March 31, 2018.
 

Research and development expenses increased to E1,522 in the current period from E599 (154.1%) in the comparative period of 2016, mainly due to the reversal of aged R&D cost accrual of E154 during the nine months ended September 2016, and subcontracting cost paid to vendor for Good Manufacturing Production launched during the nine months ended September 30, 2017.
General and administrative expenses decreased to E900 in the nine months ended September 30, 2017 from E930 (-3.2%) in the comparative period of 2016.
Foreign exchange revaluation generated a net gain of E285 during the nine months ended September 30, 2017 and a net gain of E62 during the nine months ended September 30, 2016, which is mainly due to the revaluation of existing US$ based loans from related parties.
The Company reported a net loss of (E3,031), or (E0.01) per share, for the nine months ended September 30, 2017, compared to a net loss of (E2,520), or (E0.01) per share, for the nine months ended September 30, 2016.
 
LIQUIDITY AND CAPITAL RESOURCES
 
We had cash of E830E475 at September 30, 2017March 31, 2019 compared to E1,391E479 at December 31, 2016.2018.
 
  Our first significantDuring 2018 our revenue washas been generated through the exclusive negotiation fee recorded in September 9, 2013 and the license and collaboration agreement for our RSV vaccine signed on December 27, 2013. As consideration Mymetics received an irrevocable and non-refundable upfront fee for the license of USD 5 million at the beginning of 2014 and fixed monthly collaboration and R&D fees. This license and collaboration agreement ended in 2016. For 2017, we recognized a small amount of revenue related to the Research Agreement with Sanofi Pasteur Biologics, to investigate the immunogenicity of influenza vaccines based on Mymetics’ proprietary virosome technology platform in preclinical settings and anticipate revenue related to the Horizon 2020 project. Newproject, which has now come to an end. For 2019, new significant revenues iswill not be expected, unless and until a second major licensing agreement or other commercial arrangement is entered into with respect to our technology.technology or new grant financings are awarded.
 
As of September 30, 2017,March 31, 2019, we had an accumulated deficit of approximately E79E86 million, and had net loss of E3,031E1,228 in the ninethree month period ending on that date. We expect to continue to incur net losses in the future for research, development and activities related to the future licensing of our technologies, and because of the accrual of interest payable on existing loans.
 
Net cash used infrom operating activities was E1,659E9 for the ninethree month period ended September 30, 2017March 31, 2019. During the three month period ending March 31, 2018 net cash used from operating activities was E634 mainly due to the subcontracting services paid to vendorsduring the three month period ending March 31, 2018 and final funding amount received during the three month period ending March 31, 2019, both related to the Maciviva project of E710. During the nine month period ended September 30, 2016 net cash used in operating activities was E1,270.project.
 
Net cash used infrom investing activities was (E34)NIL during the ninethree months ended September 30, 2017, related to the purchase of equipment for our laboratory in Leiden, compared to (E3) for the comparable period in 2016.March 31, 2019 and 2018.
 
FinancingNet cash provided from financing activities provided net cash of E1,150 for the nine months ended September 30, 2017, related to promissory notes from our main investors, andis NIL for the comparable periodthree months ended September 30, 2016.March 31, 2019 and 2018.
 
  Salaries and related payroll costs represent gross salaries for two executives, our CSO of Mymetics BV and seven employees. Under Executive Employment Agreements with our CEO and two CSOs, we pay our executive officers a combined amount of E65 per month.
 
  Our Swiss subsidiary, Mymetics S.A., has, besides the CEO and CSO, two additional employees on its payroll: Director of Finance and Head of Manufacturing and Quality. Mymetics BV has, besides the full time Chief Scientific Officer, three full-time technicians and one part-time assistant.
 
  We intend to continue to incur additional expenditures during the next sixnine months for additional research and development of our HIV, Influenza vaccines and Chikungunya vaccines,immunotherapy projects, which we will try to seek through collaborations with pharmaceutical companies or with not-for-profit organizations. These expenditures will relate to the continued research and testing of itsthese prototype vaccines and are included in the monthly cash outflow described above.
 
  In the past, we have financed our research and development activities primarily through debt and equity financings from various parties while the last three years our financing was generated partiallyand through a license and collaboration agreementagreements and grant agreementsagreements.
 
  We anticipate that our normal operations will require approximately E600 from existing capital resourcesE1,200 of cash in the year ending December 31, 2017. Additional promissory notes for a total of E1,150 from our main investors is received in October 2017.2019. We will seek to raise additionalthe required capital from equity or debt financings, and grants through donors and potential partnerships with major international pharmaceutical and biotechnology firms. However, there can be no assurance that we will be able to raise additional capital on satisfactory terms, or at all, to finance our operations. In the event that we are not able to obtain such additional capital, we will be required to further restrict or even cease our operations.

 
Monthly fixed and recurring expenses for "Property leases" of E13 represent the monthly lease and maintenance payments to unaffiliated third parties for our offices, of which E4 is related to our executive office located at Route de la Corniche 4, 1066 Epalinges in Switzerland (100 square meters), and E9 related to Bestewil Holding B.V. and its subsidiary Mymetics B.V operating from a similar biotechnology campus near Leiden in the Netherlands, where they occupy 120204 square meters.
 
Included in professional fees are legal fees paid to outside corporate counsel and audit and review fees paid to our independent accountants, and fees paid for investor relations.
 
Cumulative interest expense of E19,781E23,795 has been accrued on all of the Company’s outstanding notes and advances (see detailed table in Note 2 to the financial statements).
 

RECENT FINANCING ACTIVITIES
 
  During the ninethree month period ending September 30, 2017,March 31, 2019, our principal source of funds has been revenues related to the Horizon 2020 Maciviva project and the Research Agreement with Sanofi Pasteur Biologics and additionally promissory notes received in a prior quarter from our two main investors.investors and the final payment for the Maciviva project.
 
We have filed or are in the process of filing several new grant applications with U.S. and European institutions in relation to our virosome based vaccines.
 
  We anticipate using our current funds and those we receive in the future both to meet our working capital needs and for funding the ongoing vaccines pre-clinical research costs for new virosome vaccine.
 
  Management anticipates that our existing capital resources will be sufficient to fund our cash requirements through the next threefive months. We have cash presently on hand in conjunction with the collection of receivables, based upon our current levels of expenditures and anticipated needs during this period. For 2018,2019, we will need additional funding through future collaborative arrangements, licensing arrangements, and debt and equity financings under Regulation D and Regulation S under the Securities Act of 1933. We do not know whether additional financing will be available on commercially acceptable terms when needed.
 
  If management cannot raise funds on acceptable terms when needed, we may not be able to successfully commercialize our technologies, take advantage of future opportunities, or respond to unanticipated requirements. If unable to secure such additional financing when needed, we will have to curtail or suspend all or a portion of our business activities and could be required to cease operations entirely. Further, if new equity securities are issued, our shareholders may experience severe dilution of their ownership percentage.
 
  The extent and timing of our future capital requirements will depend primarily upon the rate of our progress in the research and development of our technologies, our ability to enter into a partnership agreement with a major pharmaceutical company, and the results of our present projects and future clinical trials.
 
OFF-BALANCE SHEET ARRANGEMENTS
 
None
 

 
ITEM 3.  ITEM 3.
QUANTITATIVE AND QUALITATIVE DISCLOSURES ABOUT MARKET RISK
 
INTEREST RATE RISK
 
Fluctuations in interest rates may affect the fair value of financial instruments. An increase in market interest rates may increase interest payments and a decrease in market interest rates may decrease interest payments of such financial instruments. We have no debt obligations which are sensitive to interest rate fluctuations as all our notes payable have fixed interest rates, as specified on the individual loan notes.
 
 
ITEMITEM 4.
CONTROLS AND PROCEDURES
 
EVALUATION OF DISCLOSURE CONTROLS AND PROCEDURES
 
We maintain disclosure controls and procedures that are designed to ensure that information required to be disclosed in our reports under the Exchange Act is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules and forms, and that such information is accumulated and communicated to management, as appropriate, to allow timely decisions regarding required disclosure. Our management, with the participation and supervision of our Chief Executive Officer and Chief Financial Officer, evaluated the effectiveness of our disclosure controls and procedures as of the end of the period covered by this report and determined that our disclosure controls and procedures were effective.
 
CHANGES IN INTERNAL CONTROL OVER FINANCIAL REPORTING
 
No changes of internal control over financial reporting were made in the ninethree months ended September 30, 2017.March 31, 2019.
 
INHERENT LIMITATIONS ON EFFECTIVENESS OF CONTROLS
 
Our management, Ronald Kempers, who is now both CEO and CFO, does not expect that our disclosure controls or our internal control over financial reporting will prevent or detect all error and all fraud. A control system, no matter how well designed and operated, can provide only reasonable, not absolute, assurance that the control system’s objectives will be met. The design of a control system must reflect the fact that there are resource constraints, and the benefits of controls must be considered relative to their costs. Further, because of the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that misstatements due to error or fraud will not occur or that all control issues and instances of fraud, if any, within the company have been detected.
 
These inherent limitations include the realities that judgments in decision-making can be faulty and that breakdowns can occur because of simple error or mistake. Controls can also be circumvented by the individual acts of some persons, by collusion of two or more people, or by management override of the controls. The design of any system of controls is based in part on certain assumptions about the likelihood of future events, and there can be no assurance that any design will succeed in achieving its stated goals under all potential future conditions. Projections of any evaluation of controls effectiveness to future periods are subject to risks. Over time, controls may become inadequate because of changes in conditions or deterioration in the degree of compliance with policies or procedures.
 

 
PARTPART II. 
OTHER INFORMATION
 
ITEMITEM 1.
LEGAL PROCEEDINGS
 
Neither we, nor our wholly owned subsidiaries Mymetics S.A., Bestewil Holding B.V. nor its subsidiary Mymetics B.V. are presently involved in any litigation incident to our business.
 
ITEMITEM 1A.
RISK FACTORS
 
Not Applicable
 
ITEMITEM 2.
UNREGISTERED SALES OF EQUITY SECURITIES AND USE OF PROCEEDS
 
None
 
ITEMITEM 3.
DEFAULTS UPON SENIOR SECURITIES
 
None.
 
ITEMITEM 4.
MINE SAFETY DISCLOSURES
 
None.
 
ITEMITEM 5.
OTHER INFORMATION
 
None.
 
ITEMITEM 6.
EXHIBITS
 
EXHIBIT NUMBER
DESCRIPTION
 
Rule 13a-14(a)/15d-14(a) Certification of Chief
 
Rule 13a-14(a)/15d-14(a) Certification of Chief Financial Officer
 
Section 1350 Certification of Chief Executive Officer and Chief Financial Officer
                 
101.INS 
Instance Document
 
101.SCH 
XBRL Taxonomy Extension Schema Document
 
101.CAL 
XBRL Taxonomy Extension Calculation Linkbase Document
 
101.LAB 
XBRL Taxonomy Extension Label Linkbase Document
 
101.PRE 
XBRL Taxonomy Extension Presentation Linkbase Document
 

 
SIGNATURES
 
Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
 
 MYMETICS CORPORATION 
    
Dated:  November 13, 2017May 15 2019By: /s/ Ronald Kempers 
  Chief Executive Officer / Chief Financial Officer 
    
 
 
 
 

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