UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, DC 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

 

Date of Report (Date of earliest event reported):  March 30, 2009

 

PHARMATHENE, INC.

(Exact name of registrant as specified in its charter)

 

Delaware

 

001-32587

 

20-2726770

(State or other jurisdiction
of incorporation)

 

(Commission
File Number)

 

(IRS Employer
Identification No.)

 

 

 

One Park Place, Suite 450, Annapolis, Maryland

 

21401

(Address of principal executive offices)

 

(Zip Code)

 

Registrant’s telephone number including area code: (410) 269-2600

 

 

(Former name or former address, if changed since last report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

o      Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

o      Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

o      Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

o      Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

 

 



 

Item 2.02

 

Results of Operations and Financial Condition.

 

On March 30, 2009, PharmAthene, Inc. issued a press release announcing its financial results for the fiscal year ended December 31, 2008.  A copy of the press release is furnished as Exhibit 99.1 to this report.

 

In accordance with General Instruction B.2. of Form 8-K, the information in this Current Report on Form 8-K, including Exhibit 99.1, shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, and shall not be incorporated by reference into any registration statement or other document filed under the Securities Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by specific reference in such filing.

 

Item 9.01

 

Financial Statements and Exhibits

 

(d) Exhibits

 

No.

 

Description

 

 

 

99.1

 

Press release, dated March 30, 2009, issued by PharmAthene, Inc.

 

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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 hereunto duly authorized.

 

 

 

 

PHARMATHENE, INC.
(Registrant)

 

 

 

 

Date: March 30, 2009

By:

/s/ David P. Wright

 

 

David P. Wright

 

 

President and Chief Executive Officer

 

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Exhibit 99.1

 

GRAPHIC

 

FOR IMMEDIATE RELEASE

 

Contact:

Stacey Jurchison

PharmAthene, Inc.

Phone: 410-269-2610

Stacey.Jurchison@PharmAthene.com

 

PHARMATHENE REPORTS YEAR END 2008 FINANCIAL RESULTS

 

ANNAPOLIS, MD — March 30, 2009 — PharmAthene, Inc. (NYSE Amex: PIP), a biodefense company developing medical countermeasures against biological and chemical threats, today reported operational and financial results for the year ended December 31, 2008.

 

For the years ended December 31, 2008 and 2007, the Company reported revenues of $32.9 million and $14.6 million, respectively.  Revenues for the full year 2008 consisted primarily of contract funding from the U.S. government for the development of the Company’s medical countermeasures, Protexia®, SparVax™ and RypVax™.  Revenues for the year ended December 31, 2008 increased by $11.9 million as a result of the Avecia vaccines acquisition in the second quarter of 2008, and particularly the acquired U.S. government contracts supporting the development of SparVax™, our third generation rPA anthrax vaccine candidate, and RypVax™.

 

Research and development expenses for the years ended December 31, 2008 and 2007 were $31.8 million and $16.6 million, respectively.  Expenses in 2008 resulted from research and development activities related to programs for Valortim® and Protexia® as well as from activities related to the SparVax™ and RypVax™ programs, which were acquired in the second quarter of 2008.   The increase in research and development expenses in 2008 is primarily due to programs acquired as a result of the Avecia acquisition, as well as process development, manufacturing and increased clinical activities during the year, partially offset by reduced internal resource costs.

 

General and administrative expenses for the years ended December 31, 2008 and 2007 were $19.4 million and $13.9 million, respectively.  General and administrative expenses increased as a result of additional employee costs due to the increase in headcount following the Avecia acquisition, as well as increased travel expenses, non-cash stock compensation expense, and legal and consulting expenses.

 

For the year ended December 31, 2008, the Company’s net loss attributable to common shareholders was $36.4 million or $1.59 per share, compared to net loss attributable to common shareholders of $17.7 million or $1.88 per share in the same period of 2007.

 



 

As of December 31, 2008, available cash, cash equivalents and short term investments totaled $22.9 million, excluding restricted cash totaling $13.3 million. In addition, on March 27, 2009, the Company closed on the public sale of an aggregate of 2,116,055 newly issued shares of its common stock at $2.60 per share and warrants to purchase an aggregate of 705,354 shares of its common stock at an exercise price of $3.00 per share, resulting in aggregate gross proceeds of approximately $5.5 million.

 

“The past year represented an important phase in the Company’s growth cycle, during which time we successfully executed on our milestones with the goal of transitioning from a product development company to one emphasizing procurement and delivery of next-generation medical countermeasures to the Strategic National Stockpile,” said David P. Wright, President and Chief Executive Officer of PharmAthene.

 

“Our acquisition of Avecia’s biodefense vaccines portfolio, completed in April 2008, created an expanded product portfolio that now includes five potential best-in-class, next generation product candidates, and important critical mass - - particularly with respect to our anthrax franchise,” continued Mr. Wright.

 

“We anticipate achieving important milestones in 2009 in each of these programs.  We expect our on-going Phase I clinical trial of Protexia® to be completed this year.  In addition, we also expect to commence a Phase I clinical trial of Valortim® in combination with antibiotics.  Notably, we should also hear whether SparVax™, our novel second generation recombinant protective antigen vaccine candidate, has been selected by the Biomedical Advanced Research and Development Authority (BARDA) to receive an advanced development and procurement contract,” said Mr. Wright.  In 2008 the Department of Health and Human Services issued a formal solicitation, to which PharmAthene responded, requesting advanced development and procurement of 25 million doses of a recombinant protective antigen vaccine for the Strategic National Stockpile.

 

Conference Call and Webcast Information

PharmAthene management will host a conference call to discuss the Company’s 2008 year-end results on March 30, 2009, at 4:30 p.m., E.T. The dial-in number for U.S. callers is 1-866-383-8003 and for international callers is 617-597-5330. The participant passcode is 25699583.

 

A replay of the conference call will be available for 30 days, beginning at approximately 7:30 p.m. E.T. on March 30, 2009 until approximately 11:59 p.m. E.T. April 30, 2009. The dial-in number for U.S. callers is 1-888-286-8010, and for international callers is 617-801-6888. The participant passcode is 35301584.

 

The webcast of the conference call can be accessed from the company’s website at http://www.pharmathene.com. A link to the webcast may be found on the Investor Relations section of the website.

 

About PharmAthene, Inc.

PharmAthene was formed to meet the critical needs of the United States and its allies by developing and commercializing medical countermeasures against biological and chemical weapons.  PharmAthene’s lead product development programs include:

 

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·                  SparVax - a second generation recombinant protective antigen (rPA) anthrax vaccine

·                  Valortim® - a fully human monoclonal antibody for the prevention and treatment of anthrax infection

·                  Protexia® - a novel bioscavenger for the prevention and treatment of morbidity and mortality associated with exposure to chemical nerve agents

·                  RypVax - a recombinant dual antigen vaccine for plague

·                  A third generation rPA anthrax vaccine.

 

For more information about PharmAthene, please visit www.PharmAthene.com.

 

Statement on Cautionary Factors

Except for the historical information presented herein, matters discussed may constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that are subject to certain risks and uncertainties that could cause actual results to differ materially from any future results, performance or achievements expressed or implied by such statements.  Statements that are not historical facts, including statements preceded by, followed by, or that include the words “potential”; “believe”; “anticipate”; “intend”; “plan”; “expect”; “estimate”; “could”; “may”; “should”; or similar statements are forward-looking statements.  PharmAthene disclaims, however, any intent or obligation to update these forward-looking statements.  Risks and uncertainties include risk associated with the reliability of the results of the studies relating to human safety and possible adverse effects resulting from the administration of the Company’s product candidates, unexpected funding delays and/or reductions or elimination of U.S. government funding for one or more of the Company’s development programs, including without limitation our bid related to SparVax™ under the Department of Health and Human Services  Request for Proposals for an Anthrax Recombinant Protective Antigen (rPA) Vaccine for the Strategic National Stockpile, the award of government contracts to our competitors, unforeseen safety issues, challenges related to the development, scale-up, and/or process validation of manufacturing processes for our product candidates, unexpected  determinations that these product candidates prove not to be effective and/or capable of being marketed as products, as well as risks detailed from time to time in PharmAthene’s Forms 10-K and 10-Q under the caption “Risk Factors” and in its other reports filed with the U.S. Securities and Exchange Commission (the “SEC”).

 

Copies of PharmAthene’s public disclosure filings are available from its investor relations department and our website under the investor relations tab at www.pharmathene.com.

 

Tables follow

 

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PHARMATHENE, INC.

 

CONSOLIDATED BALANCE SHEETS

 

 

 

December 31,

 

 

 

2008

 

2007

 

ASSETS

 

 

 

 

 

 

 

 

 

 

 

Current assets:

 

 

 

 

 

Cash and cash equivalents

 

$

19,752,404

 

$

40,582,643

 

Restricted Cash

 

12,000,000

 

 

Short-term investments

 

3,190,912

 

12,153,945

 

Accounts receivable

 

8,890,077

 

4,005,694

 

Other receivables

 

1,391,512

 

1,240,069

 

Prepaid expenses and other current assets

 

917,125

 

492,294

 

 

 

 

 

 

 

Total current assets

 

46,142,030

 

58,474,645

 

 

 

 

 

 

 

Long-term restricted cash

 

1,250,000

 

 

Property and equipment, net

 

5,313,219

 

6,571,024

 

Patents, net

 

925,489

 

1,312,991

 

Other long term assets

 

220,531

 

183,588

 

Deferred costs

 

37,092

 

68,884

 

Goodwill

 

2,502,909

 

 

 

 

 

 

 

 

Total assets

 

$

56,391,270

 

$

66,611,132

 

 

 

 

 

 

 

LIABILITIES AND STOCKHOLDERS’ DEFICIT

 

 

 

 

 

Current Liabilities:

 

 

 

 

 

Accounts payable

 

$

3,870,871

 

$

1,393,664

 

Accrued expenses and other liabilities

 

14,624,757

 

3,602,886

 

Convertible notes

 

13,377,505

 

 

Current portion of long term debt

 

4,000,000

 

4,000,000

 

 

 

 

 

 

 

Total current liabilities

 

35,873,133

 

8,996,550

 

Other long term liabilities

 

626,581

 

374,040

 

Long-term debt

 

928,117

 

16,668,458

 

 

 

 

 

 

 

Total liabilities

 

37,427,831

 

26,039,048

 

 

 

 

 

 

 

Stockholders’ deficit:

 

 

 

 

 

Common stock, $0.0001 par value; 100,000,000 shares authorized; 25,890,143 and 22,087,121 shares issued and outstanding at December 31, 2008 and 2007, respectively;

 

2,589

 

2,209

 

Additional paid-in capital

 

142,392,163

 

126,490,647

 

Accumulated other comprehensive income (loss)

 

386,351

 

1,481,779

 

Accumulated deficit

 

(123,817,664

)

(87,402,551

)

 

 

 

 

 

 

Total stockholders’ equity

 

18,963,439

 

40,572,084

 

 

 

 

 

 

 

Total liabilities and stockholders’ equity

 

$

56,391,270

 

$

66,611,132

 

 

4



 

PHARMATHENE, INC.

 

CONSOLIDATED STATEMENTS OF OPERATIONS

 

 

 

Year ended December 31,

 

 

 

2008

 

2007

 

 

 

 

 

 

 

Contract revenue

 

$

32,821,526

 

$

14,624,595

 

Other revenue

 

89,802

 

19,020

 

 

 

 

 

 

 

 

 

32,911,328

 

14,643,615

 

 

 

 

 

 

 

Operating expenses:

 

 

 

 

 

Research and development

 

31,812,431

 

16,559,670

 

General and administrative

 

19,397,532

 

13,882,023

 

Acquired in-process research and development

 

16,131,002

 

 

Depreciation and amortization

 

813,891

 

705,370

 

 

 

 

 

 

 

Total operating expenses

 

68,154,856

 

31,147,063

 

 

 

 

 

 

 

Loss from operations

 

(35,243,528

)

(16,503,448

)

Other income (expense):

 

 

 

 

 

Interest income

 

1,225,471

 

1,122,565

 

Gain on extinguishment of debt

 

 

886,963

 

Other income

 

58,106

 

 

Interest expense

 

(2,573,406

)

(2,122,624

)

Change in market value of derivative instruments

 

118,244

 

3,029,241

 

 

 

 

 

 

 

Total other income (expense)

 

(1,171,585

)

2,916,145

 

 

 

 

 

 

 

Net loss

 

(36,415,113

)

(13,587,303

)

Accretion of redeemable convertible preferred stock to redemptive value

 

 

(4,133,733

)

 

 

 

 

 

 

Net loss attributable to common shareholders

 

$

(36,415,113

)

$

(17,721,036

)

 

 

 

 

 

 

Basic and diluted net loss per share

 

$

(1.59

)

$

(1.88

)

 

 

 

 

 

 

Weighted average shares used in calculation of basic and diluted net loss per share

 

22,944,066

 

9,442,885

 

 

###

 

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