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 |
|
(Commission |
|
(IRS Employer |
|
|
|
||
One Park Place, Suite 450, Annapolis, Maryland |
|
21401 |
||
(Address of principal executive offices) |
|
(Zip Code) |
Registrants 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. |
2
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. |
|
|
|
|
|
|
|
Date: March 30, 2009 |
By: |
/s/ David P. Wright |
|
|
David P. Wright |
|
|
President and Chief Executive Officer |
3
Exhibit 99.1
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 Companys 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 Companys 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 Companys 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 Avecias 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 Companys 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 companys 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. PharmAthenes lead product development programs include:
2
· 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 Companys product candidates, unexpected funding delays and/or reductions or elimination of U.S. government funding for one or more of the Companys 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 PharmAthenes 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 PharmAthenes public disclosure filings are available from its investor relations department and our website under the investor relations tab at www.pharmathene.com.
Tables follow
3
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 |
|
###
5