================================================================================
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
-----------------------
FORM 10-Q
(Mark One)
|X| Quarterly Report Pursuant to Section 13 or 15(d) of
the Securities Exchange Act of 1934
For the Quarter Ended March 31, 2007
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 No. 0-23047
-----------------------
SIGA Technologies, Inc.
(Exact name of registrant as specified in its charter)
A Delaware Corporation IRS Employer No. 13-3864870
420 Lexington Avenue, Suite 408, New York, NY 10170
Telephone Number (212) 672-9100
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 |X| No |_|.
Indicate by check mark whether the registrant is a large accelerated filer, an
accelerated filer, or a non-accelerated filer. See definition of "accelerated
filer and large accelerated filer" in Rule 12b-2 of the Exchange Act. (Check
one):
Large Accelerated Filer |_| Accelerated Filer |_| Non-Accelerated Filer |X|.
Indicate by check mark whether the registrant is a shell company (as defined in
rule 12b-2 of the Exchange Act). Yes |_| No |X|.
As of April 25, 2007 the registrant had 33,014,410 shares of common stock
outstanding.
================================================================================
SIGA Technologies, Inc.
Form 10-Q
Table of Contents
Page No.
PART I FINANCIAL INFORMATION
Item 1. Financial Statements ..................................................................... 2
Item 2. Management's Discussion and Analysis of Financial Condition and Results of Operations .... 10
Item 3. Quantitative and Qualitative Disclosure About Market Risk ................................ 16
Item 4. Controls and Procedures .................................................................. 16
PART II OTHER INFORMATION
Item 1. Legal Proceedings ........................................................................ 17
Item 1A. Risk Factors ............................................................................ 17
Item 2. Changes in Securities, Use of Proceeds and Issuer Purchases of Equity Securities ......... 17
Item 3. Defaults Upon Senior Securities .......................................................... 17
Item 4. Submission of Matters to a Vote of Security Holders ...................................... 17
Item 5. Other Information ........................................................................ 17
Item 6. Exhibits ................................................................................. 17
SIGNATURES ....................................................................................... 18
1
PART I - FINANCIAL INFORMATION
Item 1 - Financial Statements
SIGA TECHNOLOGIES, INC.
CONSOLIDATED BALANCE SHEETS
Unaudited
March 31, December 31,
2007 2006
------------ ------------
ASSETS
Current assets
Cash and cash equivalents ............................................... $ 9,744,739 $ 10,639,530
Accounts receivable ..................................................... 1,278,592 617,032
Prepaid expenses ........................................................ 141,590 141,032
------------ ------------
Total current assets ................................................... 11,164,921 11,397,594
Property, plant and equipment, net ...................................... 1,102,627 1,320,315
Goodwill ................................................................ 898,334 898,334
Intangible assets, net .................................................. 144,588 165,243
Other assets ............................................................ 254,228 246,201
------------ ------------
Total assets ........................................................... $ 13,564,698 $ 14,027,687
============ ============
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities
Accounts payable ........................................................ $ 1,384,621 $ 1,357,906
Accrued expenses and other .............................................. 622,720 584,504
Notes payable ........................................................... 107,520 107,520
------------ ------------
Total current liabilities .............................................. 2,014,861 2,049,930
Non-current portion of notes payable .................................... 1,025 22,809
Common stock warrants ................................................... 6,132,266 4,673,098
------------ ------------
Total liabilities ..................................................... 8,148,152 6,745,837
Commitments and contingencies ........................................... -- --
Stockholders' equity
Common stock ($0.0001 par value, 50,000,000 shares authorized,
32,988,010 and 32,452,210 issued and outstanding at March 31, 2007
and December 31, 2006, respectively) .................................. 3,298 3,245
Additional paid-in capital .............................................. 64,822,544 63,646,224
Accumulated deficit ..................................................... (59,509,296) (56,367,619)
------------ ------------
Total stockholders' equity ............................................. 5,416,546 7,281,850
------------ ------------
Total liabilities and stockholders' equity ............................. $ 13,564,698 $ 14,027,687
============ ============
The accompanying notes are an integral part of these financial statements.
2
SIGA TECHNOLOGIES, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS (UNAUDITED)
Three Months Ended
March 31,
2007 2006
------------ ------------
Revenues
Research and development ...................................... $ 1,867,441 $ 1,394,454
------------ ------------
Operating expenses
Selling, general and administrative (include $8,306 and $92,172
of non-cash share based compensation for the three
months ended March 31, 2007 and 2006, respectively) ...... 877,116 941,540
Research and development (include $28,643 and $29,253
of non-cash share based compensation for the three
months ended March 31, 2007 and 2006, respectively) ...... 2,649,588 1,657,670
Patent preparation fees ....................................... 137,686 109,537
------------ ------------
Total operating expenses ..................................... 3,664,390 2,708,747
------------ ------------
Operating loss ............................................... (1,796,949) (1,314,293)
Decrease in fair market value of common stock rights
and common stock warrants ..................................... (1,459,168) (1,525,635)
Other income, net ............................................... 114,440 6,268
------------ ------------
Net loss ..................................................... $ (3,141,677) $ (2,833,660)
============ ============
Weighted average shares outstanding: basic and diluted 32,590,966 26,500,648
============ ============
Net loss per share: basic and diluted $ (0.10) $ (0.11)
============ ============
The accompanying notes are an integral part of these financial statements.
3
SIGA TECHNOLOGIES, INC.
CONSOLIDATED STATEMENT OF CASH FLOWS (UNAUDITED)
Three Months Ended
March 31,
2007 2006
------------ ------------
Cash flows from operating activities:
Net loss ............................................................. $ (3,141,677) $ (2,833,660)
Adjustments to reconcile net loss to net
cash used in operating activities:
Depreciation ....................................................... 257,985 39,172
Amortization of intangible assets .................................. 20,655 274,349
Increase in fair market value of rights and warrants ............... 1,459,168 1,525,635
Stock based compensation ........................................... 36,949 121,425
Changes in assets and liabilities:
Accounts receivable ............................................. (661,560) 624,872
Prepaid expenses ................................................ (558) 62,266
Other assets .................................................... (8,027) (10,158)
Deferred revenue ................................................ -- 917,037
Accounts payable and accrued expenses ........................... 70,837 (681,028)
------------ ------------
Net cash provided by (used in) operating activities ............. (1,966,228) 39,910
------------ ------------
Cash flows from investing activities:
Capital expenditures ............................................... (40,297) (307,417)
------------ ------------
Net cash used in investing activities ........................... (40,297) (307,417)
------------ ------------
Cash flows from financing activities:
Proceeds from issuance of notes payable ............................ -- 1,000,000
Net proceeds from exercise of warrants and options ................. 1,139,424 --
Repayment of notes payable ......................................... (27,690) (26,880)
------------ ------------
Net cash provided by financing activities ...................... 1,111,734 973,120
------------ ------------
Net increase (decrease) in cash and cash equivalents ................. (894,791) 705,613
Cash and cash equivalents at beginning of period ..................... 10,639,530 1,772,489
------------ ------------
Cash and cash equivalents at end of period ........................... $ 9,744,739 $ 2,478,102
============ ============
The accompanying notes are an integral part of these financial statements.
4
SIGA TECHNOLOGIES, INC.
Notes to the March 31, 2007 Consolidated Financial Statements (Unaudited)
1. Basis of Presentation
SIGA Technologies, Inc. ("SIGA" or the "Company") is a bio-defense company
engaged in the discovery, development and commercialization of products for use
in defense against biological warfare agents such as Smallpox and Arenaviruses.
The Company is also engaged in the discovery and development of other novel
anti-infectives, vaccines, and antibiotics for the prevention and treatment of
serious infectious diseases. The Company's anti-viral programs are designed to
prevent or limit the replication of viral pathogens. SIGA's anti-infectives
programs target the increasingly serious problem of drug resistant bacteria and
emerging pathogens.
The consolidated financial statements of the Company have been prepared in
accordance with accounting principles generally accepted in the United States of
America for interim financial information and the rules and regulations of the
Securities and Exchange Commission (the "SEC") for quarterly reports on Forms
10-Q and should be read in conjunction with the Company's consolidated audited
financial statements and notes thereto for the year ended December 31, 2006,
included in the 2006 Form 10-K. All terms used but not defined elsewhere herein
have the meaning ascribed to them in the Company's 2006 annual report on Form
10-K filed on March 16, 2007. The year-end condensed balance sheet data was
derived from audited financial statements, but does not include all disclosures
required by accounting principles generally accepted in the United States of
America. In the opinion of management, all adjustments (consisting of normal and
recurring adjustments) considered necessary for a fair statement of the results
of the interim periods presented have been included. The results of operations
for the three months ended March 31, 2007 are not necessarily indicative of the
results expected for the full year.
The accompanying consolidated financial statements have been prepared on a basis
which assumes that the Company will continue as a going concern and which
contemplates the realization of assets and the satisfaction of liabilities and
commitments in the normal course of business. The Company has incurred
cumulative net losses and expects to incur additional losses to perform further
research and development activities. The Company does not have commercial
products and has limited capital resources. Management's plans with regard to
these matters include continued development of its products as well as seeking
additional research support funds and future financial arrangements. Although
management will continue to pursue these plans, there is no assurance that the
Company will be successful in obtaining sufficient future financing on
commercially reasonable terms or that the Company will be able to secure funding
from anticipated government contracts and grants. Management believes that
existing cash balances combined with anticipated cash flows will be sufficient
to support its operations beyond the next twelve months, and will fund the
Company's business objectives during that period.
2. Significant Accounting Policies
Use of Estimates
The consolidated financial statements and related disclosures are prepared in
conformity with accounting principles generally accepted in the United States of
America. Management is required to make estimates and assumptions that affect
the reported amounts of assets and liabilities, the disclosure of contingent
assets and liabilities at the date of the financial statements and revenue and
expenses during the period reported. These estimates include the realization of
deferred tax assets, useful lives and impairment of tangible and intangible
assets, and the value of options and warrants granted or issued by the Company.
Estimates and assumptions are reviewed periodically and the effects of revisions
are reflected in the financial statements in the period they are determined to
be necessary. Actual results could differ from these estimates.
Cash and cash equivalents
Cash and cash equivalents consist of short term, highly liquid investments, with
original maturities of less than three months when purchased and are stated at
cost. Interest is accrued as earned.
Property, Plant and Equipment
Property, plant and equipment are stated at cost less accumulated depreciation.
Depreciation is provided on the straight-line method over the estimated useful
lives of the various asset classes. Estimated lives are 5 years for laboratory
equipment; 3 years for computer equipment; 7 years for furniture and fixtures;
and the life of the lease for leasehold improvements. Maintenance, repairs and
minor replacements are charged to expense as incurred. Upon retirement or
disposal of assets, the cost and related accumulated depreciation are removed
from the Balance Sheet and any gain or loss is reflected in the Statement of
Operations.
5
Revenue Recognition
The Company recognizes revenue from contract research and development and
research payments in accordance with SEC Staff Accounting Bulletin No. 104,
Revenue Recognition, ("SAB 104"). In accordance with SAB 104, revenue is
recognized when persuasive evidence of an arrangement exists, delivery has
occurred, the fee is fixed or determinable, collectibility is reasonably
assured, contractual obligations have been satisfied and title and risk of loss
have been transferred to the customer. The Company recognizes revenue from
non-refundable up-front payments, not tied to achieving a specific performance
milestone, over the period which the Company is obligated to perform services or
based on the percentage of costs incurred to date, estimated costs to complete
and total expected contract revenue. Payments for development activities are
recognized as revenue as earned, over the period of effort. Substantive at-risk
milestone payments, which are based on achieving a specific performance
milestone, are recognized as revenue when the milestone is achieved and the
related payment is due, providing there is no future service obligation
associated with that milestone. In situations where the Company receives payment
in advance of the performance of services, such amounts are deferred and
recognized as revenue as the related services are performed.
For the three months ended March 31, 2007 and 2006, revenues from National
Institutes of Health ("NIH") contracts and Small Business Innovation Research
("SBIR") grants were 66% and 52%, respectively, of total revenues recognized by
the Company.
Accounts Receivable
Accounts receivable are recorded net of provisions for doubtful accounts. An
allowance for doubtful accounts is based on specific analysis of the
receivables. At March 31, 2007 and December 31, 2006, the Company had no
allowance for doubtful accounts.
Research and development
Research and development expenses include costs directly attributable to the
conduct of research and development programs, including employee related costs,
materials, supplies, depreciation on and maintenance of research equipment, the
cost of services provided by outside contractors, and facility costs, such as
rent, utilities, and general support services. All costs associated with
research and development are expensed as incurred. Costs related to the
acquisition of technology rights, for which development work is still in
process, and that have no alternative future uses, are expensed as incurred.
Goodwill
Goodwill is recorded when the purchase price paid for an acquisition exceeds the
estimated fair value of the net identified tangible and intangible assets
acquired.
The Company evaluates goodwill for impairment annually, in the fourth quarter of
each year. In addition, the Company would test goodwill for recoverability
between annual evaluations whenever events or changes in circumstances indicate
that the carrying amounts may not be recoverable. Examples of such events could
include a significant adverse change in legal matters, liquidity or in the
business climate, an adverse action or assessment by a regulator or government
organization, loss of key personnel, or new circumstances that would cause an
expectation that it is more likely than not that we would sell or otherwise
dispose of a reporting unit. Goodwill impairment is determined using a two-step
approach in accordance with Statement of Financial Accounting Standards No. 142
"Goodwill and Other Intangible Assets" ("SFAS 142"). The impairment review
process compares the fair value of the reporting unit in which goodwill resides
to its carrying value. In 2006, the Company operated as one business and one
reporting unit. Therefore, the goodwill impairment analysis was performed on the
basis of the Company as a whole using the market capitalization of the Company
as an estimate of its fair value.
Identified Intangible Assets
Acquisition-related intangibles at March 31, 2007, represent acquired technology
which is amortized on a straight line basis over period 2 years.
In accordance with Statement of Financial Accounting Standards No. 144
"Accounting for the Impairment or Disposal of Long-Lived Assets" ("SFAS 144"),
the Company performs a review of its identified intangible assets to determine
if facts and circumstances exist which indicate that the useful life is shorter
than originally estimated or that the carrying amount of assets may not be
recoverable. If such facts and circumstances do exist, the Company assesses the
recoverability of identified intangible assets by comparing the projected
undiscounted net cash flows associated with the related asset or group of assets
over their remaining lives against their respective carrying amounts.
Impairment, if any, is based on the excess of the carrying amount over the fair
value of those assets. Our estimates of projected cash flows are dependent on
many factors, including general economic trends, technological developments and
projected future
6
contracts and government grants. It is reasonably likely that future cash flows
associated with our intangible assets may exceed or fall short of our current
projections, in which case a different amount for impairment would result.
Income taxes
Income taxes are accounted for under the asset and liability method prescribed
by Statement of Financial Accounting Standards No. 109, "Accounting for Income
Taxes." Deferred income taxes are recorded for temporary differences between
financial statement carrying amounts and the tax basis of assets and
liabilities. Deferred tax assets and liabilities reflect the tax rates expected
to be in effect for the years in which the differences are expected to reverse.
A valuation allowance is provided if it is more likely than not that some or the
entire deferred tax asset will not be realized.
Net loss per common share
The Company computes, presents and discloses earnings per share in accordance
with SFAS 128 "Earnings Per Share" ("EPS") which specifies the computation,
presentation and disclosure requirements for earnings per share of entities with
publicly held common stock or potential common stock. The statement defines two
earnings per share calculations, basic and diluted. The objective of basic EPS
is to measure the performance of an entity over the reporting period by dividing
income (loss) by the weighted average shares outstanding. The objective of
diluted EPS is consistent with that of basic EPS, that is to measure the
performance of an entity over the reporting period, while giving effect to all
dilutive potential common shares that were outstanding during the period. The
calculation of diluted EPS is similar to basic EPS except the denominator is
increased for the conversion of potential common shares.
The Company incurred losses for the three months ended March 31, 2007 and 2006
and as a result, certain equity instruments are excluded from the calculation of
diluted loss per share. At March 31, 2006, 68,038 shares of the Company's Series
A convertible preferred stock have been excluded from the computation of diluted
loss per share as they were anti-dilutive. These shares were converted into
shares of the Company's common stock in 2006. At March 31, 2007 and 2006
outstanding options to purchase 7,431,412 and 8,488,727 shares, respectively, of
the Company's common stock with exercise prices ranging from $0.94 to $5.50 have
been excluded from the computation of diluted loss per share as they are
anti-dilutive. At March 31, 2007 and 2006, outstanding warrants to purchase
9,166,632 and 9,478,794, shares, respectively, of the Company's common stock,
with exercise prices ranging from $1.18 to $4.99 have been excluded from the
computation of diluted loss per share as they are anti-dilutive.
Fair value of financial instruments
The carrying value of cash and cash equivalents, accounts payable and accrued
expenses approximates fair value due to the relatively short maturity of these
instruments. Common stock rights and warrants which are classified as assets or
liabilities under the provisions of EITF 00-19, are recorded at their fair
market value as of each reporting period.
Concentration of credit risk
The Company has cash in bank accounts that exceed the Federal Deposit Insurance
Corporation insured limits. The Company has not experienced any losses on its
cash accounts. No allowance has been provided for potential credit losses
because management believes that any such losses would be minimal.
Share-based Compensation
The Company accounts for its stock-based compensation programs under the
provisions of Statement of Financial Accounting Standards No. 123 (revised
2004), "Share-Based Payment" ("SFAS 123(R)"), which requires the measurement and
recognition of compensation expense for all share-based payment awards made to
employees and directors including employee stock options and employee stock
purchases related to the Employee Stock Purchase Plan ("employee stock
purchases") based on estimated fair values. The Company does not have a tock
purchase plan at the current time.
Segment information
The Company is managed and operated as one business. The entire business is
managed by a single management team that reports to the chief executive officer.
The Company does not operate separate lines of business or separate business
entities with respect to any of its product candidates. Accordingly, the Company
does not prepare discrete financial information with respect to separate product
areas or by location and only has one reportable segment as defined by SFAS No.
131, "Disclosures about Segments of an Enterprise and Related Information".
Recent accounting pronouncements
In February 2007, the FASB issued SFAS No. 159 "The Fair Value Option for
Financial Assets and Financial Liabilities" ("FAS 159"). FAS 159 permits
entities to choose to measure many financial assets and liabilities at fair
value. Unrealized gains and losses on items for which fair value option has been
elected are reported in earnings.
7
FAS 159 is effective for fiscal years beginning after November 15, 2007. The
Company is currently assessing the impact of FAS 159 on its financial position
and results of operations.
Effective January 1, 2007, the Company adopted FASB Interpretation No. 48,
Accounting for Uncertainty in Income Taxes--an Interpretation of FASB Statement
109 ("FIN 48"). FIN 48 prescribes a comprehensive model for the manner in which
a company should recognize, measure, present and disclose in its financial
statements all material uncertain tax positions that the Company has taken or
expects to take on a tax return.
Upon adoption of FIN 48 and through March 31, 2007, the Company had no
unrecognized tax benefits and, therefore, no unrecognized tax benefits that, if
recognized, would affect the effective tax rate. As of the date of adoption,
there were no tax positions for which it is reasonably possible that the total
amounts of unrecognized tax benefits will significantly increase or decrease
within twelve months from the date of adoption of FIN 48 or from March 31, 2007.
As of March 31, 2007, the only tax jurisdiction to which the Company is subject
is the United States. Open tax years relate to years in which unused net
operating losses were generated. Thus, upon adoption of FIN 48, the Company's
open tax years extend back to 1995. In the event that the Company concludes that
it is subject to interest and/or penalties arising from uncertain tax positions,
the Company will present interest and penalties as a component of income taxes.
No amounts of interest or penalties were recognized in the Company's
Consolidated Statements of Operations or Consolidated Balance Sheets upon
adoption of FIN 48 or as of and for the three months ended March 31, 2007.
3. Intangible Assets
Amortization expense recorded for the three months ended March 31, 2007 and 2006
was as follows:
Three Months Ended
March 31,
2007 2006
------------ ------------
Amortization of acquired grants $ -- $ 245,337
Amortization of customer contract and grants -- 8,357
Amortization of acquired technology 20,655 20,655
------------ ------------
$ 20,655 $ 274,349
------------ ------------
4. Stockholders' Equity
At March 31, 2007, the Company's authorized share capital consisted of
60,000,000 shares, of which 50,000,000 are designated common shares and
10,000,000 are designated preferred shares. The Company's Board of Directors is
authorized to issue preferred shares in series with rights, privileges and
qualifications of each series determined by the Board.
2006 Placement
On October 19, 2006, the Company sold 2,000,000 shares of the Company's common
stock at $4.54 per share and warrants to purchase 1,000,000 shares of the
Company's common stock. The warrants are exercisable at $4.99 per share at any
time and from time to time through and including the seventh anniversary of the
closing date. As of March 31, 2007, warrants to acquire 1,000,000 shares of
common stock were outstanding.
The Company accounted for the transaction under the provisions of EITF 00-19
which requires that free standing derivative financial instruments that require
net cash settlement be classified as assets or liabilities at the time of the
transaction, and recorded at their fair value. EITF 00-19 also requires that any
changes in the fair value of the derivative instruments be reported in earnings
or loss as long as the derivative contracts are classified as assets or
liabilities. At March 31, 2007, the fair market value of the warrants to acquire
common stock was $3.2 million. The Company applied the Black-Scholes model to
calculate the fair values of the respective derivative instruments using the
contracted term of the warrants. Management estimates the expected volatility
using a combination of the Company's historical volatility and the volatility of
a group of comparable companies. SIGA recorded a loss of $745,000 for the
increase in the instruments' fair value from December 31, 2006 to March 31,
2007.
2005 Placement
In November 2005, the Company sold 2,000,000 shares of the Company's common
stock at $1.00 per share and warrants to purchase 1,000,000 shares of the
Company's common stock at an initial exercise price of $1.18 per share, at any
time and from time to time through and including the seventh anniversary of the
closing date. The investors were also entitled to purchase additional shares of
the Company's common stock for a gross amount of $2.0 million at an initial
price of $1.10 per share for a period of 90 trading days following the
effectiveness of a registration statement. The rights to acquire additional
shares of common stock expired on August 25, 2006. As of March 31, 2007,
warrants to acquire 725,000 shares of common stock were outstanding.
The Company accounted for the transaction under the provisions of EITF 00-19. At
March 31, 2007, the fair market value of the warrants to acquire common stock
was $3.0 million. SIGA recorded a loss of $714,000 for the increase in the
instruments' fair value from December 31, 2006 to March 31, 2007.
8
5. Related Parties
During the three months ended March 31, 2007, the Company incurred costs of
$12,500 related to work performed by Transtech Pharma, Inc., a related party,
and its affiliates.
6. Stock Compensation Plans
In January 1996, the Company implemented its 1996 Incentive and Non-Qualified
Stock Option Plan (the "Plan"). The Plan as amended provides for the granting of
up to 11,000,000 shares of the Company's common stock to employees, consultants
and outside directors of the Company. The exercise period for options granted
under the Plan, except those granted to outside directors, is determined by a
committee of the Board of Directors. Stock options granted to outside directors
pursuant to the Plan must have an exercise price equal to or in excess of the
fair market value of the Company's common stock at the date of grant.
For the three months ended March 31, 2007 and 2006, the Company recorded
compensation expense of approximately $37,000 and $121,000, respectively related
to stock options. The total fair value of options vested during the three months
ended March 31, 2007 and 2006 was 188,000 and $222,000. The total compensation
cost not yet recognized related to non-vested awards at March 31, 2007 is
$832,000. The weighted average period over which total compensation cost is
expected to be recognized is 1.56 years.
The Company did not award any option grants during the three months ended March
31, 2007.
7. Commitments and Contingencies
As of March 31, 2007, our purchase obligations are not material. We lease
certain facilities and office space under operating leases. Minimum future
rental commitments under operating leases having non-cancelable lease terms in
excess of one year are as follows:
Loans and related
Year ended December 31, Lease obligations interest payable Total commitments
2007 $ 576,948 $ 107,521 $ 684,469
2008 576,948 22,809 599,757
2009 579,648 -- 579,648
2010 466,448 -- 466,448
2011 443,748 -- 443,748
------------ ------------- -------------
Total $ 2,643,740 $ 130,330 $ 2,774,070
============ ============= =============
Other
On December 20, 2006, PharmAthene, Inc. ("PharmAthene") filed an action against
the Company in the Court of Chancery in the State of Delaware, captioned
PharmAthene, Inc. v. SIGA Technologies, Inc., C.A. No. 2627-N. In its Complaint,
PharmAthene asks the Court to order the Company to enter into a license
agreement with PharmAthene with respect to SIGA-246, as well as issue a
declaration that the Company is obliged to execute such a license agreement, and
award damages resulting from the Company's supposed breach of that obligation.
PharmAthene also alleges that the Company breached an obligation to negotiate
such a license agreement in good faith, as well as seeks damages for promissory
estoppel and unjust enrichment based on supposed information, capital and
assistance that PharmAthene allegedly provided to the Company during the
negotiation process. On January 9, 2007, the Company filed a motion to dismiss
the Complaint in its entirety for failure to state a claim upon which relief can
be granted. The motion has been fully briefed and oral argument is currently
scheduled for June 1, 2007. On January 19, 2007, PharmAthene served on the
Company its first request for production of documents. The Company moved to stay
discovery on January 26, 2007 and this motion was granted on March 8, 2007. SIGA
believes that the claims are without merit and plans to defend itself
vigorously.
9
SIGA TECHNOLOGIES, INC.
Item 2. Management's Discussion and Analysis of Financial Condition and Results
of Operations
The following discussion should be read in conjunction with our financial
statements and notes to those statements and other financial information
appearing elsewhere in this Quarterly Report. In addition to historical
information, the following discussion and other parts of this Quarterly Report
contain forward-looking information that involves risks and uncertainties.
Overview
Since our inception in December 1995, SIGA has pursued the research and
development of novel products for the prevention and treatment of serious
infectious diseases, including products for use in the defense against
biological warfare agents such as Smallpox and Arenaviruses. During the third
quarter of 2006 we were awarded a 3 year, $16.5 million contract from the NIH
and an additional 3 year, $4.8 million SBIR Phase II continuation grant from the
NIH. Both awards support the continuing development of our smallpox drug
candidate, ST-246. Our efforts to develop ST-246 were also supported by previous
SBIR grants from the NIH totaling $5.8 million, a $1.0 million agreement with
Saint Louis University, and a $1.6 million contract with the U.S. Army. Our
initiative to advance SIGA's Arenavirus programs is supported by a 3 year, $6.0
million SBIR grant from the NIH, received in September 2006 and previous SBIR
grants from the NIH totaling $6.3 million.
Our anti-viral programs are designed to prevent or limit the replication
of the viral pathogen. Our anti-infectives programs are aimed at the
increasingly serious problem of drug resistance. These programs are designed to
block the ability of bacteria to attach to human tissue, the first step in the
infection process. We are also developing a technology for the mucosal delivery
of our vaccines which may allow the vaccines to activate the immune system at
the mucus lined surfaces of the body -- the mouth, the nose, the lungs and the
gastrointestinal and urogenital tracts -- the sites of entry for most infectious
agents.
We do not have commercial biomedical products, and we do not expect to
have such products for one to three years, if at all. We believe that we will
need additional funds to complete the development of our biomedical products.
Our plans with regard to these matters include continued development of our
products as well as seeking additional research support funds and financial
arrangements. Although we continue to pursue these plans, there is no assurance
that we will be successful in obtaining future financing on terms acceptable to
us. Management believes it has sufficient funds and projected cash flows to
support operations beyond the next twelve months.
Our biotechnology operations are based in our research facility in
Corvallis, Oregon. We continue to seek to fund a major portion of our ongoing
antiviral, antibiotic and vaccine programs through a combination of government
grants, contracts and strategic alliances. While we have had success in
obtaining strategic alliances, contracts and grants, there is no assurance that
we will continue to be successful in obtaining funds from these sources. Until
additional relationships are established, we expect to continue to incur
significant research and development costs and costs associated with the
manufacturing of product for use in clinical trials and pre-clinical testing. It
is expected that general and administrative costs, including patent and
regulatory costs, necessary to support clinical trials and research and
development will continue to be significant in the future.
To date, we have not marketed, or generated revenues from the commercial
sale of any products. Our biopharmaceutical product candidates are not expected
to be commercially available for several years, if at all. Accordingly, we
expect to incur operating losses for the foreseeable future. There can be no
assurance that we will ever achieve profitable operations.
Critical Accounting Estimates
The methods, estimates and judgments we use in applying our accounting
policies have a significant impact on the results we report in our consolidated
financial statements, which we discuss under the heading "Results of Operations"
following this section of our Management's Discussion and Analysis. Some of our
accounting policies require us to make difficult and subjective judgments, often
as a result of the need to make estimates of matters that are inherently
uncertain. Our most critical accounting estimates include the assessment of
recoverability of goodwill, which could impact goodwill impairments; the
assessment of recoverability of long-lived assets, which primarily impacts
operating income if impairment exists. Below, we discuss these policies further,
as well as the estimates and judgments
10
involved. Other key accounting policies, including revenue recognition, are less
subjective and involve a far lower degree of estimates and judgment.
Significant Accounting Policies
The following is a brief discussion of the more significant accounting
policies and methods used by us in the preparation of our consolidated financial
statements. Note 2 of the Notes to the Consolidated Financial Statements
includes a summary of all of the significant accounting policies.
Share-based Compensation
The Company accounts for its stock-based compensation programs under the
provisions of Statement of Financial Accounting Standards No. 123 (revised
2004), "Share-Based Payment" ("SFAS 123(R)"), which requires the measurement and
recognition of compensation expense for all share-based payment awards made to
employees and directors including employee stock options and employee stock
purchases related to the Employee Stock Purchase Plan ("employee stock
purchases") based on estimated fair values. SFAS 123(R) requires companies to
estimate the fair value of share-based awards on the grant date using an option
pricing model. The value of the portion of the award that is ultimately expected
to vest is recorded as expense over the requisite periods in the Company's
consolidated statement of operations.
Fair value of financial instruments
The carrying value of cash and cash equivalents, accounts payable and
accrued expenses approximates fair value due to the relatively short maturity of
these instruments. Common stock rights and warrants which are classified as
assets or liabilities under the provisions of EITF 00-19 are recorded at their
fair market value as of each reporting period. The Company applies the
Black-Scholes pricing model to calculate the fair values of common stock rights
and warrants using the contracted term of the instruments and expected
volatility that is calculated as a combination of the Company's historical
volatility and the volatility of a group of comparable companies.
Revenue Recognition
The Company recognizes revenue from contract research and development and
research progress payments in accordance with SEC Staff Accounting Bulletin No.
104, Revenue Recognition, ("SAB 104"). In accordance with SAB 104, revenue is
recognized when persuasive evidence of an arrangement exists, delivery has
occurred, the fee is fixed and determinable, collectibility is reasonably
assured, contractual obligations have been satisfied and title and risk of loss
have been transferred to the customer. The Company recognizes revenue from
non-refundable up-front payments, not tied to achieving a specific performance
milestone, over the period which the Company is obligated to perform services or
based on the percentage of costs incurred to date, estimated costs to complete
and total expected contract revenue. Payments for development activities are
recognized as revenue is earned, over the period of effort. Substantive at-risk
milestone payments, which are based on achieving a specific performance
milestone, are recognized as revenue when the milestone is achieved and the
related payment is due, providing there is no future service obligation
associated with that milestone. In situations where the Company receives payment
in advance of the performance of services, such amounts are deferred and
recognized as revenue as the related services are performed.
Goodwill
Goodwill is recorded when the purchase price paid for an acquisition
exceeds the estimated fair value of the net identified tangible and intangible
assets acquired.
The Company evaluates goodwill for impairment annually, in the fourth
quarter of each year. In addition, the Company would test goodwill for
recoverability between annual evaluations whenever events or changes in
circumstances indicate that the carrying amounts may not be recoverable.
Examples of such events could include a significant adverse change in legal
matters, liquidity or in the business climate, an adverse action or assessment
by a regulator or government organization, loss of key personnel, or new
circumstances that would cause an expectation that it is more likely than not
that we would sell or otherwise dispose of a reporting unit. Goodwill impairment
is determined using a two-step approach in accordance with Statement of
Financial Accounting Standards No. 142 "Goodwill and Other Intangible Assets"
("SFAS 142"). The impairment review process compares the fair value of the
reporting unit in which goodwill resides to its carrying value. In 2006, the
Company operated as one business and one reporting unit. Therefore, the goodwill
impairment analysis was performed on the basis of the Company as a whole using
the market capitalization of the Company as an estimate of its fair value. In
the past, our market capitalization has been significantly in excess of the
Company's carrying value. It is reasonably likely that the future market
capitalization of SIGA may exceed or fall short of our current market
capitalization, in which case a different amount for potential
11
impairment would result. The use of the discounted expected future cash flows to
evaluate the fair value of the Company as a whole is reasonably likely to
produce different results than the Company's market capitalization.
Intangible Assets
Acquisition-related intangibles at March 31, 2007, represent acquired
technology which is amortized on a straight line basis over a period of 2 years.
In accordance with Statement of Financial Accounting Standards No. 144
"Accounting for the Impairment or Disposal of Long-Lived Assets" ("SFAS 144"),
the Company performs a review of its identified intangible assets to determine
if facts and circumstances exist which indicate that the useful life is shorter
than originally estimated or that the carrying amount of assets may not be
recoverable. If such facts and circumstances do exist, the Company assesses the
recoverability of identified intangible assets by comparing the projected
undiscounted net cash flows associated with the related asset or group of assets
over their remaining lives against their respective carrying amounts.
Impairment, if any, is based on the excess of the carrying amount over the fair
value of those assets. Our estimates of projected cash flows are dependent on
many factors, including general economic trends, technological developments and
projected future contracts and government grants. It is reasonably likely that
future cash flows associated with our intangible assets may exceed or fall short
of our current projections, in which case a different amount for impairment
would result. If our actual cash flows exceed our estimates of future cash
flows, any impairment charge would be greater than needed. If our actual cash
flows are less than our estimated cash flows, we may need to recognize
additional impairment charges in future periods, which would be limited to the
carrying amount of the intangible assets.
Recent accounting pronouncements
In February 2007, the FASB issued SFAS No. 159 "The Fair Value Option for
Financial Assets and Financial Liabilities" ("FAS 159"). FAS 159 permits
entities to choose to measure many financial assets and liabilities at fair
value. Unrealized gains and losses on items for which fair value option has been
elected are reported in earnings. FAS 159 is effective for fiscal years
beginning after November 15, 2007. The Company is currently assessing the impact
of FAS 159 on its financial position and results of operations.
Results of Operations
Three months ended March 31, 2007 and 2006
Revenues from research and development contracts and grants for the three
months ended March 31, 2007 and 2006 were $1.9 million and $1.4 million,
respectively. Revenues recorded for the three months ended March 31, 2007
increased $0.5 million or 34% from the prior year. For the three months ended
March 31, 2007 we recorded $1.2 million from an NIH contract and NIH SBIR
grants, supporting two of our lead programs. Revenues from NIH SBIR grants and
an agreement with Saint Louis University supporting these programs during the
three months ended March 31, 2006 were $730,000. The increase is mainly due to
revenue recognized from our 3 year, $16.5 million contract with the NIH. Revenue
recognized from our programs with the USAF was $630,000 and $550,000 for the
three months ended March 31, 2007 and 2006, respectively.
Selling, general and administrative expenses ("SG&A") for the three months
ended March 31, 2007 and 2006 were $877,000 and $942,000, respectively. The
Company's legal expenses for the three months ended March 31, 2007 increased by
$140,000 as compared to the same period in 2006 mainly due to our defense
against an action filed against us by PharmAthene, Inc. This increase was offset
by a decline of $84,000 in non-cash stock-based compensation. The decline in
SG&A also relates to a charge of $115,000 recorded by the Company on March 31,
2006, reflecting a severance payment to our former Chief Executive Officer.
Research and development expenses were $2.6 million and $1.7 million for
the three months ended March 31, 2007 and 2006, respectively. The increase of
approximately $900,000 or 53% mainly reflects an increase in charges related to
clinical trials of our lead drug candidate ST-246, and higher payroll expenses
related to the expansion of the Company's research and development work force
from 38 full time employees to 40 on March 31, 2007.
During the three months ended March 31, 2007 and 2006, we spent $990,000
and $402,000, respectively, on the development of our lead drug candidate,
ST-246, an orally administered anti-viral drug that targets the smallpox virus.
For the three months ended March 31, 2007, we spent $171,000 on internal human
resources and $820,000 mainly on clinical testing. For the three months ended
March 31, 2006, we spent $191,000 on internal human resources and $211,000 on
pre-clinical testing of ST-246. From inception of the ST-246 development program
to-date, we expended a
12
total of $7.5 million related to the program, of which $1.7 million and $5.8
million were spent on internal human resources, and clinical and pre-clinical
work, respectively. These resources reflect SIGA's research and development
expenses directly related to the program. They exclude additional expenditures
such as the cost to acquire the program, patent costs, allocation of indirect
expenses, and the value of other services received from the NIH and the DoD.
R&D expenses of $257,000 and $376,000 during the three months ended March
31, 2007 and 2006, respectively, were used to support the development of ST-294,
a drug candidate which has demonstrated significant antiviral activity in cell
culture assays against arenavirus pathogens, as well as other drug candidates
for hemorrhagic fevers. For the three months ended March 31, 2007, we spent
$59,000 on internal human resources and $198,000 mainly on pre-clinical testing.
For the three months ended March 31, 2006, we spent $171,000 on internal human
resources and $204,000 on pre-clinical testing of ST-294. From inception of our
program to develop ST-294 and other drug candidates for hemorrhagic fevers,
to-date, we spent a total of $3.4 million related to the program, of which $1.6
million and $1.8 million were expended on internal human resources and
pre-clinical work, respectively. These resources reflect SIGA's research and
development expenses directly related to the program. They exclude additional
expenditures such as the cost to acquire the program, patent costs, allocation
of indirect expenses, and the value of other services received from the NIH and
the DoD.
R&D expenses related to our USAF Agreements were $251,000 and $171,000 for
internal human resources and external R&D services, respectively, during the
three months ended March 31, 2007. During the same period in 2006, we spent
$194,000 and $128,000 on internal human resources and external R&D services,
respectively. Costs related to our work on the USAF Agreements, during the term
of the agreements to-date were $2.4 million, of which we spent $1.1 million and
$1.3 million on internal human resources and external R&D services,
respectively. These resources reflect SIGA's research and development expenses
directly related to this agreement. They exclude additional expenditures such as
patent costs and allocation of indirect expenses.
Our product programs are in the early stage of development. At this stage
of development, we cannot make reasonable estimates of the potential cost for
most of our programs to be completed or the time it will take to complete the
project. Our lead product, ST-246, is an orally administered anti-viral drug
that targets the smallpox virus. In December 2005 the FDA accepted our IND
application for ST-246 and granted it Fast-Track status. In December 2006, the
FDA granted Orphan Drug designation to ST-246, for the prevention and treatment
of smallpox. We expect that costs to complete the program will approximate $15
million to $20 million, and that the project could be completed in 24 months to
36 months. There is a high risk of non-completion of any program, including
ST-246, because of the lead time to program completion and uncertainty of the
costs. Net cash inflows from any products developed from our programs is at
least one to three years away. However, we could receive additional grants,
contracts or technology licenses in the short-term. The potential cash and
timing is not known and we cannot be certain if they will ever occur.
The risk of failure to complete any program is high, as each, other than
our smallpox program which began phase I clinical trials in 2006, is in the
relatively early stage of development. Products for the biological warfare
defense market, such as the ST-246 Smallpox anti-viral, could generate revenues
in one to three years. We believe the products directed toward this market are
on schedule. We expect the future research and development cost of our
biological warfare defense programs to increase as the potential products enter
animal studies and safety testing, including human safety trials. Funds for
future development will be partially paid for by NIH contracts and SBIR grants,
additional government funding and from future financing. If we are unable to
obtain additional federal grants and contracts or funding in the required
amounts, the development timeline for these products would slow or possibly be
suspended. Delay or suspension of any of our programs could have an adverse
impact on our ability to raise funds in the future, enter into collaborations
with corporate partners or obtain additional federal funding from contracts or
grants.
Patent preparation expenses for the three months ended March 31, 2007 were
$138,000 compared to $110,000 for the three months ended March 31, 2006. We
incurred higher costs during the 2007 three months period for work performed in
connection with our two lead programs.
In connection with the sale of common stock, warrants and rights in
October 2006 and November 2005, we recorded a loss for the increase in fair
market value of common stock rights and common stock warrants. The warrants to
purchase common stock of SIGA were recorded at fair market value and classified
as liabilities at the time of the transaction. A loss of $1.5 million was
recorded by us in each of the three month periods reflecting the increase in the
fair value of warrants and rights to acquire additional shares of our common
stock, from the respective year ends.
Other income of $114,000 and $6,000 for the three months ended March 31,
2007 and 2006, respectively, reflect interest income for the period.
13
Liquidity and Capital Resources
On March 31, 2007, we had $9.7 million in cash and cash equivalents.
During the first quarter of 2007, we received net proceeds of $1.1 million from
exercises of warrants and options to purchase shares of the Company's Common
stock.
We believe that our existing cash combined with anticipated cash flows,
including receipt of future funding from government contracts and grants will be
sufficient to support our operations beyond the next twelve months, and that
sufficient cash flows will be available to meet our business objectives during
that period.
Operating activities
Net cash used in operations during the three months ended March 31, 2007
was $2.0 million compared to $40,000 generated from operations during the three
months ended March 31, 2006. During the three months ended March 31, 2006, we
received two advance payments from the USAF for a total of $1.5 million. Our
current agreements with the USAF do not include advance payments. In addition,
during the first three months of 2007, our accounts receivable balance increased
$662,000, compared with a collection of $625,000 of accounts receivable during
the same period in 2006.
Investing activities
Capital expenditures during the three months ended March 31, 2007 and 2006
were $40,000 and $307,000, respectively, and mainly supported acquisition of
laboratory equipment in 2007 and the renovation of our research facility in
Oregon during the same period in 2006.
Financing activities
Cash provided by financing activities was $1.1 million and $1.0 million
during the three months ended March 31, 2007 and 2006, respectively. During the
three months ended March 31, 2007 we received $1.1 million from the exercise of
options and warrants to purchase shares of common stock. During the three months
ended March 31, 2006, we received proceeds of $1.0 million under a note payable
to PharmAthene, Inc. The note was paid off in October 2006.
We have incurred cumulative net losses and expect to incur additional
losses to perform further research and development activities. We do not have
commercial products and have limited capital resources. Our plans with regard to
these matters include continued development of our products as well as seeking
additional working capital through a combination of collaborative agreements,
strategic alliances, research grants, equity and debt financing. Although we
continue to pursue these plans, there is no assurance that we will be successful
in obtaining future financing on commercially reasonable terms.
Our working capital and capital requirements will depend upon numerous
factors, including pharmaceutical research and development programs;
pre-clinical and clinical testing; timing and cost of obtaining regulatory
approvals; levels of resources that we devote to the development of
manufacturing and marketing capabilities; technological advances; status of
competitors; and our ability to establish collaborative arrangements with other
organizations.
Off-Balance Sheet Arrangements
SIGA does not have any off-balance sheet arrangements.
Safe Harbor Statement
This report contains certain "forward-looking statements" within the
meaning of the Private Securities Litigation Reform Act of 1995, as amended,
including statements regarding the efficacy of potential products, the timelines
for bringing such products to market and the availability of funding sources for
continued development of such products. Forward-looking statements are based on
management's estimates, assumptions and projections, and are subject to
uncertainties, many of which are beyond the control of SIGA. Actual results may
differ materially from those anticipated in any forward-looking statement.
Factors that may cause such differences include the risks that (a) potential
products that appear promising to SIGA or its collaborators cannot be shown to
be efficacious or safe in subsequent pre-clinical or clinical trials, (b) SIGA
or its collaborators will not obtain appropriate or necessary governmental
approvals to
14
market these or other potential products, (c) SIGA may not be able to obtain
anticipated funding for its development projects or other needed funding, (d)
SIGA may not be able to secure funding from anticipated government contracts and
grants, (e) SIGA may not be able to secure or enforce adequate legal protection,
including patent protection, for its products and (f) unanticipated internal
control deficiencies or weaknesses or ineffective disclosure controls and
procedures. More detailed information about SIGA and risk factors that may
affect the realization of forward-looking statements, including the
forward-looking statements in this presentation, is set forth in SIGA's filings
with the Securities and Exchange Commission, including SIGA's Annual Report on
Form 10-K for the fiscal year ended December 31, 2006, and in other documents
that SIGA has filed with the Commission. SIGA urges investors and security
holders to read those documents free of charge at the Commission's Web site at
http://www.sec.gov. Interested parties may also obtain those documents free of
charge from SIGA. Forward-looking statements speak only as of the date they are
made, and except for our ongoing obligations under the U.S. federal securities
laws, we undertake no obligation to publicly update any forward-looking
statements whether as a result of new information, future events or otherwise.
15
Item 3. Quantitative and Qualitative Disclosure About Market Risk
None
Item 4. Controls and Procedures
(a) Disclosure Controls and Procedures. The Company's management, with the
participation of the Company's Chief Financial Officer, has evaluated the
effectiveness of the Company's disclosure controls and procedures (as defined in
Rules 13a-15(e) and 15d-15(e) under the Exchange Act) as of the end of the
fiscal period covered by this Quarterly Report on Form 10-Q. Based upon such
evaluation, the Chief Executive Officer and Chief Financial Officer have
concluded that, as of the end of such period, the Company's disclosure controls
and procedures are effective.
(b) Internal Control Over Financial Reporting. There have not been any
changes in the Company's internal control over financial reporting (as such term
is defined in Rules 13a-15(f) and 15d-15(f) under the Exchange Act) during the
fiscal period covered by this Quarterly Report on Form 10-Q that have materially
affected, or are reasonably likely to materially affect, the Company's internal
control over financial reporting.
16
Part II
Other information
Item 1. On December 20, 2006, PharmAthene, Inc. ("PharmAthene") filed an action
against the Company in the Court of Chancery in the State of Delaware,
captioned PharmAthene, Inc. v. SIGA Technologies, Inc., C.A. No.
2627-N. In its Complaint, PharmAthene asks the Court to order the
Company to enter into a license agreement with PharmAthene with respect
to SIGA-246, as well as issue a declaration that the Company is obliged
to execute such a license agreement, and award damages resulting from
the Company's supposed breach of that obligation. PharmAthene also
alleges that the Company breached an obligation to negotiate such a
license agreement in good faith, as well as seeks damages for
promissory estoppel and unjust enrichment based on supposed
information, capital and assistance that PharmAthene allegedly provided
to the Company during the negotiation process. On January 9, 2007, the
Company filed a motion to dismiss the Complaint in its entirety for
failure to state a claim upon which relief can be granted. The motion
has been fully briefed and oral argument is currently scheduled for
June 1, 2007. On January 19, 2007, PharmAthene served on the Company
its first request for production of documents. The Company moved to
stay discovery on January 26, 2007 and this motion was granted on March
8, 2007. SIGA believes that the claims are without merit and plans to
defend itself vigorously.
Item 1A. Risk Factors - There were no material changes to Risk Factors disclosed
in SIGA's 2006 Form 10-K.
Item 2. Unregistered Sale of Equity Securities and Use of Proceeds - None.
Item 3. Defaults upon Senior Securities - None.
Item 4. Submission of Matters to a Vote of Security Holders - None.
Item 5. Other Information - None.
Item 6. Exhibits
* 31 Certification of Chief Executive Officer and Acting Chief
Executive Officer Pursuant to Section 302 of the Sarbanes-Oxley
Act of 2002.
* 31 Certification of Chief Financial Officer and Acting Chief
Executive Officer Pursuant to Section 302 of the Sarbanes-Oxley
Act of 2002.
* 32 Certification of Chief Executive Officer and Acting Chief
Executive Officer Pursuant to Section 906 of the Sarbanes-Oxley
Act of 2002.
* 32 Certification of Chief Financial Officer and Acting Chief
Executive Officer Pursuant to Section 906 of the Sarbanes-Oxley
Act of 2002.
* Filed herein
17
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.
SIGA Technologies, Inc.
(Registrant)
Date: May 7, 2007 By:/s/ Thomas N. Konatich
------------------------
Thomas N. Konatich
Chief Financial Officer
18
Exhibit 31.1
CERTIFICATION PURSUANT TO
SECTION 302 OF THE SARBANES-OXLEY ACT OF 2002
I, Eric A. Rose, M.D., certify that:
1. I have reviewed this quarterly report on Form 10-Q of SIGA
Technologies, Inc.;
2. Based on my knowledge, this report does not contain any untrue
statement of a material fact or omit to state a material fact
necessary to make the statements made, in light of the circumstances
under which such statements were made, not misleading with respect
to the period covered by this quarterly report;
3. Based on my knowledge, the financial statements, and other financial
information included in this quarterly report, fairly present in all
material respects the financial condition, results of operations and
cash flows of the registrant as of, and for, the periods presented
in this report;
4. The registrant's other certifying officer and I are responsible for
establishing and maintaining disclosure controls and procedures (as
defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) for the
registrant and have:
(a) Designed such disclosure controls and procedures, or caused
such disclosure controls and procedures to be designed under
our supervision, to ensure that material information relating
to the registrant, including its consolidated subsidiaries, is
made known to us by others within those entities, particularly
during the period in which this quarterly report is being
prepared;
(b) Evaluated the effectiveness of the registrant's disclosure
controls and procedures and presented in this report our
conclusions about the effectiveness of the disclosure controls
and procedures, as of the end of the period covered by this
report based on such evaluation; and
(c) Disclosed in this report any change in the registrant's
internal control over financial reporting that occurred during
the registrant's most recent fiscal quarter that has
materially affected, or is reasonably likely to materially
affect, the registrant's internal control over financial
reporting; and
5. The registrant's other certifying officer and I have disclosed,
based on our most recent evaluation of internal control over
financial reporting, to the registrant's auditors and the audit
committee of registrant's board of directors (or persons performing
the equivalent functions);
(a) All significant deficiencies and material weaknesses in the
design or operation of internal control over financial
reporting which are reasonably likely to adversely affect the
registrant's ability to record, process, summarize and report
financial information; and
(b) Any fraud, whether or not material, that involves management
or other employees who have a significant role in the
registrant's internal control over financial reporting.
Date: May 7, 2007 By: /s/ Eric A. Rose
----------------------
Eric A. Rose, M.D.
Chief Executive Officer
19
Exhibit 31.2
CERTIFICATION PURSUANT TO
SECTION 302 OF THE SARBANES-OXLEY ACT OF 2002
I, Thomas N. Konatich, certify that:
1. I have reviewed this quarterly report on Form 10-Q of SIGA
Technologies, Inc.;
2. Based on my knowledge, this report does not contain any untrue
statement of a material fact or omit to state a material fact
necessary to make the statements made, in light of the circumstances
under which such statements were made, not misleading with respect
to the period covered by this quarterly report;
3. Based on my knowledge, the financial statements, and other financial
information included in this quarterly report, fairly present in all
material respects the financial condition, results of operations and
cash flows of the registrant as of, and for, the periods presented
in this report;
4. The registrant's other certifying officer and I are responsible for
establishing and maintaining disclosure controls and procedures (as
defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) for the
registrant and have:
(a) Designed such disclosure controls and procedures, or caused
such disclosure controls and procedures to be designed under
our supervision, to ensure that material information relating
to the registrant, including its consolidated subsidiaries, is
made known to us by others within those entities, particularly
during the period in which this quarterly report is being
prepared;
(b) Evaluated the effectiveness of the registrant's disclosure
controls and procedures and presented in this report our
conclusions about the effectiveness of the disclosure controls
and procedures, as of the end of the period covered by this
report based on such evaluation; and
(c) Disclosed in this report any change in the registrant's
internal control over financial reporting that occurred during
the registrant's most recent fiscal quarter that has
materially affected, or is reasonably likely to materially
affect, the registrant's internal control over financial
reporting; and
5. The registrant's other certifying officer and I have disclosed,
based on our most recent evaluation of internal control over
financial reporting, to the registrant's auditors and the audit
committee of registrant's board of directors (or persons performing
the equivalent functions);
(a) All significant deficiencies and material weaknesses in the
design or operation of internal control over financial
reporting which are reasonably likely to adversely affect the
registrant's ability to record, process, summarize and report
financial information; and
(b) Any fraud, whether or not material, that involves management
or other employees who have a significant role in the
registrant's internal control over financial reporting.
Date: May 7, 2007 By: /s/ Thomas N. Konatich
----------------------
Thomas N. Konatich
Chief Financial Officer
20
Exhibit 32.1
CERTIFICATION PURSUANT TO
18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
In connection with the Quarterly Report of SIGA Technologies, Inc. (the
"Company") on Form 10-Q for the period ending March 31, 2007 as filed with the
Securities and Exchange Commission on the date hereof (the "Report"), I, Eric A.
Rose, Chief Executive Officer of the Company, certify, pursuant to 18 U.S.C.
ss.1350, as adopted pursuant to ss.906 of the Sarbanes-Oxley Act of 2002, that,
to the best of my knowledge:
(1) The Report fully complies with the requirements of section 13(a) or
15(d) of the Securities Exchange Act of 1934; and
(2) The information contained in the Report fairly presents, in all
material respects, the financial condition and results of operations
of the Company.
May 7, 2007
/s/ Eric A. Rose
-----------------------
Eric A. Rose, M.D.
Chief Executive Officer
21
Exhibit 32.2
CERTIFICATION PURSUANT TO
18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
In connection with the Quarterly Report of SIGA Technologies, Inc. (the
"Company") on Form 10-Q for the period ending March 31, 2007 as filed with the
Securities and Exchange Commission on the date hereof (the "Report"), I, Thomas
N. Konatich., Chief Financial Officer of the Company, certify, pursuant to 18
U.S.C. ss.1350, as adopted pursuant to ss.906 of the Sarbanes-Oxley Act of 2002,
that, to the best of my knowledge:
(3) The Report fully complies with the requirements of section 13(a) or
15(d) of the Securities Exchange Act of 1934; and
(4) The information contained in the Report fairly presents, in all
material respects, the financial condition and results of operations
of the Company.
May 7, 2007
/s/ Thomas N. Konatich
------------------------
Thomas N. Konatich
Chief Financial Officer
22
