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TEKMIRA PHARMACEUTICALS CORPORATION Unaudited Interim Condensed Consolidated Financial Statements (expressed in Canadian dollars) (Prepared in accordance with generally accepted accounting principles used in the United S

Key Takeaway: TEKMIRA PHARMACEUTICALS CORPORATION Unaudited Interim Condensed Consolidated Financial Statements (expressed in Canadian dollars) (Prepared in accordance with generally accepted accounting principles used in the United States of America (U.S. GAAP)) Three months ended March

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TEKMIRA PHARMACEUTICALS CORPORATION
Unaudited Interim Condensed Consolidated Financial
Statements (expressed in Canadian dollars)
(Prepared in accordance with generally accepted accounting principles used in the United States of
America (U.S. GAAP))
Three months ended March 31, 2011
TEKMIRA PHARMACEUTICALS CORPORATION
Condensed Consolidated Balance Sheets
(Expressed in Canadian Dollars)
(Prepared in accordance with U.S. GAAP)
March 31 2011 December 31 2010
(Unaudited)
Assets
Current assets:
Cash and cash equivalents $ 9,228,665 $ 12,346,010
Accounts receivable (note 3) 3,320,363 3,318,729
Accrued revenue 202,754 817,464
Deferred expenses 563,157 557,256
Investment tax credits receivable 403,580 403,580
Finished goods inventory 150,731
Prepaid expenses and other assets 270,621 315,057
Total current assets 13,989,140 17,908,827
Property and equipment 18,724,155 18,668,897
Less accumulated depreciation and impairment (15,794,130 ) (15,555,481 )
2,930,025 3,113,416
Total assets $ 16,919,165 $ 21,022,243
Liabilities and stockholders equity
Current liabilities:
Accounts payable and accrued liabilities (note 4) $ 4,692,242 $ 6,151,923
Deferred revenue current portion (note 2) 2,388,396 1,982,264
Total current liabilities 7,080,638 8,134,187
Deferred revenue, net of current portion (note 2) 2,113,847 2,155,478
Total liabilities 9,194,485 10,289,665
Stockholders equity:
Common shares
Authorized - unlimited number with no par value Issued and outstanding: 10,341,934 (December 31, 2010 - 10,338,703) 229,515,870 229,491,529
Additional paid-in capital 30,217,280 30,151,810
Deficit (252,008,470 ) (248,910,761 )
Total stockholders equity 7,724,680 10,732,578
Total liabilities and stockholders equity $ 16,919,165 $ 21,022,243
Basis of presentation and future operations (note 1)
Contingencies (note 5)
See accompanying notes to the condensed consolidated financial statements.
TEKMIRA PHARMACEUTICALS CORPORATION
Condensed Consolidated Statements of Operations and Comprehensive Loss
(Expressed in Canadian Dollars)
(Prepared in accordance with U.S. GAAP)
Three months ended March 31
2011 2010
Revenue (note 2)
Collaborations and contracts $ 4,343,485 $ 2,465,935
4,343,485 2,465,935
Expenses
Research, development, collaborations and contracts 5,639,575 5,456,477
General and administrative 1,541,599 995,272
Depreciation of property and equipment 238,649 237,739
7,419,823 6,689,488
Loss from operations (3,076,338 ) (4,223,553 )
Other income (losses)
Interest income 33,257 21,393
Foreign exchange gains (losses) (54,628 ) 38,669
Net loss and comprehensive loss $ (3,097,709 ) $ (4,163,491 )
Loss per common share
Basic and diluted $ (0.30 ) $ (0.40 )
Weighted average number of common shares
Basic and diluted 10,341,259 10,328,688
See accompanying notes to the
condensed consolidated financial statements.
TEKMIRA PHARMACEUTICALS CORPORATION
Condensed Consolidated Statements of Stockholders Equity
For the three months ended
March 31, 2011 (unaudited)
(Expressed in Canadian Dollars)
(Prepared in accordance with U.S. GAAP)
Number of shares Share capital Additional paid-in capital Deficit Total stockholders equity
Balance, December 31, 2010 10,338,703 $ 229,491,529 $ 30,151,810 $ (248,910,761 ) $ 10,732,578
Stock-based compensation 88,375 88,375
Issuance of common shares pursuant to exercise of options 3,231 24,341 (22,905 ) 1,436
Net loss (3,097,709 ) (3,097,709 )
Balance, March 31, 2011 10,341,934 $ 229,515,870 $ 30,217,280 $ (252,008,470 ) $ 7,724,680
See accompanying notes to the condensed consolidated financial statements.
TEKMIRA PHARMACEUTICALS CORPORATION
Condensed Consolidated Statements of Cash Flow
(Expressed in Canadian Dollars)
accordance with U.S. GAAP)
Three months ended March 31
2011 2010
OPERATING ACTIVITIES
Loss for the period $ (3,097,709 ) $ (4,163,491 )
Items not involving cash:
Depreciation of property and equipment 238,649 237,739
Stock-based compensation expense 88,375 359,817
Foreign exchange (gains) losses arising on foreign currency cash balances 4,646 (2,888 )
Net change in non-cash operating items:
Accounts receivable (1,634 ) 304,063
Accrued revenue 614,710
Deferred expenses (5,901 )
Inventory 150,731
Prepaid expenses and other assets 44,436 43,702
Accounts payable and accrued liabilities (1,459,681 ) (2,227,261 )
Deferred revenue 364,501 128,335
(3,058,877 ) (5,319,984 )
INVESTING ACTIVITIES
Acquisition of property and equipment (55,258 ) (552,570 )
(55,258 ) (552,570 )
FINANCING ACTIVITIES
Issuance of common shares pursuant to exercise of options 1,436 200
1,436 200
Foreign exchange gains (losses) arising on foreign currency cash balances (4,646 ) 2,888
Decrease in cash and cash equivalents (3,117,345 ) (5,869,466 )
Cash and cash equivalents, beginning of period 12,346,010 24,397,740
Cash and cash equivalents, end of period $ 9,228,665 $ 18,528,274
See accompanying notes to the condensed consolidated financial statements.
TEKMIRA PHARMACEUTICALS CORPORATION
Notes to interim condensed consolidated financial statements (unaudited)
(Expressed in Canadian
Three months ended March 31, 2011
Nature of business and future operations
Tekmira Pharmaceuticals Corporation (the Company ) is a Canadian biopharmaceutical business focused on advancing novel RNA interference therapeutics and providing its leading lipid nanoparticle
delivery technology to pharmaceutical partners.
The success of the Company is dependent on obtaining the necessary regulatory approvals to
bring its products to market and achieve profitable operations. The continuation of the research and development activities and the commercialization of its products are dependent on the Company s ability to successfully complete these
activities and to obtain adequate financing through a combination of financing activities and operations. It is not possible to predict either the outcome of future research and development programs or the Company s ability to fund these
programs in the future.
Basis of presentation and significant accounting policies
These unaudited interim condensed consolidated financial statements have been prepared in accordance with generally accepted accounting principles of the
United States of America ( U.S. GAAP ) for interim financial statements and accordingly, do not include all disclosures required for annual financial statements.
These statements should be read in conjunction with the Company s audited consolidated financial statements and notes thereto for the year ended December 31, 2010 and included in the 2010 Annual
The unaudited interim condensed consolidated financial statements reflect, in the opinion of management, all adjustments and
reclassifications necessary to present fairly the financial position, results of operations and cash flows at March 31, 2011 and for all periods presented.
The results of operations for the three months ended March 31, 2011 and March 31, 2010 are not necessarily indicative of the results for the full year.
These financial statements follow the same significant accounting policies as those described in the notes to the audited consolidated financial
statements of Tekmira Pharmaceuticals Corporation ( the Company ) for the year ended December 31, 2010.
include the accounts of the Company and its two wholly-owned subsidiaries, Protiva Biotherapeutics Inc. ( Protiva ) and Protiva Biotherapeutics (USA), Inc., which were acquired on May 30, 2008. All intercompany transactions and
balances have been eliminated on consolidation.
Income or loss per share
Income or loss per share is calculated based on the weighted average number of common shares outstanding. Diluted loss per share does not differ from
basic loss per share since the effect of the Company s stock options are anti-dilutive. Diluted income per share is calculated using the treasury stock method which uses the weighted average number of common shares outstanding during the period
and also includes the dilutive effect of potentially issuable common shares from outstanding stock options. At March 31, 2011, potential common shares (prior to consideration of the treasury stock method) of 1,428,763 were excluded from the
calculation of net loss per common share because their inclusion would be anti-dilutive (March 31, 2010 1,384,907).
of financial instruments
The Company s financial instruments consist of cash and cash equivalents, accounts receivable,
investment tax credits receivable, accounts payable and accrued liabilities and promissory notes.
The carrying values of cash and cash
equivalents are recorded at fair value based on quoted prices in active markets. The carrying values of accounts receivable, investment tax credits receivable and accounts payable and accrued liabilities approximate their fair values due to the
immediate or short-term maturity of these financial instruments.
TEKMIRA PHARMACEUTICALS CORPORATION
Notes to interim condensed consolidated financial statements (unaudited)
(Expressed in Canadian
Three months ended March 31, 2011
Recent accounting pronouncements
In October 2009, the Financial Accounting Standards Board (FASB) issued EITF 08-01, Revenue Arrangements with Multiple Deliverables (currently within the scope of FASB Accounting Standards
Codification (ASC) Subtopic 605-25). This statement provides principles for allocation of consideration among its multiple-elements, allowing more flexibility in identifying and accounting for separate deliverables under an arrangement. The EITF
introduces an estimated selling price method for valuing the elements of a bundled arrangement if vendor-specific objective evidence or third-party evidence of selling price is not available, and significantly expands related disclosure
requirements. This standard is effective on a prospective basis for revenue arrangements entered into or materially modified in fiscal years beginning on or after June 15, 2010. Alternatively, adoption may be on a retrospective basis, and early
application is permitted. The Company adopted this pronouncement in the three month period ending March 31, 2011. Adoption of the pronouncement did not have a material impact on the Company s financial statements.
In March 2010, the FASB ratified the EITF final consensus on Issue ASC 2010-17, Milestone Method of Revenue Recognition. The guidance in this
consensus allows the milestone method as an acceptable revenue recognition methodology when an arrangement includes substantive milestones. The guidance provides a definition of a substantive milestone and should be applied regardless of whether the
arrangement includes single or multiple deliverables or units of accounting. The scope of this consensus is limited to transactions involving milestones relating to research and development deliverables. The guidance includes enhanced disclosure
requirements about each arrangement, individual milestones and related contingent consideration, information about substantive milestones and factors considered in the determination. The consensus is effective prospectively to milestones achieved in
fiscal years, and interim periods within those years, after June 15, 2010. Early application and retrospective application are permitted. The Company adopted this pronouncement in the three month period ending March 31, 2011. Adoption of
the pronouncement did not have a material impact on the Company s financial statements.
In July 2010, the FASB issued ASU 2010-20,
Disclosures about the Credit Quality of Financing Receivables and the Allowance for Credit Losses, which amends ASC 310 by requiring more robust and disaggregated disclosures about the credit quality of an entity s financing receivables
and its allowance for credit losses. The enhanced disclosure will provide financial statement users with an improved understanding of (1) the nature of an entity s credit risk associated with its financing receivables and (2) the
entity s assessment of that risk in estimating its allowance for credit losses as well as changes in the allowance and the reasons for those changes. This standard is effective on a prospective basis for the first interim or annual period
beginning after December 15, 2010. The Company adopted this standard in the three month period ending March 31, 2011. Adoption of the standard did not have a material impact on disclosures in the Company s financial statements.
The following tables set forth revenue recognized under collaborations, contracts and licensing agreements:
Three months ended March 31
2011 2010
Collaborations and contracts
Alnylam (a) $ 917,201 $ 865,823
U.S. Government (b) 3,381,133
Roche (c) 3,520 1,265,187
BMS (d) 41,631 227,995
Other RNAi collaborators (e) 106,930
Total research and development collaborations and contracts 4,343,485 2,465,935
TEKMIRA PHARMACEUTICALS CORPORATION
Notes to interim condensed consolidated financial statements (unaudited)
(Expressed in Canadian
Three months ended March 31, 2011
The following table sets forth deferred collaborations and contracts revenue:
March 31, 2011 December 31, 2010
Alnylam (a) $ 284,739 $
U.S. Government (b) 885,837 760,924
Roche (c) 36,712 40,232
BMS current portion (d) 1,181,108 1,181,108
Deferred revenue, current portion 2,388,396 1,982,264
BMS long-term portion (d) 2,113,847 2,155,478
Total deferred revenue $ 4,502,243 $ 4,137,742
License and Collaboration Agreement with Alnylam through Tekmira
2007, the Company entered into a licensing and collaboration agreement with Alnylam ( Alnylam License and Collaboration ) giving them an exclusive license to certain of the Company s historical lipid nanoparticle intellectual property
for the discovery, development, and commercialization of ribonucleic acid interference ( RNAi ) therapeutics.
with Alnylam acquired through Protiva
As a result of the acquisition of Protiva on May 30, 2008, the Company acquired a
Last updated: May 10, 2011