Delaware
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001-34637
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20-1852016
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(State or Other Jurisdiction of
Incorporation)
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(Commission File Number)
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(I.R.S. Employer
Identification No.)
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25801 Industrial Boulevard, Suite B, Hayward,
California
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94545
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(Address of Principal Executive Offices)
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(Zip Code)
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Item 2.02
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Results of Operations and Financial Condition.
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Item 9.01
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Financial Statements and Exhibits.
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Exhibit No.
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Description
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99.1
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Press Release dated July 30, 2013
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Anthera Pharmaceuticals, Inc.
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By:
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/s/May Liu
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May Liu
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Principal Accounting Officer and
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Senior Vice President, Finance
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& Administration |
·
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The Company initiated its Phase 2 BRIGHT-SC study in patients with IgA nephropathy. The primary endpoint of the study will be a reduction in proteinuria at 32 weeks. The Company plans to conduct an interim analysis of proteinuria after all patients have completed 8 weeks of therapy (N=48). The interim data analysis is planned for the fourth quarter of this year. Secondary endpoints will include the effects of blisibimod on estimated Glomerular Filtration Rate (eGFR), plasma B cells, and other biomarkers of kidney disease.
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·
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Anthera completed its Open-Label Extension (“OLE”) of the PEARL-SC study to evaluate the long-term safety of blisibimod. The analysis of certain biomarkers, including proteinuria, complement C3, IgG and IgM beyond the 24 week PEARL-SC study will provide further insights on the potential effectiveness and safety of blisibimod. Data from the OLE study will be presented at an upcoming scientific conference.
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·
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In May, the Company met with the US FDA to discuss the IgA nephropathy development plan, with a specific focus on the use of proteinuria as an endpoint in studies of IgA nephropathy. The positive response from the US FDA, combined with the proteinuria data from the PEARL-SC study, provide a manageable path forward for the development of blisibimod.
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·
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In June, the Company met with the Japanese Pharmaceuticals and Medical Devices Agency (“PMDA”) to examine development strategies for blisibimod in Asia. Like the US FDA, the PMDA was receptive to proteinuria as an endpoint for the basis of approval. “The prevalence of IgA nephropathy is highest in Asia. Therefore, the concurrence between the US FDA and PMDA in terms of proteinuria as an endpoint provides a great deal of clarity for the continued global development of blisibimod for this disease,” said Dr. Colin Hislop, Anthera’s Chief Medical Officer.
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·
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In April 2013, the Company strengthened its financial position by securing a $20.0 million debt financing facility through a syndicate led by MidCap Financial SBIC, LP ("MidCap Financial"). The Company used the loan proceeds to repay the remaining principal of the loan agreement previously entered into with Hercules Technology Growth Capital. The Company also entered into an $18.5 million common stock purchase agreement with Lincoln Park Capital Fund, LLC ("LPC") a Chicago-based institutional investor. Upon executing the agreement, LPC made an initial purchase of $2 million in common stock from the Company. As of June 30, 2013, there was $16.5 million available under the purchase agreement.
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·
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The Company effectuated a 1-for-8 reverse stock split of its common stock on July 15, 2013, resulting in a decrease of the number of shares issued and outstanding from approximately 152.9 million to 19.1 million.
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·
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The NASDAQ Hearings Panel has determined to allow continued listing of the shares of the Company on the NASDAQ Global Market, as the Company has regained compliance with the minimum bid price continued listing requirements.
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Three months ended
June 30,
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Six months ended
June 30,
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2013
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2012
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2013
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2012
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Operating expenses:
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Research and development
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$ | 5,265 | $ | 14,865 | $ | 10,194 | $ | 32,603 | ||||||||
General and administrative
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1,688 | 1,799 | 3,660 | 4,121 | ||||||||||||
Total operating expenses
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6,953 | 16,664 | 13,854 | 36,724 | ||||||||||||
Loss from operations
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(6,953 | ) | (16,664 | ) | (13,854 | ) | (36,724 | ) | ||||||||
Other Income (expense):
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Other income (expense) - net
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(6 | ) | (28 | ) | 19 | (38 | ) | |||||||||
Interest expense
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(1,322 | ) | (908 | ) | (2,026 | ) | (1,751 | ) | ||||||||
Total other (expense) - net
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(1,328 | ) | (936 | ) | (2,007 | ) | (1,789 | ) | ||||||||
Net loss
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$ | (8,281 | ) | $ | (17,600 | ) | $ | (15,861 | ) | $ | (38,513 | ) | ||||
(1) Net loss per basic and diluted:
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$ | (0.43 | ) | $ | (3.43 | ) | $ | (0.92 | ) | $ | (7.51 | ) | ||||
(1) Weighted-average number of shares used in
per share calculation-basic and diluted
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19,059,130 | 5,137,218 | 17,297,098 | 5,131,126 |
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(1)
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Common stock and per share data adjusted to reflect reverse split of stock effectuated on July 15, 2013.
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ANTHERAPHARMACEUTICALS, INC.
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(A Development Stage Company)
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BALANCE SHEET DATA
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(in thousands, except share data)
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(unaudited)
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June 30,
2013
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December 31,
2012
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Cash and cash equivalents
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$ | 37,304 | $ | 19,431 | ||||
Short term investments
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$ | 1,142 | $ | 5,322 | ||||
Restricted cash
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$ | 10,000 | $ | — | ||||
Total assets
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$ | 50,246 | $ | 26,445 | ||||
Total current liabilities, excluding current portion of notes payable
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$ | 3,387 | $ | 9,421 | ||||
Total notes payable
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$ | 19,264 | $ | 20,550 | ||||
Deficit accumulated during development stage
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$ | (276,239 | ) | $ | (260,378 | ) | ||
Total shareholders' equity (deficit)
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$ | 27,595 | $ | (3,526 | ) | |||
(2) Common shares outstanding
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19,115,189 | 9,893,949 |