10-K – Annual report [Section 13 and 15(d), not S-K Item 405]

Verastem has filed a 10-K – Annual report [Section 13 and 15(d), not S-K Item 405] with the U.S. Securities and Exchange Commission (Filing, 10-K, Verastem, MAR 10, 2015, View Source [SID1234502516]).

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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10-K – Annual report [Section 13 and 15(d), not S-K Item 405]

Sophiris Bio has filed a 10-K – Annual report [Section 13 and 15(d), not S-K Item 405] with the U.S. Securities and Exchange Commission (Filing, 10-K, Sophiris Bio, MAR 10, 2015, View Source [SID1234502509]).

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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10-K – Annual report [Section 13 and 15(d), not S-K Item 405]

Radius has filed a 10-K – Annual report [Section 13 and 15(d), not S-K Item 405] with the U.S. Securities and Exchange Commission (Filing, 10-K, Radius, MAR 10, 2015, View Source [SID1234502500]).

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8-K – Current report

On March 9, 2015 Heat Biologics reported that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation for HS-410 (vesigenurtacel-L) for the treatment of non-muscle invasive bladder cancer (NMIBC) (Filing, 8-K, Heat Biologics, MAR 10, 2015, View Source [SID:1234502283]). HS-410 is Heat’s NMIBC product candidate and is based on its breakthrough Immune Pan Antigen Cytotoxic Therapy ("ImPACT") platform that is designed to generate killer T cells to attack cancers. HS-410 is currently being evaluated in a randomized Phase 2 trial in combination with BCG and as monotherapy for the treatment of NMIBC.

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"We are very pleased that FDA has granted this important designation for HS-410," said Melissa Price, Ph.D., Heat’s Vice President of Clinical Development and Regulatory Affairs. "The decision underscores the unmet need for bladder cancer treatments and serves as an additional validation for our clinical program. Currently there are limited therapeutic treatment options available for this patient population, with no new treatments approved in this setting in over 30 years."

Asterias Biotherapeutics Reports Fourth Quarter and Full Year 2014 Financial and Operating Results

Asterias continues development and scale-up of the AST-VAC2 manufacturing process and expects to complete transfer of the resulting cGMP-compatible process to development partner Cancer Research UK (CRUK) in the second quarter of 2015 (Press release, BioTime, MAR 10, 2015, View Source;p=RssLanding&cat=news&id=2024391 [SID:1234502238]). Following completion of the technology transfer, CRUK will, at its own cost, manufacture clinical grade AST-VAC2 and conduct the Phase 1/2a clinical trial in patients with non-small cell lung cancer in the UK, subject to regulatory approval.

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