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BioWorld - Monday, December 29, 2025
Home » Authors » Catherine Shaffer

Articles by Catherine Shaffer

Onyx Public Offering Will Beef Up Kyprolis Marketing Push

Jan. 17, 2013
By Catherine Shaffer
Onyx Pharmaceuticals Inc.'s new multiple myeloma drug Kyprolis (carfilzomib) will get a $358.6 million boost following a new public offering of stock from the South San Francisco-based company.
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Versartis' $25M Series C to Fund HGH Trial in Children

Jan. 16, 2013
By Catherine Shaffer
Versartis Inc., of Redwood City, Calif., closed a $25 million Series C financing round through Aisling Capital, Index Ventures, New Leaf Venture Partners and Advent Venture Partners to support clinical trials of VRS-317 for growth hormone deficiency in children.
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Oculus Spinout Ruthigen Focusing on Infection Drug

Jan. 15, 2013
By Catherine Shaffer
Oculus Innovative Sciences Inc., of Petaluma, Calif., spun out a new biotechnology business to develop a drug candidate for infection in trauma and surgical procedures.
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Morphotek's Ovarian Cancer Drug Fails in Phase III Study

Jan. 14, 2013
By Catherine Shaffer
Morphotek Inc.'s promising ovarian cancer drug farletuzumab yielded disappointing results in a Phase III trial in ovarian cancer. The study, which combined farletuzumab with carboplatin and taxane in platinum-sensitive epithelial ovarian cancer, did not meet its primary endpoint of progression-free survival (PFS).
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Cell Therapeutics' Pacritinib Phase III Program Takes Off

Jan. 10, 2013
By Catherine Shaffer
Cell Therapeutics Inc., of Seattle, began a much-anticipated Phase III trial for its JAK2 inhibitor, pacritinib, in myelofibrosis.
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BIND, Amgen Ink $180.5M Nanomedicine Partnership

Jan. 9, 2013
By Catherine Shaffer
BIND Biosciences Inc., of Cambridge, Mass., signed a deal with Amgen Inc., of Thousand Oaks, Calif., worth up to $180.5 million. to collaborate on development of a nanotechnology-based therapeutic for solid tumors.
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Peregrine Redeemed: Phase II Bavi Discrepancies Minimal

Jan. 8, 2013
By Catherine Shaffer
Peregrine Pharmaceuticals Inc.'s internal review of vial coding discrepancies from a Phase II trial of bavituximab in non-small-cell lung cancer (NSCLC) showed that the errors were isolated to placebo and 1-mg/kg treatment arms, leaving the 3-mg/kg treatment arm unaffected.
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Qsymia Set for Fourth-Quarter Launch with Reasonable REMS

Jan. 4, 2013
By Catherine Shaffer

Vivus Inc. shared details of its launch plans and risk evaluation and management strategy (REMS) for newly approved weight loss drug Qsymia (phentermine/topiramate) on an investor call Wednesday morning. Vivus is aiming for a fourth-quarter launch with a REMS that includes a medication guide delivered with each prescription, a health provider training program and distribution of the drug through certified pharmacies only.

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Streamlined, simplified SBIR regulations effective next month

Dec. 28, 2012
By Catherine Shaffer

Streamlined, Simplified SBIR Regulations Effective January

Dec. 28, 2012
By Catherine Shaffer
Updated regulations by the U.S. Small Business Administration (SBA) regarding the size and eligibility for Small Business Innovation Research (SBIR) and Small Business Technology Transfer programs may make the programs significantly more competitive when they take effect Jan. 28.
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