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BioWorld - Saturday, February 7, 2026
Home » Authors » Catherine Shaffer

Articles by Catherine Shaffer

Alzheimer's imaging agent Amyvid wins approval on second try

April 11, 2012
By Catherine Shaffer

4s3 Exploiting Delivery Method for Treating Muscle Diseases

April 11, 2012
By Catherine Shaffer
It can be difficult to deliver proteins and other large molecules to muscle tissue. But 4s3 Bioscience Inc., of Medford, Mass., said it believes it has found a back door into those cells using its 3E10-targeting antibody along with the ENT2 nucleoside transporter, which is naturally enriched in skeletal muscle fibers.
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Amgen Boosts Pipeline, Adds SHPT Drug in $315M KAI Buy

April 11, 2012
By Catherine Shaffer
Wowed by stunning Phase IIa results for nephrology candidate KAI-4169, Thousand Oaks, Calif.-based Amgen Inc. tendered an offer of $315 million in cash to buy KAI Pharmaceuticals Inc., of San Francisco.
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Alzheimer's Imaging Agent Amyvid Finally Wins Approval

April 10, 2012
By Catherine Shaffer
A year makes all the difference. In March 2011, the FDA sent Amyvid (florbetapir) back to its manufacturer, Avid Radiopharmaceuticals Inc., a wholly owned subsidiary of Eli Lilly and Co. Inc., of Indianapolis, to develop a reader training program for interpretation of scans made with Amyvid.
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Spectrum Acquiring Allos on Heels of Apaziquone Failure

April 6, 2012
By Catherine Shaffer
It was a tumultuous day at the market for Spectrum Pharmaceuticals Inc. and Allos Therapeutics Inc., as investors responded simultaneously to news of the two companies' merger and the failure of Spectrum's cancer drug apaziquone in two Phase III trials.
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CBLI in Damage Control Mode After Surprise BARDA Rejection

April 5, 2012
By Catherine Shaffer
For Cleveland BioLabs Inc., of Buffalo, N.Y., the question of the day was phrased by its vice president of pharmaceutical development, Ed Venkat, who asked, "Why did BARDA reject our white paper proposals?"
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Amylin's Long-Awaited Therapy For Lipodystrophy Goes to FDA

April 4, 2012
By Catherine Shaffer
Nearly eclipsed by the lengthy approval process for Bydureon (exenatide once-weekly), Amylin Pharmaceuticals Inc.'s metreleptin (recombinant methionyl human leptin) in diabetes lipodystrophy may soon get its moment in the sun.
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AlloCure Closes $25M Series B for Kidney Injury

April 3, 2012
By Catherine Shaffer
AlloCure Inc. raised $25 million for a Series B venture financing, welcoming new investor Lundbeckfond Ventures, as well as previous investors SV Life Sciences and Novo A/S.
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Top-Line Results for Genentech/ Immunogen's T-DM1 No Surprise

April 2, 2012
By Catherine Shaffer
The Genentech Inc. unit of Roche AG announced that its Phase III (EMILIA) trial of Immunogen Inc.-partnered asset trastuzumab emtansine (T-DM1) showed positive results. Patients randomized to treatment with T-DM1 had a significantly longer duration of progression-free survival than those receiving the control therapy, lapatinib plus capecitabine.
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Merrimack Pharmaceuticals Aims to Raise $100M in IPO

March 30, 2012
By Catherine Shaffer
Merrimack Pharmaceuticals Inc., which has initiated six new clinical trials since August 2011, priced an initial public offering (IPO) of 14.3 million shares of common stock at $7 per share, for a total anticipated raise of about $100 million.
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