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BioWorld - Monday, February 2, 2026
Home » Authors » Catherine Shaffer

Articles by Catherine Shaffer

FDA Issues CRL to Salix/ Progenics Constipation Drug

July 31, 2012
By Catherine Shaffer
A day of anticipation ended in disappointment as Salix Pharmaceuticals Ltd. and Progenics Pharmaceuticals Inc. received a complete response letter late Friday from the FDA for injectable Relistor (methylnaltrexone bromide) for opioid-induced constipation in adult patients with chronic, noncancer pain, which has not responded to treatment with laxatives.
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Gilead Sciences Shoots for 1st All-Oral Hepatitis C Regimen

July 30, 2012
By Catherine Shaffer
Four months after passing on an opportunity to pursue Phase III trials of its hepatitis C drug GS-7977 in combination with Bristol-Myers Squibb Co.'s daclatasvir, Gilead Sciences Inc. has confirmed that it will go it alone instead, pressing ahead with its in-house NS5A inhibitor GS-5885.
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Rising Revlimid Demand Helps Celgene's Second-Quarter EPS

July 27, 2012
By Catherine Shaffer
Celgene Corp., of Summit, N.J., exceeded analysts' estimates modestly in its second-quarter earnings report, turning in total revenues of $1.367 billion, a 16 percent increase over the second quarter of 2011. Those revenue increases were led by growing sales of multiple myeloma blockbuster Revlimid (lenolidomide).
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Regeneron's Revenues Nearly Triple; Eylea Launch Still Strong

July 26, 2012
By Catherine Shaffer
A strong launch of Eylea (aflibercept injection) for age-related macular degeneration led Regeneron Pharmaceuticals Inc.'s revenues for the second quarter, with $194 million in sales.
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Thursday's Adcom Eyeballs 2 New Drugs for Ocular Diseases

July 25, 2012
By Catherine Shaffer
The FDA released briefing documents for two products on the slate for consideration at Thursday's meeting of the dermatologic and ophthalmologic drugs advisory committee.
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Investors Step Up for PTC's $30M Round for DMD Trials

July 24, 2012
By Catherine Shaffer
Following encouraging results from a Phase III trial, PTC Therapeutics Inc., of South Plainfield, N.J., completed a $30 million financing to support late-stage development of ataluren. The drug has showed clinically meaningful trends in Duchenne's and Becker muscular dystrophy and cystic fibrosis.
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Regeneron and Sanofi Begin 'ODYSSEY' for Cholesterol mAb

July 23, 2012
By Catherine Shaffer
Sanofi SA and Regeneron Pharmaceuticals Inc. began enrolling patients for several trials within its Phase III program for REGN727, an antibody for lowering LDL cholesterol.
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Acucela Kicks off U.S. Study of Japanese Dry Eye Drug

July 20, 2012
By Catherine Shaffer
Acucela Inc., of Seattle, began a Phase III trial of 2 percent rebamipide ophthalmic suspension for dry eye syndrome. The trial will support eventual U.S. regulatory submission for the product, already launched in Japan as Mucosta by Otsuka Pharmaceutical Co. Ltd.
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Juventas Preps for Phase II Studies with $22M Series B

July 17, 2012
By Catherine Shaffer
Juventas Therapeutics Inc., of Cleveland, is funded through the end Phase II trials for its biologic product, JVS-100, now that it has closed a $22.2 million Series B financing round co-led by Triathlon Medical Venture Partners and New Science Ventures.
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Merck Terminates Odanacatib Trial Early on Positive Results

July 13, 2012
By Catherine Shaffer
Some investors were puzzled when shares of Quest Diagnostics Inc. surged nearly 5 percent Thursday morning for apparently no reason. They could hardly be blamed for not knowing that Madison, N.J.-based Quest is entitled to a rather large payday upon commercialization of Merck & Co. Inc.'s odanacatib, which just blasted through its Phase III study goals upon interim analysis.
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