Dendreon Announces Fourth Quarter and 2013 Year End Results

On March 3, 2014 Dendreon Corporation reported results for the fourth quarter and full year ended December 31, 2013. Net product revenue for the year ended December 31, 2013 was $283.7 million compared to $325.3 million for the year ended December 31, 2012 (Press release Dendreon, MAR 3, 2014, View Source [SID:1234500204]). Net product revenue for the fourth quarter ended December 31, 2013 was $74.8 million compared to $81.6 million on a pro-forma basis for the fourth quarter ended December 31, 2012, which excludes a $3.8 million favorable adjustment to the Company’s chargebacks reserve due to a change in estimate.
New commercial model in place to improve execution with Silvio Pacheco as Chief Customer Officer and Bill Jenkinson as Chief Marketing Officer. Dendreon is advancing automation efforts in the U.S. which is key to lower COGS in U.S. and also more efficiently make PROVENGE available worldwide. As a first step, Dendreon will make PROVENGE available in Europe through Centers of Excellence using Contract Manufacturing Organization (PharmaCell), beginning with Germany and the United Kingdom.

Roche provides update on phase III study of onartuzumab in people with specific type of lung cancer

On March 3, 2014 Roche announced that an independent data monitoring committee has recommended that the Phase III METLung study be stopped due to a lack of clinically meaningful efficacy (Press release Hoffmann-La Roche, MAR 3, 2014, View Source [SID:1234500215]).
The study evaluated if onartuzumab (MetMab) in combination with Tarceva (erlotinib) helped patients with previously treated, advanced non-small cell lung cancer (NSCLC) whose tumors were identified as MET-positive live longer compared to Tarceva alone. Overall adverse event rates were generally similar between the two groups. Data will be submitted for presentation at a forthcoming medical meeting.
Roche is evaluating the implications of the METLung study results across the ongoing onartuzumab clinical programme.

8-K – Current report

Lexicon has during 2013 initiated a companion study of telotristat etiprate in carcinoid syndrome (Filing 8K, Lexicon Pharmaceuticals, FEB 28, 2014, View Source [SID:1234500200]).

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MEI Pharma Receives Orphan Status For Lead Drug Candidate Pracinostat For Treatment Of Acute Myeloid Leukemia

On February 28, 2014 MEI Pharma announced that the U.S. Food and Drug Administration (FDA) has granted orphan drug designation to the company’s investigational drug Pracinostat for the treatment of acute myeloid leukemia (AML) (Press release MEI Pharma, FEB 28, 2014, View Source [SID:1234500202]).

(Filing, 20-F, Theratechnologies, FEB 27, 2014, View Source [SID:1234504821])

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