Puma Biotech Delays Breast Cancer Drug Filing to FDA

By |2017-04-25T18:03:51+00:00December 3rd, 2014|Pharma News|

Puma Biotechnology Inc. (PBYI) said it will delay filing for U.S. regulatory approval of its experimental breast cancer treatment by as much as a year. The company’s shares fell 15 percent to $192.36 at 9:36 a.m. in New York, the most since June. The drugmaker announced yesterday that it would apply for Food and Drug [...]

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Studyops is aggressively recruiting Rheumatologist Principal Investigators for RA trials

By |2014-12-03T17:56:36+00:00December 3rd, 2014|Pharma News|

Studyops, San Francisco California, is aggressively seeking a Rheumatologist to become the lead investigator on Clinical Trials. There are currently 1800 studies for RA listed on clinicaltrials.gov and 500 for Lupis. This is a huge area of development in the R&D space and an excellent opportunity for a Rheumatologist to participate in the advancement of [...]

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Otsuka expands in neurologic diseases with deal to buy Avanir for $3.5 billion

By |2014-12-02T19:43:45+00:00December 2nd, 2014|Pharma News|

Ref: PR Newswire, Financial Times, Bloomberg, Yahoo!Finance, The Wall Street Journal, The New York Times, ABC News, Otsuka) December 2nd, 2014 By: Matthew Dennis Otsuka announced Tuesday a definitive agreement to acquire Avanir Pharmaceuticals for $17.00 per share in cash, or approximately $3.5 billion, expanding its presence in neurologic diseases. The transaction, which has been [...]

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Groundbreaking research is uncovering better ways to keep AIDS at bay

By |2017-04-25T18:03:51+00:00December 2nd, 2014|Pharma News|

The Biggest HIV/AIDS Research Breakthroughs Of 2014   http://www.huffingtonpost.com/2014/12/01/2014-hiv-aids-research_n_6251388.html

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Should The FDA Force Drug Makers To Discuss Their Clinical Trials?

By |2017-04-25T18:03:53+00:00December 1st, 2014|Pharma News|

http://www.forbes.com/sites/johnlamattina/2014/12/01/should-the-fda-force-drug-makers-to-discuss-their-clinical-trials/ Companies are not required to meet with the FDA to discuss their trial design. Nor are they required to follow their recommendations. As revealed in a recent research letter to the Journal of the American Medical Association (JAMA) ), of the 35 drugs approved from February 1, 2011 to February 29, 2012, companies met [...]

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