After spending $257 million and pushing into Phase III trials for a rare thyroid cancer, Bristol-Myers Squibb ends its deal. Exelixis CEO George Scangos says: "There is no smoking gun." read more
The standard exercise test is a problem for many pediatric patients, and FDA's Cardiovascular and Renal Drugs Advisory Committee will assess alternatives. read more
After a futile confirmatory trial, Pfizer will review ongoing studies to see if they can be refined to indentify patients that could benefit from the drug, oncology VP Eagle says. read more
Phase III data for Affymax/Takeda's anemia drug for chronic kidney failure signals potential regulatory hurdles in non-dialysis use. read more
GSK's Witty urges European companies to work with government payers. read more
A deal that would combine two smaller specialty pharmas into one will result in a company with four main business areas. read more
Wyeth challenged whether testimony of expert witness in hormone replacement therapy litigation was admissible; Ortho Biotech argued former sales rep was not an original source of kickback claims. read more
Multiple firms are racing to develop an affordable whole-genome sequencing product as a marketable diagnostics tool, but clinicians and genetics experts told a government advisory panel last week that the practice is not yet ready for clinical application read more
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