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Hemosol eyes IGIV market

The company expects to file an investigational new drug application (IND) in late 2005 or early 2006, followed by a biologic license application in the second half of

Varisolve trials given FDA go-ahead

The FDA intervened in 2003 to stop trials of Varisolve amid fears that the treatment could increase the risk of embolism in patients. In March 2005, Provensis submitted

FDA report says Able falsified drugs data

The report gives twelve observations that raise concerns about the quality control and reporting procedures within Able. Most pertinently the report claims “the quality unit and senior management

Corixa stockholders approve Glaxo deal

As part of the $300 million takeover, shareholders will receive $4.40 in cash for each share of common stock, $517.65 in cash for each share of Series A

Caprion and Boehringer agree research partnership

“This collaboration represents yet another important disease biomarker discovery program for Caprion,” noted Dr Daniel Chelsky, chief scientific officer of Caprion Pharmaceuticals. “This study reflects how Caprion’s biomarker

Genentech profits continue to soar

Operating revenues for the second quarter of 2005 of $1.53 billion represent a 35% increase on revenues of $1.12 billion for the same period in 2004. This has