Article: Clinic Roundup.

o Actelion Ltd., of Allschwil, Switzerland, reported a preliminary analysis of its 413-patient, Phase IIb dose-finding study showing that its intravenous clazosentan reached statistical significance vs. placebo at all three doses tested - 15 mg/hour, 5 mg/hour and 1 mg/hour. All met the primary endpoint of reducing the occurrence of moderate or severe cerebral vasospasm, as measured by cerebral angiography at day nine post-aneurysm rupture compared to placebo. However, results also showed a lack of clinical benefit in patients who had experienced subarachnoid hemorrhage, and that news dropped Actelion's stock by more than 12 percent Monday. Treatment with clazosentan, an ...

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