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AstraZeneca's Galida Filing Delayed Until 2007 Due To PPAR Safety Concerns

This article was originally published in The Pink Sheet Daily

Executive Summary

Long-term patient follow-up is extended to two years in light of regulatory concerns about PPAR class safety, firm tells analysts. News is setback for AstraZeneca's near-term cardiovascular pipeline and a boost for Bristol/Merck's muraglitazar.

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