US FDA delays verdict on Pfizer/BMS stroke prevention drug
This article was originally published in Scrip
The US FDA has delayed by three months its decision on the new drug application (NDA) for Bristol-Myers Squibb's and Pfizer's experimental anticoagulant Eliquis (apixaban) as a therapy to reduce the risk of stroke and systemic embolism in patients with nonvalvular atrial fibrillation.
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