Ampyra Lower-Dose Post-Market Study Misses Endpoint
By Catherine Shaffer
Staff Writer
Staff Writer
Monday, August 13, 2012
A post-market study by Acorda Therapeutics Inc. designed to compare a lower 5-mg dose of Ampyra (dalfampridine) to the approved 10-mg dose failed to show any benefit for the 5-mg dose and missed its primary endpoint altogether at both doses. The drug is approved for use in patients with multiple sclerosis.
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