Shots:
- The approval is based on the P-III OLE trial involves assessing Nurtec ODT (rimegepant, 75 mg) vs PBO in patients with episodic migraine who experience less than 15 headache days/mos.
- The 1EPs & 2EPs of the trial demonstrate a reduction in monthly migraine days by 4.3 days/mos. after 3mos. treatment, 50% patients reported at least >50% reduction in moderate-to-severe migraine days /mos., 95% of all US migraine patients experience less than 15 headache days/ mos.
- Nurtec ODT (rimegepant) is the first and only CGRP receptor antagonist approved by the FDA for migraine as a dual therapy for both the acute and preventive treatment
Click here to read full press release/ article | Ref: PR Newswire | Image: PR Newswire
The post Biohaven’s Nurtec ODT (rimegepant) Receives the US FDA’s Approval for Treatment of Migraine first appeared on PharmaShots.
