AbbVie Publishes Results for Ubrelvy (ubrogepant) in P-III Trial for Migraine in ‘The Lancet’
Shots:
- The P-III (PRODROME) clinical trial evaluates the safety, efficacy & tolerability of Ubrelvy (100mg) vs PBO in patients (n=518) experiencing 2-8 migraine attacks with moderate-to-severe headache/month. The results from the trials were published in ‘The Lancet’
- The results from the trial depicted a significant reduction in headache frequency within 24hrs. & 48hrs., with 46% vs 29% & 41% vs 25% of qualifying prodrome events being absent whereas the intensity of headache was also significantly reduced within 24hrs. after 24% vs 14% of qualifying prodrome events
- Ubrelvy is an orally administered calcitonin gene-related peptide (CGRP) receptor antagonist (gepant) developed for the acute treatment of migraine with or without aura in adults
Ref: PR Newswire | Image: AbbVie
Related News:- Allergan's Ubrelvy (ubrogepant) Receives the US FDA's Approval for Acute Treatment of Migraine with or without Aura in Adults
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Shivani is a content writer at PharmaShots. She has a keen interest in recent innovations in the life sciences industry. She covers news related to Product approvals, clinical trial results, and updates. She can be contacted at connect@pharmashots.com.
