AbbVie Presents P-III Study (ELEVATE) Results of Qulipta (atogepant) for the Preventive Treatment of Episodic Migraine at AAN 2023
Shots:
- The P-III study evaluating atogepant (60mg, qd) vs PBO in 315 adult patients. The trial met its 1EPs i.e., patients treated with atogepant (60mg, qd) experienced a decrease of 4.20 days vs 1.85 days in MMDs @12wk
- The trial also met its 2EPs i.e., achievement of ≥50% reduction in MMDs, change from baseline in MMDs, and change from baseline in acute medication use days across 12wks.
- The therapy was well tolerated, and the safety results were consistent with the known safety profile of atogepant. Qulipta (CGRP receptor antagonist) was approved in the US to prevent episodic and chronic migraines in adults. Throughout the year, the company will continue to pursue regulatory submissions for atogepant on all global markets
Ref: AbbVie | Image: AbbVie
Related News:- AbbVie Reports P-III Study (INSPIRE) Results of Skyrizi (risankizumab) in P-III Induction Study (INSPIRE) for Ulcerative Colitis
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