Lundbeck tries to rush its FDA-approved migraine drug to China but fails PhIII trial
Sales of Lundbeck’s CGRP inhibitor Vyepti, first approved in the US in 2020 and earlier this year in Europe, doubled to more than $50 million in the first half of 2022. But the up-and-coming migraine drug faces a crowded field and the company disclosed Thursday that it failed to beat out placebo in a smaller Phase III trial based in Asia.
The setback may not mean much in terms of introducing the drug into Asian countries more widely, but it’s a setback nonetheless.
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