Ubrogepant: First Approval

Author:

Scott Lesley J.

Abstract

AbstractUbrogepant (Ubrelvy™) is an orally administered, small molecule, highly-selective, calcitonin gene-related peptide (CGRP) antagonist that was developed by Allergan under license to Merck & Co. as an acute treatment for migraine. In December 2019, ubrogepant received its first global approval in the USA for the acute treatment of migraine (± aura) in adults. This article summarizes the milestones in the development of ubrogepant leading to its first global approval for the acute treatment of migraine (± aura) in adults.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical)

Reference25 articles.

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4. Allergan, Merck. Allergan enters into licensing agreement with Merck to obtain exclusive worldwide rights to CGRP migraine development program [media release]. 7 Jul 2015.

5. US Food & Drug Administration. FDA approves new treatment for adults with migraine [media release]. 23 Dec 2019. https://www.fda.gov/news-events/press-announcements/fda-approves-new-treatment-adults-migraine.

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