Rimegepant
This article may contain excessive or inappropriate references to self-published sources. (June 2020) |
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Trade names | Nurtec ODT |
Other names | BHV-3000, BMS-927711 |
AHFS/Drugs.com | Monograph |
MedlinePlus | a620031 |
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Routes of administration | By mouth |
Drug class | calcitonin gene-related peptide receptor antagonist |
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Formula | C28H28F2N6O3 |
Molar mass | 534.568 g·mol−1 |
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Rimegepant, sold under the brand name Nurtec ODT, is a medication for the treatment of an acute migraine with or without aura in adults.[1] It is not used prophylactically.[2]
Taken by mouth to dissolve on or under the tongue,[2] rimegepant takes effect within an hour and can provide relief from migraine headache for up to 48 hours. It is not a narcotic and has no addictive potential; thus it is not designated as a controlled substance.
This article needs additional citations for verification. (August 2020) |
It works by blocking CGRP receptors.
Approved for use in the United States in February 2020, rimegepant is produced and marketed by Biohaven Pharmaceuticals, based in New Haven, Connecticut.[3][1]
Mechanism of action
Rimegepant is a small molecule calcitonin gene-related peptide (CGRP) receptor antagonist.[4]
History
Originally discovered at Bristol-Myers Squibb,[5] rimegepant was developed by Biohaven Pharmaceuticals, which markets the drug in the United States after receiving FDA approval in February 2020.[6] Approval was based on evidence from one clinical trial of 1,351 subjects with migraine headaches.[1]
References
- ^ a b c "Drug Trials Snapshots: Nurtec ODT". U.S. Food and Drug Administration (FDA). 27 February 2020. Retrieved 19 March 2020. This article incorporates text from this source, which is in the public domain.
- ^ a b "Nurtec ODT - rimegepant sulfate tablet, orally disintegrating". DailyMed. 19 February 2020. Retrieved 19 March 2020.
- ^ "Nurtec ODT: FDA-Approved Drugs". U.S. Food and Drug Administration (FDA). Retrieved 28 February 2020.
- ^ Diener HC, Charles A, Goadsby PJ, Holle D (October 2015). "New therapeutic approaches for the prevention and treatment of migraine". The Lancet. Neurology. 14 (10): 1010–22. doi:10.1016/S1474-4422(15)00198-2. PMID 26376968.
- ^ "Rimegepant - Biohaven Pharmaceuticals Holding Company". Adis Insight. Springer Nature Switzerland AG.
- ^ "Biohaven's Nurtec ODT (rimegepant) Receives FDA Approval for the Acute Treatment of Migraine in Adults" (Press release). Biohaven Pharmaceuticals Holding Company Ltd. 27 February 2020 – via PR Newswire.
External links
- "Rimegepant". Drug Information Portal. U.S. National Library of Medicine.
- Clinical trial number NCT03461757 for "Trial in Adult Subjects With Acute Migraines" at ClinicalTrials.gov
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