Clinical data | |
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Trade names | Nurtec ODT, Vydura |
Other names | BHV-3000, BMS-927711 |
AHFS/Drugs.com | Monograph |
MedlinePlus | a620031 |
License data |
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Routes of administration | By mouth |
Drug class | Calcitonin gene-related peptide receptor antagonist |
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Chemical and physical data | |
Formula | C28H28F2N6O3 |
Molar mass | 534.568 g·mol−1 |
3D model (JSmol) | |
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Rimegepant, sold under the brand name Nurtec ODT among others, is a medication used for the acute treatment of migraine with or without aura in adults and the prophylactic/ preventive treatment of episodic migraine in adults. [6] [8] It is taken by mouth to dissolve on or under the tongue. [6] It works by blocking CGRP receptors. [9]
In the United States, rimegepant was approved for treating acute migraine in February 2020, [10] and its approval was extended to preventing episodic migraine in June 2021. [6] It is produced and marketed by Pfizer. [11] In March 2021, rimegepant was approved for medical use in the United Arab Emirates and in Israel. [12] [13] [14] It was approved for medical use in Canada in December 2023. [3]
Rimegepant is indicated for the treatment of acute migraine with or without aura in adults and for the preventative treatment of episodic migraine in adults. [6] [8] [7]
Rimegepant is a small molecule calcitonin gene-related peptide (CGRP) receptor antagonist. [9]
Rimegepant was developed by Biohaven Pharmaceuticals, which markets the drug in the United States after receiving FDA approval in February 2020. [10] [15] Approval was based on evidence from one clinical trial of 1,351 subjects with migraine headaches. [8]
On 24 February 2022, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion, recommending the granting of a marketing authorization for the medicinal product Vydura, intended for the prophylaxis and acute treatment of migraine. [16] The applicant for this medicinal product is Biohaven Pharmaceutical Ireland DAC. [16] Rimegepant was approved for medical use in the European Union in April 2022. [7] [17]
The European Medicines Agency (EMA) is an agency of the European Union (EU) in charge of the evaluation and supervision of pharmaceutical products. Prior to 2004, it was known as the European Agency for the Evaluation of Medicinal Products or European Medicines Evaluation Agency (EMEA).
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