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    Home > Active Ingredient News > Study of Nervous System > Express Delivers Positive Results from Pivotal Clinical Trial of Oral CGRP Receptor Antagonist for Migraine Patients in Asia Pacific

    Express Delivers Positive Results from Pivotal Clinical Trial of Oral CGRP Receptor Antagonist for Migraine Patients in Asia Pacific

    • Last Update: 2022-03-07
    • Source: Internet
    • Author: User
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    ▎WuXi AppTec Content Team Editors On February 14, 2022, Biohaven Pharmaceutical and Pfizer announced positive top-line results from a Phase 3 clinical trial of rimegepant in adults with acute migraine
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    Rimegepant is a small molecule oral calcitonin gene-related peptide (CGRP) receptor antagonist that has been approved by the US FDA for both acute treatment of migraine attacks and as a preventive treatment to reduce the frequency of migraine attacks.
    Nurtec
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    According to the press release, rimegepant is the first oral CGRP receptor antagonist to achieve positive results in a pivotal clinical trial in the Asia-Pacific region
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    Migraine is a very common chronic disease
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    According to the World Health Organization (WHO), one in ten people in the world suffers from migraine, and women suffer three times as often as men
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    Patients often experience flare-ups with symptoms including headache, photophobia, phonophobia, hallucinations, and nausea
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    Small-molecule CGRP receptor inhibitors represent a new class of drugs for the treatment of migraine, and the activity of CGRP is thought to pathologically contribute to migraine
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    Rimegepant's fast-dissolving oral tablet formulation works by blocking CGRP receptors
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    This is the fourth Phase 3 clinical trial of rimegepant for the acute treatment of migraine, and the first in the Asia-Pacific region, led by BioShin, a wholly-owned subsidiary of Biohaven in the Asia-Pacific region.

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    The trial met its co-primary endpoints of no pain and no most bothersome migraine-related symptoms (MBS, including nausea, phonophobia, or photophobia)
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    A single oral dose of 75 mg rimegepant significantly relieved migraine symptoms and returned patients to normal function within 2 hours
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    Also, the drug provides sustained efficacy for up to 48 hours in many patients
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    In terms of safety, rimegepant showed a favorable safety and tolerability profile, consistent with the results of previous clinical trials in the United States
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    Detailed data from the study will be presented at a future medical meeting
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    Dr.
    Vlad Coric, Chief Executive Officer and Chairman of the Board of Directors of Biohaven, commented: "These top-line trial results clearly demonstrate the consistent clinical performance of rimegepant in migraine relief and recovery of patients' normal function
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    Through our partnership with Pfizer, we have Committed to rapidly expanding the accessibility of rimegepant to patients around the world
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    Migraine is a common condition and a leading cause of disability, especially in the Asia Pacific region
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    " Nick Lagunowich, Global President, Pfizer Internal Medicine, said: "Seeing rimegepant It is very exciting to see the successful completion of the first Phase 3 clinical trial in Asia Pacific with positive results
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    Millions of patients in the region are affected by this debilitating neurological disease, and these results provide a hope for patients in need.
    hope for a potentially effective novel acute treatment
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    "Reference: [1] Biohaven and Pfizer Announce Positive Topline Results of Pivotal Trial of Rimegepant for the Acute Treatment of Migraine in China and South Korea.
    Retrieved February 14, 2022, from https:// releases/biohaven-and-pfizer-announce-positive-topline-results-of-pivotal-trial-of-rimegepant-for-the-acute-treatment-of-migraine-in-china-and-south-korea-301481322.
    html Disclaimer: The WuXi AppTec content team focuses on introducing the progress of global biomedical health research
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    This article is for information exchange purposes only.
    The views in this article do not represent WuXi AppTec's position, nor do they support or oppose the views in the article
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    This article is not Recommended treatment plan
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    If you need treatment plan guidance, please go to a regular hospital for treatment
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