Biohaven Enrolls First Patient In Phase 3 Clinical Trial To Evaluate Rimegepant Zydis® ODT In The Acute Treatment Of Migraine
- Category: Small Molecules
- Published on Tuesday, 06 March 2018 11:21
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NEW HAVEN, CT, USA I March 6, 2018 I Biohaven Pharmaceutical Holding Company Ltd. (NYSE: BHVN) announced today that it has enrolled the first patient in a Phase 3 clinical trial of the Zydis® orally dissolving tablet ("ODT") formulation of rimegepant for the acute treatment of migraine. Rimegepant is a potent, orally available small molecule calcitonin gene-related peptide ("CGRP") receptor antagonist in late stage development for the treatment of migraine.
The Phase 3 clinical trial will assess the onset of action, patient satisfaction, efficacy and safety of the fast-dissolve Zydis® ODT formulation of rimegepant. Biohaven has been working with Catalent U.K. Swindon Zydis Limited, a subsidiary of Catalent, Inc. (NYSE: CTLT) ("Catalent") to develop this new ODT formulation of rimegepant and extend additional delivery formulations across its CGRP platform. Biohaven has entered into an exclusive agreement with Catalent for the use of the Zydis® ODT formulation technology in the development of small molecule CGRP receptor antagonists. The trial will randomize approximately 850 patients across two treatment arms, rimegepant 75 mg ODT versus placebo.
Vlad Coric, M.D., Chief Executive Officer at Biohaven, commented, "Biohaven is committed to bringing the most differentiated oral, small molecule CGRP receptor antagonist to patients suffering from migraine. The fast-dissolving Zydis® ODT rimegepant formulation is designed to conveniently enable people experiencing a migraine attack to promptly initiate their acute treatment without the need for taking with liquids. We believe that rimegepant Zydis® ODT has the potential to be a best-in-class therapy option for the acute treatment of migraine."
Robert Croop, M.D., Chief Development Officer – Neurology, at Biohaven, added, "This clinical trial with the new fast-dissolve Zydis® ODT formulation complements our ongoing work with rimegepant. We are very pleased to incorporate the trial into our ongoing Phase 3 clinical program. We believe that the rimegepant Zydis® ODT will be a desirable new approach for the acute treatment of migraine."
Biohaven continues to expect topline results from its two pivotal Phase 3 trials examining the efficacy of rimegepant 75 mg oral tablet versus placebo by the end of the first quarter of 2018, and expects topline results from the Phase 3 trial with rimegepant Zydis® ODT in the fourth quarter of 2018.
Biohaven is a clinical-stage biopharmaceutical company with a portfolio of innovative, late-stage product candidates targeting neurological diseases, including rare disorders. Biohaven has combined internal development and research with intellectual property licensed from companies and institutions including Bristol-Myers Squibb Company, AstraZeneca AB, Yale University, Catalent, Rutgers, ALS Biopharma LLC and Massachusetts General Hospital. Currently, Biohaven's lead development programs include multiple compounds across its CGRP receptor antagonist and glutamate modulation platforms. The Company's common shares are listed on the New York Stock Exchange and traded under the ticker symbol BHVN. More information about Biohaven is available at www.biohavenpharma.com.
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