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Biohaven Enrolls First Patient in Phase 3 Troriluzole Trial
americanpharmaceuticalreview
February 21, 2019
Biohaven has enrolled its first patient in a Phase 3 clinical trial assessing the efficacy and safety of troriluzole in generalized anxiety disorder (GAD).....
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Biohaven Reaches Targeted Therapeutic Exposures of BHV-3500
americanpharmaceuticalreview
February 19, 2019
Biohaven announced that administration of intranasal BHV-3500 in a Phase 1 clinical trial has achieved targeted therapeutic exposures and that the compound will advance into a Phase 2 trial to evaluate efficacy for the acute treatment of migraine....
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Biohaven Receives FDA May Proceed Letter for BHV-3241 Trial
americanpharmaceuticalreview
January 25, 2019
Biohaven announced the U.S. Food and Drug Administration (FDA) has notified the company that it may proceed with its clinical investigation of BHV-3241 ....
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Biohaven Announces Positive Results from Rimegepant Safety Study
americanpharmaceuticalreview
December 11, 2018
Biohaven announced initial positive results from its ongoing long-term, open-label safety study of its oral calcitonin gene-related peptide (CGRP) receptor antagonist, rimegepant.....
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Biohaven Delivers Positive Phase 3 Results with Rimegepant Zydis ODT
americanpharmaceuticalreview
December 04, 2018
Biohaven announced positive topline results from a randomized, controlled Phase 3 clinical trial (BHV3000-303 or Study 303) evaluating the efficacy ......
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Biohaven Announces Formation of Bioshin
americanpharmaceuticalreview
November 30, 2018
Biohaven has advanced the formation of a wholly owned subsidiary, BioShin, a Shanghai based limited liability company, to develop and commercialize its late-stage migraine....
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Biohaven Announces Submission of IND for BHV-3500
americanpharmaceuticalreview
September 13, 2018
Biohaven has submitted an Investigational New Drug (IND) application to the U.S. Food and Drug Administration (FDA) to evaluate the safety and tolerability of BHV-3500, the first small molecule calcitonin gene-related peptide (CGRP) receptor antagonist to
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Biohaven Reports Positive Results from BHV-0223 Trial
americanpharmaceuticalreview
August 17, 2018
Biohaven announced positive results from a double-blind, placebo-controlled, proof of concept clinical trial evaluating the effect of BHV-0223 in patients diagnosed with social anxiety disorder and public speaking anxiety while performing an anxiety-provo
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Too scared to speak in public? Biohaven says it has a drug that can help
fiercebiotech
August 17, 2018
Biohaven’s new formulation of amyotrophic lateral sclerosis drug riluzole has helped people with social anxiety face the challenge of speaking in public.
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Biohaven Announces Positive Results From Bioequivalence Study With Sublingual BHV-0223 Zydis Orally
biospace
January 10, 2018
Biohaven announced positive results today from its bioequivalence study with BHV-0223, an innovative sublingual formulation of riluzole.