Therapy Areas: Central Nervous System
Biohaven Reports Positive Results from Double-Blind, Placebo-Controlled, Investigator Initiated, Proof Of Concept Trial Of BHV-0223 For Anxiety
17 August 2018 - - US-based biopharmaceutical company Biohaven Pharmaceutical Holding company Ltd. (NYSE: BHVN) has seen 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-provoking speech task (clinicaltrials.gov identifier: NCT03017508), the company said.

The investigator-initiated trial was performed at Yale University School of Medicine and treated 21 subjects who had a diagnosis of social anxiety disorder and participated in an anxiety-provoking, speech task in a double-blind, crossover design.

In the pre-specified, primary analysis, BHV-0223 reduced anxiety by 8.3 points relative to placebo on the 100-point Visual Analogue Scale.

The observed reduction in anxiety was significant (p=0.056), relative to the protocol specified level of p= 0.10.

A likelihood-based analysis, that analyzed the change in the VAS from the pre-speech baseline, found that BHV-0223 had a 14.4-point advantage relative to placebo (p=0.0259).

In addition, BHV-0223 was safe and well-tolerated during this study. Biohaven expects to present additional results from this trial at upcoming scientific meetings over the next year.

Biohaven has an exclusive license agreement with Yale University under Yale's patent rights for the commercial development, manufacture, distribution, use and sale of products and methods related to the use of riluzole in treating a range of central nervous system disorders including generalized anxiety disorder, social anxiety disorder and panic disorder.

In addition to BHV-0223, Biohaven also owns worldwide patents and patent applications covering a broad library of prodrugs of riluzole designed for optimized safety, tolerability and pharmacokinetics.

These include troriluzole (BHV-4157), currently in late-stage clinical trials in spinocerebellar ataxia, obsessive compulsive disorder, and Alzheimer's disease.

Biohaven anticipates submitting a New Drug Application for BHV-0223 for the treatment of amyotrophic lateral sclerosis to the US Food and Drug Administration in 3Q18.

The primary purpose of the trial was to examine the acute anti-anxiety potential of BHV-0223 as compared to placebo in subjects with social anxiety disorder and public speaking anxiety while performing a 10-minute anxiety-provoking speech task.

Twenty-one subjects who met DSM-5 criteria for social anxiety disorder and clinically significant public speaking anxiety on the Impromptu Speech Task were enrolled in a public speaking challenge study. Subjects were treated with BHV-0223 35mg or placebo under double-blind crossover conditions one hour prior to performing each of two impromptu speech tasks, which were separated by two to ten days to allow for medication washout.

The trial was powered at 80%, to detect an effect size of 0.58, at an alpha of p=0.10, on the primary endpoint of self-reported anxiety measured on the VAS during the Impromptu Speech Task. Baseline anxiety was measured on the VAS prior to the speaking exercise.

Based upon these trial results, Biohaven plans to expand its glutamate modulating platform development program to include the treatment of GAD.

Biohaven's glutamate modulating platform includes agents targeting glutamate transporters on glia and NMDA antagonism. Sublingual riluzole (BHV-0223) and the third generation prodrug troriluzole (BHV-4157) are being developed across a variety of neurologic and neuropsychiatric disorders.

BHV-0223 is a sublingual formulation of riluzole which employs the Zydis orally dissolving tablet technology.

It is administered under the tongue, where it dissolves in seconds and does not require swallowing or administration with liquids.

In addition to exclusive intellectual property rights related to the use of riluzole in certain neuropsychiatric disorders licensed from Yale University, Biohaven has worldwide exclusive rights from Catalent to the use of Zydis orally dissolving tablet technology in riluzole products. Troriluzole is currently being evaluated in Phase 2/3 clinical trials in SCA, OCD and AD.


Biohaven's low-trapping NMDA antagonist (BHV-5000) was in-licensed from AstraZeneca and potential development programs include Rett syndrome, treatment-resistant depression and chronic pain disorders.

Biohaven is a clinical-stage biopharmaceutical company with a portfolio of innovative, late-stage product candidates targeting neurological diseases, including rare disorders.

The company combined internal development and research with intellectual property licensed from companies and institutions including Bristol-Myers Squibb Company, AstraZeneca AB, Yale University, Catalent, ALS Biopharma LLC and Massachusetts General Hospital.

Currently, Biohaven's lead development programs include multiple compounds across its CGRP receptor antagonist and glutamate modulating platforms.

The company's common shares are listed on the New York Stock Exchange and traded under the ticker symbol BHVN.
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