Study to Determine if BHV-7000 is Effective and Safe in Adults With Refractory Focal Onset Epilepsy

Description

The purpose of this study is to determine whether BHV-7000 is effective in the treatment of refractory focal epilepsy.

Conditions

Focal Epilepsy

Study Overview

Study Details

Study overview

The purpose of this study is to determine whether BHV-7000 is effective in the treatment of refractory focal epilepsy.

A Phase 2/3 Multicenter, Randomization, Double-Blind, Placebo-Controlled, Study to Evaluate the Efficacy, Safety and Tolerability of BHV-7000 in Subjects With Refractory Focal Onset Epilepsy

Study to Determine if BHV-7000 is Effective and Safe in Adults With Refractory Focal Onset Epilepsy

Condition
Focal Epilepsy
Intervention / Treatment

-

Contacts and Locations

Phoenix

Xenoscience, Inc., Phoenix, Arizona, United States, 85004

Phoenix

ARENSIA Exploratory Medicine, Phoenix, Arizona, United States, 85015

Lancaster

Amicis Research Center, Lancaster, California, United States, 93534

Long Beach

Memorialcare Miller Children's & Women's Hospital Long Beach, Long Beach, California, United States, 90806

Poway

Profound Research LLC, Poway, California, United States, 92065

Aurora

Kaiser Permanente, Aurora, Colorado, United States, 80011

Farmington

UConn Health, Farmington, Connecticut, United States, 06030

Washington

Children's National Medical Center, Washington, District of Columbia, United States, 20010

Kissimmee

Dm Healthworks, Kissimmee, Florida, United States, 34741

Miami

Y&L Advance Health Care, Inc d/b/a Elite Clinical Research, Miami, Florida, United States, 33144

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Male and Female participants 18 to 75 years of age at time of consent.
  • 2. Diagnosis of Focal Onset Epilepsy at least 1 year prior to screening visit defined by 2017 International League Against Epilepsy (ILAE) Classification and based on requirements of Epilepsy Adjudication criteria.
  • 3. Subject meets the 2009 ILAE definition of drug resistant epilepsy, failure of adequate trials of two tolerated and appropriately chosen and used anti-seizure medication (ASM) schedules (whether as monotherapies or in combination) to achieve sustained seizure freedom.
  • 4. Ability to keep accurate seizure diaries
  • 5. Current treatment with at least 1 and up to 3 ASMs and 4 epilepsy treatments in total (e.g., 3 ASMs + 1 diet regimen; 2 ASMs + 1 diet regimen + 1 device, etc.)
  • 1. History of status epilepticus (convulsive status epilepticus for \> 5 minutes or focal status epilepticus with impaired conscious for \> 10 minutes) within the last 6 months prior to screening visit that is not consistent with the subject's habitual seizure.
  • 2. History of repetitive/cluster seizures (where individual seizures cannot be counted) within the last 6 months prior to screening visit and during observation phase.
  • 3. Resection neurosurgery for seizures \<4 months prior to the screening visit.
  • 4. Radiosurgery performed \<2 years prior to the screening visit.
  • 5. Subjects with only focal aware nonmotor seizures which involve subjective sensory or psychic phenomena only, without impairment of consciousness or awareness (formally called simple partial seizures), with or without ictal EEG correlation with clinical symptoms.
  • 6. Any condition that would interfere with the subject's ability to comply with study instructions, place the subject at unacceptable risk, and/or confound the interpretation of safety or efficacy data from the study, as judged by the Investigator

Ages Eligible for Study

18 Years to 75 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Biohaven Therapeutics Ltd.,

Study Record Dates

2025-09