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Study to Determine if BHV-7000 is Effective and Safe in Adults With Refractory Focal Onset Epilepsy
NCT06309966 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to determine whether BHV-7000 is effective in the treatment of refractory focal epilepsy.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG BHV-7000
Study Locations (20)
Florida
- EZR Research, LLC — Boca Raton
- Nova Clinical Research, LLC — Bradenton
- Las Mercedes Medical Research — Hialeah
- Coral Clinic Research — Homestead
- Dm Healthworks — Kissimmee
- Y&L Advance Health Care, Inc d/b/a Elite Clinical Research — Miami
California
- Amicis Research Center — Lancaster
- Memorialcare Miller Children's & Women's Hospital Long Beach — Long Beach
- Tri Valley Neurology Medical Associates, Inc. — Mission Hills
- Stanford University — Palo Alto
- Profound Research LLC — Poway
Arizona
- Onyx Clinical Trials — Peoria
- Xenoscience, Inc. — Phoenix
- University of Arizona / Banner University Medical Center Phoenix — Phoenix
- ARENSIA Exploratory Medicine — Phoenix
Alabama
- Accel Research — Birmingham
Arkansas
- Clinical Trials, Inc. — Little Rock
Colorado
- Kaiser Permanente — Aurora
Connecticut
- UConn Health — Farmington
District of Columbia
- Children's National Medical Center — Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 390 participants |
| Start Date | 2024-05-13 |
| Est. Completion | 2026-05 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06309966
The ClinicalTrials.gov registry entry for NCT06309966 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 390 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Biohaven Therapeutics, which has 65 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Focal Epilepsy appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06309966 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Florida, California, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06309966 about?
NCT06309966 is a clinical study titled "Study to Determine if BHV-7000 is Effective and Safe in Adults With Refractory Focal Onset Epilepsy". The purpose of this study is to determine whether BHV-7000 is effective in the treatment of refractory focal epilepsy.
What is the current status of trial NCT06309966?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 390 participants. The study started on 2024-05-13. Estimated completion is 2026-05.
What conditions does trial NCT06309966 study?
This clinical trial studies the following conditions: Focal Epilepsy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06309966?
The interventions under investigation include: Placebo (DRUG), BHV-7000 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06309966?
This trial is sponsored by Biohaven Therapeutics, which has 65 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06309966 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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