NCT06419582CompletedPhase 2/3
BHV-7000 Acute Treatment of Bipolar Mania
A Phase 2/3, Multicenter, Inpatient, Placebo-Controlled, Double-blind Trial of BHV-7000 for the Acute Treatment of Manic Episodes, With or Without Mixed Features, Associated With Bipolar I Disorder
Source: ClinicalTrials.gov · Last updated 16 Dec 2025
Brief summary (registry, in English)
The purpose of this study is to determine whether BHV-7000 is a safe and effective acute treatment for manic episodes in bipolar disorder I.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2/3
- Study type
- Interventional
- Enrollment
- 274 (actual)
- First submitted
- 14 May 2024
- Start date
- 28 May 2024
- Primary completion date
- 15 Jan 2025
- Lead sponsor
- Biohaven Therapeutics Ltd.
- Diseases
- Bipolar disorder
- NCT number
- NCT06419582
What you commit to
- Study type: Interventional · Phase 2/3
- Participants enrolled: 274
- From 28 May 2024 to the primary completion date, 15 Jan 2025
- 32 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Participants with a confirmed lifetime history of schizophrenia, psychotic disorders, dementia, delirium, amnesia, neurodegenerative disease, traumatic brain injury with clinically significant sequalae, seizure disorder, or other neurocognitive disorder. Previous diagnosis of psychotic spectrum disorders are allowable if the Investigator deems the diagnosis to be describing symptoms related to bipolar disorder.
Other illness
- Any medical condition, based on the judgement of the Investigator, that would confound the ability to adequately assess safety and efficacy outcome measures.
Other
- Rapid cycling is excluded as defined herein by subjects who have experienced ≥ 6 distinct mood episodes in a year. Consecutive mood episodes must be demarcated either by a partial or full remission of at least 2 months' duration or by a switch to an episode of opposite polarity. Each manic or mixed episode must have lasted at least 1 week, and each hypomanic episode must have lasted at least 4 days.
Who the study is looking for
- Participant must be voluntarily hospitalized for a current manic episode.
- Male and female participants 18 years to 75 years of age at the time of the screening visit.
- Body Mass Index (BMI) must be ≥ 18 kg/m2 and ≤ 35 kg/m2.
- Meets DSM-5 criteria for bipolar disorder type I, with or without mixed features, as confirmed by MINI interview with at least one well- defined prior mood episode (in addition to the current episode). The most recent prior manic episode must have occurred in the last 2 years.
- Episode of mania must not exceed 12 weeks in duration.
- Participants must be able and willing to discontinue all other psychotropic medications during the Screening Phase (e.g., antidepressant, antimanic, antipsychotic medications).
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (32)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Advanced Research Center, Inc. Coordinator of this site? Confirm its status | Anaheim | United States | Unknown status |
| Atlanta Center for Medical Research Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| Community Clinical Research, Inc. Coordinator of this site? Confirm its status | Austin | United States | Unknown status |
| CIT LA Coordinator of this site? Confirm its status | Bellflower | United States | Unknown status |
| Pillar Clinical Research LLC Coordinator of this site? Confirm its status | Bentonville | United States | Unknown status |
| Pillar Clinical Research Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| Uptown Research Institute Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| ProScience Research Group Coordinator of this site? Confirm its status | Culver City | United States | Unknown status |
| Midwest Clinical Research Center Coordinator of this site? Confirm its status | Dayton | United States | Unknown status |
| CenExel iResearch, LLC Coordinator of this site? Confirm its status | Decatur | United States | Unknown status |
| InSite Clinical Research, LLC Coordinator of this site? Confirm its status | DeSoto | United States | Unknown status |
| Precise Clinical Research Coordinator of this site? Confirm its status | Flowood | United States | Unknown status |
| CBH Health Coordinator of this site? Confirm its status | Gaithersburg | United States | Unknown status |
| CenExel CNS Coordinator of this site? Confirm its status | Garden Grove | United States | Unknown status |
| Segal Trials - Larkin Behavioral Health Services-Inpatient & Early Phase Site Coordinator of this site? Confirm its status | Hollywood | United States | Unknown status |
| CenExel RCA Coordinator of this site? Confirm its status | Hollywood | United States | Unknown status |
| Synergy San Diego Coordinator of this site? Confirm its status | Lemon Grove | United States | Unknown status |
| WIRG Coordinator of this site? Confirm its status | Little Rock | United States | Unknown status |
| Hassman Research Institute Coordinator of this site? Confirm its status | Marlton | United States | Unknown status |
| LCC Medical Research Inst Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Floridian Neuroscience Institute Coordinator of this site? Confirm its status | Miami Lakes | United States | Unknown status |
| Segal Trials - Miami Lakes Medical Research-Inpatient & Early Phase Site Coordinator of this site? Confirm its status | Miami Lakes | United States | Unknown status |
| NBCR Coordinator of this site? Confirm its status | North Canton | United States | Unknown status |
| NRC Research Institute Coordinator of this site? Confirm its status | Orange | United States | Unknown status |
| Pillar Clinical Research, LLC Coordinator of this site? Confirm its status | Richardson | United States | Unknown status |
| CIT IE Coordinator of this site? Confirm its status | Riverside | United States | Unknown status |
| WRN Coordinator of this site? Confirm its status | Rogers | United States | Unknown status |
| CenExel iResearch, LLC Coordinator of this site? Confirm its status | Savannah | United States | Unknown status |
| RBA Coordinator of this site? Confirm its status | Staten Island | United States | Unknown status |
| Arch Clinical Trials Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
| Cenexel CNS Coordinator of this site? Confirm its status | Torrance | United States | Unknown status |
| Neuroscience Research Institute Coordinator of this site? Confirm its status | West Palm Beach | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.