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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.
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

Full criteria on ClinicalTrials.gov

Sites (32)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Advanced Research Center, Inc.
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AnaheimUnited StatesUnknown status
Atlanta Center for Medical Research
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AtlantaUnited StatesUnknown status
Community Clinical Research, Inc.
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AustinUnited StatesUnknown status
CIT LA
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BellflowerUnited StatesUnknown status
Pillar Clinical Research LLC
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BentonvilleUnited StatesUnknown status
Pillar Clinical Research
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ChicagoUnited StatesUnknown status
Uptown Research Institute
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ChicagoUnited StatesUnknown status
ProScience Research Group
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Culver CityUnited StatesUnknown status
Midwest Clinical Research Center
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DaytonUnited StatesUnknown status
CenExel iResearch, LLC
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DecaturUnited StatesUnknown status
InSite Clinical Research, LLC
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DeSotoUnited StatesUnknown status
Precise Clinical Research
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FlowoodUnited StatesUnknown status
CBH Health
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GaithersburgUnited StatesUnknown status
CenExel CNS
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Garden GroveUnited StatesUnknown status
Segal Trials - Larkin Behavioral Health Services-Inpatient & Early Phase Site
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HollywoodUnited StatesUnknown status
CenExel RCA
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HollywoodUnited StatesUnknown status
Synergy San Diego
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Lemon GroveUnited StatesUnknown status
WIRG
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Little RockUnited StatesUnknown status
Hassman Research Institute
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MarltonUnited StatesUnknown status
LCC Medical Research Inst
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MiamiUnited StatesUnknown status
Floridian Neuroscience Institute
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Miami LakesUnited StatesUnknown status
Segal Trials - Miami Lakes Medical Research-Inpatient & Early Phase Site
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Miami LakesUnited StatesUnknown status
NBCR
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North CantonUnited StatesUnknown status
NRC Research Institute
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OrangeUnited StatesUnknown status
Pillar Clinical Research, LLC
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RichardsonUnited StatesUnknown status
CIT IE
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RiversideUnited StatesUnknown status
WRN
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RogersUnited StatesUnknown status
CenExel iResearch, LLC
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SavannahUnited StatesUnknown status
RBA
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Staten IslandUnited StatesUnknown status
Arch Clinical Trials
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St LouisUnited StatesUnknown status
Cenexel CNS
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TorranceUnited StatesUnknown status
Neuroscience Research Institute
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West Palm BeachUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.