A Study to Determine if BHV-8000 is Effective, Safe and Tolerable as a Treatment for Adults Living With Early Parkinson's Disease

Part of paid clinical trials in Birmingham, Alabama.

Sponsor
Biohaven Therapeutics Ltd.
Study ID
NCT06976268
Phase
PHASE2/PHASE3
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
40 Years - 85 Years
Healthy Volunteers
Not accepted

Interventions

  • BHV-8000 — DRUG
    BHV-8000 10 mg. Participants will take blinded investigational product (IP) once daily
  • BHV-8000 — DRUG
    BHV-8000 20 mg. Participants will take blinded investigational product (IP) once daily
  • Placebo — DRUG
    Matching placebo taken once daily

Study Details

A study to determine if BHV-8000 is efficacious, safe and tolerable in adults diagnosed with early Parkinson's disease.

Key Dates

Start date
May 28, 2025
Status verified
Jan 2026
Primary completion
Aug 31, 2027
Completion
Sep 30, 2027

Study Design

Enrollment
550 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: BHV-8000 10 mg
  • Experimental: BHV-8000 20 mg
  • Placebo Comparator: Placebo

Primary Outcome Measure

Time to first qualifying worsening event on Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part II [ Time Frame: Up to 48 Weeks ]

Central Contacts

Locations (15)

FacilityCityStateZIPSite coordinators
Site-049BirminghamAlabama35294-
Site-041Los AngelesCalifornia90033-
Site-031FarmingtonConnecticut06030-
Site-028New HavenConnecticut06510-
Site-038AtlantisFlorida33462-
Site-017Boca RatonFlorida33486-
Site-051MaitlandFlorida32751-
Site-027ChicagoIllinois60611-
Site-071BostonMassachusetts02114-
Site-015Farmington HillsMichigan48334-
Site-044ChesterfieldMissouri63005-
Site-005New YorkNew York10021-
Site-091PortlandOregon97210-
Site-043Round RockTexas78681-
Site-007BellevueWashington98007-

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