Study of BHV-1400 in IgA Nephropathy
Part of paid clinical trials in Farmington, Connecticut.
- Sponsor
- Biohaven Therapeutics Ltd.
- Study ID
- NCT07054684
- Phase
- PHASE1
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- BHV-1400 — DRUGBHV-1400 is delivered subcutaneously (SC)
Study Details
The purpose of this study is to determine if BHV-1400 is a safe and tolerable treatment in participants with IgA Nephropathy (IgAN).
Key Dates
- Start date
- Jul 30, 2025
- Status verified
- May 2026
- Primary completion
- Jul 31, 2027
- Completion
- Jul 31, 2027
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: BHV-1400
Primary Outcome Measure
Number of participants with Serious AEs (SAEs), AEs leading to discontinuation, deaths [ Time Frame: Up to 1 year ]
Central Contacts
- Chief Medical Officer203-404-0410
Locations (14)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Site-001 | Farmington | Connecticut | 06030 | - |
| Site-003 | Miami Lakes | Florida | 33016 | - |
| Site-011 | Miami Lakes | Florida | 33172 | - |
| Site-013 | Orlando | Florida | 32806 | - |
| Site-005 | Pembroke Pines | Florida | 33029 | - |
| Site-008 | Lawrenceville | Georgia | 30046 | - |
| Site-009 | Hinsdale | Illinois | 60521 | - |
| Site-012 | Indianapolis | Indiana | 46268 | - |
| Site-015 | Shelby | Michigan | 48316 | - |
| Site-006 | Chesterfield | Missouri | 63017 | - |
| Site-002 | Dakota Dunes | South Dakota | 57049 | - |
| Site-004 | Houston | Texas | 77099 | - |
| Site-014 | Houston | Texas | 77027 | - |
| Site-016 | Salt Lake City | Utah | 84115 | - |
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