A Phase 1/2 Study of BHV-1510 (Previously PBI-410) in Advanced Solid Tumors
Public ClinicalTrials.gov record NCT06384807. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
A Phase 1/2, First in Human, Dose Escalation and Dose Expansion Study of BHV-1510 (Previously PBI-410) as Monotherapy and in Combination With Anti-Cancer Agents in Participants With Advanced Solid Tumors
Study identification
- NCT ID
- NCT06384807
- Recruitment status
- Recruiting
- Study type
- Interventional
- Phase
- Phase 1, Phase 2
- Lead sponsor
- Biohaven Therapeutics Ltd.
- Industry
- Enrollment
- 500 participants
Conditions and interventions
Conditions
Interventions
- BHV-1510 Drug
- Cemiplimab Drug
Drug
Eligibility (public fields only)
- Age range
- 18 Years and older
- Sex
- All
- Healthy volunteers
- Healthy volunteers not accepted
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Apr 21, 2024
- Primary completion
- Jan 31, 2028
- Completion
- Jan 31, 2028
- Last update posted
- Mar 10, 2026
2024 – 2028
United States locations
- U.S. sites
- 17
- U.S. states
- 13
- U.S. cities
- 17
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Site-113 | Duarte | California | 91010 | Recruiting |
| Site-112 | La Jolla | California | 92093 | Recruiting |
| Site-111 | Palo Alto | California | 94304 | Recruiting |
| Site-114 | Washington D.C. | District of Columbia | 20016 | Recruiting |
| Site-103 | Miami | Florida | 33176 | Recruiting |
| Site-105 | Orlando | Florida | 32827 | Recruiting |
| Site-115 | Tampa | Florida | 33612 | Recruiting |
| Site-110 | Augusta | Georgia | 30912 | Recruiting |
| Site-109 | Detroit | Michigan | 48201 | Recruiting |
| Site-101 | St Louis | Missouri | 63108 | Recruiting |
| Site-117 | New York | New York | 10021 | Recruiting |
| Site-116 | Oklahoma City | Oklahoma | 73117 | Recruiting |
| Site-108 | Philadelphia | Pennsylvania | 19107 | Recruiting |
| Site-107 | Nashville | Tennessee | 37203 | Recruiting |
| Site-104 | Dallas | Texas | 75231 | Recruiting |
| Site-106 | West Valley City | Utah | 84119 | Recruiting |
| Site-102 | Fairfax | Virginia | 22031 | Recruiting |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT06384807, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Mar 10, 2026 · Synced Jul 21, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT06384807 live on ClinicalTrials.gov.