drugset / Trial / NCT06874335

A Phase 1 Study of BHV-1530 in Advanced Solid Tumors

NCT06874335

Phase 1 Recruiting 140 enrolled Biohaven Therapeutics Ltd.
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a Phase 1, first in human (FIH), Open-Label, Dose Escalation, Dose Expansion and Dose Optimization Study of BHV-1530 as Monotherapy and in Combination with Other Anti-Cancer Agents in Adult Participants with Advanced or Metastatic Solid Tumors

Timeline

Start
2025-03-20
Primary completion
2029-03
Completion
2029-03

Drugs

EvaluationDrugModalityDoseRoute
Subject BHV-1530 Unknown Intravenous
Subject Cemiplimab Monoclonal antibody 350 mg Intravenous

Indications