drugset / Trial / NCT06233942

Phase 1a/1b First-in-Human Study of BG-C9074 Alone and in Combination With Other Anticancer Therapies in Patients With Advanced Solid Tumors

NCT06233942

Phase 1 Recruiting 308 enrolled BeOne Medicines
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a first-in-human, dose finding and dose expansion study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-C9074 alone and in combination with other anticancer therapies in patients with advanced solid tumors.

Timeline

Start
2024-04-12
Primary completion
2027-09-28
Completion
2028-05-15

Drugs

EvaluationDrugModalityDoseRoute
Subject BG-C9074 Unknown Intravenous
Subject Bevacizumab Monoclonal antibody Intravenous
Subject Tislelizumab Monoclonal antibody Intravenous

Indications