drugset / Trial / NCT05351697

Clinical Study of BR105 Injection

NCT05351697 ↗

Phase 1 Terminated 31 enrolled BioRay Pharmaceutical Co., Ltd.
NaSequentialOpen-labelOther

Summary

A phase 1, dose escalation and dose expansion study of BR105 in patients with advanced malignancies.

Timeline

Start
2022-04-19
Primary completion
2025-10-30
Completion
2025-10-30

Outcome

Outcome not reported

Stopped (Business): “Company R\&D Strategy Adjustment”

Drugs

EvaluationDrugModalityDoseRoute
Subject LUMISTOBART Monoclonal antibody 0.2 mg/kg Intravenous
Subject LUMISTOBART Monoclonal antibody 1 mg/kg Intravenous
Subject LUMISTOBART Monoclonal antibody 3 mg/kg Intravenous
Subject LUMISTOBART Monoclonal antibody 10 mg/kg Intravenous
Subject LUMISTOBART Monoclonal antibody 20 mg/kg Intravenous
Subject LUMISTOBART Monoclonal antibody 30 mg/kg Intravenous
Subject LUMISTOBART Monoclonal antibody 40 mg/kg Intravenous

Indications