drugset / Trial / NCT05212896

An Exploratory Clinical Study of BC006 in Patients With Advanced Solid Tumors

NCT05212896 ↗

Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a first in human, open-label, exploratory phase I clinical study including dose escalation (Ia) and dose expansion (Ib) stage. It aims to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of BC006 in giant cell tumor of tendon sheath (GCTTS) and other advanced solid tumors.

Timeline

Start
2021-11-26
Primary completion
2024-12
Completion
2024-12

Drugs

EvaluationDrugModalityDoseRoute
Subject BC006 Monoclonal antibody 0.08 mg/kg Intravenous
Subject BC006 Monoclonal antibody 0.3 mg/kg Intravenous
Subject BC006 Monoclonal antibody 1 mg/kg Intravenous
Subject BC006 Monoclonal antibody 3 mg/kg Intravenous
Subject BC006 Monoclonal antibody 10 mg/kg Intravenous
Subject BC006 Monoclonal antibody 20 mg/kg Intravenous