drugset / Trial / NCT04630522

Efficacy and Safety of JMT103 in Patients With Bone Metastases From Solid Tumors

NCT04630522

Phase 1 Completed 295 enrolled Shanghai JMT-Bio Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a randomized, open-label, dose-finding, multi-centre, phase Ⅰb study to evaluate the efficacy and safety of JMT103 in patients with bone metastases from solid tumors.

Timeline

Start
2020-10-31
Primary completion
2023-03-31
Completion
2023-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject JMT103 Monoclonal antibody 120 mg Subcutaneous
Subject JMT103 Monoclonal antibody 180 mg Subcutaneous