drugset / Trial / NCT04859569

Efficacy and Safety of LY01011 and Xgeva® in Patients With Bone Metastases From Solid Tumors

NCT04859569

Phase 3 Unknown 850 enrolled Luye Pharma Group Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter,randomized, double-blind, active-controlled, parallel-group study comparing efficacy and safety of LY01011 (recombinant anti-RANKL human monoclonal antibody injection) and Xgeva® in patients with bone metastases from solid tumors.

Timeline

Start
2021-04-30
Primary completion
2022-12-31
Completion
2023-06-30

Drugs

EvaluationDrugModalityDoseRoute
Comparator Denosumab Monoclonal antibody 120 mg Subcutaneous
Subject LY01011 Monoclonal antibody 120 mg Subcutaneous