Clinical Trial

A Comparative Study to Valuating the Efficacy and Safety of QL1206 and Prolia®

Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
This study is a multicenter, randomized, double-blind comparative study to valuating the efficacy and safety of QL1206 and Prolia® in postmenopausal women with osteoporosis at high risk of fracture.
Trial Details
NCT Number NCT07062978
Lead Sponsor Qilu Pharmaceutical Co., Ltd.
Conditions Postmenopausal Women With Osteoporosis at High Risk of Fracture
Enrollment 278 participants
Start Date 2025-06-27
Primary Completion 2027-01 (estimated)
Study Completion 2027-01 (estimated)
Updated on ClinicalTrials.gov 2025-07-14