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A Comparative Study to Valuating the Efficacy and Safety of QL1206 and Prolia®
Sponsor: Qilu Pharmaceutical Co., Ltd.
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.
Official title: 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
Key Details
Gender
FEMALE
Age Range
50 Years - 85 Years
Study Type
INTERVENTIONAL
Enrollment
278
Start Date
2025-06-27
Completion Date
2027-01
Last Updated
2025-07-14
Healthy Volunteers
No
Interventions
QL1206
QL1206 Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.
Prolia®
Prolia® Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.
Locations (1)
Zhejiang Provincial People's Hospital Bijie Hospital
Guizhou, China