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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
278
QL1206 Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.
Prolia® Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.
Zhejiang Provincial People's Hospital Bijie Hospital
Guizhou, China
RECRUITINGPercent Change From Baseline in lumbar spine(LS)-BMD at Month 12
Percent Change From Baseline in lumbar spine(LS)-BMD at Month 12
Time frame: Baseline and 12 months
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