This study is a multicenter, randomized, double-blinded, parallel-group Phase III clinical study to compare the clinical efficacy, safety, and immunogenicity of 9MW0311 and Prolia® in Chinese postmenopausal women with osteoporosis at high risk for fracture.
278 patients are randomized 1:1 to receive 9MW0311 and Prolia® every 6 months for 12 months. The primary efficacy endpoint is the percentage change from baseline in BMD at the lumbar spine(LS) in month 12.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
280
9MW0311 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.
Mabwell (Shanghai) Bioscience Co., Ltd.
Beijing, China
Percent Change From Baseline in lumbar spine(LS)-BMD at Week 53 (Month 12)
Percent Change From Baseline in LS-BMD at Week 53 (Month 12)
Time frame: Baseline and 12 months
Percent Change From Baseline in LS-BMD at Week 27 (Month 6)
Percent Change From Baseline in LS-BMD at Week 27 (Month 6)
Time frame: Baseline and Month 6
Percent change in BMD at the total hip, femoral neck from Baseline up to week 27 (Month 6) and Week 53 (Month 12 )
Percent change in BMD at the total hip, femoral neck from Baseline up to week 27 (Month 6) and Week 53 (Month 12 )
Time frame: Baseline, Month6 and Month 53
Percent Change in Serum Carboxy-terminal Cross-linking Telopeptide of Type I Collagen (s-CTX) and Serum type I procollagen N-terminal propeptide (s-PINP) from Baseline up to 12 months
Percent Change in Serum Carboxy-terminal Cross-linking Telopeptide of Type I Collagen (s-CTX) and Serum type I procollagen N-terminal propeptide (s-PINP) from Baseline up to 12 months
Time frame: Baseline, Month1, Month3, Month6, Month9 and Month 12
Proportion of subjects with new fragility fractures (e.g., vertebrae, hip, non-vertebrae)
Proportion of subjects with new fragility fractures (e.g., vertebrae, hip, non-vertebrae)
Time frame: From baseline to Month12
Number of participants with AE, SAE, with abnormal vital signs, abnormal physical examination findings, abnormal oral examination findings, abnormal laboratory tests results and abnormal 12-lead ECG readings
AE, SAE, vital signs, physical examination, oral examination, laboratory examination (blood routine, urine routine/urine sediment, blood biochemistry, coagulation function), 12-lead ECG
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Time frame: From baseline to Month12
ADA positive rate and ADA titer (if applicable)
ADA positive rate and ADA titer (if applicable)
Time frame: Baseline and Month 1, Month3, Month6, Month12
NAb positive rate (if applicable)
NAb positive rate (if applicable)
Time frame: Baseline and Month 1, Month3, Month6, Month12