A Study on Efficacy, Safety and Immunogenicity of 9MW0311 in Postmenopausal Women With Osteoporosis
A Randomized, Double-blind, Parallel-group, Phase III Study to Compare the Clinical Efficacy, Safety, and Immunogenicity of Denosumab Injection 9MW0311 With Prolia® in Postmenopausal Women With Osteoporosis
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 3
Contacts and Locations
Study Contact
Study Contact
- Name: Zhitian Hu
- Phone Number: 86-10-87708016
- Email: zhitian.hu@Mabwell.com
Study Locations
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-
-
Beijing, China
- Mabwell (Shanghai) Bioscience Co., Ltd.
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Women who can walk freely (≥50 and ≤80 years);
- As measured by DXA, the absolute value of BMD at lumbar spine, femoral neck or total hip was -4.0<T value ≤-2.5;
- Subjects must have at least one of the following other risk factors: 1) history of previous fragility fractures; 2) Either or both parents have a history of hip fragility fracture; 3) Increased bone turnover rate during screening; 4) Low body weight; 5) Old age(≥70); 6) Currently smoking.
- The duration of spontaneous amenorrhea was >2 years or >2 years after bilateral oophorectomy. If the status of bilateral oophorectomy is unknown or if the ovaries are preserved after hysterectomy, follicle stimulating hormone (FSH) levels >40mIU/mL may be used to confirm the status of postoperative menopause.
Exclusion Criteria:
- Bone/metabolic disease
- Hyperparathyroidism or hypoparathyroidism
- Thyroid condition: Hyperthyroidism or hypothyroidism
- Rheumatoid arthritis
- Malignant tumors
- Malabsorption syndrome
- Liver cirrhosis, active hepatitis B or hepatitis C, and unstable liver disease; serum aspartate aminotransferase and alanine aminotransferase ≥ 2.0 times the upper limit of normal (ULN); alkaline phosphatase or total bilirubin ≥ 1.5 ULN;
- Renal disease - severe impairment of kidney function
- Clinically significant cardiovascular and cerebrovascular diseases (such as myocardial infarction, unstable angina or stroke, NYHA class III or IV heart failure in the 12 months prior to screening) and hematopoietic system disease judged by the investigator;
- Hypercalcemia or hypocalcemia ;
- vitamin D deficiency (25-hydroxyvitamin D, 25OHD <20 ng/mL);
- Oral or dental diseases: previous or current evidence of mandibular osteomyelitis or osteonecrosis; Acute dental or mandibular disease requiring oral surgery; Planning invasive dental surgery; Failure to recover from dental or oral surgery;
- Use of intravenous bisphosphonates within the previous 2 years;
- oral bisphosphonates (used for at least 2 years, or used for less than 2 years but more than 3 months, with the last use occurring <1 year before the screening);
Use of any of the following drugs within 6 weeks prior to screening that may affect bone metabolism:
- parathyroid hormone (PTH) or PTH derivatives, such as teriparatide;
- anabolic hormones or testosterone;
- glucocorticoids (equivalent dose more than 5mg/ day of prednisone and continuous use for more than 10 days);
- Selective estrogen receptor modulators (SERMs), such as raloxifene;
- Menopausal hormone therapy (such as estrogen, estrogen + progesterone, tibolone);
- Active vitamin D and its analogues (cumulative use of more than 30 days);
- Other bone-active drugs include antiepileptic drugs (except benzodiazepines) and heparin;
- Long-term systemic use of ketoconazole, adrenocorticotropin (ACTH), aluminum, lithium, protease inhibitors, methotrexate, gonadotropin releasing hormone agonists;
- Chinese patent medicines for osteoporosis related treatment are clearly described in the instructions, such as Xianling Gubao capsule (tablet), Gushukang capsule (granule), Jintiange capsule and Qianggu capsule."
- History of more than two vertebral fractures.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Quadruple
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: 9MW0311
9MW0311 Denosumab injection(60 mg)
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9MW0311 Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.
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|
Active Comparator: Prolia®
Prolia® Denosumab injection(60 mg)
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Prolia® Denosumab injection(60 mg) was administered subcutaneously once every 6 months for a maximum of 2 consecutive doses throughout the trial.
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What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percent Change From Baseline in lumbar spine(LS)-BMD at Week 53 (Month 12)
Time Frame: Baseline and 12 months
|
Percent Change From Baseline in LS-BMD at Week 53 (Month 12)
|
Baseline and 12 months
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percent Change From Baseline in LS-BMD at Week 27 (Month 6)
Time Frame: Baseline and Month 6
|
Percent Change From Baseline in LS-BMD at Week 27 (Month 6)
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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 )
Time Frame: Baseline, Month6 and Month 53
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Percent change in BMD at the total hip, femoral neck from Baseline up to week 27 (Month 6) and Week 53 (Month 12 )
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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
Time Frame: Baseline, Month1, Month3, Month6, Month9 and Month 12
|
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
|
Baseline, Month1, Month3, Month6, Month9 and Month 12
|
|
Proportion of subjects with new fragility fractures (e.g., vertebrae, hip, non-vertebrae)
Time Frame: From baseline to Month12
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Proportion of subjects with new fragility fractures (e.g., vertebrae, hip, non-vertebrae)
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From baseline to Month12
|
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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
Time Frame: From baseline to Month12
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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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From baseline to Month12
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ADA positive rate and ADA titer (if applicable)
Time Frame: Baseline and Month 1, Month3, Month6, Month12
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ADA positive rate and ADA titer (if applicable)
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Baseline and Month 1, Month3, Month6, Month12
|
|
NAb positive rate (if applicable)
Time Frame: Baseline and Month 1, Month3, Month6, Month12
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NAb positive rate (if applicable)
|
Baseline and Month 1, Month3, Month6, Month12
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Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- 9MW0311-2024-CP302
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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