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NCT06804590CompletedPhase 3

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

Source: ClinicalTrials.gov · Last updated 7 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
280 (actual)
First submitted
9 Dec 2024
Start date
16 Nov 2024
Primary completion date
24 Apr 2026
Lead sponsor
Mabwell (Shanghai) Bioscience Co., Ltd.
Diseases
Osteoporosis
NCT number
NCT06804590

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 280
  • From 16 Nov 2024 to the primary completion date, 24 Apr 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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;
  • 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;
  • 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."

Other illness

  • Bone/metabolic disease
  • Thyroid condition: Hyperthyroidism or hypothyroidism
  • Malignant tumors
  • Malabsorption syndrome
  • Renal disease - severe impairment of kidney function
  • History of more than two vertebral fractures.

Lab values

  • 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;

Other

  • Hyperparathyroidism or hypoparathyroidism
  • Rheumatoid arthritis
  • Hypercalcemia or hypocalcemia ;
  • vitamin D deficiency (25-hydroxyvitamin D, 25OHD \<20 ng/mL);
  • 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);

Who the study is looking for

  • 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.

Age in the registry: 50 years to 80 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mabwell (Shanghai) Bioscience Co., Ltd.
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.