Postmenopausal Osteoporosis
Conditions
Brief summary
CMAB807 is a human monoclonal antibody targeting the key bone resorption mediator RANKL. The drug is administered via subcutaneous injection once six months and is approved for various indications, including the treatment of postmenopausal women with osteoporosis at increased/high risk of fracture. This phase 1 clincical study investigates the pharmacokinetics, safety and immnogenicity of CMAB807,compared to prolia®, in healthy Chinese male subjects.
Detailed description
This is a phase 1 single center, randomized, double-masked, parallel-group clinical trial. The primary objective is to assess the pharmacokinetics similarity of single and subcutaneous injection of CMAB807 injection or Prolia® in health volunteers. The secondary objectives are to assess the clinical safety and immnogenicity similarity of single and subcutaneous injection of CMAB807 or Prolia® in healty volunteers. Meanwhile, exploring the pharmacodynamic similarities of CMAB807 and Prolia®. Subjects will receive a single 60mg of CMAB807 or Prolia® through subcutaneous injection.
Interventions
DRUGProlia®
mAb targeting RANKL. human monoclonal antibody targeting RANKL.
DRUGCMAB807
human monoclonal antibody targeting RANKL.
Sponsors
Shanghai Biomabs Pharmaceutical Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Masking description
subjects, investigator, sponsor
Intervention model description
Randomized, Double-masked, Parallel-group
Eligibility
Sex/Gender
MALE
Age
18 Years to 65 Years
Healthy volunteers
Yes
Inclusion criteria
* Fully understand and voluntary sign the informed consent form,and be able to complete the study according to the protocol; * 18 years ≤ age ≤65 years; * Physical examination, vital signs, clinical laboratory examination and various examinations are normal or abnormal without clinical significance; * Agree to take effective contraceptive measures throughout the study period (including not limited to: physical contraception, hormonal drugs of pregnancy, surgery, abstinence, etc.,) until at least 10 months after the last study is administered; * Body weight ≥50 kg, 19kg/m2≤BMI≤26kg/m2; * Serum calcium level between 2.15\ 2.55mmol/L（including the boundary value）; * Normal or clinically acceptable electrocardiogram (12-lead ECG), QTcB\<450msec.
Exclusion criteria
* Drink 14 units of alcohol per week within 3 months prior to administration, or take any alcohol substance within 48 hours before subcutaneous injection; * Substance abuse within 5 years before subcutaneous injection; * Smoke more than 5 cigarettes per day or the same amount of tobacco within 3 months before subcutaneous injection; * Allergic constitution; * Drink excessive amounts of tea, coffee or caffeinated beverages within 30 days before subcutaneous injection; * Use any prescription, over-the-counter, vitamin or herbal medicine within 30 days before subcutaneous injection; * Bone surgery was performed within 30 days before administration; * History of osteomyelitis or osteonecrosis of the jaw; * Inflammation or abnormalities in or around the site of administration; * Needle or blood sickness; * Dental disease or jaw disease requiring oral surgery, dental surgery; or plan to have dental surgery during the study; * Received the study drug(including Xgeva and Prolia), or participated in a clinical trial within 3 months prior to administration； * Received living viraL vaccine within 3 months prior to administration; * Blood donation or blood loss \>400ml within 3 months prior to administration; * Hepatitis B surface antigen was positive, and/or hepatitis C antibody was positive; * The HIV antibody test was not negative; * Syphilitic test was positive; * Drug was detected in the urine; * Hyperparathyroidism, hypothyroidism, rheumatoid arthritis, Ankylosing Spondylitis, osteomalacia, Paget's disease, or fracture within 6 months; * History of severe lumbar disc herniation; * Insanity or legal problem are exist; * Plan to engage in strenuous physical labor or exercise during the study; * Other conditions that made it difficult to participate the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| AUC0-t | 0~126 day | Area Under Curve(AUC)0-t |
| Cmax | 0~126 day | Maximum Concentration |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of Adverse Event | 0~126 day | measured by common terminology criteria for adverse events grading |
| Antidrug Antibody | 0~126 day | Percentage of Subjects Positive for Antidrug Antibody |
| Serum type 1 C-telopeptide(CTX1) | 0~126 day | explore the pharmacodynamic profile by detect the serum concentration of CTX1 |
Countries
China
Outcome results
None listed