A Randomized, Double-blind, Parallel-group, Active-controlled Study to Compare the Efficacy, Pharmacokinetics, Pharmacodynamics, Safety, and Immunogenicity of MAB-22 Versus Prolia® Sourced from the European Union in Postmenopausal Women with Osteoporosis

Trial details

Who runs it

Xentria Inc.

Trial code

EU 2024-512417-41-00

Record updated

2024. szeptember 30.

Original description

To compare MAB-22 and Prolia® (EU-authorized) in postmenopausal women with osteoporosis to demonstrate biosimilarity with respect to the following: - Efficacy profile in terms of bone mineral density (BMD). - Pharmacodynamic (PD) profile in terms of serum cross-linked C telopeptide of type I collagen (sCTX).Read full original descriptionShow less

To compare MAB-22 and Prolia® (EU-authorized) in postmenopausal women with osteoporosis to demonstrate biosimilarity with respect to the following: - Efficacy profile in terms of bone mineral density (BMD). - Pharmacodynamic (PD) profile in terms of serum cross-linked C telopeptide of type I collagen (sCTX).

Inclusion: Individuals must meet all of the following inclusion criteria to be included in the study: Signed informed consent must be obtained before participation in the study; Postmenopausal women diagnosed with osteoporosis (consistent with a LS BMD [L1-L4] or TH-BMD T-score of ≤ -2.5 and ≥ -4.0 as measured by DXA at screening). Postmenopausal status is defined as at least 12 consecutive months of amenorrhea before date of screening, for which there is no other obvious pathological or physiological cause; Between ≥55 and ≤80 years of age at screening; Body weight ≥50 kg and ≤90 kg at screening; At least 3 vertebrae in the L1-L4 region (vertebrae to be assessed by local reading of lateral spine x-ray at screening) and at least one hip joint are evaluable by DXA; Adequate organ function as defined by the following criteria: a. Serum aspartate aminotransferase (AST) and serum alanine aminotransferase (ALT) ≤2.5 × upper limit of normal (ULN). b. Total serum bilirubin ≤1.5 × ULN. c. Absolute neutrophil count ≥1500 cells/µL (SI units: ≥1.5 × 109/L). d. Platelet count ≥100,000 cells/µL (SI units: ≥100 × 109/L) and ≤ULN. e. Hemoglobin ≥11 g/dL and ≤ULN. f. Albumin-adjusted serum calcium within the normal range for the testing laboratory. g. Estimated glomerular filtration rate >45 mL/min.

Exclusion: Individuals meeting any of the following exclusion criteria are ineligible to participate in this study: Previous exposure to denosumab (Prolia®, Xgeva®, or biosimilar denosumab); Use of other investigational drugs within 2 months of screening (or 5 half-lives of the drug or until the expected PD effect of the drug has returned to baseline, whichever is longer) or longer if required by local regulations; Oral or dental conditions: osteomyelitis or history and/or presence of osteonecrosis of the jaw (ONJ), presence of risk factors for ONJ (e.g., periodontal disease, poorly fitting dentures, invasive dental procedures such as tooth extractions in 6 months before screening), active dental or jaw condition which requires oral surgery and/or planned invasive dental procedure; History and/or presence of significant cardiac disease as per investigator’s discretion, including but not restricted to: ECG abnormalities at screening indicating significant risk of safety for participants participating in the study, history and/or presence of myocardial infarction within 6 months before screening, history and/or presence of New York Heart Association (NYHA) class III or IV heart failure; History of prior allogeneic transplantation; Have a history of alcohol or drug abuse in the judgment of the investigator within the previous 12 months before screening; Unstable systemic disease including active infection, uncontrolled hypertension, unstable angina, congestive heart failure, or myocardial infarction within 6 months before randomization; Have major surgery (including surgery to bone), or significant traumatic injury occurring within 4 weeks before randomization; Other bone active drugs including heparin, anti-convulsives (with the exception of benzodiazepines), systemic ketoconazole, adrenocorticotropic hormone, lithium, gonadotropin releasing hormone agonists, and anabolic steroids, within the past 3 months before the first administration of study treatment; Systemic glucocorticosteroids (≥5 mg prednisone equivalent per day for ≥10 days or a total cumulative dose of ≥50 mg) within the past 3 months before screening; History and/or presence of a severe allergic reaction (e.g., anaphylaxis); Has a hepatitis B surface antigen, hepatitis C antibody, or human immunodeficiency virus (HIV) antibody positive at screening; History of hypersensitivity to any recombinant protein drugs or any of the excipients used in MAB-22 or Prolia®; Malignancy within the 5 years before screening (except cervical carcinoma in situ or basal cell carcinoma, which are acceptable); Vitamin D deficiency (25-[OH] vitamin D serum level <20 ng/mL). Vitamin D repletion is permitted at the discretion of the investigator, and participants will be rescreened to reevaluate vitamin D level post-repletion; Known intolerance to, or malabsorption of calcium or vitamin D supplements; History and/or presence of bone metastases, bone disease, or metabolic disease, other than osteoporosis, which could interfere with the interpretation of the findings (e.g., osteogenesis imperfecta, osteopetrosis, osteomalacia, rheumatoid arthritis, Paget’s disease, ankylosing spondylitis, Cushing’s disease, hyperprolactinemia, malabsorption syndrome, hypoparathyroidism or hyperparathyroidism [irrespective of current controlled or uncontrolled status], hypocalcemia or hypercalcemia [based on albumin-adjusted serum calcium]); Ongoing use of any osteoporosis treatment (other than calcium and vitamin D supplements); Recent tooth extraction (within 6 months of the screening visit). Edentulous participants are permitted to enroll in the study, as long as the most recent tooth extraction occurred >6 months of the screening visit; History and/or presence of 1 severe or more than 2 moderate vertebral fractures or hip fractures (as determined by local reading of lateral spine x-ray at screening). Osteoporotic-related fracture (i.e., crush or wedge vertebral fracture or hip fracture) known or suspected to have occurred within 6 months of randomization; Recent long bone fracture (within 6 months) before screening. Presence of active healing fracture according to assessment of investigators.

EU CTIS 2024-512417-41-00