TY - GEN AU - Singh, Inderjeet AU - Jose, Vinu TI - Denosumab biosimilar in postmenopausal osteoporotic women: A randomized, assessor‑blind, active‑controlled clinical trial PY - 2021/// CY - Mumbai PB - Wolter Kluwer KW - PHARMACOLOGY N2 - OBJECTIVE: The study assessed the efficacy, safety, pharmacokinetic (PK), and immunogenicity profiles of denosumab‑biosimilar and denosumab‑reference in postmenopausal osteoporotic women from India. MATERIALS AND METHODS: In this randomized, assessor‑blind, active‑control, multicenter trial, 114 patients were randomly allocated to receive denosumab‑biosimilar (n = 58) or denosumab‑reference (n = 56) at a subcutaneous dose of 60 mg every 6 months, for a year. Vitamin D and oral calcium were given daily. Lumbar spine bone mineral density (BMD) change was the primary end point. RESULTS: Of 114 randomized patients, 111 (denosumab‑biosimilar, n = 56; denosumab‑reference, n = 55) completed the study. All 114 patients were part of safety and immunogenicity analyses, 110 (denosumab‑biosimilar, n = 56; denosumab‑reference, n = 54) were part of efficacy analysis, and 20 (denosumab‑biosimilar, n = 10; denosumab‑reference, n = 10) were part of PK analysis. The bone mineral density (BMD) (lumbar spine) percent change at 1 year with denosumab‑biosimilar and denosumab‑reference (7.22 vs. 7.62; difference:−0.40; 95% confidence interval: −5.92, 5.12) showed no statistically relevant difference. Likewise, alkaline phosphatase (bone‑specific) and PK parameters also did not show statistically relevant differences. Adverse events were reported in 44.83% of patients on denosumab‑biosimilar versus 33.93% of patients on denosumab‑reference; most events were mild or moderate and not related to the study drugs. No patients showed anti‑denosumab antibody positivity. CONCLUSIONS: Denosumab‑biosimilar and denosumab‑reference showed biosimilarity in osteoporotic postmenopausal women. Availability of denosumab‑biosimilar provides a treatment alternative for patients UR - https://www.ijp-online.com/temp/IndianJPharmacol5316-1576306_042243.pdf ER -