.Pharmacolibrary.Drugs.ATC.M.M05BX04

Information

name:Denosumab
ATC code:M05BX04
route:subcutaneous
n-compartments2

Denosumab is a fully human monoclonal antibody that inhibits RANK ligand (RANKL), a key mediator of osteoclast formation, function, and survival, thus reducing bone resorption and increasing bone mass. It is approved for the treatment of osteoporosis in postmenopausal women and men at increased risk of fractures, as well as for bone loss associated with certain cancers and for prevention of skeletal-related events in patients with bone metastases.

Pharmacokinetics

Pharmacokinetic parameters reported for adults (including postmenopausal women with osteoporosis) after subcutaneous administration of denosumab 60 mg.

References

  1. Zhang, S, et al., & Jiang, Z (2024). Efficacy, Safety, and Population Pharmacokinetics of MW032 Compared With Denosumab for Solid Tumor-Related Bone Metastases: A Randomized, Double-Blind, Phase 3 Equivalence Trial. JAMA oncology 10(4) 448–455. DOI:10.1001/jamaoncol.2023.6520 PUBMED:https://pubmed.ncbi.nlm.nih.gov/38329745

  2. Vogg, B, et al., & Sekhar, S (2024). Pharmacokinetics and pharmacodynamics of the proposed biosimilar denosumab GP2411 and reference denosumab in healthy males. Expert opinion on biological therapy 24(1-2) 91–100. DOI:10.1080/14712598.2024.2308645 PUBMED:https://pubmed.ncbi.nlm.nih.gov/38269652

  3. Gibiansky, L, et al., & Pérez-Ruixo, JJ (2012). Population pharmacokinetic analysis of denosumab in patients with bone metastases from solid tumours. Clinical pharmacokinetics 51(4) 247–260. DOI:10.2165/11598090-000000000-00000 PUBMED:https://pubmed.ncbi.nlm.nih.gov/22420579

Revisions


Generated at 2025-07-20T18:21:09Z by OpenModelicaOpenModelica 1.25.1 using GenerateDoc.mos