Prolia denosumab APPROVED
Drug Profile
ModalityMonoclonal antibody
RouteSC
Therapy AreaCVRM
Launch2010-06-01
Peak Sales Est$4500M
Formulations[{"id":"prolia-sc","doses":"60mg/mL prefilled syringe","route":"SC","setting":"HCP_ADMINISTERED","fr
Companies
AMGN (ORIGINATOR)100%
Mechanism: RANK ligand inhibitor
Expert: Fully human IgG2 monoclonal antibody targeting RANK ligand (RANKL). Inhibits osteoclast formation, function, and survival, reducing bone resorption.
Everyday: Blocks a signal (RANKL) that tells bone-eating cells to break down bone. Without this signal, your bones stay stronger and denser — like telling the demolition crew to stop working.
Targets: ["RANKL"]
Revenue History
PeriodRevenue ($M)
2024$4,374M
2025$4,414M
Q4 2024$1,165M
Q4 2025$1,054M
Programs (1)
IndicationStageKey StudyRegional Status
Postmenopausal osteoporosisAPPROVEDFREEDOM[{"stage":"APPROVED","region":"US","approval_date":"2010-06-01"}]
Notes
BIOSIMILAR RISK: 8+ denosumab biosimilars approved. Analysts expect 28% decline in 2026. SC biologic may erode slower than IV (compliance advantage with Q6M dosing).
Data from Supabase · Updated 2026-03-24