Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: M05BX04

Bilprevda(denosumab)

Giant Cell Tumor of Bone;Neoplasms, Bone Tissue

Marketing Authorisation Holder: Sciencepharma Sp. z o.o

EMA Authorisation: 17/09/2025

INN: denosumab

Indication

Prevention of skeletal related events (pathological fracture, radiation to bone, spinal cord compression or surgery to bone) in adults with advanced malignancies involving bone.Treatment of adults and skeletally mature adolescents with giant cell tumour of bone that is unresectable or where surgical resection is likely to result in severe morbidity. 

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.