Advice

Following a full submission:

denosumab 60mg solution for injection in a pre-filled syringe (Prolia) is accepted for restricted use in NHSScotland. Indication under review: treatment of osteoporosis in postmenopausal women at increased risk of fractures.  Denosumab significantly reduces the risk of vertebral, non vertebral and hip fractures.

SMC restriction: use only in patients with a bone mineral density (BMD) T-score < -2.5 and ≥ -4.0 for whom oral bisphosphonates are unsuitable due to contraindication, intolerance or inability to comply with the special administration instructions.

Treatment with denosumab for three years significantly reduced the incidence of new vertebral, non-vertebral and hip fractures compared with placebo in postmenopausal women at increased risk of fractures.

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Medicine details

Medicine name:
denosumab (Prolia)
SMC ID:
651/10
Indication:
Osteoporosis in postmenopausal women at increased risk of fractures
Pharmaceutical company
Amgen Ltd
BNF chapter
Endocrine system
Submission type
Full
Status
Restricted
Date advice published
13 December 2010
Additional notes
After the SMC advice for denosumab (Prolia) was published, the manufacturer provided SMC with minor revisions to the economic case initially submitted. The effect of these changes was a slight improvement in the cost effectiveness results that are reported in the Detailed Advice Document (DAD). Note that the DAD has not been updated.