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liraglutide (Saxenda®)

 

Status: Superseded

AWMSG ADVICE SUPERSEDED BY NICE GUIDANCE ISSUED OCTOBER 2020. Refer to TA664: Liraglutide for managing overweight and obesity for full guidance on NICE recommendations, including any specific restrictions on the use of the technology. AWMSG documentation provided for reference only.

 Statement of Advice (SOA) liraglutide (Saxenda) 1799 (PDF, 120Kb)

Medicine details

Medicine name liraglutide (Saxenda®)
Formulation 6 mg/ml solution for injection
Reference number 1799
Indication

Adjunct to a reduced-calorie diet and increased physical activity for weight management in adult patients with an initial Body Mass Index (BMI) of ≥ 30 kg/m² (obese), or ≥ 27 kg/m² to < 30 kg/m² (overweight) in the presence of at least one weight-related comorbidity such as dysglycaemia (pre-diabetes or type 2 diabetes mellitus), hypertension, dyslipidaemia or obstructive sleep apnoea. Treatment with Saxenda should be discontinued after 12 weeks on the 3.0 mg/day dose if patients have not lost at least 5% of their initial body weight

Company Novo Nordisk Ltd
BNF chapter Central nervous system
Submission type Non-submission
Status Superseded
Date of issue 15/07/2015
NICE guidance

TA664: Liraglutide for managing overweight and obesity

Commercial arrangement PAS
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