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levodopa/carbidopa/entacapone (Lecigon®)

 

Following a full submission

AWMSG advice

Status: Recommended with restrictions

This product is not currently marketed in the UK.

Levodopa-carbidopa-entacapone (Lecigon®) is recommended as an option for restricted use within NHS Wales.

Levodopa-carbidopa-entacapone (Lecigon®) is licensed for the treatment of advanced Parkinson’s disease with severe motor fluctuations and hyperkinesia or dyskinesia when available oral combinations of Parkinson medicinal products have not given satisfactory results.

Levodopa-carbidopa-entacapone (Lecigon®) is restricted within the licensed indication for patients who are not eligible for deep brain stimulation.

Levodopa-carbidopa-entacapone (Lecigon®) is not recommended for use within NHS Wales outside of this subpopulation.

This recommendation applies only in circumstances where the approved Wales Patient Access Scheme (WPAS) is utilised or where the list/contract price is equivalent or lower than the WPAS price.

 Final Recommendation: levodopa carbidopa entacapone (Lecigon) 4871 (PDF, 567Kb)
 Appraisal Report: levodopa carbidopa entacapone (Lecigon) 4871 (PDF, 860Kb)
 Equality impact assessment: levodopa/carbidopa/entacapone (Lecigon®) 4871 (PDF, 293Kb)

Medicine details

Medicine name levodopa/carbidopa/entacapone (Lecigon®)
Formulation 20 mg/ml 5 mg/ml 20 mg/ml intestinal gel
Reference number 4871
Indication

Treatment of advanced Parkinson's disease with severe motor fluctuations and hyperkinesia or dyskinesia when available oral combinations of Parkinson medicinal products have not given satisfactory results

Company Britannia Pharmaceuticals
BNF chapter Central nervous system
Submission type Full
Status Recommended with restrictions
Advice number 0223
NMG meeting date 01/03/2023
AWMSG meeting date 19/04/2023
Date of issue 27/04/2023
Commercial arrangement WPAS
Further information

This product is not currently marketed in the UK.

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