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levodopa-carbidopa intestinal gel (Duodopa®)

 

Status: Recommended with restrictions

Levodopa-carbidopa intestinal gel (Duodopa®) is recommended as an option for restricted use within NHS Wales. Levodopa-carbidopa intestinal gel (Duodopa®) should be restricted for use in the following subpopulation within its licensed indication for the treatment of advanced levodopa-responsive Parkinson’s disease with severe motor fluctuations and hyper-/dyskinesia when available combinations of Parkinson medicinal products have not given satisfactory results:

  • Patients not eligible for deep brain stimulation.

Levodopa-carbidopa intestinal gel (Duodopa®) 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 intestinal gel (Duodopa) 3397 (PDF, 341Kb)
 Appraisal Report: levodopa-carbidopa intestinal gel (Duodopa) 3397 (PDF, 287Kb)

Medicine details

Medicine name levodopa-carbidopa intestinal gel (Duodopa®)
Formulation 20 mg/ml and 5 mg/ml intestinal gel
Reference number 3397
Indication

Treatment of advanced levodopa-responsive Parkinson’s disease with severe motor fluctuations and hyper-/dyskinesia when available combinations of Parkinson medicinal products have not given satisfactory results and patients are not eligible for deep brain stimulation

Company AbbVie Ltd
BNF chapter Central nervous system
Submission type Resubmission
Status Recommended with restrictions
Advice number 0518
NMG meeting date 04/10/2017
AWMSG meeting date 14/03/2018
Date of issue 22/03/2018
Date of last review March 2021
Commercial arrangement WPAS
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