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Decision-making process for opicapone’s bedtime regimen

A. Falcão, A. Santos, J. Ferreira, A. Lees, B. Hernandez, F. Rocha, P. Soares-da-Silva (Coimbra, Portugal)

Meeting: 2017 International Congress

Abstract Number: 1429

Keywords: COMT inhibitors

Session Information

Date: Thursday, June 8, 2017

Session Title: Parkinson’s Disease: Clinical Trials, Pharmacology And Treatment

Session Time: 1:15pm-2:45pm

Location: Exhibit Hall C

Objective: To clarify the decision-making process for opicapone’s bedtime regímen.

Background: OPC, a new once-daily COMT inhibitor, was shown to be effective in the treatment of motor fluctuations in Parkinson’s disease patients.

Methods: Review of opicapone, levodopa, carbidopa and benserazide pharmacokinetic data. Five phase 1 studies were selected on the basis of concomitant, alone or 1-hour apart administration between oral single-doses of opicapone (25, 50 and 100mg) and immediate- (IR) or controlled-release (CR) levodopa/carbidopa (LC, 100/25) or levodopa/benserazide (LB, 100/25).

Results: In studies conducted with concomitant administration between opicapone and IR/CR LB, an increase in rate (as assessed by Cmax) and extent (as assessed by AUC) to levodopa and benserazide occurred at all doses of opicapone. The increase was statistically significant for IR formulation. Levodopa Cmax decreased when doses of opicapone increased. In studies conducted with concomitant administration between opicapone and IR/CR LC, a statistically significant increase in Cmax and AUC to levodopa, but not to carbidopa, occurred at all doses of opicapone. Levodopa Cmax decreased (more pronounced with CR formulation) when doses of opicapone increased. Finally, similar levodopa and carbidopa Cmax was observed when opicapone (50mg) was administered 1-hour apart from IR LC. In all studies, Cmax and AUC to opicapone increased in a dose-proportional manner but an important variability was observed between different levodopa formulations and the use of carbidopa or benserazide.

Conclusions: The pharmacokinetic data suggest a certain degree of interaction at absorption phase that was minimized by separating both administrations for at least 1-hour. Opicapone was developed as an add-on to levodopa and, taking into consideration that Parkinson’s disease patients may well necessitate several daily doses of levodopa, a bedtime regimen for opicapone was proposed to better allow the physician to individually tailor the levodopa daily regimen without any concern of a potential absorption interaction.

To cite this abstract in AMA style:

A. Falcão, A. Santos, J. Ferreira, A. Lees, B. Hernandez, F. Rocha, P. Soares-da-Silva. Decision-making process for opicapone’s bedtime regimen [abstract]. Mov Disord. 2017; 32 (suppl 2). https://www.mdsabstracts.org/abstract/decision-making-process-for-opicapones-bedtime-regimen/. Accessed June 14, 2025.
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