Evidence map›Paper›PMID 42133843›Full record

ArticleClinical neuropharmacology

Opicapone Improves the Pharmacokinetics of Levodopa Administered as Extended-Release Capsules.

Peter A LeWitt, Olga Klepitskaya, Kurt Olson, Grace Liang, Gordon Loewen

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Article in Clinical neuropharmacology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Peter A LeWittWayne State University School of Medicine, Sastry Foundation Endowed Chair in Parkinson's Disease Research, Detroit, MI.
Olga KlepitskayaNeurocrine Biosciences, Inc., San Diego, CA.
Kurt OlsonNeurocrine Biosciences, Inc., San Diego, CA.
Grace LiangNeurocrine Biosciences, Inc., San Diego, CA.
Gordon LoewenNeurocrine Biosciences, Inc., San Diego, CA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveBoth a catechol-O-methyltransferase inhibitor and extended-release (ER) levodopa formulations may enhance levodopa treatment through a more continuous levodopa delivery to the striatum; the combination of these therapies has not undergone a pharmacokinetic study. We evaluated the effects of once-daily opicapone 50 mg on levodopa plasma pharmacokinetics when added to a carbidopa/levodopa (CD/LD)-ER formulation (RYTARY®). MATERIALS AND

methodsThis was an exploratory, open-label study of levodopa's pharmacokinetics measured over 24 hours in healthy adults. Enrolled individuals received CD/LD-ER three times daily (TID) alone for 3 days, followed by once-daily opicapone for 14 days. On the last 3 days of the opicapone regimen, participants received CD/LD ER TID again. Pharmacokinetic parameters were evaluated after the 3-day exposure to CD/LD-ER alone and with concomitant administration of opicapone.

resultsEighteen healthy adults (9 male, 9 female) entered and completed the study. Levodopa exposure (area under the time-concentration curve) was higher with opicapone than with CD/LD-ER alone across all dosing intervals, including between 21:00 and 07:00 (10801.5 vs. 5153.3 ng/mL·h). Over 24 hours, mean levodopa trough concentration (Ctrough) was higher with opicapone versus CD/LD-ER alone (677.2 vs. 266.8 ng/mL), as was minimum Ctrough (302.9 vs. 41.3 ng/mL). There was a greater increase in Ctrough (208%) than in maximum plasma concentration (75%), decreasing the fluctuation index by 38%.

conclusionsAdding opicapone to CD/LD-ER enhanced levodopa pharmacokinetics in healthy adults, by increasing levodopa trough levels. Notably, opicapone increased overnight and morning levodopa concentrations and decreased daily levodopa concentrations, sub-therapeutic for Parkinson disease patients.

Indexed as

Antiparkinson AgentsCatechol O-Methyltransferase InhibitorsLevodopaOxadiazolesAdultCapsulesCarbidopaDelayed-Action PreparationsDrug CombinationsFemaleHumansMaleMiddle AgedYoung AdultAntiparkinson AgentsCapsulesCarbidopacarbidopa, levodopa drug combinationCatechol O-Methyltransferase InhibitorsDelayed-Action PreparationsDrug CombinationsLevodopaopicaponeOxadiazolescatechol O-methyltransferaselevodopaopicaponeParkinson diseasepharmacokinetics

Identifiers

PMID42133843
PMCPMC13166064

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.