Evidence map›Paper›PMID 36081875›Full record

ArticleFrontiers in neurology2022

The safety/tolerability of opicapone when used early in Parkinson's disease patients with levodopa-induced motor fluctuations: A

José-Francisco Rocha, Georg Ebersbach, Andrew Lees, Eduardo Tolosa, Joaquim J Ferreira, Werner Poewe, Olivier Rascol, Fabrizio Stocchi, Angelo Antonini, Diogo Magalhães and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 9 institutions in 7 countries.

José-Francisco RochaBIAL-Portela & Ca S.A., Coronado, Portugal.
Georg EbersbachMovement Disorders Clinic, Beelitz-Heilstätten, Germany.
Andrew LeesNational Hospital for Neurology and Neurosurgery, London, United Kingdom.
Eduardo TolosaParkinson Disease and Movement Disorder Unit, Neurology Service, Hospital Clínic de Barcelona, Institut d'Investigacions Biomédiques August Pi i Sunyer (IDIBAPS), University of Barcelona (UB), Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Barcelona, Spain.
Joaquim J FerreiraLaboratory of Clinical Pharmacology and Therapeutics, Faculty of Medicine, University of Lisbon, Lisbon, Portugal.
Werner PoeweDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Olivier RascolToulouse Parkinson Expert Center, Departments of Neurosciences and Clinical Pharmacology, Centre d'Investigation Clinique de Toulouse CIC1436, NS-Park/FCRIN Network, and NeuroToul COEN Center, University Hospital of Toulouse, INSERM, University of Toulouse 3, Toulouse, France.
Fabrizio StocchiDepartment of Neurology, IRCCS San Raffaele Pisana, Rome, Italy.
Angelo AntoniniParkinson and Movement Disorders Unit, Center for Neurodegenerative Disease (CESNE), Department of Neurosciences, University of Padova, Padova, Italy.
Diogo MagalhãesBIAL-Portela & Ca S.A., Coronado, Portugal.
Helena GamaBIAL-Portela & Ca S.A., Coronado, Portugal.
Patrício Soares-da-SilvaBIAL-Portela & Ca S.A., Coronado, Portugal.
Bial (Portugal) · PTBiomedical Research Networking Center on Neurodegenerative Diseases · ESInnsbruck Medical University · ATInserm · FRIstituto di Ricovero e Cura a Carattere Scientifico San RaffaeleNational Hospital for Neurology and Neurosurgery · GBNeurologisches Fachkrankenhaus für Bewegungsstörungen/Parkinson · DEUniversity of Lisbon · PTUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Materials and methods: Data from matching treatment arms in BIPARK-I and II were combined for the placebo (PLC) and OPC 50 mg groups and exploratory Results: The Safety Set included 522 patients (PLC, Conclusion: OPC 50 mg was generally well-tolerated when used to treat patients with PD with end-of-dose fluctuations, with an even more favorable tolerability profile in patients who were earlier, as opposed to later, in their disease course and levodopa treatment pathway, further supporting its use as an early adjunct to levodopa in PD.

Indexed as

catechol-O-methyltransferase inhibitorlevodopamotor fluctuationsopicaponeParkinson's diseasesafety/tolerabilitywearing off

Identifiers

PMID36081875
PMCPMC9446144
OpenAlexW4292708034

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.