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Study identifier: NCT06922175 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

REACH: RWE Retrospective Study to Evaluate Cenobamate Impact on Health Care Resource Utilization

Condition: Epilepsy With Uncontrolled Focal-onset Seizures  ·  Sponsor: Aziende Chimiche Riunite Angelini Francesco S.p.A

PhaseN/A
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The Study is an observational, retrospective study which aim is to assess cenobamate's healthcare resources utilization (HCRU) in the management of uncontrolled focal onset seizures. The amin objective is to compare the resource utilization before and after the use of cenobamate. Data from medical charts will be used and inserted into the eCRF from which the analyses will be conducted. Data from 200 patients from 10 sites in 5 countries are included.

This description comes directly from the study's public registry record.

Talk to the study team

Lars Nicklasson  ·  +46 702528077  ·  Lars.nicklasson@angelinipharma.com

Always discuss trial participation with your own doctor first.

Locations (10)

Epilepsiezentrums am Neurozentrum des Universitätsklinikum FreiburgFreiburg im Breisgau, Germany, GermanyNot Yet Recruiting
EpileptologicumHamburg, Germany, GermanyNot Yet Recruiting
Diakonie Kork, EpilepsiezentrumKork, Germany, GermanyNot Yet Recruiting
Kempenhaeghe - Academisch Centrum voor EpilepsieHeeze, Netherlands, NetherlandsNot Yet Recruiting
Epilepsy Unit - Neurology Department Valle de Hebron HospitalBarcelona, Spain, SpainRecruiting
Epilepsy Unit of the Neurology Department of the Hospital Clínico San CarlosMadrid, Spain, SpainRecruiting
Consorcio Hosp. General Universitario ValenciaValencia, Spain, SpainRecruiting
Department of Neurology, University Hospital ZurichZurich, Switzerland, SwitzerlandRecruiting
Institute of Neurosciences NHS Greater Glasgow and ClydeGlasgow, UK, United KingdomRecruiting
Epilepsies - The Royal Wolverhampton NHS TrustWolverhampton, UK, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT06922175