Catalyst Wire Dossier Catalyst Wire Dossier
CLINICAL_TRIALS ClinicalTrials.gov record update

A Post Marketing Observational Study to Evaluate the Safety and Efficacy of Fycompa® (Perampanel) as Add-on Therapy in Epilepsy Patients

This page presents selected fields from the linked source record. It does not add a medical interpretation.

Open original source record ↗

Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT04230044
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:37:26.768622+00:00
Published At
2020-01-18T00:00:00+00:00
Record Updated At
2020-01-18
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Epilepsy", "Partial-onset Seizures"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2020-01-18"
protocolSection.identificationModule.nctId
"NCT04230044"
protocolSection.identificationModule.officialTitle
"A Post Marketing Observational Study to Evaluate the Safety and Efficacy of Fycompa\u00ae (Perampanel) as Add-on Therapy in Epilepsy Patients"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Epilepsy (protocolSection.conditionsModule.conditions)
  • Partial-onset Seizures (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.