Study to Investigate Dosage, Efficacy, and Safety of Fycompa in Routine Clinical Care of Patients With Epilepsy

NCT03208660 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2019-04-11

No results posted yet for this study

Summary

This study is conducted to assess the retention rate of Fycompa when given in routine clinical care.

Conditions

Interventions

DRUG

Fycompa

Oral suspension

Sponsors & Collaborators

  • Eisai Inc.

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-04-07
Primary Completion
2019-03-15
Completion
2019-03-15
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03208660 on ClinicalTrials.gov