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NCT04608799

The Efficacy of Fycompa (Perampanel) in Children With Epilepsy

Completed Last updated 29 October 2020
What this trial tests

trial testing Perampanel in Neurologic Disorder in 38 participants. Completed in 19 March 2020.

Timeline
1 January 2018
Primary endpoint
19 March 2020
19 March 2020

Quick facts

Lead sponsorNational Taiwan University Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment38
Start date1 January 2018
Primary completion19 March 2020
Estimated completion19 March 2020
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

National Taiwan University Hospital

Who can join

Adults 0 to 18, any sex, with Neurologic Disorder. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Fycompa (Perampanel), a new anti-epileptic drug that uses a new mechanism-AMPA receptor antagonist. Its initial indication is for local or generalized epilepsy in children and adults over 12 years old, but its effectiveness in the treatment of epilepsy in children At present, more evidence is still needed. We will study the effectiveness of Fycompa (Perampanel) in the treatment of epilepsy in children under the age of 18. It is expected that the clinical use of Fycompa (Parampanel) in Taiwan will be able to analyze and study the effectiveness of the clinical use of Fycompa (Parampanel) in the treatment of epilepsy in children, and compare it with foreign reports.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Perampanel

Trials testing the same drug.

Other recruiting trials for Neurologic Disorder

Currently open trials in the same condition.

Other National Taiwan University Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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