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NCT02849626 · ClinicalTrials.gov registry record · Phase 3

Perampanel as Adjunctive Therapy in Pediatrics With Partial Onset Seizures or Primary Generalized Tonic Clonic Seizures

A Phase 3 study, sponsored by Eisai.

Completed
Registry status
Phase 3
Development phase
180
Enrollment target

NCT02849626: Completed Phase 3 study, sponsored by Eisai.

NCT02849626 is a Phase 3 study that has completed, run by Eisai. The registered enrollment target is 180 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02849626, a Phase 3 study, has completed, sponsored by Eisai.

COMPLETED
Registry status
Phase 3
Development phase
180 participants
Enrollment target

Study Summary

This is an open-label, multicenter study with an Extension Phase to evaluate the safety and tolerability of perampanel oral suspension when administered as an adjunctive therapy in children (ages 4 to less than \[\<\] 12 years) with inadequately controlled partial onset seizures (POS) or primary generalized tonic clonic (PGTC) seizures.

Interventions

  • DRUG Perampanel

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2016-11-16
Est. Completion 2021-12-06
Phase Phase 3
Eisai

287 total trials

What the finished NCT02849626 record still lists

NCT02849626 is an interventional study that assigns participants to a tested intervention. The registered 180 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 1 intervention - of which Perampanel is the first listed.

NCT02849626 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02849626 about?

NCT02849626 is a clinical study titled "Perampanel as Adjunctive Therapy in Pediatrics With Partial Onset Seizures or Primary Generalized Tonic Clonic Seizures". This is an open-label, multicenter study with an Extension Phase to evaluate the safety and tolerability of perampanel oral suspension when administered as an adjunctive therapy in children (ages 4 to less than \[\<\] 12 years) with inadequately controlled partial onset seizures (POS) or primary gen...

What is the current status of trial NCT02849626?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 180 participants. The study started on 2016-11-16. Estimated completion is 2021-12-06.

What interventions are being tested in trial NCT02849626?

The interventions under investigation include: Perampanel (DRUG).

Who is sponsoring clinical trial NCT02849626?

This trial is sponsored by Eisai, which has 287 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02849626's enrollment target sits among peer trials

180 1422nd of 2000 higher than 564 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02849626, the US trial registry maintained by the National Library of Medicine. NCT02849626 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.