Clinical Trials Directory

Trials / Completed

CompletedNCT06450236

Bioequivalence Study of Perampanel Tablets 10 mg

An Open-label, Balanced, Randomized, Two Treatment, Two Sequence, Two Period, Two Way Cross-over, Single Dose Bioequivalence Study of Perampanel Tablets 10 mg of Humanis Sağlık A.Ş., Turkey and Fycompa 10 mg Film-coated Tablets of Eisai GmbH Edmund-Rumpler-Straße 3 60549 Frankfurt am Main Deutschland in Normal, Healthy, Adult, Human Subjects Under Fasting Condition

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Humanis Saglık Anonim Sirketi · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

An open-label, balanced, randomized, two treatment, two sequence, two period, two way cross-over, single dose bioequivalence study of Perampanel Tablets 10 mg of Humanis Sağlık A.ġ., Turkey and Fycompa 10 mg film-coated tablets of Eisai GmbH Edmund-Rumpler-Straße 3 60549 Frankfurt am Main Deutschland in normal, healthy, adult, human subjects under fasting condition.

Conditions

Interventions

TypeNameDescription
DRUGPerampanel 10 MG1 tablet of Perampanel Tablets 10mg
DRUGFycompa 10Mg Tablet1 tablet of Perampanel Tablets 10mg

Timeline

Start date
2023-11-22
Primary completion
2023-11-26
Completion
2024-02-06
First posted
2024-06-10
Last updated
2024-06-10

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT06450236. Inclusion in this directory is not an endorsement.