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
| Type | Name | Description |
|---|---|---|
| DRUG | Perampanel 10 MG | 1 tablet of Perampanel Tablets 10mg |
| DRUG | Fycompa 10Mg Tablet | 1 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.