An Extended Access Program for Perampanel

• Conditions: Partial Onset Seizures

• Registration Number: NCT01871233
• Lead Sponsor: Eisai Inc.

Brief Summary

The Extended Access Program (EAP) is a managed access programme for Perampanel. The main objective of this EAP is to ensure that patients participating in studies E2007-A001-207, E2007-G000-307, or E2007-G000-235 continue to have access to perampanel until such time perampanel tablets become commercially available for the treatment of Partial Onset Seizures (POS) in the country in which they reside. This EAP will consist of 2 phases:

* Screening: The patient will start the program once the Screening assessments are completed and the patient is qualified for participation.

* Treatment: Additional assessments, physical examinations, and dosage changes will be clinically determined by the treating physician.

Patients will enter this program on the same dose of perampanel that they were receiving at the end of their participation in previous study. Doses of perampanel and of concomitant anti-epileptic drugs (AEDs) can be adjusted (i.e., added,removed, or changed in dose) based on clinical judgment.

Treatment will be prescribed as long as clinically appropriate according to the judgement of the treating physician and the approved Summary of Product Characteristics (SmPC).

The program will complete in a staggered fashion, country by country, as and when perampanel becomes commercially available for the treatment of POS in each country.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2013-06-04
• Study First Submitted QC: 2013-06-04
• Study First Posted: 2013-06-06
• Status Verified: 2020-03
• Last Update Submitted: 2020-04-15
• Last Update Posted: 2020-04-16

Recruitment & Eligibility

• Status: NO_LONGER_AVAILABLE
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Patients who are participating in either Study 207, Study 307, or Study 235 and who in the opinion of the treating physician, continue to benefit from treatment with perampanel (revised per Amendment 01)
• Patients who provide informed consent where applicable per local requirements.
• Female patients of childbearing potential must agree for the duration of the program and for a period of at least 1 month following last dose of perampanel to be abstinent or to commit to the consistent and correct use of a medically acceptable method of birth control (e.g., a double-barrier method [condom plus spermicide, condom plus diaphragm with spermicide])

Exclusion Criteria

• Patients residing in countries where perampanel is commercially available for the treatment of POS
• Female patients who are lactating, pregnant, or planning to become pregnant

Study & Design

• Study Type: EXPANDED_ACCESS
• Study Design: Not specified

Trial Locations

Locations (41)

Fundacion Cerebro Y Mente; 🇦🇷 Mendoza, Provincia De Mendoza, Argentina

Hospital General De Agudos José María Ramos Mejia; 🇦🇷 Buenos Aires, Argentina

Centro De Estudio Y Tratamiento De La Epilepsia Y Sueno - Cetes S.A.; 🇦🇷 Cordoba, Argentina

St Vincent's Hospital Melbourne; 🇦🇺 Fitzroy, Australia

Clinical Trials, Epilepsy Research Centre, Melbourne Brain Centre; 🇦🇺 Heidelberg, Australia

Royal Melbourne Hospital; 🇦🇺 Parkville, Australia

Uz Antwerpen; 🇧🇪 Edegem, Belgium

Uz Gent; 🇧🇪 Ghent, Belgium

Foothills Medical Center; 🇨🇦 Calgary, Albert, Canada

London Health Sciences Center; 🇨🇦 London, Ontario, Canada

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