MedPath

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

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
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (41)

St Vincent's Hospital Melbourne

๐Ÿ‡ฆ๐Ÿ‡บ

Fitzroy, Australia

Fakultni Nemocnice U Sv. Anny V Brne

๐Ÿ‡จ๐Ÿ‡ฟ

Brno, Czechia

Royal Melbourne Hospital

๐Ÿ‡ฆ๐Ÿ‡บ

Parkville, Australia

Centro De Estudio Y Tratamiento De La Epilepsia Y Sueno - Cetes S.A.

๐Ÿ‡ฆ๐Ÿ‡ท

Cordoba, Argentina

Clinical Trials, Epilepsy Research Centre, Melbourne Brain Centre

๐Ÿ‡ฆ๐Ÿ‡บ

Heidelberg, Australia

Uz Antwerpen

๐Ÿ‡ง๐Ÿ‡ช

Edegem, Belgium

Hospital Dr. Sรณtero Del Rรญo

๐Ÿ‡จ๐Ÿ‡ฑ

Santiago, Chile

Hospital Base Valdivia Servicio De Neurologรญa

๐Ÿ‡จ๐Ÿ‡ฑ

Valdivia, Chile

Kempenhaeghe

๐Ÿ‡ณ๐Ÿ‡ฑ

Heeze, Netherlands

Oy Neurodiagnostika Ap

๐Ÿ‡ช๐Ÿ‡ช

Tallinn, Estonia

Childrens Clinical University Hospital

๐Ÿ‡ฑ๐Ÿ‡ป

Riga, Latvia

Azienda Ospedaliera Universitaria Federico Ii

๐Ÿ‡ฎ๐Ÿ‡น

Napoli, Italy

Outpatient Clinic 'Valmieras Veselibas Centrs'

๐Ÿ‡ฑ๐Ÿ‡ป

Valmiera, Latvia

Fakultni Nemocnice V Motole

๐Ÿ‡จ๐Ÿ‡ฟ

Prague, Czechia

Fakultni Nemocnice Hradec Kralove

๐Ÿ‡จ๐Ÿ‡ฟ

Hradec Kralove, Czechia

Rambam Medical Center

๐Ÿ‡ฎ๐Ÿ‡ฑ

Haifa, Israel

Stichting Epilepsie Instellingen Nederland

๐Ÿ‡ณ๐Ÿ‡ฑ

Hoofddorp, Netherlands

University Malaya Medical Centre

๐Ÿ‡ฒ๐Ÿ‡พ

Kuala Lumpur, Malaysia

Edith Wolfson Medical Center

๐Ÿ‡ฎ๐Ÿ‡ฑ

Holon, Israel

West Tallinn Central Hospital

๐Ÿ‡ช๐Ÿ‡ช

Tallinn, Estonia

Tallinn Children's Hospital

๐Ÿ‡ช๐Ÿ‡ช

Tallinn, Estonia

Tartu University Hospital

๐Ÿ‡ช๐Ÿ‡ช

Tartu, Estonia

Akademickie Centrum Kliniczne - Szpital Akademii Medycznej W Gdansku

๐Ÿ‡ต๐Ÿ‡ฑ

Gdansk, Poland

Srinagarind Hospital

๐Ÿ‡น๐Ÿ‡ญ

Khonkaen, Thailand

Hospital Universitari I Politรจcnis La Fe Bulevar Sur

๐Ÿ‡ช๐Ÿ‡ธ

Valencia, Spain

Barzilai Medical Center

๐Ÿ‡ฎ๐Ÿ‡ฑ

Ashkelon, Israel

Hospital Clinico San Carlos

๐Ÿ‡ช๐Ÿ‡ธ

Madrid, Spain

Hospital Of Lithuanian University Of Health Sciences Kaunas Clinics

๐Ÿ‡ฑ๐Ÿ‡น

Kaunas, Lithuania

Klaipeda University Hospital

๐Ÿ‡ฑ๐Ÿ‡น

Klaipeda, Lithuania

Vilnius University Hospital Santariskes Clinics

๐Ÿ‡ฑ๐Ÿ‡น

Vilnius, Lithuania

Fundacion Jimenez Diaz

๐Ÿ‡ช๐Ÿ‡ธ

Madrid, Spain

Hospital Universitario San Cecilio

๐Ÿ‡ช๐Ÿ‡ธ

Granada, Spain

King Chulalongkorn Memorial Hospital, Chulalongkorn University

๐Ÿ‡น๐Ÿ‡ญ

Bangkok, Thailand

Phramongkutklao Hospital

๐Ÿ‡น๐Ÿ‡ญ

Bangkok, Thailand

Maharaj Nakorn Chiang Mai, Chiang Mai University

๐Ÿ‡น๐Ÿ‡ญ

Chiang Mai, Thailand

Fundacion Cerebro Y Mente

๐Ÿ‡ฆ๐Ÿ‡ท

Mendoza, Provincia De Mendoza, Argentina

Hospital General De Agudos Josรฉ Marรญa Ramos Mejia

๐Ÿ‡ฆ๐Ÿ‡ท

Buenos Aires, Argentina

London Health Sciences Center

๐Ÿ‡จ๐Ÿ‡ฆ

London, Ontario, Canada

Youthdale Treatment Centers

๐Ÿ‡จ๐Ÿ‡ฆ

Toronto, Ontario, Canada

Uz Gent

๐Ÿ‡ง๐Ÿ‡ช

Ghent, Belgium

Foothills Medical Center

๐Ÿ‡จ๐Ÿ‡ฆ

Calgary, Albert, Canada

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