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An Extended Access Program (EAP) for Participants Who Have Completed Rufinamide Study E2080-G000-303

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Eisai

Status

Conditions

Lennox Gastaut Syndrome

Treatments

Drug: Rufinamide

Study type

Expanded Access

Funder types

Industry

Identifiers

NCT03778424
E2080-E044-501

Details and patient eligibility

About

This is an extended access study for participants who have completed Rufinamide Study E2080-G000-303 to continue to have access to rufinamide until it becomes commercially available in Poland or until no participants remain in the EAP.

Sex

All

Ages

4+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants who were on rufinamide treatment and have completed Study E2080-G000-303 in Poland.

Exclusion criteria

  • Participants were randomized to the other antiepileptic drug (AED) treatment group in study E2080-G000-303.

Trial contacts and locations

2

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Central trial contact

Eisai Medical Information

Data sourced from clinicaltrials.gov

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