CompletedPhase 3NCT01146951
A Placebo-Controlled, Double-Blind Comparative Study of E2080 in Lennox-Gastaut Syndrome Patients (Study E2080-J081-304)
Studying Lennox-Gastaut syndrome
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Eisai Limited
- Principal Investigator
- Hiroki TakanoNeuroscience Clinical Development Section. JAC PCU. Eisai Co., Ltd.
- Intervention
- Rufinamide (E2080)(drug)
- Enrollment
- 66 enrolled
- Eligibility
- 4-30 years · All sexes
- Timeline
- 2010 – 2011
Study locations (23)
- Nagoya, Aichi-ken, Japan
- Matsuyama, Ehime, Japan
- Fukuoka, Fukuoka, Japan
- Hiroshima, Hiroshima, Japan
- Sapporo, Hokkaido, Japan
- Kobe, Hyōgo, Japan
- Yokohama, Kanagawa, Japan
- Goshi-shi, Kumamoto, Japan
- Iwamuma-shi, Miyagi, Japan
- Omura-shi, Nagasaki, Japan
- Nara, Nara, Japan
- Niigata, Niigata, Japan
- Yufu-shi, Oita Prefecture, Japan
- Okayama, Okayama-ken, Japan
- Neyagawa, Osaka, Japan
- +8 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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