Double-Blind, Placebo-Controlled, Efficacy and Safety Study of Clobazam (0.25, 0.5 and 1.0 mg/kg/day) in Patients with Lennox-Gastaut Syndrome.

Registry ID
EUCTR2007-004322-24
Source registry
EUCTR
Status
Completed
Phase
PHASE3
Sponsor
Lundbeck Inc
Start date
2008-03-17
Completion date
2010-04-23
Last update
2026-08-16

Conditions

Summary

1. To determine the efficacy of clobazam (CLB) in the reduction of drop seizures at three dose levels when compared to baseline during 12 weeks maintenance dosing in a placebo controlled trial in patients with Lennox-Gastaut Syndrome (LGS). 2. To determine the safety of CLB when administered for up to 18 weeks at three different dose levels in patients with LGS.

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