drugset / Trial / NCT01995838
A Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group, Bayesian Adaptive Randomization Design, Dose Response Study of the Efficacy of E2006 in Adults and Elderly Subjects With Chronic Insomnia
RandomizedParallel-groupDouble-blindTreatment
Summary
This is a multicenter, multiple dose, randomized, double-blind, placebo-controlled, parallel-group, Bayesian adaptive, dose response study in subjects with chronic insomnia. Subjects will be randomized to 1 of 6 doses of E2006 (1 mg, 2.5 mg, 5 mg, 10 mg, 15 mg, or 25 mg) or placebo.
Timeline
- Start
- 2013-11-13
- Primary completion
- 2014-04-29
- Completion
- 2014-04-29
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lemborexant | Small molecule | 1 mg | Oral |
| Subject | Lemborexant | Small molecule | 2.5 mg | Oral |
| Subject | Lemborexant | Small molecule | 5 mg | Oral |
| Subject | Lemborexant | Small molecule | 10 mg | Oral |
| Subject | Lemborexant | Small molecule | 15 mg | Oral |
| Subject | Lemborexant | Small molecule | 25 mg | Oral |