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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT01995838

Public ClinicalTrials.gov record NCT01995838. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 9:09 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT01995838
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eisai Inc.
Industry
Enrollment
291 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 13, 2013 (Actual)
Primary completion
Apr 29, 2014 (Actual)
Completion
Apr 29, 2014 (Actual)
Last update posted
Jan 31, 2020

2013 – 2014

United States locations

U.S. sites
29
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Not listed Glendale Arizona 85306 —
Not listed Phoenix Arizona 85006 —
Not listed Fountain Valley California 92708 —
Not listed Oceanside California 92054 —
Not listed San Diego California 92103 —
Not listed San Diego California 92123 —
Not listed Thousand Oaks California 91360 —
Not listed Colorado Springs Colorado 80907 —
Not listed Colorado Springs Colorado 80909 —
Not listed Brandon Florida 33511 —
Not listed Hallandale Florida 33009 —
Not listed Hollywood Florida 33024 —
Not listed South Miami Florida 33143 —
Not listed Atlanta Georgia 30342 —
Not listed Chicago Illinois 60634 —
Not listed Chicago Illinois 60637 —
Not listed Overland Park Kansas 66212 —
Not listed Glen Burnie Maryland 21061 —
Not listed Las Vegas Nevada 89104 —
Not listed New York New York 10019 —
Not listed Raleigh North Carolina 27612 —
Not listed Cincinnati Ohio 45212 —
Not listed Cincinnati Ohio 45255 —
Not listed Philadelphia Pennsylvania 19118 —
Not listed Columbia South Carolina 29201-2953 —
Not listed Austin Texas 78731 —
Not listed Austin Texas 78744 —
Not listed Dallas Texas 75230 —
Not listed Vienna Virginia 22182 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01995838, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 31, 2020 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01995838 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →