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A 2-Part Single Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2006

Primary Purpose

Insomnia

Status

Completed

Phase

Phase 1

Locations

United States

Study Type

Interventional

Intervention

E2006 1.0 mg

E2006 2.5 mg

E2006 5.0 mg

E2006 10.0 mg

E2006 25.0 mg

E2006 50.0 mg

E2006 100 mg

E2006 200 mg

Zolpidem 10 mg

E2006 Matched Placebo or Zolpidem Matched Placebo

E2006 Matched Placebo

About this trial

This is an interventional treatment trial for Insomnia

Eligibility Criteria

18 Years - 64 Years (Adult)All SexesAccepts Healthy Volunteers

Key Inclusion Criteria:

Healthy Subjects:

With habitual time in bed > 7 hours, with lights out 2200 to 2400 and lights on 0600 to 0800
Who report typical sleep latency of </= 30 minutes
With typical total sleep time (TST) >/= 420 minutes

Primary Insomnia Subjects:

Otherwise healthy adult male and female subjects with a diagnosis of primary insomnia (as defined by the Diagnostic and Statistical Manual of Mental Disorders-IV-Text Revision [DSM-IV-TR]) present at the time of Screening for at least 3 months
With a score of > 15 on the Insomnia Severity Index (ISI) at Screening
Who report taking >/= 30 minutes to fall asleep on at least 3 nights per week for the past month
Who report 6.5 hours sleep or less on at least 3 nights per week for the past month
With mean latency to persistent sleep (LPS) on both baseline nights of >/= 20 minutes with neither night < 15 minutes
With mean wake after sleep onset (WASO) >/= 20 minutes on both baseline nights, with neither night < 15 minutes or mean TST > 420 minutes

Key Exclusion Criteria:

With a current history of sleep disorders (e.g., obstructive sleep apnea, restless leg syndrome [RLS], narcolepsy, or circadian rhythm disorder) other than primary insomnia (for Part B)
Subjects with any clinically abnormal symptom or organ impairment found in medical history, symptoms/signs, vital signs, ECG finding, or laboratory test results which require medical treatment
All females must be of non-childbearing potential
With a known history of significant neurological or serious psychiatric illness

Sites / Locations

Clinilabs, Inc.
Community Research

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm 9

Arm 10

Arm 11

Arm 12

Arm 13

Arm 14

Arm Type

Experimental

Arm Label

Part A: E2006 1.0 mg

Part A: E2006 2.5 mg

Part A: E2006 5.0 mg

Part A: E2006 10.0 mg

Part A: E2006 25.0 mg

Part A: E2006 50.0 mg

Part A: E2006 100 mg

Part A: E2006 200 mg

Part B: Zolpidem 10 mg

Part B: E2006 Matched Placebo or Zolpidem Matched Placebo

Part A: E2006 Matched Placebo

Part B: E2006 2.5 mg

Part B: E2006 10 mg

Part B: E2006 25 mg

Arm Description

Outcomes

Primary Outcome Measures

Part A: Number of Participants With Treatment Emergent Adverse Events (AEs) and Treatment Emergent Serious Adverse Events (SAEs)

Part A: Number of Participants With Markedly Abnormal Laboratory Parameter Values

Part A: Number of Participants With Significant Change From Baseline in Vital Sign Values

Part A: Number of Participants With Clinically Significant Change From Baseline in Electrocardiogram (ECG) Parameter Values

Part A: Number of Participants With Any Suicidality Assessed Using Columbia-Suicide Severity Rating Scale (C-SSRS)

The C-SSRS (mapped to Columbia Classification Algorithm of Suicide Assessment [C-CASA]) is an interview-based rating scale to systematically assess any suicidality, any suicidal behavior, any suicidal ideation. Any suicidality: emergence of any suicidal ideation or suicidal behavior. Any suicidal behavior: when response is "yes" for any these questions- actual attempt to suicide, engaged in non-suicidal self-injurious behavior, interrupted attempt, aborted attempt, preparatory acts. Any suicidal ideation: when response is "yes" for any of these questions- wish to be dead, non-specific active suicidal thoughts, active suicidal ideation with methods without intent to act or some intent to act, without specific plan or with specific plan and intent to suicide. Number of Participants with any suicidality has been reported for this outcome measure.

Part B: Change From Baseline in Latency to Persistent Sleep (LPS) Assessed Using Polysomnography (PSG) Measurement at Day 1

LPS was the duration of time in minutes from lights off to the first 30 seconds of recording (epoch) of 20 consecutive epochs of non-wakefulness as measured by PSG.

Part B: Change From Baseline in Total Sleep Time (TST) Assessed Using PSG at Day 1

TST was the duration in minutes including rapid eye movement (REM) sleep plus non-rapid eye movement (NREM) sleep during the time spent in bed.

Part B: Change From Baseline in Sleep Efficiency Assessed Using PSG at Day 1

Sleep efficiency was defined as the TST divided by the time in bed (minutes) multiplied by 100. TST was the duration in minutes including REM sleep plus NREM sleep during the time spent in bed.

Part B: Change From Baseline in Wake After Sleep Onset (WASO) Assessed Using PSG at Day 1

WASO was defined as the duration (in minutes) of wakefulness from onset of persistent sleep to lights-on.

Part B: Change From Baseline in Number of Awakenings After Persistent Sleep (NAW) Assessed Using PSG at Day 1

Number of awakenings was determined from LPS to lights-on. LPS was the duration of time measured from lights off to the first 30 seconds of PSG measurement recording (epoch) of 20 consecutive epochs of non-wake. An awakening was defined as a PSG recording of at least two consecutive wake epochs.

Part B: Change From Baseline in Percentage of Each Sleep Stage Duration Assessed Using PSG at Day 1

Sleep stages included NREM sleep and REM (dreaming) sleep. Non-REM sleep is comprised of the sum of Stage N1 (light sleep), N2 (also fairly light, with sudden increases in brain wave frequency known as sleep spindles) and N3 or slow wave sleep (deep sleep). Sleep was staged in sequential 30-second epochs.

Part B: Change From Baseline in Duration (in Minutes) of Each Sleep Stage Assessed Using PSG at Day 1

Part B: Change From Baseline in Mean Total Number of Shift in Sleep Stages Assessed Using PSG at Day 1

Part B: Change From Day 1 in Waketime Questionnaire Parameters: How Long Did You Sleep Last Night at Day 6

Participants were asked to answer the following question using Waketime Questionnaire: How long did you sleep last night, number of awakening after falling asleep, time to fall asleep last night, time spent awake after falling asleep, rate quality of your sleep (using Likert scale, ranged from 0 = very sound or restful, to 4 = very restless where lower score indicates better outcome). The primary purpose of the Waketime Questionnaire was to confirm anticipated reports of poor sleep. In this outcome measure, data for question "How long did you sleep last night" has been reported.

Part B: Change From Day 1 in Waketime Questionnaire Parameters: Time to Fall Asleep Last Night at Day 6

Part B: Change From Day 1 in Waketime Questionnaire Parameters: Number of Awakening After Falling Asleep at Day 6

Participants were asked to answer the following question using Waketime Questionnaire: How long did you sleep last night, number of awakening after falling asleep, time to fall asleep last night, time spent awake after falling asleep, rate quality of your sleep (using Likert scale, ranged from 0 = very sound or restful, to 4 = very restless where lower score indicates better outcome). The primary purpose of the Waketime Questionnaire was to confirm anticipated reports of poor sleep. In this outcome measure, data for question "Number of awakening after falling asleep" has been reported.

Part B: Change From Day 1 in Waketime Questionnaire Parameters: Time Spent Awake After Falling Asleep at Day 6

Participants were asked to answer the following question using Waketime Questionnaire: How long did you sleep last night, number of awakening after falling asleep, time to fall asleep last night, time spent awake after falling asleep, rate quality of your sleep (using Likert scale, ranged from 0 = very sound or restful, to 4 = very restless where lower score indicates better outcome). The primary purpose of the Waketime Questionnaire was to confirm anticipated reports of poor sleep. In this outcome measure, data for question "Time spent awake after falling asleep" has been reported.

Part B: Change From Day 1 in Waketime Questionnaire Parameters: Rate Quality of Your Sleep at Day 6

Part B: Change From Day 1 (Pre-dose) in Digit Symbol Substitution Test (DSST) Score at Day 6

DSST is a cognitive test designed to assess psychomotor speed of performance requiring visual perception, spatial decision-making, and motor skills. It consists of 133 digits and requires the participant to substitute each digit with a simple symbol in a 90-second period. Each correct symbol is counted, and the total score ranges from 0 (less than cognitive functioning) to 133 (greater than cognitive functioning) as a description of DSST. An increase in score represents an improvement in an integrated measure of cognitive function.

Part B: Change From Day 1 (Pre-dose) in Number of Lapses of Greater Than (>) 500- Milliseconds (Msec) Assessed by Psychomotor Vigilance Test (PVT) at Day 6

Part B: Change From Day 1 (Pre-dose) in Score on Karolinska Sleepiness Scale (KSS) at Day 6

Secondary Outcome Measures

Part A: Maximum Plasma Concentration (Cmax) of E2006

Part A: Time to Reach Maximum Plasma Concentration (Tmax) of E2006

Part A: Area Under the Plasma Concentration-time Curve From Time Zero to 24 Hours (AUC0-24) of E2006

Part A: Area Under the Plasma Concentration-time Curve From Time Zero to t Hours (AUC0-t) of E2006

Part A: Area Under the Plasma Concentration-time Curve From Time Zero to Infinity (AUC0-inf) of E2006

Part A: Terminal Half-life (t1/2) of E2006 in Plasma

Part A: Apparent Total Clearance of E2006 From Plasma (CL/F)

Part A: Apparent Volume of Distribution of E2006 in Plasma (Vz/F)

Part A: Cumulative Amount of Unchanged Drug E2006 Excreted Into the Urine (Ae)

Part A: Renal Clearance (CLR) of Drug E2006

Part A: Maximum Change From Day 1 (Pre-dose) in Digit Symbol Substitution Test (DSST) Score at Day 6

Part A: Maximum Change From Day 1 (Pre-dose) in Number of Lapses of > 500 Msec Assessed by Psychomotor Vigilance Test (PVT) at Day 6

PVT, a computer-based test, is a chronometric measure of an individual's reaction to specified small changes in a labile environment. Participants were instructed to respond to a digital signal on a computer terminal by pressing a key. Errors of omission and commission are recorded. When a participant did not respond to the PVT signal within 500 msec, it was termed a lapse. The higher the number of lapses the greater the impairment. In this outcome measure, data for participants who received placebo matched to "1 mg, 2.5 mg, 5 mg E2006" and matched to "10 mg, 25 mg, 50 mg, 100 mg, and 200 mg E2006", has been presented separately.

Part A: Maximum Change From Day 1 (Pre-dose) in Karolinska Sleepiness Scale (KSS) Score at Day 6

KSS is a 9-point scale, on which the participant has to mark his or her sleepiness during the previous 10 minutes. The scale ranges from 1, which indicates "extremely alert", to 9, which indicates "extremely sleepy, can't stay awake". Higher numbers indicating sleepier and lower numbers more alert. In this outcome measure, data for participants who received placebo matched to "1 mg, 2.5 mg, 5 mg E2006" and matched to "10 mg, 25 mg, 50 mg, 100 mg, and 200 mg E2006", has been presented separately.

Part A: Change From Day 1 in Waketime Questionnaire Parameters: How Long Did You Sleep Last Night at Day 6

Participants were asked to answer the following question using Waketime Questionnaire: How long did you sleep last night, number of awakening after falling asleep, time to fall asleep last night, time spent awake after falling asleep, rate quality of your sleep (using Likert scale, ranged from 0 = very sound or restful, to 4 = very restless where lower score indicates better outcome). The primary purpose of the Waketime Questionnaire was to confirm a lack of sleep disturbance. In this outcome measure, data for question "How long did you sleep last night" has been reported.

Part A: Change From Day 1 in Waketime Questionnaire Parameters: Time to Fall Asleep Last Night at Day 6

Participants were asked to answer the following question using Waketime Questionnaire: How long did you sleep last night, number of awakening after falling asleep, time to fall asleep last night, time spent awake after falling asleep, rate quality of your sleep (using Likert scale, ranged from 0 = very sound or restful, to 4 = very restless where lower score indicates better outcome). The primary purpose of the Waketime Questionnaire was to confirm a lack of sleep disturbance. In this outcome measure, data for question "Time to fall asleep last night" has been reported.

Part A: Change From Day 1 in Waketime Questionnaire Parameters: Number of Awakening After Falling Asleep at Day 6

Participants were asked to answer the following question using Waketime Questionnaire: How long did you sleep last night, number of awakening after falling asleep, time to fall asleep last night, time spent awake after falling asleep, rate quality of your sleep (using Likert scale, ranged from 0 = very sound or restful, to 4 = very restless where lower score indicates better outcome). The primary purpose of the Waketime Questionnaire was to confirm a lack of sleep disturbance. In this outcome measure, data for question "Number of awakening after falling asleep" has been reported.

Part A: Change From Day 1 in Waketime Questionnaire Parameters: Time Spent Awake After Falling Asleep at Day 6

Participants were asked to answer the following question using Waketime Questionnaire: How long did you sleep last night, number of awakening after falling asleep, time to fall asleep last night, time spent awake after falling asleep, rate quality of your sleep (using Likert scale, ranged from 0 = very sound or restful, to 4 = very restless where lower score indicates better outcome). The primary purpose of the Waketime Questionnaire was to confirm a lack of sleep disturbance. In this outcome measure, data for question "Time spent awake after falling asleep" has been reported.

Part A: Change From Day 1 in Waketime Questionnaire Parameters: Rate Quality of Your Sleep at Day 6

Participants were asked to answer the following question using Waketime Questionnaire: How long did you sleep last night, number of awakening after falling asleep, time to fall asleep last night, time spent awake after falling asleep, rate quality of your sleep (using Likert scale, ranged from 0 = very sound or restful, to 4 = very restless where lower score indicates better outcome). The primary purpose of the Waketime Questionnaire was to confirm a lack of sleep disturbance. In this outcome measure, data for question "Rate quality of your sleep" has been reported.

Part B: Number of Participants With Treatment Emergent Adverse Events (AEs) and Treatment Emergent Serious Adverse Events (SAEs)

Part B: Number of Participants With Markedly Abnormal Laboratory Parameter Values

Part B: Number of Participants With Significant Change From Baseline in Vital Sign Values

Part B: Number of Participants With Clinically Significant Change From Baseline in ECG Parameter Values

Part B: Number of Participants With Any Suicidality Assessed Using Columbia-Suicide Severity Rating Scale (C-SSRS)

The C-SSRS (mapped to Columbia Classification Algorithm of Suicide Assessment [C-CASA]) is an interview-based rating scale to systematically assess any suicidality, any suicidal Behavior, any suicidal ideation. Any suicidality: emergence of any suicidal ideation or suicidal behavior. Any suicidal behavior: when response is "yes" for any these questions- actual attempt to suicide, engaged in non-suicidal self-injurious, behavior, interrupted attempt, aborted attempt, preparatory acts. Any suicidal ideation: when response is "yes" for any of these questions-wish to be dead, non-specific active suicidal thoughts, active suicidal ideation with methods without intent to act or some intent to act, without specific plan or with specific plan and intent to suicide. Number of participants with any suicidality has been reported for this outcome measure.

Full Information

NCT ID

NCT01463098

First Posted

October 26, 2011

Last Updated

January 3, 2020

Sponsor

Eisai Inc.

1. Study Identification

Unique Protocol Identification Number

NCT01463098

Brief Title

A 2-Part Single Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2006

Official Title

A 2-Part, Randomized, Double-Blind, Placebo- and Active- Controlled, Single Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of E2006 in Healthy Subjects and Otherwise Healthy Subjects With Primary Insomnia

Study Type

Interventional

2. Study Status

Record Verification Date

March 2013

Overall Recruitment Status

Completed

Study Start Date

October 5, 2011 (Actual)

Primary Completion Date

August 11, 2012 (Actual)

Study Completion Date

August 11, 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Sponsor

Name of the Sponsor

Eisai Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Yes

Data Monitoring Committee

5. Study Description

Brief Summary

Part A: The purpose of this study is to evaluate the safety and tolerability of single oral doses of E2006 administered in the morning to healthy male and female subjects. Part B: The purpose of this study is to evaluate selected pharmacodynamic (PD) parameters (e.g., polysomnographically defined sleep measures) with regard to dose response in subjects with primary insomnia following single oral dosing of E2006 in the evening approximately 30 minutes prior to the sleep period, compared with 10 mg zolpidem and placebo.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Insomnia

7. Study Design

Primary Purpose

Treatment

Study Phase

Phase 1

Interventional Study Model

Parallel Assignment

Masking

ParticipantInvestigatorOutcomes Assessor

Allocation

Randomized

Enrollment

122 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Part A: E2006 1.0 mg

Arm Type

Experimental

Arm Title

Part A: E2006 2.5 mg

Arm Type

Experimental

Arm Title

Part A: E2006 5.0 mg

Arm Type

Experimental

Arm Title

Part A: E2006 10.0 mg

Arm Type

Experimental

Arm Title

Part A: E2006 25.0 mg

Arm Type

Experimental

Arm Title

Part A: E2006 50.0 mg

Arm Type

Experimental

Arm Title

Part A: E2006 100 mg

Arm Type

Experimental

Arm Title

Part A: E2006 200 mg

Arm Type

Experimental

Arm Title

Part B: Zolpidem 10 mg

Arm Type

Experimental

Arm Title

Part B: E2006 Matched Placebo or Zolpidem Matched Placebo

Arm Type

Experimental

Arm Title

Part A: E2006 Matched Placebo

Arm Type

Experimental

Arm Title

Part B: E2006 2.5 mg

Arm Type

Experimental

Arm Title

Part B: E2006 10 mg

Arm Type

Experimental

Arm Title

Part B: E2006 25 mg

Arm Type

Experimental

Intervention Type

Drug

Intervention Name(s)

E2006 1.0 mg

Other Intervention Name(s)

Lemborexant

Intervention Description

E2006 1.0 mg capsule.

Intervention Type

Drug

Intervention Name(s)

E2006 2.5 mg

Other Intervention Name(s)

Lemborexant

Intervention Description

E2006 2.5 mg capsule.

Intervention Type

Drug

Intervention Name(s)

E2006 5.0 mg

Other Intervention Name(s)

Lemborexant

Intervention Description

E2006 5.0 mg (2 capsules of 2.5 mg each).

Intervention Type

Drug

Intervention Name(s)

E2006 10.0 mg

Other Intervention Name(s)

Lemborexant

Intervention Description

E2006 10.0 mg capsule.

Intervention Type

Drug

Intervention Name(s)

E2006 25.0 mg

Other Intervention Name(s)

Lemborexant

Intervention Description

E2006 25.0 mg (2 capsules of 10 mg each and 2 capsules of 2.5 mg each).

Intervention Type

Drug

Intervention Name(s)

E2006 50.0 mg

Other Intervention Name(s)

Lemborexant

Intervention Description

E2006 50.0 mg capsule.

Intervention Type

Drug

Intervention Name(s)

E2006 100 mg

Other Intervention Name(s)

Lemborexant

Intervention Description

E2006 100 mg (2 capsules of 50 mg each).

Intervention Type

Drug

Intervention Name(s)

E2006 200 mg

Other Intervention Name(s)

Lemborexant

Intervention Description

E2006 200 mg (4 capsules of 50 mg each).

Intervention Type

Drug

Intervention Name(s)

Zolpidem 10 mg

Intervention Description

Zolpidem 10 mg immediate release tablet.

Intervention Type

Drug

Intervention Name(s)

E2006 Matched Placebo or Zolpidem Matched Placebo

Intervention Description

E2006-matched placebo capsules or zolpidem-matched placebo tablets.

Intervention Type

Drug

Intervention Name(s)

E2006 Matched Placebo

Intervention Description

E2006-matched placebo capsule.

Primary Outcome Measure Information:

Title

Part A: Number of Participants With Treatment Emergent Adverse Events (AEs) and Treatment Emergent Serious Adverse Events (SAEs)

Time Frame

Baseline up to Day 11

Title

Part A: Number of Participants With Markedly Abnormal Laboratory Parameter Values

Time Frame

Baseline up to Day 6

Title

Part A: Number of Participants With Significant Change From Baseline in Vital Sign Values

Time Frame

Baseline up to Day 11

Title

Part A: Number of Participants With Clinically Significant Change From Baseline in Electrocardiogram (ECG) Parameter Values

Time Frame

Baseline up to Day 11

Title

Part A: Number of Participants With Any Suicidality Assessed Using Columbia-Suicide Severity Rating Scale (C-SSRS)

Description

Time Frame

Baseline, Day 11

Title

Part B: Change From Baseline in Latency to Persistent Sleep (LPS) Assessed Using Polysomnography (PSG) Measurement at Day 1

Description

LPS was the duration of time in minutes from lights off to the first 30 seconds of recording (epoch) of 20 consecutive epochs of non-wakefulness as measured by PSG.

Time Frame

Baseline, Day 1

Title

Part B: Change From Baseline in Total Sleep Time (TST) Assessed Using PSG at Day 1

Description

TST was the duration in minutes including rapid eye movement (REM) sleep plus non-rapid eye movement (NREM) sleep during the time spent in bed.

Time Frame

Baseline, Day 1

Title

Part B: Change From Baseline in Sleep Efficiency Assessed Using PSG at Day 1

Description

Sleep efficiency was defined as the TST divided by the time in bed (minutes) multiplied by 100. TST was the duration in minutes including REM sleep plus NREM sleep during the time spent in bed.

Time Frame

Baseline, Day 1

Title

Part B: Change From Baseline in Wake After Sleep Onset (WASO) Assessed Using PSG at Day 1

Description

WASO was defined as the duration (in minutes) of wakefulness from onset of persistent sleep to lights-on.

Time Frame

Baseline, Day 1

Title

Part B: Change From Baseline in Number of Awakenings After Persistent Sleep (NAW) Assessed Using PSG at Day 1

Description

Time Frame

Baseline, Day 1

Title

Part B: Change From Baseline in Percentage of Each Sleep Stage Duration Assessed Using PSG at Day 1

Description

Time Frame

Baseline, Day 1

Title

Part B: Change From Baseline in Duration (in Minutes) of Each Sleep Stage Assessed Using PSG at Day 1

Description

Time Frame

Baseline, Day 1

Title

Part B: Change From Baseline in Mean Total Number of Shift in Sleep Stages Assessed Using PSG at Day 1

Description

Time Frame

Baseline, Day 1

Title

Part B: Change From Day 1 in Waketime Questionnaire Parameters: How Long Did You Sleep Last Night at Day 6

Description

Time Frame

Day 1, Day 6

Title

Part B: Change From Day 1 in Waketime Questionnaire Parameters: Time to Fall Asleep Last Night at Day 6

Description

Time Frame

Day 1, Day 6

Title

Part B: Change From Day 1 in Waketime Questionnaire Parameters: Number of Awakening After Falling Asleep at Day 6

Description

Participants were asked to answer the following question using Waketime Questionnaire: How long did you sleep last night, number of awakening after falling asleep, time to fall asleep last night, time spent awake after falling asleep, rate quality of your sleep (using Likert scale, ranged from 0 = very sound or restful, to 4 = very restless where lower score indicates better outcome). The primary purpose of the Waketime Questionnaire was to confirm anticipated reports of poor sleep. In this outcome measure, data for question "Number of awakening after falling asleep" has been reported.

Time Frame

Day 1, Day 6

Title

Part B: Change From Day 1 in Waketime Questionnaire Parameters: Time Spent Awake After Falling Asleep at Day 6

Description

Participants were asked to answer the following question using Waketime Questionnaire: How long did you sleep last night, number of awakening after falling asleep, time to fall asleep last night, time spent awake after falling asleep, rate quality of your sleep (using Likert scale, ranged from 0 = very sound or restful, to 4 = very restless where lower score indicates better outcome). The primary purpose of the Waketime Questionnaire was to confirm anticipated reports of poor sleep. In this outcome measure, data for question "Time spent awake after falling asleep" has been reported.

Time Frame

Day 1, Day 6

Title

Part B: Change From Day 1 in Waketime Questionnaire Parameters: Rate Quality of Your Sleep at Day 6

Description

Time Frame

Day 1, Day 6

Title

Part B: Change From Day 1 (Pre-dose) in Digit Symbol Substitution Test (DSST) Score at Day 6

Description

Time Frame

Day 1 (Pre-dose), Day 6

Title

Part B: Change From Day 1 (Pre-dose) in Number of Lapses of Greater Than (>) 500- Milliseconds (Msec) Assessed by Psychomotor Vigilance Test (PVT) at Day 6

Description

Time Frame

Day 1 (Pre-dose), Day 6

Title

Part B: Change From Day 1 (Pre-dose) in Score on Karolinska Sleepiness Scale (KSS) at Day 6

Description

Time Frame

Day 1 (Pre-dose), Day 6

Secondary Outcome Measure Information:

Title

Part A: Maximum Plasma Concentration (Cmax) of E2006

Time Frame