Eisai Clinical Trials

A Randomized, Double-Blind, Single-Dose, 5-Period Crossover Study to Evaluate the Efficacy, Safety, and Tolerability of E2086 Compared to Placebo and Active Comparator in Adult Subjects With Narcolepsy Type 1

E2086-A001-101

Study Overview

E2086
N/A
NCT06462404
Jun 2024 - Mar 2025
Narcolepsy Type 1
1. Mean Sleep Latency (MSL) as Assessed by the 4 Maintenance of Wakefulness Tests (MWTs) for E2086 Versus Placebo at Day 1 [Time Frame: At Day 1]

2. MSL as Assessed by the 4 MWTs for E2086 Versus Placebo at Day 5 [Time Frame: At Day 5]

3. MSL as Assessed by the 4 MWTs for E2086 Versus Placebo at Day 9 [Time Frame: At Day 9]

4. MSL as Assessed by the 4 MWTs for E2086 Versus Placebo at Day 13 [Time Frame: At Day 13]

  • Males and females 18 Years and older (Adult, Older Adult)

  • Completed

  • Phase 1

  • Canada, United States See more

Clinical Trial Documents

Clinical Study Report Synopsis

No download available

Plain Language Protocol Synopsis (PLPS)

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Plain Language Summary of Results (PLS)

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Publication reference citation

Data Sharing

ClinicalStudyDataRequest.com (CSDR) is a multi sponsor site through which qualified researchers who wish to access clinical trial data and associated information in order to conduct further research can submit their research proposal or enquiry.

CSDR Sharing is not available for this study.

CSDR Availability
Clinical Trial Data

Redacted documents may be available upon request for this study.

Document type Availability
Protocol
SAP
Sample CRF
Full CSR