Condition: Narcolepsy · Sponsor: Eisai Inc.
The primary purpose of this study is to evaluate the optimal doses of E2086 compared to placebo in participants with narcolepsy for reduction of excessive daytime sleepiness (EDS) as assessed by Mean Sleep Latency (MSL) (measured from the first 4 maintenance of wakefulness tests \[MWTs\]).
This description comes directly from the study's public registry record.
Eisai Medical Information · +1-888-274-2378 · esi_medinfo@eisai.com
Always discuss trial participation with your own doctor first.
| SDS Clinical Trials, Inc-California-Santa Ana | Santa Ana, California, United States | Not Yet Recruiting |
| Meris Clinical Research-310 Oakfield Dr | Brandon, Florida, United States | Not Yet Recruiting |
| Hope Research Network Trials -6500 NW 77th CT | Medley, Florida, United States | Not Yet Recruiting |
| Vitaly Clinical Research LLC | Miami, Florida, United States | Not Yet Recruiting |
| Anchor Medical Research LLC | Miami, Florida, United States | Not Yet Recruiting |
| New Access Research & Medical Services Inc - Kendall | Miami, Florida, United States | Not Yet Recruiting |
| NeuroTrials Research, Inc | Atlanta, Georgia, United States | Not Yet Recruiting |
| Sleep Practitioners, LLC | Macon, Georgia, United States | Not Yet Recruiting |
| Clinical Research Institute Stockbridge | Stockbridge, Georgia, United States | Not Yet Recruiting |
| Wu Lab at Johns Hopkins University | Baltimore, Maryland, United States | Not Yet Recruiting |
| Midwest Center for Sleep Disorders (MWCSD) | Lansing, Michigan, United States | Not Yet Recruiting |
| Henry Ford Medical Center - Columbus | Novi, Michigan, United States | Not Yet Recruiting |
+ 45 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07493265