Condition: Excessive Daytime Sleepiness · Sponsor: Centessa Pharmaceuticals (UK) Limited
Characterize the safety, tolerability and pharmacokinetics of ORX142 following single and multiple doses.
This description comes directly from the study's public registry record.
ORX142 Centessa Program Lead · 617-468-5770 · ORX142-0101study@centessa.com
Always discuss trial participation with your own doctor first.
| Site #1 | Lincoln, Nebraska, United States | Recruiting |
| Site #2 | Eatontown, New Jersey, United States | Recruiting |
| Site #3 | New York, New York, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07082829