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Study identifier: NCT07082829 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study of ORX142 in Healthy Adult Subjects, Including Subjects 18 to 80 Years of Age

Condition: Excessive Daytime Sleepiness  ·  Sponsor: Centessa Pharmaceuticals (UK) Limited

PhasePhase 1
Planned participants208
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersYes

About this study

Characterize the safety, tolerability and pharmacokinetics of ORX142 following single and multiple doses.

This description comes directly from the study's public registry record.

Talk to the study team

ORX142 Centessa Program Lead  ·  617-468-5770  ·  ORX142-0101study@centessa.com

Always discuss trial participation with your own doctor first.

Locations (3)

Site #1Lincoln, Nebraska, United StatesRecruiting
Site #2Eatontown, New Jersey, United StatesRecruiting
Site #3New York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07082829