RecruitingAccepts healthy volunteersPhase 1
A Study of ORX489 in Healthy Adult Participants, Aged 18 to 60 Years
Centessa Pharmaceuticals (UK) Limited · NCT07413666
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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–60 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 1
- Target enrollment
- 212
- US sites recruiting
- 1
- Study start
- February 25, 2026
- Record last updated
- February 25, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Characterize the safety, tolerability and pharmacokinetics of ORX489 following single and multiple doses.
Being studied: ORX489 Tablets; Placebo Tablets
Conditions: Healthy Adult Male and Female Volunteers
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Healthy males or females as determined by assessments at the Screening Visit.
- For Parts A, B, C, and D: Participants must be at least 18 years of age and no more than 60 years of age at the Screening
Exclusion Criteria
- Presence of significant cardiac, pulmonary, gastrointestinal, hepatic, renal, hematological, malignancy, endocrine, neurological, or psychiatric disease, as determined by medical history, physical examination, and screening investigations.
- History of seizure disorder, any other condition that increases the risk of seizure
- Has a clinically significant sleep disorder, including insomnia or sleep apnea
Recruiting US locations
Celerion
Lincoln, NE 68502
Study contacts (from the official record)
- ORX489 Centessa Program Lead ORX489 Centessa Program Lead · 617-468-5770 · ORX489-101study@centessa.com
- Celerion Program Lead CA49982 United States, Nebraska [Recruiting]
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