A Study of ORX489 in Healthy Adult Participants, Aged 18 to 60 Years
- Age
- 18 – 60
- Sex
- Any
- Trial phase
- Phase 1
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 212 (estimated)
- Sponsor
- Centessa Pharmaceuticals (UK) Limited · Industry
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Check Your EligibilityCharacterize the safety, tolerability and pharmacokinetics of ORX489 following single and multiple doses.
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ORX489 Centessa Program Lead ORX489 Centessa Program Lead
617-468-5770
CONTACT
Celerion Program Lead CA49982 United States, Nebraska [Recruiting]
CONTACT