drugset / Trial / NCT07413666

A Study of ORX489 in Healthy Adult Participants, Aged 18 to 60 Years

NCT07413666 ↗

Phase 1 Recruiting 212 enrolled Centessa Pharmaceuticals (UK) Limited
RandomizedParallel-groupDouble-blindTreatment

Summary

Characterize the safety, tolerability and pharmacokinetics of ORX489 following single and multiple doses.

Timeline

Start
2026-02-25
Primary completion
2027-06-30
Completion
2027-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ORX489 Unknown — —

Indications

No indication recorded.