A First-in-Human Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Single and Multiple Oral Doses of Debio 1453P in Healthy Adults

Recruiting now · Phase 1 · Has a placebo group

Conditions studied: Healthy Participants

In brief

The main purpose of this study is to evaluate the safety, tolerability and pharmacokinetics (PK) of Debio 1453P compared to placebo across different dose levels in healthy adults after single and repeated oral dosing.

Key facts

Study ID
NCT07035769
Run by
Debiopharm International SA
People needed
88
Starts
2025-06-18
Expected to finish
2026-11-01
Last updated by the study team
2026-07-24

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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