A Study to Evaluate Single and Multiple Doses of SEP-479 in Healthy Adult Participants
Recruiting now · Phase 1 · Has a placebo group
Conditions studied: Healthy Volunteers
In brief
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and food effects of oral SEP-479 in healthy adult participants.
Key facts
- Study ID
- NCT07433179
- Run by
- Septerna, Inc.
- People needed
- 150
- Starts
- 2026-03-04
- Expected to finish
- 2027-02-01
- Last updated by the study team
- 2026-04-22
Who can join
Age: 21 and older, up to 60. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Subjects who are able and willing to provide informed consent
- Aged 21 to 60 years at the time of consent
- Have a BMI within the range 18.0 to 32.0 kg/m2
- In general good health
You may not qualify if…
- Any condition, which in the investigator's opinion might jeopardize participant's safety or compliance with the protocol.
- Have clinically significant abnormalities on clinical laboratory results.
- Participation in other clinical trials recently/currently
Where it is running
- Nucleus Network — Melbourne, Australia (enrolling)
Full record on ClinicalTrials.gov
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