Safety Follow-up Study of Participants Dosed With INV-347 in Study INV-CL-108
Recruiting now · Phase 1
Conditions studied: Obesity
In brief
The study looks at the safety and blood levels of the study drug INV-347 in participants who were previously dosed with INV-347 in study INV-CL-108. Participants will not get any study drug in this study as it looks into the safety of a drug previously dosed. The study will last until visit 21.
Key facts
- Study ID
- NCT07153172
- Run by
- Novo Nordisk A/S
- People needed
- 91
- Starts
- 2025-08-06
- Expected to finish
- 2027-09-15
- Last updated by the study team
- 2026-03-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Informed consent obtained before any study-related activities. Study-related activities are any procedures that are carried out as part of the study, including activities to determine suitability for the study.
- Male or female (sex at birth).
- Age 18 years or above at the time of signing the informed consent.
- Previously dosed with INV-347 in study INV-CL-108 and with measurable INV-347 concentration in plasma at enrolment [above lower limit of qualification (LLOQ) of 0.5 nanogram per milliliter (ng/mL)].
You may not qualify if…
- The study has no exclusion criteria.
Where it is running
- Syneos Health Clinique — Québec, Canada (enrolling)
Full record on ClinicalTrials.gov
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