Safety Follow-up Study of Participants Dosed With INV-347 in Study INV-CL-108
← catalyst calendarNCT07153172 · readout in 392 d
Sponsored by Novo Nordisk A/S (industry) · NVO — their whole pipeline →.
Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Na · None · Other
Enrollment
91estimated
Sites
1
Country
Canada
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2025-08-06 | actual | When the study began enrolling |
| Primary completion | 2027-09-15 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-09-15 | estimated | The whole study's end, after follow-up |
| First posted | 2025-09-03 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-03-06 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Obesity
Intervention
- Drug: INV-347
Primary outcome
what the primary-completion date above is the date OFNumber of adverse events
measured From the end-of-study participation in INV-CL-108 (week 0) to completion of the end-of-study visit (up to week 104 from enrolment)
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