A Study to Assess a New Medicine Called IPN01195 When Administered Alone in Adults With Advanced Solid Tumours
← catalyst calendarNCT06833008 · readout in 775 d
Sponsored by Ipsen (industry) · IPN.PA — their whole pipeline →.
Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
85estimated
Sites
13
Countries
France, Italy, Spain +1
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 | 2025-03-14 | actual | When the study began enrolling |
| Primary completion | 2028-10-03 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2028-10-03 | estimated | The whole study's end, after follow-up |
| First posted | 2025-02-18 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-07-30 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Advanced Solid Tumor
Intervention
- Drug: IPN01195
Primary outcomes
what the primary-completion date above is the date OFPart A: Percentage of participants with dose limiting toxicity (DLT)
measured Part A: within 28 days of first dose.
Part A and B: Percentage of participants experiencing treatment emergent adverse events (TEAEs) and treatment emergent serious adverse events (TE SAEs).
measured From the first IPN01195 administration to 30 days after last dose.
Part A and B: Percentage of participants with dose interruptions and permanent treatment discontinuations
measured From the first study drug administration to 30 days after last dose.
Part B: Objective response rate (ORR)
measured Part B: At end of study (up to approximately 3 years)
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