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A Study to Assess a New Medicine Called IPN01195 When Administered Alone in Adults With Advanced Solid Tumours

← catalyst calendar

NCT06833008 · 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
DateFiledBasisWhat it is
Start2025-03-14actualWhen the study began enrolling
Primary completion2028-10-03estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-10-03estimatedThe whole study's end, after follow-up
First posted2025-02-18actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-30actualThe 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 OF
Part 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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