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A Study to Assess the Safety, Tolerability, Pharmacokinetic, Pharmacodynamic, Immunogenicity and Antitumour Activity of IPN60300 in Adults With Locally Advanced or Metastatic Solid Tumours

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NCT07213817 · readout in 803 d

Sponsored by Ipsen (industry) · IPN.PA — their whole pipeline →.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
114estimated
Sites
12
Countries
France, Spain, United States

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
Start2025-12-05actualWhen the study began enrolling
Primary completion2028-10-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-10-30estimatedThe whole study's end, after follow-up
First posted2025-10-09actualWhen 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

Conditions

  • Locally Advanced Solid Tumor
  • Metastatic Solid Tumor

Intervention

  • Biological: IPN60300

Primary outcomes

what the primary-completion date above is the date OF
Phase Ia: Percentage of participants with dose limiting toxicity (DLT)
measured within 21 days following study drug administration.
Phase Ia and Ib: Percentage of participants experiencing Treatment Emergent Adverse Events (TEAEs) and Treatment Emergent Serious Adverse Events (TE SAEs).
measured From the first IPN60300 administration until 30 days after the last dose
Phase Ib: Objective response rate (ORR)
measured At end of study (up to approximately 3 years )

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