Clinical trial
An Open-Label, Phase I/II First-in-Human, Dose Escalation, Dose Optimisation and Dose Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetic, Pharmacodynamic, Immunogenicity and Antitumour Activity of IPN60300 as Single Agent in Adult Participants With Locally Advanced or Metastatic Solid Tumours.
NCT07213817 is registered in ClinicalTrials.gov with Ipsen as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- An Open-Label, Phase I/II First-in-Human, Dose Escalation, Dose Optimisation and Dose Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetic, Pharmacodynamic, Immunogenicity and Antitumour Activity of IPN60300 as Single Agent in Adult Participants With Locally Advanced or Metastatic Solid Tumours.
- Lead sponsor
- Ipsen
- Phase
- Phase 1/2
- Overall status
- Recruiting
- Start date
- December 5, 2025
- Completion date
- October 30, 2028
- Enrollment
- 114 (estimated)
- Sites
- 12
Conditions
As the registry lists them; a condition with its own page is linked.
locally advanced solid tumor, metastatic solid tumor