Safety and Tolerability of IPH4502 in Patients With Advanced Solid Tumors
Running, not enrolling · Phase 1
Conditions studied: Advanced or Metastatic Solid Tumors
In brief
This is a first-in-human, open-label, multicenter, Phase 1 study to evaluate the safety, tolerability and preliminary efficacy of IPH4502 and to determine the recommended Phase 2 dose (RP2D) in advanced solid tumors that are known to express Nectin-4
Key facts
- Study ID
- NCT06781983
- Run by
- Innate Pharma
- People needed
- 145
- Starts
- 2025-01-24
- Expected to finish
- 2029-04-01
- Last updated by the study team
- 2026-07-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Massachusetts General Hospital - Boston — Boston, Massachusetts, United States
- John Theurer Cancer Center — Hackensack, New Jersey, United States
- Mount Sinai Tisch Cancer Center — New York, New York, United States
- NEXT Oncology - Dallas — Dallas, Texas, United States
- NEXT Oncology - Virginia — Fairfax, Virginia, United States
- Centre Léon Bérard — Lyon, France
- Gustave Roussy Cancer Institute — Villejuif, France
Full record on ClinicalTrials.gov
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