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OncoMatch/Clinical Trials/NCT06781983

Safety and Tolerability of IPH4502 in Patients With Advanced Solid Tumors

Is NCT06781983 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies IPH4502 for advanced or metastatic solid tumors.

Phase 1RecruitingInnate PharmaNCT06781983Data as of May 2026

Treatment: IPH4502This 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

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Extracted eligibility criteria

Cancer type

Tumor Agnostic

Biomarker criteria

Required: NECTIN4 overexpression

Prior therapy

Min 1 prior line

Must have received: systemic therapy — locally advanced or metastatic

Prior systemic treatment for locally advanced or metastatic disease

Lab requirements

Blood counts

adequate hematological function

Kidney function

adequate organ function

Liver function

adequate organ function

Adequate organ function and hematological function.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Massachusetts General Hospital - Boston · Boston, Massachusetts
  • John Theurer Cancer Center · Hackensack, New Jersey
  • Mount Sinai Tisch Cancer Center · New York, New York
  • NEXT Oncology - Dallas · Dallas, Texas
  • NEXT Oncology - Virginia · Fairfax, Virginia

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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