Safety and Tolerability of IPH4502 in Patients With Advanced Solid Tumors

Phase 1

Recruiting

• Conditions: Advanced or Metastatic Solid Tumors
• Interventions: Drug: IPH4502

• Registration Number: NCT06781983
• Lead Sponsor: Innate Pharma

Brief Summary

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

Detailed Description

This is a first-in-human, open-label, multicenter, single-arm Phase 1 study, with a part 1 dose escalation guided by a Bayesian optimal interval design with backfilling (BOIN-BF), followed by a part 2 dose optimization in up to 2 selected indications. This study is to measure the safety, tolerability, pharmacokinetics, and preliminary efficacy of escalating doses of IPH4502 in patients with advanced solid tumors that are known to express Nectin-4.

Study Timeline

• Study First Submitted: 2025-01-08
• Study First Submitted QC: 2025-01-13
• Study First Posted: 2025-01-17
• Study Start: 2025-01-24
• Status Verified: 2025-05
• Last Update Submitted: 2025-05-01
• Last Update Posted: 2025-05-02
• Primary Completion: 2028-04
• Study Completion: 2029-04

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 105

Inclusion Criteria

• Histologically confirmed, unresectable, locally advanced or metastatic solid tumors that are known to express Nectin-4
• Prior systemic treatment for locally advanced or metastatic disease, yet no therapy with demonstrated clinical benefit for the tumor type is available.
• Measurable disease according to RECIST 1.1.
• Archival tumor tissue obtained within 4 months of screening and since the last anticancer therapy prior to the study or agree to undergo a tumor biopsy at baseline.
• Adequate organ function and hematological function.

Main

Exclusion Criteria

• Known or suspected brain metastases.
• Participants with an active infection, Any other infection requiring systemic treatment or latent infection.
• Participants with clinically significant comorbidity(s).
• History of treatment for, or suspicion or confirmed interstitial lung disease (ILD) at baseline.
• Condition being treated with systemic corticosteroids or immunosuppressive therapy during IPH4502 treatment.
• Thromboembolic event requiring anticoagulation therapy ≤14 days prior to the first dose of IPH4502.
• Clinically significant cardiovascular disease and/or cardiac repolarization abnormality.
• Participants with symptomatic heart failure, Acute coronary syndromes
• Participant is receiving or has received anticancer therapy prior to enrolment that may have impact on the assessment of IPH4502.
• Major surgery ≤28 days and minor surgery ≤7 days prior to first dose of IPH4502 or 6 months for coronary artery bypass surgery.
• Concomitant medications or vaccines : Live-attenuated vaccines ≤ 6 weeks prior to first dose of IPH4502; systemic corticosteroids or other immunosuppressive agents within 14 days prior to the first dose of IPH4502; systemic use of moderate or strong CYP 3A4 inhibitors; systemic use of moderate or strong CYP 3A4 inducers.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
IPH4502 Monotherapy	IPH4502	-

Primary Outcome Measures

Name	Time	Method
Safety and Tolerability	From time of first dose through treatment period, including the follow-up: up to 24 months	To evaluate the incidence of AEs, SAEs, TEAEs, and DLTs.

Secondary Outcome Measures

Name	Time	Method
Maximum Observed Plasma Concentration (Cmax)	From time of informed consent through treatment period, including the follow-up: up to 24 months	To characterize and evaluate the pharmacokinetic profile of IPH4502.
Area Under the Plasma Concentration (AUC)	From time of informed consent through treatment period, including the follow-up: up to 24 months	To characterize and evaluate the pharmacokinetic profile of IPH4502.
Incidence of antidrug antibodies (ADA) against IPH4502	From time of informed consent through treatment period, including the follow-up: up to 24 months	To evaluate the immunogenicity of IPH4502.
Objective Response Rate (ORR)	From time of informed consent through treatment period, including the follow-up: up to 24 months	To investigate any preliminary antitumor activity of IPH4502.
Duration Of Response (DoR)	From time of informed consent through treatment period, including the follow-up: up to 24 months	To investigate any preliminary antitumor activity of IPH4502.
Progression Free Survival (PFS)	From time of informed consent through treatment period, including the follow-up: up to 24 months	To investigate any preliminary antitumor activity of IPH4502.

Trial Locations

Locations (5)

Gustave Roussy Cancer Institute; 🇫🇷 Villejuif, France

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