Innate Pharma Highlights Antibody Drug Conjugate IPH4502 Abstract Selected for the AACR 2025 Annual Meeting

On March 26, 2025 Innate Pharma SA (Euronext Paris: IPH; Nasdaq: IPHA) ("Innate" or the "Company") reported that an abstract regarding IPH4502, its novel and differentiated topoisomerase I inhibitor Antibody Drug Conjugate (ADC) targeting Nectin-4, has been selected for the American Association for Cancer Research (AACR) (Free AACR Whitepaper) Annual Meeting 2025, taking place April 25-30 in Chicago, Illinois (Press release, Innate Pharma, MAR 26, 2025, View Source [SID1234651496]).

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In addition, Jonathan Dickinson, CEO of Innate Parma, will present in a showcase session at the AACR (Free AACR Whitepaper) Oncology Industry Partnering Event, to give an update on Innate’s pipeline and strategy.

Presentation details

AACR 2025 ANNUAL MEETING

IPH4502, a differentiated Nectin-4 exatecan antibody-drug conjugate

Abstract Number: 5443

Session Type: Poster session

Session Category: Experimental and Molecular Therapeutics

Session Title: Antibody-Based Cancer Therapeutics 3

Session Date/Time: Tuesday Apr 29, 2025 2:00 PM – 5:00 PM

More information can be found on the AACR (Free AACR Whitepaper) website.

AACR ONCOLOGY INDUSTRY PARTNERING EVENT

Showcase Session 2 | W192

Presenter: Jonathan Dickinson, Chief Executive Officer

Date and Time: Thursday Apr 24, 2025 4:50 PM

Location: McCormick Place Convention Center West Building, Chicago, Illinois

More information can be found on the AACR (Free AACR Whitepaper) Oncology Industry Partnering Event website.

About IPH4502

IPH4502 is a novel and differentiated topoisomerase I inhibitor Antibody Drug Conjugate (ADC) conjugated to exatecan targeting Nectin-4, a cell adhesion molecule that is overexpressed in several types of solid tumors, such as urothelial carcinoma, breast cancer, non-small cell lung cancer or gastro-intestinal tract cancer.

IPH4502 is currently investigated in a Phase 1 trial in advanced solid tumors. The Phase 1 trial includes a dose escalation part 1 and a dose optimization part 2 and will assess the safety, tolerability, and preliminary efficacy of IPH4502 in different solid tumors known to express Nectin-4, including but not limited to urothelial carcinoma, non-small cell lung, breast, ovarian, gastric, esophageal, and colorectal cancers. The study plans to enroll approximately 105 patients.

In preclinical models, IPH4502 demonstrates strong bystander killing effect, and efficient internalization, enabling a potent anti-tumor activity in models with various Nectin-4 expression levels. Additionally, IPH4502 shows efficacy in models resistant to MMAE-ADC. These results support its potential for development beyond UC and in cancer patients treated with MMAE-based ADCs.