Leerink Global Healthcare Conference 2026
Logotype for Innate Pharma S.A.

Innate Pharma (IPH) Leerink Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for Innate Pharma S.A.

Leerink Global Healthcare Conference 2026 summary

9 Mar, 2026

Nectin-4 ADC (IPH4502) program updates

  • Differentiation from competitors is based on a superior antibody and linker, enabling efficacy in low Nectin-4 expression tumors and a potentially wider therapeutic window compared to Lilly and Hengrui compounds.

  • Ongoing phase I basket study uses adaptive design to identify promising tumor types, with expansion to 120+ patients and focus on triple-negative breast, prostate, and non-small cell lung cancers.

  • Study aims to enrich for PADCEV-treated patients, targeting a post-PADCEV label and potential accelerated approval in this high unmet need setting.

  • Decision pending on timing of data release: early basket data or more robust, tumor-specific results with longer follow-up, with a preference for the latter.

  • Study remains on track, with strong patient demand and rapid cohort enrollment.

Lacutamab clinical and strategic progress

  • Accelerated approval path agreed with FDA for Sézary syndrome, with a phase III umbrella protocol including cohorts for Sézary and mycosis fungoides, both using active comparators.

  • Confirmatory study ready to initiate pending funding, with BLA submission targeted for early 2027 and potential approval by late 2027.

  • Strategic partnership, royalty financing, and equity raise options are being evaluated to fund the program.

  • Strong PFS data in mycosis fungoides supports confidence in outperforming standard of care in the confirmatory trial.

  • Investigator-initiated studies planned to explore use in earlier-stage patients, aiming to prevent disease progression and expand market potential.

Lacutamab in PTCL and future directions

  • Phase II investigator-initiated study ongoing in PTCL with GemOx combination, with data expected before year-end and potential for first-line development.

  • LYSA group, with a strong track record, is leading the study and aims to develop an L-CHOP regimen for PTCL.

  • Interim analysis has been seen by the company, but not yet by regulators.

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