Innate Pharma (IPH) Investor Update summary
Event summary combining transcript, slides, and related documents.
Investor Update summary
30 Jun, 2026Strategic and Clinical Development Update
Focused on three priority assets: lacutamab, IPH4502, and monalizumab, with streamlined R&D and a 30% organizational reduction to align with new strategy.
Lacutamab, a first-in-class anti-KIR3DL2 antibody, is advancing toward accelerated approval in Sézary syndrome, with confirmatory Phase III protocols for both SS and MF submitted to the FDA.
Monalizumab, partnered with AstraZeneca, is in a Phase III study (PACIFIC-9) with data expected in 2026 and significant milestone and royalty potential.
IPH4502, a Nectin-4 targeted ADC, is in Phase I with early clinical activity and data expected by early next year.
Clinical Efficacy, Safety, and Unmet Needs in CTCL
CTCL, especially Sézary syndrome and advanced mycosis fungoides, has poor prognosis and significant unmet need for effective, well-tolerated systemic therapies.
TELLOMAK Phase II data showed lacutamab delivers rapid, durable responses and significant quality of life improvements in SS and MF, regardless of KIR3DL2 expression.
In SS post-mogamulizumab, lacutamab achieved a global ORR of 42.9%, median PFS of 8.3 months, and median DoR of 25.6 months.
In MF, lacutamab induced deep responses with a global clinical benefit rate of 86% and median PFS of 10.2 months.
Safety profile is favorable, with low rates of serious adverse events and treatment discontinuation, supporting long-term use.
Regulatory Progress and Milestones
Regulatory designations include FDA Breakthrough Therapy, Orphan Drug, Fast Track, and EMA PRIME, enabling accelerated approval and market exclusivity.
No new data required for accelerated approval in SS; Phase III design includes two cohorts (SS and MF) with primary endpoint of progression-free survival.
Key milestones include US accelerated approval in 2027 for SS and potential US approval for MF in 2029.
Upcoming catalysts: Phase I data for IPH4502, PACIFIC-9 readout for monalizumab, and BLA submissions for lacutamab and monalizumab.
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