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Immutep (IMM) investor relations material
Immutep Q2 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Entered strategic collaboration with Dr. Reddy's for efti commercialization outside North America, Europe, Japan, and Greater China, receiving ~A$30 million upfront and eligibility for up to ~A$528 million in milestones plus royalties.
Strong operational progress in TACTI-004 (KEYNOTE-F91) Phase III trial for 1L NSCLC, with futility analysis on track for Q1 CY2026.
Positive clinical data across multiple trials, including INSIGHT-003 (NSCLC), EFTISARC-NEO (soft tissue sarcoma), and AIPAC-003 (metastatic breast cancer).
IMP761 Phase I trial in autoimmune diseases showed dose-dependent immunosuppressive effects and favorable safety.
Received A$4.6 million R&D tax incentive from the French government.
Financial highlights
Cash, cash equivalents, and term deposits totaled A$99.1 million as of 31 December 2025; pro-forma balance of A$129.3 million after Dr. Reddy's upfront payment.
Net cash used in operating activities for the quarter was A$9.4 million, down from A$19.0 million in Q1 FY26.
Cash used in R&D activities was A$9.9 million, compared to A$15.8 million in the previous quarter.
Payments to related parties totaled A$474k for the quarter.
Cash reach extended well into Q2 CY2027, excluding future milestone payments.
Outlook and guidance
Cash position expected to fund operations well into Q2 CY2027.
Additional updates on IMP761 Phase I trial anticipated in H1 CY2026.
TACTI-004 futility analysis expected in Q1 CY2026; 50% patient enrollment target anticipated soon.
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