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Immuneering (IMRX) investor relations material
Immuneering Q2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Atebimetinib advanced in Phase 2a trials, showing 94% OS and 72% PFS at six months in first-line pancreatic cancer; median OS and PFS not reached.
Regulatory feedback on pivotal trial plans expected in Q4 2025, with trial initiation planned for 2026.
Strategic focus shifted to atebimetinib after pausing IMM-6-415; partnership opportunities for IMM-6-415 are being explored.
U.S. composition of matter patent granted for atebimetinib, providing exclusivity into 2042 and potential extension to 2044.
Net loss for the six months ended June 30, 2025 was $29.5 million, with an accumulated deficit of $253.8 million and $26.4 million in cash and cash equivalents.
Financial highlights
Net loss was $14.4 million for Q2 2025, up 2.5% year-over-year; net loss for the six months ended June 30, 2025 was $29.5 million, up 3.9% year-over-year.
R&D expenses for Q2 2025 were $10.5 million, slightly down from $10.7 million in Q2 2024; for the six months, R&D expenses were $21.9 million, up 0.3% year-over-year.
G&A expenses for Q2 2025 were $4.3 million, unchanged from Q2 2024; for the six months, G&A expenses were $8.3 million, down 0.8% year-over-year.
Cash used in operating activities was $23.5 million for the six months ended June 30, 2025; net cash provided by financing activities was $13.7 million, mainly from ATM equity sales.
Cash and cash equivalents were $26.4 million as of June 30, 2025, down from $36.1 million at December 31, 2024.
Outlook and guidance
Existing cash and cash equivalents expected to fund operations into 2026; additional capital will be required to continue beyond that point.
Updated OS and PFS data from the Phase 2a atebimetinib trial expected in Q3 2025.
Plans to initiate a registrational trial for atebimetinib in combination with mGnP in 2026, pending regulatory feedback.
If unable to raise additional capital, significant reductions in spending or operational scale-back may be necessary.
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