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Immuneering (IMRX) investor relations material
Immuneering Q3 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Q3 net loss widened to $24.2M from $15.0M YoY as late-stage atebimetinib development, particularly MAPKeeper 301, drove higher R&D spending.
Cash, cash equivalents and marketable securities totaled $166.1M at Sept. 30, 2026; expected runway was revised from 2029 to Q4 2028.
Atebimetinib is in Phase 3 first-line pancreatic cancer and Phase 1/2a advanced solid tumor trials; no product candidates are approved for sale.
Phase 2 atebimetinib plus mGnP follow-up was extended as patients lived longer than projected; updated data for 55 patients is expected in 1H 2027.
Financial highlights
Q3 2026 operating expenses and operating loss were $25.8M vs. $15.4M YoY; net loss was $24.2M vs. $15.0M.
9M 2026 operating expenses and operating loss were $60.1M vs. $45.6M YoY; net loss was $54.9M vs. $44.4M.
Q3 R&D rose 90.7% to $20.7M from $10.9M, primarily due to higher lead-program clinical costs, including $8.5M in higher MAPKeeper 301 costs.
Q3 G&A increased 12.3% to $5.1M from $4.5M; 9M G&A rose 15.1% to $14.7M, mainly from employee-related and stock-based compensation costs.
Q3 basic and diluted loss per share was $0.37 vs. $0.38; 9M loss per share was $0.85 vs. $1.20.
Outlook and guidance
Existing liquidity is expected to fund operations into Q4 2028, versus prior guidance into 2029; the estimate may prove incorrect and additional capital will be needed thereafter.
Runway revision reflects extended Phase 1/2a activity, larger and faster MAPKeeper 301 enrollment, and commercial-readiness costs; R&D and G&A expenses are expected to increase.
MAPKeeper 301 enrollment target rose from 510 to 570 patients and is ahead of schedule; topline data remain planned for mid-2028, with potential acceleration.
Updated Phase 2 atebimetinib plus mGnP data for N=55 is expected in 1H 2027; the extended follow-up reflects longer-than-projected survival.
First patient dosing in the atebimetinib plus cemiplimab (Libtayo) NSCLC trial and additional anti-PD-1 preclinical data are expected in Q4 2026; next-program IND-enabling work is planned for mid-2027.
- Atebimetinib delivers 17.3 months median OS in first-line pancreatic cancer with high tolerability.IMRX
H.C. Wainwright 28th Annual Global Investment Conference - Atebimetinib nearly doubles survival in first-line pancreatic cancer with superior tolerability.IMRX
12th Annual Cantor Fitzgerald Global Healthcare Conference - Pivotal trial for atebimetinib advanced, with strong interim data and cash runway into 2029.IMRX
Q2 2026 - Atebimetinib shows strong survival and tolerability in pancreatic cancer, with pivotal phase III underway.IMRX
25th Annual Needham Virtual Healthcare Conference - Atebimetinib nearly doubles 12-month survival in First-Line pancreatic cancer with strong tolerability.IMRX
Leerink Global Healthcare Conference 2026 - Director elections and auditor ratification were approved without stockholder questions.IMRX
AGM 2026 - Atebimetinib plus mGnP achieved 94% 6-month OS and strong tolerability in pancreatic cancer.IMRX
Study Update - 40% response and 80% disease control seen with IMM-1-104 combo in early pancreatic cancer trial.IMRX
Study Update - IMM-1-104 achieved 43% ORR and 86% DCR with strong tolerability in first-line pancreatic cancer.IMRX
Study Result
Next Immuneering earnings date
Next Immuneering earnings date
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