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Elicio Therapeutics (ELTX) investor relations material
Elicio Therapeutics Q1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Clinical-stage biotech focused on immunotherapies for mKRAS-positive cancers, with lead candidate ELI-002 7P in Phase 2 for pancreatic cancer and a pipeline targeting additional solid tumors.
Focus remains on advancing the Phase 2 AMPLIFY-7P trial for ELI-002 7P in post-resection KRAS-driven PDAC, with primary disease-free survival (DFS) analysis expected mid-year 2026.
Durability of T-cell responses and favorable clinical observations support ELI-002 7P's potential as monotherapy in adjuvant PDAC.
Net loss for Q1 2026 was $11.8 million, with an accumulated deficit of $245.5 million and cash/cash equivalents of $14.9 million as of March 31, 2026.
Substantial doubt exists about ability to continue as a going concern beyond Q4 2026 without additional financing.
Financial highlights
Research and development expenses decreased 13% year-over-year to $6.8 million, primarily due to lower clinical trial costs as patients moved to follow-up phase.
General and administrative expenses increased 30% year-over-year to $3.8 million, mainly from higher headcount and personnel costs.
Net loss per share improved to $0.65 from $0.87 year-over-year, with weighted average shares outstanding increasing to 18.2 million.
Cash and cash equivalents were $14.9 million as of March 31, 2026, compared to $18.6 million at year-end 2025.
Raised $13.0 million in Q1 and Q2 2026 to date through at-the-market program.
Outlook and guidance
Cash runway expected to fund operations into Q4 2026, but additional capital will be required to continue development programs and operations beyond that point.
Event-driven primary DFS analysis for AMPLIFY-7P Phase 2 trial anticipated mid-year 2026.
Plans to seek additional funding through equity, debt, or strategic transactions; failure to secure capital may require scaling back or liquidation.
Plans to request End-of-Phase 2 meeting with FDA to align on Phase 3 trial design and advance toward a registrational study.
- Reduced net loss, strong cash position, and key clinical milestones expected in 2026.ELTX
Q4 202513 Mar 2026 - Biotech seeks $400M for cancer immunotherapy pipeline, with ongoing trials and going concern risk.ELTX
Registration Filing12 Mar 2026 - Phase II data for a lymph node-targeted KRAS immunotherapy show robust T cell responses and safety.ELTX
TD Cowen 46th Annual Health Care Conference4 Mar 2026 - Shelf registration allows ongoing securities offerings with robust governance protections.ELTX
Registration Filing2 Mar 2026 - Biotech seeks up to $400M via flexible securities shelf to advance immunotherapy pipeline.ELTX
Registration Filing27 Feb 2026 - 2.25 million shares registered for resale by a board-controlled entity after recent private placements.ELTX
Registration Filing16 Dec 2025 - Biotech seeks up to $200M, including $40M at-the-market, to fund immunotherapy pipeline.ELTX
Registration Filing16 Dec 2025 - Registration enables resale of shares from a $20M convertible note, with no proceeds to the company.ELTX
Registration Filing16 Dec 2025 - Registering 103,225 shares for resale from a warrant linked to a $10M note, with Phase 2 cancer immunotherapy in focus.ELTX
Registration Filing16 Dec 2025
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