Bank of America Global Healthcare Conference 2026
Logotype for Elicio Therapeutics Inc

Elicio Therapeutics (ELTX) Bank of America Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for Elicio Therapeutics Inc

Bank of America Global Healthcare Conference 2026 summary

14 May, 2026

Corporate and pipeline overview

  • Focus on immunotherapeutics using the AMP platform to enhance lymphatic targeting and immune response against cancers, with broad applicability across cancer types.

  • Lead program ELI-002 targets mutated KRAS, present in 25% of solid tumors, with phase I data in pancreatic and colorectal cancer and ongoing phase II in adjuvant pancreatic cancer.

  • Pipeline includes assets targeting other high-frequency mutations such as BRAF and P53, with early-stage programs in development.

  • AMP platform aims to overcome historical challenges in immunotherapy by improving antitumor immune responses and enabling off-the-shelf solutions.

  • Personalized tumor immunity observed through antigen spreading, expanding immune response beyond targeted mutations.

Clinical trial results and differentiation

  • Phase I studies in pancreatic and colorectal cancer showed robust immune responses, with T-cell activity strongly correlated to clinical benefit.

  • ELI-002 demonstrated favorable relapse-free and overall survival compared to historical controls, with 100% of patients generating mutant KRAS-specific T-cells.

  • 7-peptide formulation covers a broader range of KRAS mutations, maintaining strong safety and tolerability with no dose-limiting toxicities.

  • Antigen spreading led to 70% of patients generating immune responses against additional tumor mutations.

Ongoing and future studies

  • Phase II trial in adjuvant pancreatic cancer is randomized, focusing on disease-free survival as the primary endpoint, with final analysis expected mid-2026.

  • Interim analysis confirmed safety and preliminary activity, supporting progression to phase III planning in alignment with FDA guidance.

  • Secondary endpoints show 99% of patients generating KRAS-specific T-cell responses, with 80% exceeding the threshold previously linked to clinical benefit.

  • Antigen spreading observed in 87% of patients in phase II, supporting broad applicability.

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