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ELTX — Elicio Therapeutics Inc.

ELTX (Elicio Therapeutics Inc.) stock: $1.51, $40.9M market cap, $30.9M cash, $19.6M EV, $54.5M fully diluted market cap. Lead program: ELI-002 7P (Pancreatic Ductal Adenocarcinoma), Phase 2. Data from Fully Diluted's biotech stocks database.

What they do

We are a clinical-stage biotechnology company advancing novel immunotherapies for the treatment of cancer, including mutant Kirsten rat sarcoma viral oncogene homolog (“mKRAS”) - positive pancreatic cancer, colorectal cancer (“CRC”), lung cancer and other mKRAS positive cancers.

Source: 10-K FY2025 via SEC EDGAR

Share price
$1.51
Market cap
$40.9M
Cash
$30.9M
Enterprise value
$19.6M

Balance sheet

Cash$30.9M
Debt$9.6M
Net cash$21.3M
Enterprise value$19.6M
Basic shares28.3M shares
Fully diluted shares36.1M shares
Fully diluted market cap$54.5M
Cash per share$1.09
Quarterly burn$8.2M
Cash runway4.3 quarters

Cash figures as of 2026-09-30. Database snapshot: 2026-11-07.

Share structure

Common
26.3M
Pre-funded warrants
2.6M
Options
3.1M
RSUs
0.2M
Warrants
3.6M
Converts
0.0M
Conv preferred
0.0M
ESPP reserve
0.3M
FDSO
36.1M

Cap table as of 2026-08-11.

Price history

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Recently reported

ELI-002 7P Phase 2 Positive · 2026-10-23
AMPLIFY-7P
Primary: Disease-free survival (DFS) in the intent-to-treat population — Did not meet its pre-specified primary disease-free survival (DFS) endpoint in the intent-to-treat (ITT) population (HR 0.85)
· Baseline ctDNA positivity was more prevalent in the camupepimut arm (20.8% vs. 12.5%)
· ctDNA-negative (n=93): median DFS not reached vs. 21.2 months (HR 0.51; nominal p=0.0280); recurrence or death 27.4% (17/62) vs. 48.4% (15/31)
· ctDNA-positive (n=26): median DFS 4.3 months vs. 1.9 months (HR 0.57; nominal p=0.0489)
· No prior radiation (n=106): median DFS 23.8 months vs. 10.4 months (HR 0.59; nominal p=0.0221)
· Multivariable adjusted HR 0.47; p=0.0086
· Mutant KRAS-specific T-cell responses in 99% of evaluable treated patients
Safety: Generally well tolerated, no new safety signals; Grade 3 or higher adverse events 10.4% vs. 14.6% under observation, serious adverse events 6.3% and 8.3% respectively, no adverse events led to withdrawal
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