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LGVN — Longeveron Inc.

LGVN (Longeveron Inc.) stock: $1.81, $5.8M market cap, $10.1M cash, -$4.3M EV, $139.8M fully diluted market cap. Lead program: Lomecel-B medicinal signaling cells (Hypoplastic Left Heart Syndrome), Phase 2. Data from Fully Diluted's biotech stocks database.

What they do

Our lead investigational product candidate is laromestrocel, also referred to as Lomecel-B ® . Laromestrocel is a proprietary, scalable, allogeneic cellular therapy that has multiple potential modes of action that include pro-vascular, pro-regenerative, and anti-inflammatory mechanisms that collectively appear to promote tissue repair and healing.

Source: 10-K FY2025 via SEC EDGAR

Share price
$1.81
Market cap
$5.8M
Cash
$10.1M
Enterprise value
-$4.3M

Balance sheet

Cash$10.1M
Debt$0.0M
Net cash$10.1M
Enterprise value-$4.3M
Basic shares30.4M shares
Fully diluted shares77.3M shares
Fully diluted market cap$139.8M
Cash per share$0.33
Quarterly burn$5.7M
Cash runway1.8 quarters

Cash figures as of 2026-06-30. Database snapshot: 2026-11-07.

Share structure

Common
30.4M
Pre-funded warrants
0.0M
Options
0.8M
RSUs
2.6M
Warrants
21.2M
Converts
0.0M
Conv preferred
22.2M
ESPP reserve
—
FDSO
77.3M

Cap table as of 2026-06-30.

Price history

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Recently reported

laromestrocel Phase 2 Mixed · 2026-10-26
hypoplastic left heart syndrome
Primary: Change from baseline in right ventricular ejection fraction (RVEF) at Month 12 in the ELPIS II Phase 2b trial of laromestrocel in hypoplastic left heart syndrome (HLHS) — Did not meet the primary endpoint: mean RVEF decreased by 3.3 (SD=8.4) percentage points in the laromestrocel group and 2.6 (SD=10.5) in the standard of care group (baseline adjusted difference=-1.36, 95% CI: -8.0 - 6.7, p=0.68)
· Pre-specified secondary clinical outcome endpoint major adverse cardiac events (MACE) achieved statistical significance: 8 events in the standard of care arm versus 1 in the laromestrocel treatment arm (P=0.043)
· 40 randomized infants in the intention-to-treat population; baseline and Month 12 CMR available for 28 infants (15 standard of care, 13 laromestrocel)
· Company intends to request a meeting with the FDA to review the results and determine potential next steps
· Results selected for the Late-Breaking Science Program podium presentation at the AHA 2026 Scientific Sessions
Safety: Favorable safety and tolerability profile through 12 months, with no treatment-related serious adverse events identified
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