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COAG — Hemab Therapeutics Holdings Inc.

COAG (Hemab Therapeutics Holdings Inc.) stock: $49.02, $2.29B market cap, $457.5M cash, $1.83B EV, $2.54B fully diluted market cap. Lead program: Sutacimig (Congenital Factor VII Deficiency), Phase 2. Data from Fully Diluted's biotech stocks database.

What they do

Hemab Therapeutics Holdings, Inc. (the “Company”) is a clinical-stage biotechnology company developing therapies that reimagine the treatment of blood coagulation disorders to sustain life and human resilience.

Source: 10-Q FY2026 via SEC EDGAR

Share price
$49.02
Market cap
$2,289.8M
Cash
$457.5M
Enterprise value
$1,832.3M

Balance sheet

Cash$457.5M
Debt$0.0M
Net cash$457.5M
Enterprise value$1,832.3M
Basic shares46.7M shares
Fully diluted shares51.8M shares
Fully diluted market cap$2,538.2M
Cash per share$9.79
Quarterly burn$22.6M
Cash runway20.2 quarters

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

Share structure

Common
46.7M
Pre-funded warrants
0.0M
Options
0.3M
RSUs
0.0M
Warrants
4.3M
Converts
0.0M
Conv preferred
0.0M
ESPP reserve
0.4M
FDSO
51.8M

Cap table as of 2026-06-30.

Price history

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Next catalyst

HMB-003 · Jun 11 - Jul 23 in 7 mo · Phase 1 · Healthy Adult Participants

Recently reported

Sutacimig Phase 2 Mixed · 2026-11-04
HMB-001-201 · congenital factor vii deficiency
Primary: Pharmacokinetic and pharmacodynamic results (prothrombin time and endogenous FVII(a) accumulation) after a single subcutaneous dose in the single-ascending-dose cohort — Both participants had a baseline prothrombin time of ≥180 seconds, which shortened by more than 50% following dosing; in the participant with PK/PD data available to date, sutacimig produced sustained accumulation (~5x) of endogenous total FVII(a), with exposure maintained through Day 22
· 2 participants with severe congenital FVIID had received a single subcutaneous dose as of July 24, 2026
· Phase 2b study HMB-001-201 (NCT07347249), conducted at a single site in the UK
· Abstract Number: abs26-10755, to be presented at ASH on December 14, 2026
Safety: Adverse events were low grade and assessed as not related to treatment
Source release →
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