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IRON — Disc Medicine Inc.

IRON (Disc Medicine Inc.) stock: $78.91, $3.50B market cap, $682.8M cash, $2.88B EV, $3.49B fully diluted market cap. Lead program: DISC-1459 (Erythropoietic Protoporphyria), Phase 3. Data from Fully Diluted's biotech stocks database.

What they do

We are a clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of novel treatments for patients suffering from serious hematologic diseases. We have assembled a portfolio of clinical and preclinical product candidates that aim to modify fundamental biological pathways associated with the formation and function of red blood cells, specifically heme biosynthesis and iron homeostasis.

Source: 10-K FY2025 via SEC EDGAR

Share price
$78.91
Market cap
$3,503.0M
Cash
$682.8M
Enterprise value
$2,879.9M

Balance sheet

Cash$682.8M
Debt$59.7M
Net cash$623.1M
Enterprise value$2,879.9M
Basic shares38.4M shares
Fully diluted shares44.2M shares
Fully diluted market cap$3,486.0M
Cash per share$17.78
Quarterly burn$44.2M
Cash runway16.2 quarters

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

Share structure

Common
38.4M
Pre-funded warrants
0.4M
Options
3.7M
RSUs
1.3M
Warrants
0.0M
Converts
0.0M
Conv preferred
0.0M
ESPP reserve
0.3M
FDSO
44.2M

Cap table as of 2026-06-30.

Price history

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Next catalyst

DISC-0974 · Nov 12 - Dec 24 in 5d · Phase 2 · Inflammatory Bowel Disease (IBD); Anemia

Recently reported

Bitopertin Phase 3 Positive · 2026-10-19
APOLLO · erythropoietic protoporphyria (epp), x-linked protoporphyria (xlp)
Primary: Co-primary endpoints: reduction in whole-blood metal-free PPIX from baseline and increase in average monthly total time in light without pain during month 6 (bitopertin 60 mg QD vs placebo, n=183, EPP/XLP, age 12+) — PPIX -41.4% vs placebo (p<0.0001); average monthly total time in light without pain in month 6 +12.2 hours vs placebo (p=0.0010)
· Phototoxic reaction incidence rate reduced vs placebo (p<0.0001)
· Cumulative total time in light without pain over the 6-month treatment period increased vs placebo (p<0.0001)
· Average daily sunlight exposure time to prodrome increased vs placebo (p=0.0077, adults only)
· Patient Global Impression of Change (PGIC) score improved vs placebo (p<0.0001)
· Patient Global Impression of Severity (PGIS) score improved vs placebo (p<0.0001)
· Disc plans to resubmit an NDA to FDA by end of 2026, with an FDA decision anticipated by mid-2027
Safety: Generally well tolerated; dizziness was the most common TEAE (50%), mild or moderate and generally transient; no TEAEs above Grade 3; no new safety signals
Source release →
DISC-3405 Phase 2 Mixed · 2026-09-10
RESTORE-PV · polycythemia vera (pv)
Source release →
DISC-1459 Mixed · 2026-06-12
Source release →
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