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Disc Medicine, Inc./$IRON

1D1W1M3M6MYTD1Y5YMAX

About Disc Medicine, Inc.

Disc Medicine Inc is a clinical-stage biopharmaceutical company focused on the discovery, development, and commercialization of novel treatments for hematologic diseases. It aims to modify fundamental biological pathways associated with the formation and function of red blood cells, specifically heme biosynthesis and iron homeostasis. Its pipeline includes bitopertin for erythropoietic porphyrias (EPs), including erythropoietic protoporphyria (EPP), X-linked protoporphyria (XLP), and Diamond-Blackfan Anemia (DBA); DISC-0974 for the treatment of anemia of myelofibrosis (MF) and anemia of chronic kidney disease (CKD); and DISC-3405 for the treatment of polycythemia vera (PV) and other hematologic disorders. In addition, the Company's preclinical programs include DISC-0998.
Ticker
$IRON
Sector
Health
Primary listing
NASDAQ
Employees
165

IRON Metrics

BasicAdvanced
$3.6B
-
-$6.56
2.05
-

What the Analysts think about IRON

Analyst ratings (Buy, Hold, Sell) for Disc Medicine, Inc. stock.
Analyst projections of the future price of Disc Medicine, Inc. stock.

Bulls say / Bears say

Bitopertin cleared a major hurdle: the 183-patient APOLLO Phase 3 met both co-primary and all secondary endpoints, including a placebo-adjusted 12.2-hour monthly gain in pain-free time outdoors at month six. The results give Disc a strong basis to resubmit its application. (Disc Medicine)
Selcodebart produced meaningful anaemia responses in Phase 2 across transfusion groups and whether patients were taking a JAK inhibitor. For example, 55% of patients who were not transfusion-dependent achieved a major response, supporting its potential as a second growth driver. (Disc Medicine)
DISC-3405 showed an encouraging early signal in polycythaemia vera: among 13 patients completing 26 weeks, average phlebotomies fell from 4.0 to 0.6, and 61.5% needed none during that period. This could offer patients an alternative to frequent blood removal if larger studies confirm the benefit. (Disc Medicine)
Bitopertin still needs regulatory approval. The FDA previously rejected the application because earlier trials did not establish that lowering PPIX predicted clinical benefit; APOLLO strengthens the case, but Disc still plans to resubmit and expects an FDA decision only by mid-2027. (SEC)
Evidence for the other programmes is still preliminary: the open-label RALLY-MF study had 50 patients in its response analysis, while the headline RESTORE-PV results came from 13 patients who completed 26 weeks. These small, uncontrolled groups may not predict results in larger trials. (Disc Medicine, Disc Medicine)
Disc has no product sales and continues to incur substantial losses; its Q2 2026 net loss was $59.5 million. Its roughly $718 million cash balance provides a long runway, but continued development spending leaves profitability dependent on successful approvals and future sales. (SEC, Disc Medicine)
Data summarised monthly by Lightyear AI. Last updated on 19 Oct 2026.

IRON Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

IRON Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise
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