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IR

NASDAQ · IRON

Disc Medicine, Inc.

Healthcare · Biotechnology

$67.30

Up+$1.59 (+2.36%)

Updated Sep 16, 2026, 2:59 PM

SID Score

4.0/10

Composite research score

Smart Money

58/100

Neutral

Market cap
3.53B
P/E ratio
-18.17
Dividend yield
0.00%
52-week range
$40.00 – $99.50
Volume
603.9K
Avg. volume
503.23K

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Overview

Company profile and research snapshot.

Company profile

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.

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Analyst outlook

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Consensus
Average target
$123.50
Implied upside
Analysts
IRON recent ratings
DateFirmRatingTarget
Sep 10, 2026WedbushOutperform
Sep 2, 2026WedbushOutperform
Aug 6, 2026HC Wainwright & Co.Buy
Jun 16, 2026Morgan StanleyOverweight
Jun 10, 2026WedbushOutperform
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Yahoo · Sep 9, 2026

Disc Medicine Presents Initial Results from RESTORE-PV Phase 2 Trial in Patients with Polycythemia Vera (PV) at the 14th Society of Hematologic Oncology (SOHO) Annual Meeting

Initial results from RESTORE-PV show DISC-3405 increased hepcidin and lowered serum iron, translating to controlled hematocrit, reduced phlebotomy, and improved symptoms in PV patientsDISC-3405 is the first monoclonal antibody targeting TMPRSS6 that has demonstrated phlebotomy reduction in patients with PVDisc also presented an encore of the positive results from the Phase 2 RALLY-MF trial of selcodebart (DISC-0974) in patients with anemia of myelofibrosis (MF) and a new systematic literature re

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