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Disc Medicine Reports Fourth Quarter and Full Year 2023 Financial Results and Provides Business Update Top-line results from AURORA, the placebo-controlled phase 2 study of bitopertin in erythropoietic porphyrias (EPP),

Key Takeaway: Disc Medicine, Inc. has reported its fourth quarter and full year 2023 financial results, highlighting a significant year of progress. The company demonstrated positive clinical trial results for its therapies, including bitopertin and DISC-0974. Additionally, it advanced DISC-3405 into clinical studies and improved its financial standing. However, the company also reported a substantial net loss, raising concerns about operating expenses and financial sustainability moving forward.

Market Sentiment Analysis

POSITIVE FACTORS

  • Reported positive results from clinical studies for bitopertin and DISC-0974.
  • Successfully advanced the new program DISC-3405 into clinical trials.
  • Fortified financial position with a stronger balance sheet.

CONCERNS & RISKS

  • Significant operating loss increased from $46.8 million in 2022 to $76.4 million in 2023.
  • High research and development expenses indicate ongoing financial risk.

Full Press Release Details

Disc Medicine Reports Fourth Quarter and Full Year 2023 Financial Results and Provides Business Update
WATERTOWN, Mass. (March 21, 2024) Disc Medicine, Inc. (NASDAQ:IRON), a clinical-stage biopharmaceutical
company focused on the discovery, development, and commercialization of novel treatments for patients suffering from serious hematologic diseases, today reported financial results for the fourth quarter and full year ended December 31, 2023,
and provided an update on recent program and corporate developments.
The past year has been truly remarkable for Disc and marks another important
chapter in our company s story. During 2023, we provided the first evidence of the therapeutic potential of our programs, with positive read-outs in patients for both bitopertin and DISC-0974. In addition, we advanced a third program,
DISC-3405, into the clinic and fortified our balance sheet, so we can execute our strategy with confidence, said John Quisel, J.D., Ph.D., President and Chief Executive Officer of Disc. These achievements have positioned us well for
2024, which promises to be another transformational year, and I want to express my deep gratitude to our team for their determination and hard work. We re looking forward to sharing AURORA data in the coming weeks, as well as updated data for
DISC-0974 in MF and initial data for DISC-3405 in healthy volunteers in the first half of this year.
Recent Business Highlights and Upcoming
Bitopertin: GlyT1 Inhibitor (Heme Synthesis Modulator)
DISC-0974: Anti-Hemojuvelin Antibody (Hepcidin Suppression)
DISC-3405: Anti-TMPRSS6 Antibody (Hepcidin Induction)
Full Year 2023 Financial Results:
Disc Medicine (NASDAQ:IRON) is a
clinical-stage biopharmaceutical company committed to discovering, developing, and commercializing novel treatments for patients who suffer from serious hematologic diseases. We are building a portfolio of innovative, potentially first-in-class therapeutic candidates that aim to address a wide spectrum of hematologic diseases by targeting fundamental biological pathways of red blood cell biology,
specifically heme biosynthesis and iron homeostasis. For more information, please visit www.discmedicine.com.
Available Information
Disc announces material information to the public about the Company, its products and services, and other matters through a variety of means, including filings
with the U.S. Securities and Exchange Commission (SEC), press releases, public conference calls, webcasts and the investor relations section of the Company website at ir.discmedicine.com in order to achieve broad,
non-exclusionary distribution of information to the public and for complying with its disclosure obligations under Regulation FD.
Disc Cautionary Statement Regarding Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including, but
not limited to, express or implied statements regarding Disc s expectations with respect to its AURORA phase 2 and BEACON phase 2 clinical studies of bitopertin and the results thereof, and its phase 1b/2 study of bitopertin in Diamond-Blackfan
Anemia, its phase 1b/2 clinical studies of DISC-0974 in patients with MF and NDD-CKD patients with anemia, its phase 1 clinical study of DISC-3405 in healthy volunteers; projected timelines for the initiation
and completion of its clinical trials, anticipated timing of release of data, and other clinical activities; Disc s business plans, objectives and expected contributions of management; and Disc s beliefs about operating expenses and that
it will have capital to fund Disc well into 2026. The use of words such as, but not limited to, believe, expect, estimate, project, intend, future, potential,
continue, may, might, plan, will, should, seek, anticipate, or could or the negative of these terms and other similar words or expressions
that are intended to identify forward-looking statements. Forward-looking statements are neither historical facts nor assurances of future performance. Instead, they are based on Disc s current beliefs, expectations and assumptions regarding
the future of Disc s business, future plans and strategies, clinical results and other future conditions. New risks and uncertainties may emerge from time to time, and it is not possible to predict all risks and uncertainties. No
representations or warranties (expressed or implied) are made about the accuracy of any such forward-looking statements.
Disc may not actually achieve
the plans, intentions or expectations disclosed in these forward-looking statements, and investors should not place undue reliance on these forward-looking statements. Actual results or events could differ materially from the plans, intentions and
expectations disclosed in the forward-looking statements as a result of a number of material risks and uncertainties including but not limited to: the adequacy of Disc s capital to support its future operations and its ability to successfully
initiate and complete clinical trials; the nature, strategy and focus of Disc; the difficulty in predicting the time and cost of development of Disc s product candidates; Disc s plans to research, develop and commercialize its current and
future product candidates; that enrollment timelines of both the BEACON
and AURORA studies may not necessarily be predictive of future enrollment timelines; the timing of initiation of Disc s planned clinical trials; Disc s ability to retain and recognize
the intended incentives conferred by Fast Track Designation for its product candidates including DISC-3405 and DISC-0974; Disc s ability to retain and recognize the intended incentives conferred by Orphan Drug Designation for DISC-3405 and
bitopertin; the timing of the availability of data from Disc s clinical trials; Disc s ability to identify additional product candidates with significant commercial potential and to expand its pipeline in hematological diseases; the timing
and anticipated results of Disc s preclinical studies and clinical trials and the risk that the results of Disc s clinical trials may not be predictive of future results in connection with future studies or clinical trials and may not
support further development and marketing approval; the other risks and uncertainties described in the Risk Factors section of our Annual Report on Form 10-K for the year ended December 31,
2023, and other documents filed by Disc from time to time with the SEC, as well as discussions of potential risks, uncertainties, and other important factors in Disc s subsequent filings with the SEC. Any forward-looking statement speaks only
as of the date on which it was made. None of Disc, nor its affiliates, advisors or representatives, undertake any obligation to publicly update or revise any forward-looking statement, whether as result of new information, future events or
otherwise, except as required by law.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(In thousands, except share and per share amounts)
Year Ended December 31,
2023 2022
Operating expenses:
Research and development $ 69,264 $ 33,437
General and administrative 21,861 14,038
Total operating expenses 91,125 47,475
Loss from operations (91,125 ) (47,475 )
Other income (expense), net 14,795 648
Income tax expense (99 )
Net loss $ (76,429 ) $ (46,827 )
Weighted-average common shares outstanding-basic and diluted 22,315,877 1,039,490
Net loss per share-basic and diluted $ (3.42 ) $ (45.05 )
CONDENSED CONSOLIDATED BALANCE SHEETS
December 31, December 31,
2023 2022
Assets
Cash and cash equivalents $ 360,382 $ 194,611
Other current assets 5,280 3,880
Total current assets 365,662 198,491
Non-current assets 2,334 1,714
Total assets $ 367,996 $ 200,205
Liabilities and Stockholders Equity
Current liabilities $ 21,439 $ 22,578
Non-current liabilities 1,436 1,027
Total liabilities 22,875 23,605
Total stockholders equity 345,121 176,600
Total liabilities and stockholders equity $ 367,996 $ 200,205
Verge Scientific Communications
Investor Relations Contact
Stern Investor Relations

Frequently Asked Questions

What were Disc Medicine's 2023 financial results?

Disc Medicine reported a net loss of $76.4 million for 2023.

What are the main products of Disc Medicine?

Disc's primary products include bitopertin, DISC-0974, and DISC-3405.

What significant achievements did Disc Medicine report for 2023?

In 2023, Disc showed positive results for bitopertin and DISC-0974 and launched DISC-3405.

What is the focus of Disc Medicine's research?

Disc Medicine focuses on treatments for serious hematologic diseases.

When will Disc share data from their clinical programs?

Disc plans to share AURORA data and updates on DISC-0974 in early 2024.

Last updated: Mar 21, 2024