Breakdown | ||||
TTM | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
-136.00K | -100.00K | -300.00K | -192.00K | -322.00K | EBIT |
-129.72M | -91.13M | -47.48M | -30.93M | -34.04M | EBITDA |
-108.27M | -91.03M | -46.53M | -35.78M | -33.69M | Net Income Common Stockholders |
-109.36M | -76.43M | -46.09M | -41.01M | -47.66M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
360.38M | 360.38M | 194.61M | 88.04M | 1.21M | Total Assets |
368.00M | 368.00M | 200.21M | 92.41M | 122.09M | Total Debt |
2.10M | 2.10M | 1.33M | 1.65M | 21.64M | Net Debt |
-358.28M | -358.28M | -193.28M | -86.38M | 20.43M | Total Liabilities |
22.88M | 22.88M | 23.61M | 156.61M | 4.82M | Stockholders Equity |
345.12M | 345.12M | 176.60M | -64.20M | 117.27M |
Cash Flow | Free Cash Flow | |||
-94.43M | -73.55M | -42.40M | -27.60M | -32.73M | Operating Cash Flow |
-93.93M | -73.46M | -42.25M | -27.53M | -32.71M | Investing Cash Flow |
-292.33M | -89.00K | -151.00K | -68.00K | -22.00K | Financing Cash Flow |
218.31M | 239.38M | 148.98M | 89.93M | 34.25M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
61 Neutral | $2.73B | ― | -31.68% | ― | 32.29% | 64.39% | |
50 Neutral | $3.20B | ― | -93.55% | ― | 97.02% | 64.32% | |
49 Neutral | $6.90B | 0.01 | -53.76% | 2.46% | 24.91% | -3.11% | |
48 Neutral | $1.86B | ― | -27.73% | ― | ― | -14.19% | |
48 Neutral | $22.52M | ― | -436.16% | ― | 0.44% | 16.44% | |
45 Neutral | $591.93M | ― | -42.91% | ― | ― | 2.90% | |
37 Underperform | $46.58M | ― | -71.81% | ― | -100.00% | -5.05% |
On January 21, 2025, Disc Medicine announced positive feedback from the FDA regarding their APOLLO post-marketing confirmatory trial for bitopertin, a treatment for erythropoietic protoporphyria (EPP) and X-linked protoporphyria (XLP). The meeting resulted in alignment on the trial design, which includes key features such as co-primary endpoints and a double-blind, placebo-controlled study. The company plans to initiate the trial by mid-2025 and anticipates submitting a New Drug Application in the second half of 2025 under the Accelerated Approval Program. This development marks a significant step forward in potentially providing a life-changing therapy for EPP patients, enhancing Disc Medicine’s position in the biopharmaceutical industry.
Disc Medicine announced strategic priorities for 2025, highlighting progress in its hematology portfolio. The company reported a material weakness in IT controls impacting financial reporting but identified no misstatements. Key developments include a potential accelerated approval path for bitopertin in erythropoietic protoporphyria, phase 2 studies for DISC-0974 in anemia of myelofibrosis and chronic kidney disease, and initiation of a phase 2 trial for DISC-3405 in polycythemia vera. Strengthened financial position with approximately $178 million from equity offering and debt facility, supporting growth through 2027.