Breakdown | |||||
TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
-110.00K | -156.00K | -100.00K | -300.00K | -192.00K | -322.00K | EBIT |
-138.20M | -129.72M | -91.13M | -47.48M | -30.93M | -34.04M | EBITDA |
-109.89M | -108.27M | -91.03M | -46.53M | -35.78M | -33.69M | Net Income Common Stockholders |
-116.49M | -109.36M | -76.43M | -46.09M | -41.01M | -47.66M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
694.66M | 489.88M | 360.38M | 194.61M | 88.04M | 1.21M | Total Assets |
709.27M | 496.77M | 368.00M | 200.21M | 92.41M | 122.09M | Total Debt |
30.64M | 30.00M | 2.10M | 1.33M | 1.65M | 21.64M | Net Debt |
-92.03M | -162.43M | -358.28M | -193.28M | -86.38M | 20.43M | Total Liabilities |
48.90M | 53.19M | 22.88M | 23.61M | 156.61M | 4.82M | Stockholders Equity |
660.36M | 443.59M | 345.12M | 176.60M | -64.20M | 117.27M |
Cash Flow | Free Cash Flow | ||||
-102.99M | -94.43M | -73.55M | -42.40M | -27.60M | -32.73M | Operating Cash Flow |
-101.70M | -93.93M | -73.46M | -42.25M | -27.53M | -32.71M | Investing Cash Flow |
-564.90M | -292.33M | -89.00K | -151.00K | -68.00K | -22.00K | Financing Cash Flow |
446.67M | 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 |
---|---|---|---|---|---|---|---|
66 Neutral | $2.15B | ― | 18.68% | ― | 41.67% | 75.79% | |
61 Neutral | $2.07B | 3.17 | 60.26% | ― | 25.96% | ― | |
61 Neutral | $1.65B | ― | -5.78% | ― | 25.50% | 64.63% | |
54 Neutral | $5.34B | 3.27 | -45.10% | 3.30% | 16.80% | 0.02% | |
52 Neutral | $1.60B | ― | -70.58% | ― | 100.03% | 64.22% | |
45 Neutral | $1.67B | ― | -38.04% | ― | -82.38% | -164.76% | |
43 Neutral | $1.80B | ― | -23.34% | ― | ― | -14.19% |
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.