| 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 | -40.00K | -156.00K | -100.00K | -300.00K | -192.00K | -322.00K |
| EBITDA | -133.34M | -108.27M | -91.03M | -47.39M | -30.90M | -33.69M |
| Net Income | -145.39M | -109.36M | -76.43M | -46.83M | -35.97M | -40.84M |
Balance Sheet | ||||||
| Total Assets | 665.06M | 496.77M | 368.00M | 200.21M | 92.41M | 122.09M |
| Cash, Cash Equivalents and Short-Term Investments | 649.97M | 489.88M | 360.38M | 194.61M | 88.04M | 1.21M |
| Total Debt | 30.92M | 30.00M | 2.10M | 1.33M | 1.65M | 21.64M |
| Total Liabilities | 50.90M | 53.19M | 22.88M | 23.61M | 156.61M | 4.82M |
| Stockholders Equity | 614.16M | 443.59M | 345.12M | 176.60M | 77.65M | -21.86M |
Cash Flow | ||||||
| Free Cash Flow | -135.56M | -94.43M | -73.55M | -42.40M | -27.60M | -32.73M |
| Operating Cash Flow | -134.23M | -93.93M | -73.46M | -42.25M | -27.53M | -32.71M |
| Investing Cash Flow | -293.46M | -292.33M | -89.00K | -151.00K | -68.00K | -22.00K |
| Financing Cash Flow | 274.37M | 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 |
|---|---|---|---|---|---|---|---|
60 Neutral | $3.04B | ― | -28.35% | ― | 182.44% | 47.21% | |
59 Neutral | $2.33B | ― | -27.57% | ― | 36.26% | -158.98% | |
59 Neutral | $2.94B | ― | -28.17% | ― | 129.21% | 80.35% | |
54 Neutral | $3.05B | ― | -410.78% | ― | 114.22% | 77.02% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
43 Neutral | $3.22B | ― | -26.36% | ― | ― | -22.19% | |
41 Neutral | $2.17B | ― | -86.34% | ― | 30.14% | -10.08% |
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.