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 |
---|---|---|---|---|---|---|---|
58 Neutral | $2.13B | 3.32 | 64.05% | ― | 30.57% | ― | |
58 Neutral | $1.67B | ― | -5.38% | ― | 26.90% | 62.72% | |
53 Neutral | $1.92B | ― | -57.33% | ― | 99.50% | 65.91% | |
51 Neutral | $7.46B | -0.25 | -46.00% | 2.25% | 22.77% | -2.14% | |
50 Neutral | $1.77B | ― | 18.68% | ― | 45.85% | 76.36% | |
43 Neutral | $2.05B | ― | -26.36% | ― | ― | -22.19% | |
41 Neutral | $1.78B | ― | -41.94% | ― | -82.90% | -155.64% |
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.