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 | |||
1.21M | 360.38M | 194.61M | 88.04M | 1.21M | Total Assets |
9.82M | 368.00M | 200.21M | 92.41M | 122.09M | Total Debt |
0.00 | 2.10M | 1.33M | 1.65M | 21.64M | Net Debt |
-1.21M | -358.28M | -193.28M | -86.38M | 20.43M | Total Liabilities |
4.82M | 22.88M | 23.61M | 156.61M | 4.82M | Stockholders Equity |
5.00M | 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 |
---|---|---|---|---|---|---|---|
59 Neutral | $1.31B | ― | -13.92% | ― | 24.19% | 10.51% | |
57 Neutral | $1.73B | ― | -113.76% | ― | 229.74% | 70.23% | |
56 Neutral | $1.51B | 2.31 | 57.29% | ― | 36.07% | ― | |
52 Neutral | $1.41B | ― | 18.68% | ― | 36.00% | 63.50% | |
48 Neutral | $6.36B | 1.28 | -45.04% | 2.64% | 19.24% | 1.69% | |
41 Neutral | $1.34B | ― | -27.73% | ― | ― | -14.19% | |
39 Underperform | $1.63B | ― | -43.94% | ― | -83.18% | -144.95% |
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.