Breakdown | |||||
TTM | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 | Dec 2019 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
0.00 | 0.00 | 0.00 | 18.94M | 0.00 | 0.00 | Gross Profit |
-153.00K | -310.00K | -93.00K | 18.89M | -62.00K | -70.00K | EBIT |
-196.92M | -191.09M | 144.65M | -67.95M | -60.34M | -22.27M | EBITDA |
-196.61M | -190.34M | 151.41M | -67.90M | -60.27M | -22.20M | Net Income Common Stockholders |
-167.38M | -153.16M | 111.21M | -65.04M | -50.85M | -20.04M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
398.98M | 467.07M | 550.12M | 430.86M | 210.21M | 98.63M | Total Assets |
621.82M | 484.18M | 561.12M | 437.19M | 214.71M | 100.46M | Total Debt |
2.15M | 3.59M | 5.19M | 0.00 | 0.00 | 0.00 | Net Debt |
-80.85M | -94.84M | -544.93M | -430.86M | -168.20M | -63.25M | Total Liabilities |
31.50M | 30.29M | 26.09M | 11.81M | 291.05M | 140.37M | Stockholders Equity |
590.33M | 453.70M | 535.03M | 422.58M | -77.64M | -40.77M |
Cash Flow | Free Cash Flow | ||||
-145.30M | -134.48M | -127.80M | -44.02M | -29.78M | -20.92M | Operating Cash Flow |
-145.30M | -134.28M | -126.66M | -43.43M | -29.77M | -20.90M | Investing Cash Flow |
-136.31M | 35.81M | 248.97M | -333.77M | -5.42M | -35.40M | Financing Cash Flow |
266.19M | 40.75M | -25.93M | 268.78M | 140.14M | 85.72M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
62 Neutral | $1.52B | ― | -9.85% | ― | 56.60% | -403.56% | |
49 Neutral | $6.90B | -0.08 | -53.01% | 2.43% | 24.84% | -3.06% | |
48 Neutral | $3.72B | ― | -19.20% | ― | -89.95% | -123.71% | |
48 Neutral | $244.69M | ― | 322.49% | ― | -33.83% | 27.89% | |
44 Neutral | $425.63M | ― | -54.15% | ― | ― | ― | |
42 Neutral | $476.88M | ― | -32.06% | ― | ― | 15.34% | |
42 Neutral | $129.44M | ― | -98.10% | ― | -58.64% | -40.05% |
On January 28, 2025, Cullinan Therapeutics, in collaboration with Taiho Pharmaceutical and Taiho Oncology, announced that their REZILIENT1 trial successfully met its primary endpoint of overall response rate. The trial involved zipalertinib monotherapy for patients with non-small cell lung cancer harboring EGFR exon 20 insertion mutations. The results, consistent with previous data presentations, are from the Phase 2b part of the study, with plans to present full results at an upcoming international medical conference. The companies intend to seek U.S. regulatory approval in the latter half of 2025.