Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
67.42M | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
67.42M | -1.39M | -1.43M | -544.00K | -160.00K | EBIT |
-191.19M | -248.99M | -227.29M | -216.54M | -118.79M | EBITDA |
-186.17M | -275.50M | -219.87M | -164.01M | -117.94M | Net Income Common Stockholders |
-165.84M | -292.19M | -220.83M | -164.26M | -118.55M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
351.91M | 482.92M | 437.37M | 339.89M | 338.50M | Total Assets |
430.34M | 551.69M | 539.31M | 454.51M | 365.56M | Total Debt |
39.58M | 43.15M | 45.17M | 45.91M | 2.00M | Net Debt |
5.68M | 15.11M | 2.10M | -13.80M | -52.95M | Total Liabilities |
93.15M | 114.30M | 105.29M | 90.03M | 32.18M | Stockholders Equity |
337.19M | 437.28M | 434.02M | 364.48M | 333.38M |
Cash Flow | Free Cash Flow | |||
-171.08M | -208.41M | -166.30M | -160.20M | -87.58M | Operating Cash Flow |
-170.86M | -207.82M | -163.75M | -154.09M | -86.83M | Investing Cash Flow |
176.56M | -44.46M | -114.18M | -18.11M | -284.83M | Financing Cash Flow |
108.00K | 237.30M | 261.04M | 178.52M | 360.44M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
51 Neutral | $5.19B | 3.12 | -41.08% | 2.95% | 17.98% | 2.02% | |
43 Neutral | $88.74M | ― | -45.58% | ― | 71.44% | 43.22% | |
42 Neutral | $94.81M | ― | 149.62% | ― | -31.04% | 11.34% | |
41 Neutral | $92.64M | ― | -42.83% | ― | ― | 48.92% | |
41 Neutral | $85.02M | ― | -46.26% | ― | ― | -61.95% | |
40 Underperform | $80.39M | ― | -80.74% | ― | ― | ― | |
35 Underperform | $81.15M | ― | -94.52% | ― | ― | 2.98% |
Zentalis Pharmaceuticals presented updated clinical data at the Society of Gynecologic Oncology 2025 Annual Meeting, highlighting the potential of azenosertib in treating platinum-resistant ovarian cancer (PROC). The data from the DENALI Part 1b clinical trial showed a median duration of response of 6.3 months and an objective response rate of approximately 35% in response-evaluable patients. The company plans to initiate Part 2 of the trial in the first half of 2025, with topline data expected by the end of 2026, potentially supporting accelerated approval. The presentation also emphasized the role of Cyclin E1 protein overexpression as a predictive biomarker for identifying patients who could benefit from azenosertib.
On January 29, 2025, Zentalis Pharmaceuticals announced the development plan for their WEE1 inhibitor product candidate, azenosertib, focusing on patients with Cyclin E1-positive platinum-resistant ovarian cancer (PROC). The company, aligned with the FDA, intends to initiate the DENALI Part 2 study in the first half of 2025, with the potential for accelerated approval. Clinical results highlighted meaningful azenosertib activity, showing an objective response rate (ORR) of approximately 35% in heavily-pretreated patients, with a median duration of response of about 5.5 months. The safety profile was consistent with previous findings, showing no new safety signals.
On January 22, 2025, Zentalis Pharmaceuticals announced a strategic restructuring, including a workforce reduction of approximately 40%, to support the late-stage development of its WEE1 inhibitor product candidate, azenosertib. The restructuring aims to extend the company’s cash runway beyond the anticipated 2026 data readout from the DENALI Part 2 study. The company expects to incur one-time costs of approximately $7.0–8.0 million due to the workforce reduction, which is expected to be largely completed by the second quarter of 2025. This move is intended to efficiently allocate resources to advance azenosertib’s development and potentially bring it to market for patients with gynecological malignancies, thereby solidifying Zentalis’ position in the oncology therapeutics market.