Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 88.38M | 54.55M | 76.99M | 38.63M | 29.75M | 17.82M |
Gross Profit | 79.93M | 38.12M | 63.33M | 27.82M | 23.67M | -48.67M |
EBITDA | -217.88M | -196.60M | -141.41M | -173.06M | -111.80M | -62.80M |
Net Income | -207.32M | -193.57M | -143.95M | -180.36M | -117.19M | -43.24M |
Balance Sheet | ||||||
Total Assets | 591.55M | 669.34M | 355.60M | 416.76M | 476.77M | 396.34M |
Cash, Cash Equivalents and Short-Term Investments | 485.78M | 609.58M | 287.91M | 309.14M | 295.72M | 281.15M |
Total Debt | 51.93M | 28.30M | 30.61M | 11.96M | 13.04M | 0.00 |
Total Liabilities | 143.95M | 142.35M | 155.10M | 113.06M | 134.47M | 106.07M |
Stockholders Equity | 447.60M | 526.99M | 200.49M | 303.70M | 342.30M | 290.27M |
Cash Flow | ||||||
Free Cash Flow | -225.79M | -181.86M | -89.77M | -172.05M | -90.03M | -4.63M |
Operating Cash Flow | -215.18M | -172.58M | -81.36M | -159.81M | -84.36M | -80.00K |
Investing Cash Flow | -65.12M | -257.71M | 68.30M | 27.20M | -108.25M | -254.40M |
Financing Cash Flow | 247.77M | 485.67M | 3.22M | 117.19M | 153.88M | 339.02M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
55 Neutral | $796.08M | ― | -53.16% | ― | 636.99% | 27.10% | |
55 Neutral | $1.25B | ― | -56.95% | ― | 14.99% | 14.42% | |
54 Neutral | $1.15B | ― | -50.34% | ― | 6.07% | -2.28% | |
53 Neutral | $2.52B | ― | -63.21% | ― | ― | -32.33% | |
51 Neutral | $7.91B | -0.36 | -41.71% | 2.23% | 23.45% | -1.86% | |
50 Neutral | $558.71M | ― | -35.41% | ― | ― | ― | |
47 Neutral | $697.22M | ― | -50.67% | ― | 41.86% | 10.48% |
Nurix Therapeutics announced plans to meet with securities analysts and investors starting September 3, 2025, to discuss updates on their clinical development plans for bexobrutideg. This drug is being tested in a Phase 1 trial and has shown potential in treating B cell malignancies by overcoming resistance mutations and crossing the blood-brain barrier. The announcement highlights the company’s strategic focus on advancing treatments for unmet medical needs, potentially impacting its market positioning and offering significant implications for stakeholders.
On August 19, 2025, Nurix Therapeutics announced that Lori A. Kunkel, M.D., would resign from her position as a Class III director and chair of the Clinical and Commercialization Committee, effective September 1, 2025. Her resignation was not due to any disagreements with the company. In response, the board appointed Roy D. Baynes to take over as chair of the Clinical and Commercialization Committee, also effective September 1, 2025.
On June 12, 2025, Nurix Therapeutics announced positive clinical data from its Phase 1 trial of bexobrutideg (NX-5948) at the European Hematology Association Congress. The data showed an objective response rate of 80.9% in patients with relapsed or refractory chronic lymphocytic leukemia (CLL) and 84.2% in patients with Waldenström macroglobulinemia (WM), with bexobrutideg demonstrating a favorable safety profile and potential as a treatment for patients with high unmet medical needs. The company plans to initiate pivotal trials in 2025, reinforcing its scientific leadership in targeted protein degradation.