| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 1.40M | 200.00K | 1.80M | 2.19M | 7.13M | 12.81M |
| Gross Profit | -1.21M | -2.08M | 609.00K | -107.99M | 4.44M | -60.69M |
| EBITDA | -143.47M | 1.70B | -206.69M | -125.82M | -75.37M | -63.80M |
| Net Income | -155.09M | 1.69B | -241.36M | -145.23M | -81.77M | -75.64M |
Balance Sheet | ||||||
| Total Assets | 177.47M | 180.77M | 307.89M | 290.88M | 150.45M | 143.74M |
| Cash, Cash Equivalents and Short-Term Investments | 153.09M | 152.60M | 277.92M | 273.87M | 131.30M | 128.66M |
| Total Debt | 6.99M | 8.05M | 210.14M | 207.10M | 72.14M | 37.45M |
| Total Liabilities | 140.64M | 47.18M | 264.39M | 232.82M | 98.07M | 68.27M |
| Stockholders Equity | 36.83M | 133.58M | 43.50M | 58.06M | 52.38M | 75.47M |
Cash Flow | ||||||
| Free Cash Flow | -143.44M | -197.01M | -197.90M | -115.99M | -81.19M | -49.33M |
| Operating Cash Flow | -143.39M | -194.41M | -193.31M | -115.30M | -80.32M | -47.97M |
| Investing Cash Flow | -44.00K | -2.60M | -4.59M | -686.00K | -809.00K | -1.36M |
| Financing Cash Flow | 100.19M | 71.68M | 201.96M | 258.55M | 83.77M | 166.46M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
66 Neutral | $698.07M | 10.04 | 66.76% | ― | -10.26% | 144.62% | |
62 Neutral | $1.27B | -7.63 | -144.07% | ― | ― | ― | |
55 Neutral | $6.65B | 3.83 | -15.92% | 6.20% | 10.91% | 7.18% | |
52 Neutral | $1.05B | 53.96 | 9.28% | ― | 1112.27% | ― | |
50 Neutral | $521.07M | -1.82 | -67.63% | ― | -91.16% | -112.24% | |
42 Neutral | $206.51M | -4.73 | ― | ― | ― | 82.23% | |
33 Underperform | $326.10M | -10.49 | -70.17% | ― | ― | 68.53% |
Inhibrx Biosciences announced updates on its clinical trials for INBRX-106 and ozekibart. The INBRX-106 Phase 2/3 trial, in combination with Keytruda, is progressing with 46 out of 60 patients enrolled for treating head and neck squamous cell carcinoma, with data expected to mature by the second half of 2026. The ozekibart trials have completed enrollment for colorectal cancer and are progressing for Ewing sarcoma, with potential discussions for accelerated FDA approval in 2026.
On October 23, 2025, Inhibrx Biosciences announced positive topline results from its ChonDRAgon study, showing that ozekibart significantly improved median progression-free survival in patients with advanced chondrosarcoma compared to placebo. This marks the first investigational therapy to demonstrate such benefits in this disease, which lacks approved systemic treatments. The company also reported promising interim data from expansion cohorts for colorectal cancer and Ewing sarcoma, indicating high response and disease control rates in heavily pretreated patients. Inhibrx plans to file a biologics license application with the FDA in the second quarter of 2026, potentially enhancing its positioning in the oncology market.