| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 9.29M | 9.99M | 34.48M | 13.85M | 9.60M | 12.36M |
| Gross Profit | -21.20M | 6.07M | 30.95M | 10.21M | 8.61M | -22.06M |
| EBITDA | -140.02M | -162.69M | -112.53M | -95.71M | -65.61M | -35.21M |
| Net Income | -157.13M | -149.10M | -102.07M | -99.42M | -66.92M | -34.31M |
Balance Sheet | ||||||
| Total Assets | 194.98M | 313.31M | 432.21M | 373.76M | 442.36M | 36.05M |
| Cash, Cash Equivalents and Short-Term Investments | 147.26M | 209.54M | 328.83M | 247.66M | 375.83M | 15.95M |
| Total Debt | 25.46M | 26.49M | 27.11M | 27.75M | 259.00K | 1.58M |
| Total Liabilities | 53.14M | 60.36M | 63.81M | 72.89M | 54.53M | 59.48M |
| Stockholders Equity | 141.84M | 252.95M | 368.40M | 300.87M | 387.82M | -23.44M |
Cash Flow | ||||||
| Free Cash Flow | -127.73M | -144.71M | -104.90M | -97.42M | -35.64M | -34.53M |
| Operating Cash Flow | -125.64M | -138.20M | -93.29M | -90.97M | -32.52M | -33.22M |
| Investing Cash Flow | 100.20M | 86.61M | -68.18M | -93.25M | -176.40M | 6.36M |
| Financing Cash Flow | 4.61M | 16.72M | 154.30M | 2.13M | 433.43M | 1.74M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
54 Neutral | $362.52M | ― | -31.07% | ― | 158.54% | 66.90% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
47 Neutral | $202.08M | -1.22 | -74.28% | ― | -19.00% | -2.72% | |
45 Neutral | $162.39M | ― | -480.02% | ― | -37.13% | 40.47% | |
39 Underperform | $227.19M | ― | -101.06% | ― | ― | -17.21% | |
33 Underperform | $226.34M | ― | ― | ― | ― | -1072.48% | |
30 Underperform | $149.50M | -2.19 | ― | ― | ― | 17.36% |
On November 3, 2025, Caribou Biosciences announced positive results from its ANTLER phase 1 trial, demonstrating that its allogeneic CAR-T cell therapy, vispacabtagene regedleucel (vispa-cel), shows efficacy and durability comparable to autologous CAR-T therapies in treating relapsed or refractory B cell non-Hodgkin lymphoma. The trial results highlight vispa-cel’s potential as a best-in-class therapy due to its off-the-shelf availability and favorable safety profile, which allows for outpatient administration. Additionally, the company shared data from its CaMMouflage phase 1 trial for CB-011, targeting multiple myeloma, and announced plans for a phase 3 trial for vispa-cel in large B cell lymphoma patients ineligible for transplant.