| 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 | -104.78M | -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 | 0.00 | 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 |
|---|---|---|---|---|---|---|---|
57 Neutral | $308.38M | ― | -31.07% | ― | 158.54% | 66.90% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
39 Underperform | $222.37M | ― | -101.06% | ― | ― | -17.21% | |
39 Underperform | $138.30M | ― | -480.02% | ― | -37.13% | 40.47% | |
38 Underperform | $202.08M | -1.22 | -74.28% | ― | -19.00% | -2.72% | |
33 Underperform | $204.51M | ― | ― | ― | ― | -1072.48% | |
30 Underperform | $149.50M | -2.19 | ― | ― | ― | 17.36% |
Caribou Biosciences, Inc. is a clinical-stage biopharmaceutical company specializing in CRISPR genome-editing technologies to develop transformative therapies, particularly focusing on allogeneic CAR-T cell therapies for hematologic malignancies. In its latest earnings report, Caribou Biosciences revealed a net loss of $121.6 million for the nine months ending September 30, 2025, compared to a net loss of $113.6 million in the same period in 2024. The company’s revenue from licensing and collaboration slightly decreased to $7.2 million from $7.9 million year-over-year. Despite the financial losses, the company continues to invest heavily in research and development, with expenses totaling $85.6 million for the nine months ended September 30, 2025. Caribou Biosciences also reported a significant impairment charge of $12.2 million, primarily due to the full impairment of its investment in Edge Animal Health. Looking forward, Caribou Biosciences’ management remains focused on advancing its product candidates through clinical development and securing additional capital to support its operations, with existing cash and marketable securities expected to fund operations for at least the next 12 months.
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.
The most recent analyst rating on (CRBU) stock is a Hold with a $2.50 price target. To see the full list of analyst forecasts on Caribou Biosciences stock, see the CRBU Stock Forecast page.
Study Overview: Caribou Biosciences, Inc. is conducting a Phase 1 clinical trial titled ‘A Phase 1, Multicenter, Open-Label Study of CB-011, a CRISPR-Edited Allogeneic Anti-BCMA CAR-T Cell Therapy in Patients With Relapsed/Refractory Multiple Myeloma’ (CaMMouflage Trial). The study aims to evaluate the safety, optimal dosing, and efficacy of CB-011 in treating relapsed or refractory multiple myeloma, a condition where the disease returns or does not respond to existing treatments.
Caribou Biosciences, Inc. is conducting a long-term follow-up study titled ‘An Observational Long-Term Follow-up Study of Patients Who Received Prior Caribou Cell Therapy.’ The study aims to evaluate the long-term safety of investigational Caribou therapies in patients who participated in previous Caribou-sponsored clinical studies or special access programs. This research is significant as it seeks to ensure the safety and efficacy of treatments over a 15-year period post-infusion, focusing on conditions like Non-Hodgkin Lymphoma and other hematologic malignancies.
Caribou Biosciences, Inc. is conducting a Phase 1 clinical trial titled ‘A Phase 1, Multicenter, Open-Label Study of CB-010, a CRISPR-Edited Allogeneic Anti-CD19 CAR-T Cell Therapy in Patients With Relapsed/Refractory B Cell Non-Hodgkin Lymphoma (ANTLER)’. The study aims to evaluate the safety, emerging efficacy, pharmacokinetics, and immunogenicity of CB-010 in adults with relapsed or refractory B cell non-Hodgkin lymphoma. This study is significant as it explores innovative gene-editing technology to potentially offer new treatment options for patients with limited alternatives.