| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 37.36M | 35.00M | 371.21M | 436.00K | 913.08M | 543.00K |
| Gross Profit | -81.06M | -75.25M | 240.96M | -109.81M | 895.13M | -268.86M |
| EBITDA | -511.48M | -447.31M | -202.70M | -648.99M | 391.48M | -345.25M |
| Net Income | -467.80M | -366.25M | -153.61M | -650.17M | 377.66M | -348.87M |
Balance Sheet | ||||||
| Total Assets | 2.03B | 2.24B | 2.23B | 2.24B | 2.75B | 1.83B |
| Cash, Cash Equivalents and Short-Term Investments | 1.72B | 1.90B | 1.69B | 1.82B | 2.38B | 1.69B |
| Total Debt | 215.45M | 223.69M | 238.63M | 244.02M | 225.03M | 61.43M |
| Total Liabilities | 318.59M | 309.95M | 346.77M | 367.58M | 352.42M | 163.73M |
| Stockholders Equity | 1.71B | 1.93B | 1.88B | 1.88B | 2.40B | 1.66B |
Cash Flow | ||||||
| Free Cash Flow | -325.57M | -144.68M | -272.35M | -532.93M | 457.27M | -256.72M |
| Operating Cash Flow | -324.77M | -142.77M | -260.38M | -495.74M | 538.97M | -238.37M |
| Investing Cash Flow | -5.55M | -280.48M | 374.65M | -258.65M | -1.04B | -541.17M |
| Financing Cash Flow | 39.36M | 331.98M | 62.66M | 38.59M | 250.94M | 1.02B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
83 Outperform | $1.77B | 9.87 | 25.93% | ― | 21.13% | 50.86% | |
59 Neutral | $2.94B | ― | -28.17% | ― | 129.21% | 80.35% | |
52 Neutral | ― | ― | ― | ― | 271.44% | 26.65% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $1.31B | ― | -56.95% | ― | 14.99% | 14.42% | |
46 Neutral | $2.31B | ― | -47.19% | ― | -84.07% | -157.71% | |
41 Neutral | $5.13B | ― | -25.34% | ― | -81.18% | -69.19% |
Study Overview: The clinical study titled A Long-term Follow-up Study of Subjects With Malignancies Treated With CRISPR CAR T Cellular Therapies aims to evaluate the long-term safety and efficacy of CRISPR CAR T cellular therapies in subjects with hematologic and solid malignancies. This study is significant as it seeks to provide insights into the durability and safety of these innovative therapies over an extended period.
On October 15, 2025, CRISPR Therapeutics AG announced the filing of a prospectus supplement with the SEC to offer and sell additional common shares worth up to $600 million through Jefferies LLC. This move aligns with the company’s strategic financial initiatives, potentially impacting its market position and stakeholder interests by providing additional capital for its operations and growth.
The most recent analyst rating on (CRSP) stock is a Buy with a $86.00 price target. To see the full list of analyst forecasts on Crispr Therapeutics AG stock, see the CRSP Stock Forecast page.
Study Overview: The study titled A Long-term Follow-up Study of Subjects With Malignancies Treated With CRISPR CAR T Cellular Therapies aims to assess the long-term safety and efficacy of CRISPR CAR T cellular therapies. This observational study is significant as it seeks to gather data on the long-term outcomes of patients with hematological and solid malignancies who have undergone these innovative treatments.
Study Overview: The clinical study titled A Phase 1 Dose Evaluation Study of the Safety and Preliminary Efficacy of Anti-CD19 Allogeneic CRISPR-Cas9-Engineered T Cells (CTX112) in Adult Subjects With Refractory Autoimmune Disease aims to assess the safety and initial effectiveness of CTX112 in adults suffering from challenging autoimmune conditions like systemic lupus erythematosus, systemic sclerosis, and idiopathic inflammatory myopathy. This study is significant as it explores innovative gene-editing technology to potentially transform treatment options for these refractory diseases.
Study Overview: The clinical study titled ‘A Phase 1 Dose Evaluation Study of the Safety and Preliminary Efficacy of Anti-CD19 Allogeneic CRISPR-Cas9-Engineered T Cells (CTX112) in Adult Subjects With Refractory Autoimmune Disease’ aims to assess the safety and initial effectiveness of CTX112. This study is significant as it targets challenging autoimmune diseases like systemic lupus erythematosus, systemic sclerosis, and idiopathic inflammatory myopathy, offering hope for patients with limited treatment options.
CRISPR Therapeutics is a biopharmaceutical company specializing in gene-based medicines for serious diseases, leveraging the CRISPR/Cas9 technology to develop transformative therapies across various medical fields.