| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 0.00 | 251.00K | 33.49M | 4.93M | 2.00M | 0.00 |
| Gross Profit | -662.00K | 251.00K | 33.49M | 4.93M | 2.00M | 0.00 |
| EBITDA | -82.23M | -64.85M | -28.41M | -58.67M | -71.58M | -17.52M |
| Net Income | -72.31M | -58.49M | -27.70M | -58.39M | -71.83M | -17.99M |
Balance Sheet | ||||||
| Total Assets | 148.86M | 209.58M | 105.11M | 133.05M | 169.93M | 29.23M |
| Cash, Cash Equivalents and Short-Term Investments | 122.97M | 185.43M | 76.97M | 102.53M | 160.92M | 25.44M |
| Total Debt | 11.69M | 14.35M | 16.91M | 19.45M | 1.74M | 2.12M |
| Total Liabilities | 19.64M | 22.94M | 267.13M | 273.75M | 258.78M | 50.80M |
| Stockholders Equity | 129.22M | 186.64M | -162.01M | -140.70M | -88.86M | -21.57M |
Cash Flow | ||||||
| Free Cash Flow | -78.91M | -55.67M | -50.69M | -57.13M | -17.03M | -13.82M |
| Operating Cash Flow | -76.67M | -55.03M | -47.43M | -50.83M | -15.30M | -13.54M |
| Investing Cash Flow | 46.41M | -120.46M | -25.98M | -6.30M | -1.72M | -284.00K |
| Financing Cash Flow | 100.00K | 162.23M | 24.39M | -1.26M | 152.75M | 37.40M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
53 Neutral | $76.47M | -0.69 | -49.78% | ― | -82.16% | 14.58% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
44 Neutral | $87.69M | -1.16 | -47.96% | ― | ― | ― | |
43 Neutral | $68.53M | -12.64 | -40.32% | ― | 56.52% | 75.22% | |
37 Underperform | $98.83M | -0.47 | -64.27% | ― | ― | 14.19% | |
35 Underperform | $47.01M | ― | -191.12% | ― | ― | -24.38% | |
27 Underperform | $105.79M | -0.53 | -71.73% | ― | ― | 25.89% |
Artiva Biotherapeutics, Inc. is a biopharmaceutical company focused on developing off-the-shelf, allogeneic NK cell-based therapies for autoimmune diseases and cancers, headquartered in San Diego, California. In its latest earnings report for the quarter ending September 30, 2025, Artiva Biotherapeutics reported a net loss of $21.5 million, reflecting an increase from the $17.5 million loss in the same period last year. The company has not yet generated revenue from product sales, as its therapies are still in the development phase. Key financial highlights include a decrease in cash and cash equivalents to $25.5 million from $40.2 million at the end of 2024, and a reduction in short-term investments from $145.2 million to $97.5 million. Operating expenses rose to $22.9 million, driven by increased research and development costs. Despite the financial losses, Artiva Biotherapeutics continues to focus on advancing its lead product candidate, AlloNK, through clinical development. Looking ahead, the company remains committed to its strategic goals of developing and commercializing its NK cell therapies, with management expressing confidence in securing additional funding to support ongoing operations.
On November 12, 2025, Artiva Biotherapeutics announced positive initial safety and translational data from clinical trials of AlloNK in combination with rituximab or obinutuzumab for treating autoimmune diseases. The trials demonstrated that AlloNK was well tolerated, with no serious adverse events, and showed consistent B-cell depletion, comparable to CD19-auto-CAR-T therapies. This data supports the feasibility of administering AlloNK in outpatient and community settings, potentially addressing unmet needs in refractory rheumatoid arthritis, with plans for further clinical response data and FDA interactions in 2026.
The most recent analyst rating on (ARTV) stock is a Hold with a $3.50 price target. To see the full list of analyst forecasts on Artiva Biotherapeutics, Inc. stock, see the ARTV Stock Forecast page.
Artiva Biotherapeutics, Inc. is conducting a Phase 2a clinical study titled ‘An Open-label Phase 2a Study to Evaluate the Safety and Efficacy of AlloNK®, an Allogeneic Cord Blood-derived NK Cell Therapy, in Combination With Rituximab in Relapsing Forms of B-cell Dependent Rheumatologic Diseases.’ The study aims to assess the safety and efficacy of AlloNK®, a non-genetically modified NK cell therapy, combined with Rituximab for treating refractory rheumatoid arthritis, Sjögren’s disease, idiopathic inflammatory myopathies, and systemic sclerosis. This research is significant as it explores innovative treatments for challenging rheumatologic conditions.
Artiva Biotherapeutics, Inc. is conducting a Phase 1 clinical trial titled A Phase 1 Study to Evaluate the Efficacy and Safety of AB-101, an Allogeneic Cord Blood-Derived NK-Cell Therapy in Combination With B-Cell Depleting mAb in Patients Who Failed Treatment for Class III or IV Lupus Nephritis or Other Forms of Refractory Systemic Lupus Erythematosus. The study aims to assess the safety, tolerability, and preliminary activity of AB-101, a natural killer cell therapy, in combination with B-cell depleting monoclonal antibodies in patients with relapsed or refractory lupus nephritis or systemic lupus erythematosus.
Study Overview: The clinical study titled A Phase 1, Multicenter Trial to Assess the Safety, Tolerability, and Preliminary Efficacy of GCC2005 With Lymphodepleting Chemotherapy in Treatment of Patients With Relapsed or Refractory NK and T-cell Malignancies aims to evaluate the safety, tolerability, and preliminary efficacy of GCC2005 in patients with relapsed or refractory NK and T-cell malignancies. This study is significant as it targets patients who have undergone at least two prior lines of therapy, offering a potential new treatment avenue.
Artiva Biotherapeutics, Inc. is a clinical-stage biotechnology company focused on developing accessible cell therapies for autoimmune diseases and cancers, utilizing its lead program AlloNK® to enhance treatment efficacy.