| 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 | 0.00 | 251.00K | 33.49M | 4.93M | 2.00M | 0.00 |
| EBITDA | -79.71M | -64.85M | -28.41M | -58.67M | -71.58M | -17.72M |
| Net Income | -68.25M | -58.49M | -27.70M | -58.39M | -71.83M | -17.99M |
Balance Sheet | ||||||
| Total Assets | 169.39M | 209.58M | 105.11M | 133.05M | 169.93M | 29.23M |
| Cash, Cash Equivalents and Short-Term Investments | 142.37M | 185.43M | 76.97M | 102.53M | 160.92M | 25.44M |
| Total Debt | 13.22M | 14.35M | 16.91M | 19.45M | 1.74M | 2.12M |
| Total Liabilities | 20.35M | 22.94M | 267.13M | 273.75M | 258.78M | 50.80M |
| Stockholders Equity | 149.04M | 186.64M | -162.01M | -140.70M | -88.86M | -21.57M |
Cash Flow | ||||||
| Free Cash Flow | -70.81M | -55.67M | -50.69M | -57.13M | -17.03M | -13.82M |
| Operating Cash Flow | -69.08M | -55.03M | -47.43M | -50.83M | -15.30M | -13.54M |
| Investing Cash Flow | -100.50M | -120.46M | -25.98M | -6.30M | -1.72M | -284.00K |
| Financing Cash Flow | 164.01M | 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 |
|---|---|---|---|---|---|---|---|
56 Neutral | $76.47M | -0.69 | -69.96% | ― | -99.64% | -59.17% | |
52 Neutral | $87.69M | -1.16 | -86.18% | ― | ― | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
43 Neutral | $68.53M | -12.64 | -39.93% | ― | 186.84% | 89.16% | |
37 Underperform | $98.83M | -0.47 | -67.55% | ― | ― | -9.87% | |
35 Underperform | $50.54M | -0.30 | -146.87% | ― | ― | -17.96% | |
27 Underperform | $105.79M | -0.53 | -64.39% | ― | ― | 48.45% |
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.