| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 454.07M | 329.00M | 233.66M | 2.79M | 6.69M | 152.00K |
| Gross Profit | 394.85M | 290.52M | 219.11M | 2.52M | 5.90M | 152.00K |
| EBITDA | 97.09M | 49.90M | 26.10M | -187.63M | -341.97M | -272.68M |
| Net Income | 60.46M | 23.38M | 12.67M | -198.34M | -348.10M | -279.38M |
Balance Sheet | ||||||
| Total Assets | 702.61M | 577.69M | 329.59M | 193.57M | 379.63M | 625.64M |
| Cash, Cash Equivalents and Short-Term Investments | 251.87M | 311.00M | 217.51M | 161.68M | 314.76M | 605.43M |
| Total Debt | 253.72M | 254.38M | 110.80M | 83.06M | 79.05M | 41.98M |
| Total Liabilities | 426.18M | 355.33M | 169.09M | 134.99M | 142.48M | 106.29M |
| Stockholders Equity | 276.43M | 222.36M | 160.50M | 58.59M | 237.15M | 519.35M |
Cash Flow | ||||||
| Free Cash Flow | -59.24M | -40.56M | -31.41M | -176.18M | -296.04M | -214.86M |
| Operating Cash Flow | -59.13M | -40.52M | -31.41M | -176.17M | -295.63M | -214.51M |
| Investing Cash Flow | -10.47M | -1.04M | -50.65M | -20.01M | -332.00K | -24.51M |
| Financing Cash Flow | 115.84M | 128.53M | 72.70M | -391.00K | 41.42M | 679.83M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
65 Neutral | $5.40B | 11.97 | 111.96% | ― | 100.88% | ― | |
58 Neutral | $8.36B | ― | -9.06% | ― | 4.14% | -179.96% | |
57 Neutral | $12.10B | -43.30 | -39.99% | ― | 20.39% | 34.00% | |
54 Neutral | $6.80B | ― | -275.50% | ― | 65.83% | 28.50% | |
52 Neutral | $6.64B | ― | -240.36% | ― | 54.92% | 28.47% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
43 Neutral | $6.70B | ― | -38.79% | ― | ― | -52.84% |
TG Therapeutics is a biopharmaceutical company focused on developing and commercializing novel treatments for B-cell diseases, with a particular emphasis on therapies for multiple sclerosis. In its latest earnings report, TG Therapeutics announced a strong third quarter for 2025, with total revenue reaching $161.7 million, driven primarily by the success of its product BRIUMVI in the U.S. market. The company has raised its full-year revenue guidance to $600 million, reflecting continued strong demand for BRIUMVI. Key financial highlights include a significant increase in net income to $390.9 million for the quarter, largely due to a non-recurring income tax benefit. The company also reported substantial growth in product revenue, with BRIUMVI U.S. net revenue experiencing an 84% increase compared to the same period in 2024. Additionally, TG Therapeutics has expanded its commercialization efforts internationally and achieved several pipeline development milestones. Looking ahead, TG Therapeutics remains focused on expanding patient awareness, advancing clinical trials, and driving long-term shareholder value, as indicated by the authorization of an additional $100 million share repurchase program.
The clinical study titled ‘Ublituximab in Pediatric Participants With Relapsing Forms of Multiple Sclerosis (RMS)’ aims to assess the pharmacokinetics and pharmacodynamics of ublituximab in children aged 10 to under 18 with relapsing multiple sclerosis. The study also seeks to compare the efficacy of ublituximab with fingolimod, a current treatment option, and evaluate its long-term safety and efficacy.
Study Overview: TG Therapeutics is conducting a Phase 3 study titled A Phase 3, Non-Inferiority, Randomized, Open-Label, Parallel Group, Multicenter Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, Radiological and Clinical Effects of Subcutaneous Ublituximab Versus Intravenous Ublituximab in Patients With Multiple Sclerosis. The study aims to compare the pharmacokinetics of subcutaneous versus intravenous administration of ublituximab in patients with relapsing multiple sclerosis (RMS), a significant endeavor to enhance treatment options for this condition.
The recent clinical study update from TG Therapeutics focuses on evaluating the safety, efficacy, and pharmacokinetics of a modified regimen of ublituximab in patients with Relapsing Multiple Sclerosis (RMS). Officially titled ‘Evaluating Safety, Efficacy and Pharmacokinetics of a Modified Regimen of Ublituximab (ENHANCE)’, the study aims to measure the impact of this treatment on T1 Gadolinium-enhancing lesions, a key indicator of disease activity in RMS.
Study Overview: TG Therapeutics is conducting a study titled BRIUMVI® Pregnancy Registry: A Prospective Study of Pregnancy and Infant Outcomes in Patients Treated With BRIUMVI®. The study aims to evaluate the prevalence of major congenital malformations (MCM) in pregnant participants with Multiple Sclerosis (MS) who are exposed to BRIUMVI® compared to those who are not. This research is significant as it seeks to provide crucial insights into the safety of BRIUMVI® during pregnancy.
Study Overview: TG Therapeutics is conducting a study titled ‘REal World ExperieNce With BRIUMVI® (UblituximAB-xiiy) Treated Patients: A Longitudinal REgistry Study (ENABLE)’ to assess the safety, effectiveness, and treatment experience of BRIUMVI® (ublituximab-xiiy) in patients with Relapsing Multiple Sclerosis (RMS). This study is significant as it aims to provide real-world insights into the drug’s performance outside of controlled clinical trials.
Study Overview: TG Therapeutics is conducting a post-marketing study titled ‘A Study Evaluating the Presence and Concentration of BRIUMVI™ (Ublituximab) in Breast Milk’ (PROVIDE). The study aims to assess the presence and concentration of BRIUMVI™ in breast milk among breastfeeding participants who are receiving the drug for the treatment of relapsing forms of multiple sclerosis (RMS). This research is significant as it addresses safety concerns for breastfeeding mothers undergoing treatment.
Study Overview: TG Therapeutics is conducting a Phase 1 study titled ‘A Phase 1, Open-label Study to Evaluate the Safety and Clinical Activity of Azercabtagene Zapreleucel in Participants With B-cell Mediated Autoimmune Disorders.’ The primary goal is to determine the recommended phase 2 dose of Azercabtagene zapreleucel (azer-cel), highlighting its potential significance in treating B-cell mediated autoimmune disorders.
TG Therapeutics faces significant business risks associated with the incorporation of AI technology into its operations, primarily due to the rapidly evolving regulatory landscape. The uncertainty surrounding AI regulations, both in the U.S. and internationally, could lead to increased compliance costs and potential legal liabilities. Changes in implementation standards and enforcement practices may impact TG Therapeutics’ ability to effectively utilize AI, potentially affecting its operational efficiency and financial performance. Additionally, challenges related to intellectual property rights and potential litigation further compound the risks, potentially allowing competitors to capitalize on TG Therapeutics’ innovations.
The latest earnings call for TG Therapeutics showcased a positive sentiment, underscored by strong commercial performance and strategic advancements. The company highlighted the success of BRIUMVI and its subcutaneous version, although it acknowledged increased operating expenses and potential challenges from payer preferences for subcutaneous therapies.
TG Therapeutics is a biopharmaceutical company focused on developing and commercializing novel treatments for B-cell diseases, with a particular emphasis on therapies for multiple sclerosis (MS). The company is known for its innovative approach in the healthcare sector, particularly with its flagship product BRIUMVI, an anti-CD20 monoclonal antibody therapy.