TG Therapeutics Announces BRIUMVI Data Presentation Schedule at CMSC 2026
Written by Emily J. Thompson, Senior Investment Analyst
Updated: 34 minutes ago
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Source: Newsfilter
- Presentation Schedule: TG Therapeutics will showcase four data presentations on BRIUMVI at the 2026 Consortium of Multiple Sclerosis Centers annual meeting, emphasizing its clinical advantages in relapsing multiple sclerosis (RMS), which is expected to attract industry attention and enhance the company's reputation.
- Clinical Research Findings: New analyses from the ENABLE Phase 4 study indicate significant improvements in patient-reported outcomes, including treatment satisfaction and physical and psychological impact measures, observed as early as Day 15 and sustained through Week 48, highlighting BRIUMVI's long-term benefits for patient experience.
- Real-World Data: The data reveals that 99.4% of patients remained relapse-free after transitioning to BRIUMVI, with a low annualized relapse rate of 0.011, showcasing the drug's exceptional performance in disease control and patient satisfaction, potentially driving market share growth.
- Clinical Trial Background: The ULTIMATE I and II trials enrolled a total of 1,094 patients, demonstrating low rates of infusion-related reactions and consistent infusion times, further solidifying BRIUMVI's competitive edge in RMS treatment.
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Analyst Views on TGTX
Wall Street analysts forecast TGTX stock price to rise
4 Analyst Rating
3 Buy
0 Hold
1 Sell
Moderate Buy
Current: 39.240
Low
15.00
Averages
43.50
High
60.00
Current: 39.240
Low
15.00
Averages
43.50
High
60.00
About TGTX
TG Therapeutics, Inc. is a fully integrated, commercial stage biotechnology company focused on the acquisition, development and commercialization of novel treatments for B-cell diseases. Its products include Ublituximab IV (anti-CD20 mAb), Ublituximab IV Simplified Dosing Schedule, Ublituximab Subcutaneous (anti-CD20 mAb), and Azer-cel. It is engaged in late-stage clinical development of BRIUMVI. BRIUMVI is an anti-CD20 monoclonal antibody that can be administered to adults with relapsing forms of multiple sclerosis (RMS) in a one-hour infusion every 24 weeks, following the starting dose. It is used for treatment of adults with clinically isolated syndrome, relapsing-remitting disease, and active secondary progressive disease. The Company is also engaged in ULTIMATE I & II Trials Evaluating Single Agent Ublituximab in RMS. Its ENHANCE Phase 3b Trial is an ongoing, multi-center, open-label study designed to evaluate alternative dosing regimens for BRIUMVI in patients with RMS.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
- Presentation Schedule: TG Therapeutics will showcase four data presentations on BRIUMVI at the 2026 Consortium of Multiple Sclerosis Centers annual meeting, emphasizing its clinical advantages in relapsing multiple sclerosis (RMS), which is expected to attract industry attention and enhance the company's reputation.
- Clinical Research Findings: New analyses from the ENABLE Phase 4 study indicate significant improvements in patient-reported outcomes, including treatment satisfaction and physical and psychological impact measures, observed as early as Day 15 and sustained through Week 48, highlighting BRIUMVI's long-term benefits for patient experience.
- Real-World Data: The data reveals that 99.4% of patients remained relapse-free after transitioning to BRIUMVI, with a low annualized relapse rate of 0.011, showcasing the drug's exceptional performance in disease control and patient satisfaction, potentially driving market share growth.
- Clinical Trial Background: The ULTIMATE I and II trials enrolled a total of 1,094 patients, demonstrating low rates of infusion-related reactions and consistent infusion times, further solidifying BRIUMVI's competitive edge in RMS treatment.
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- Revenue Beat: TG Therapeutics reported approximately $195 million in U.S. BRIUMVI net product revenue for Q1 2026, exceeding guidance of $185 million to $190 million, indicating strong market performance and sustained growth potential.
- Share Buyback Program: The company repurchased $100 million of its stock this quarter, which not only enhances shareholder value but also reflects management's confidence in future growth, likely increasing market recognition of its shares.
- Guidance Upgrade: Following a strong Q1, the company raised its 2026 U.S. revenue guidance to $885 million to $900 million, with global revenue guidance increased to approximately $925 million, signaling optimism about future performance.
- Clinical Trial Progress: Management expects to release top-line data from the ENHANCE study in the coming weeks and plans to launch subcutaneous BRIUMVI by 2028, pending regulatory approval, which could open new market opportunities for the company.
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