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Sep 30, 2024

TG Therapeutics Q3 2024 Earnings Report

TG Therapeutics reported Q3 2024 financial results, highlighting BRIUMVI's strong performance and raised full-year revenue guidance.

Key Takeaways

TG Therapeutics reported a successful third quarter in 2024, driven by strong U.S. BRIUMVI net revenue of $83.3 million. The company raised its full-year 2024 U.S. BRIUMVI net revenue target to $300 - $305 million and continues to advance its clinical programs.

BRIUMVI U.S. net product revenue reached $83.3 million in Q3 2024, reflecting approximately 15% quarter-over-quarter growth and over 230% growth from the same quarter last year.

The company raised its full-year 2024 U.S. BRIUMVI net revenue target to $300 to $305 million.

Updated data from the ULTIMATE I & II Phase 3 trials showed 92% of patients were free from disability progression after five years of BRIUMVI treatment.

A phase 1 clinical trial evaluating subcutaneous ublituximab in RMS was initiated.

Total Revenue
$83.9M
Previous year: $166M
-49.4%
EPS
$0.02
Previous year: $0.73
-97.3%
R&D Expense
$20.1M
Previous year: $14.8M
+35.8%
SG&A Expense
$42M
Previous year: $32.8M
+28.0%
Gross Profit
$74.5M
Previous year: $162M
-54.1%
Cash and Equivalents
$341M
Previous year: $229M
+48.8%
Free Cash Flow
-$12.2M
Previous year: $83.7M
-114.6%
Total Assets
$586M
Previous year: $331M
+77.0%

TG Therapeutics

TG Therapeutics

Forward Guidance

TG Therapeutics raised its full year 2024 U.S. BRIUMVI net product revenue target to $300 to $305 million and anticipates several development pipeline milestones.

Positive Outlook

  • Continued strong commercial launch of BRIUMVI.
  • Potential for continued growth into the end of the year and into 2025.
  • Focus on improving the treatment experience for individuals living with relapsing forms of multiple sclerosis.
  • Advancement of clinical programs, including shortening infusion times and developing a subcutaneous BRIUMVI option.
  • Development of novel treatments such as allogeneic CD19 CAR-T.

Challenges Ahead

  • Risks associated with maintaining a commercial infrastructure for BRIUMVI.
  • Potential failure to obtain and maintain payor coverage.
  • Uncertainties inherent in research and development.
  • Reliance on third parties for manufacturing, distribution, and supply.
  • Potential regulatory challenges in seeking marketing approval outside of the U.S.