TG Therapeutics (TGTX) H.C. Wainwright 28th Annual Global Investment Conference summary
Event summary combining transcript, slides, and related documents.
H.C. Wainwright 28th Annual Global Investment Conference summary
14 Sep, 2026Market landscape and commercial performance
Relapsing multiple sclerosis sees about 40,000 new patients annually, with 65%-70% opting for IV therapies and 30%-35% for subcutaneous options.
The IV segment is growing, with over one-third market share and consistent outperformance of sales guidance, targeting a $1 billion run rate by year-end.
Key revenue drivers are new patient starts and persistence, with gross-to-net fluctuations impacting quarterly results.
Patient distribution among naive, non-CD20, and CD20-switchers is now nearly equal, with naive patient uptake increasing over time.
Shared decision-making is prevalent, with patients choosing between self-injection and infusion based on preference.
Product development and competitive positioning
Enhanced dosing protocol consolidating initial doses is expected to simplify administration and drive growth in 2027.
Supplemental BLA for the enhanced protocol is imminent.
Subcutaneous formulation phase I data showed over 60% bioavailability, supporting confidence for phase III, with pivotal data expected late 2024 or early 2025.
Quarterly auto-injector is positioned as highly competitive versus monthly or bimonthly alternatives.
Ex-U.S. commercialization is progressing well, especially in markets where subcutaneous options dominate over 50% of share.
Industry trends and future outlook
IV and subcutaneous markets are both seen as having significant growth potential, with subcutaneous possibly surpassing IV.
OCREVUS patent expiry in 2028 and competitor moves to on-body injectors are being monitored.
Oral BTK inhibitors are expected to have minimal impact on the anti-CD20 market, which retains about 50%-55% dynamic share.
Upcoming catalysts include supplemental BLA approval, phase III subcutaneous data, schizophrenia trial results, and potential 2028 subcutaneous approval.
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