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Positive subcutaneous delivery data implies expansion of addressable market and potential regulatory upside; immediate price reaction supports a bullish stance, though execution risk remains until Phase 3 results.
What happened, with direct paths to the underlying reporting
TG Therapeutics reported Phase 1 data on a high-concentration subcutaneous formulation showing >60% bioavailability relative to IV, with B-cell depletion comparable to IV and no new safety signals. Pharmacokinetic modeling supports quarterly SC dosing, and Phase 3 is fully enrolled. Topline data are expected late 2026 or early 2027, with regulatory approval potential by 2028, expanding the addressable market.
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