TG Therapeutics' (TGTX) subcutaneous formulation of ublituximab showed "positive" pharmacokinetic, pharmacodynamic, safety, and tolerability data from a phase 1 clinical trial comparing the multiple sclerosis therapy to the drug's intravenous version, the company said Wednesday.
The high-concentration, low-volume subcutaneous version of ublituximab, the active agent in Briumvi, was also well-tolerated in the trial, which involved more than 100 patients, the company said.
The company expects to report data from a phase 3 trial of the self-administered therapy later this year or early next year and said it could advance toward potential approval in 2028 if successful.
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