drugset / Trial / NCT07503873

A Study to Evaluate Pharmacokinetics (PK) and Safety of Subcutaneous (SC) Ublituximab Administered at Various Injection Sites and Relative Bioavailability Via Autoinjector (AI) Versus Syringe Subcutaneously in Participants With Multiple Sclerosis (MS)

NCT07503873

Phase 2 Recruiting 350 enrolled TG Therapeutics, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the PK and safety of ublituximab SC at different sites of administration and relative bioavailability of ublituximab SC administered with a prefilled pen versus syringe.

Timeline

Start
2026-04-01
Primary completion
2027-05-30
Completion
2029-05-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Ublituximab Monoclonal antibody Subcutaneous

Indications