drugset / Trial / NCT07211633

A Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, Radiological and Clinical Effects of Subcutaneous Ublituximab in Participants With Relapsing Multiple Sclerosis (RMS)

NCT07211633

Phase 3 Active not recruiting 360 enrolled TG Therapeutics, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the pharmacokinetics of ublituximab when administered subcutaneously (SC) compared to intravenous (IV) administration in participants with RMS.

Timeline

Start
2025-07-09
Primary completion
2026-10-31
Completion
2028-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Ublituximab Monoclonal antibody Intravenous

Indications