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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)

Not yet recruiting Phase 2 Last updated 31 March 2026
What this trial tests

Phase 2 trial testing Ublituximab in Multiple Sclerosis in 350 participants. Not yet recruiting.

Timeline
21 March 2026
Primary endpoint
31 July 2027
30 May 2029

Quick facts

Lead sponsorTG Therapeutics, Inc.
PhasePhase 2
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment350
Start date21 March 2026
Primary completion31 July 2027
Estimated completion30 May 2029

Drugs / interventions tested

Conditions studied

Sponsor

TG Therapeutics, Inc. — full company profile →

Who can join

Adults 18 to 65, any sex, with Multiple Sclerosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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 with an AI device versus syringe.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Ublituximab

Trials testing the same drug.

Other recruiting trials for Multiple Sclerosis

Currently open trials in the same condition.

Other TG Therapeutics, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07503873.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing