NCT07503873Phase 2Recruiting

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)

Study sponsor: TG Therapeutics, Inc. · TGTX

Compare the available registry edits below. Primary completion is the date data collection ends for the main study measures; it does not tell you when results will be published.

Primary completion2027-07-31Estimated
Enrollment · participants350Estimated
Source updated2026-09-21Last update listed in the registry record
Version history

Changes to this trial

Last 12 months
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· 1 field changed

Primary completion date changed

− Before

30 May 2027

+ After

31 Jul 2027

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· 2 fields changed

Main study measure wording changed

Text changed; whether the study measures changed has not been verified. Saved text may be shortened.

Compare wording
− Before

Measure: Part 2: Area under the curve (AUC) From Week 0 to Week 12 [AUC(0-W12)] of Ublituximab

+ After

Measure: Part 2: Area under the curve (AUC) at Steady State [AUCss] of Ublituximab

Primary completion date changed

− Before

31 Jul 2027

+ After

30 May 2027

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· 1 field changed

Recruitment status changed

− Before

Not yet recruiting

+ After

Recruiting

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