A Phase 3, Randomized, Multi-center, Double-blinded, Active-controlled Study to Assess the Efficacy and Safety/Tolerability of Ublituximab (TG-1101; UTX) as Compared to Teriflunomide in Subjects With Relapsing Multiple Sclerosis (RMS)



Status:Active, not recruiting
Conditions:Neurology, Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:18 - 55
Updated:1/31/2019
Start Date:August 1, 2017
End Date:September 30, 2021

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UbLiTuximab In Multiple Sclerosis Treatment Effects (ULTIMATE I STUDY)

This is a Phase 3, randomized, multi-center, double-blinded, active-controlled study that is
primarily designed to assess the Annualized Relapse Rate (ARR) and safety/tolerability of
ublituximab/oral placebo (TG-1101; UTX) as compared to teriflunomide/IV placebo in subjects
with Relapsing MS.


Inclusion Criteria:

- 18-55 age

- Diagnosis of RMS (McDonald criteria 2010)

- Active disease

- Expanded disability status scale (EDSS) 0-5.5 (inclusive) at screening

Exclusion Criteria:

- Treatment with prior Anti-CD20 or other B cell directed treatment

- Treatment with the following therapies at any time prior to randomization:
Alemtuzumab, Natalizumab, Teriflunomide, Leflunomide and Stem cell transplantation

- Diagnosed with Primary Progressive MS (PPMS)

- Pregnant or nursing
We found this trial at
14
sites
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Stanford, CA
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Amherst, NY
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Carlsbad, CA
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Dallas, TX
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Detroit, MI
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Franklin, TN
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Kansas City, KS
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Knoxville, TN
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Long Beach, California 90808
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Long Beach, CA
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Miami, FL
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Northbrook, IL
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Pasadena, CA
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Round Rock, TX
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Westerville, OH
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