Oral Ponesimod Versus Teriflunomide In Relapsing MUltiple Sclerosis



Status:Active, not recruiting
Conditions:Neurology, Neurology, Multiple Sclerosis
Therapuetic Areas:Neurology, Other
Healthy:No
Age Range:18 - 55
Updated:12/22/2018
Start Date:June 4, 2015
End Date:May 15, 2019

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Multicenter, Randomized, Double-blind, Parallel-group, Active-controlled, Superiority Study to Compare the Efficacy and Safety of Ponesimod to Teriflunomide in Subjects With Relapsing Multiple Sclerosis

International clinical trial to compare ponesimod and teriflunomide in relapsing multiple
sclerosis


Inclusion Criteria:

Male and female subjects aged 18 to 55 years with established diagnosis of MS McDonald 2010
with relapsing course from onset (i.e., RRMS and SPMS with superimposed relapses).

Subjects must have active disease evidenced by one or more MS attacks with onset within the
period of 12 to 1 months prior to randomization, or by two or more MS attacks with onset
within the 24 to 1 months prior to randomization, or with one or more gadolinium-enhancing
(Gd+) lesion(s) of the brain on an MRI performed within 6 months prior to randomization.

Enrolled subjects must be ambulatory (EDSS score of up to 5.5 inclusive) and may be
treatment-naïve or previously treated with MS disease modifying therapy.

Exclusion Criteria:

Subjects with significant medical conditions or therapies for such conditions (e.g.,
cardiovascular, pulmonary, immunological, hepatic,ophthalmological conditions) or lactating
or pregnant women are not eligible to enter the study.

Subjects with contraindications to MRI or with clinically relevant medical or surgical
conditions that, in the opinion of the investigator, would put the subject at risk by
participating in the study are not eligible to enter the study.
We found this trial at
12
sites
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Raleigh, NC
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Carlsbad, CA
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Denver, CO
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Franklin, TN
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Grodno,
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Indianapolis, IN
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Pomona, CA
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Tampa, FL
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