Multiple Sclerosis Clinical Trial

Oral Ponesimod Versus Teriflunomide In Relapsing MUltiple Sclerosis

Summary

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

View Eligibility Criteria

Eligibility Criteria

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.

Study is for people with:

Multiple Sclerosis

Phase:

Phase 3

Estimated Enrollment:

1133

Study ID:

NCT02425644

Recruitment Status:

Completed

Sponsor:

Actelion

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There are 155 Locations for this study

See Locations Near You

Investigator Site 8045
Carlsbad California, 92011, United States
Investigator Site 8311
Pomona California, 91767, United States
Investigator Site 8036
Denver Colorado, 80209, United States
Investigator Site 8065
Ormond Beach Florida, 32174, United States
Investigator Site 8018
Tampa Florida, 33612, United States
Investigator Site 8013
Indianapolis Indiana, 46256, United States
Investigator Site 8040
Raleigh North Carolina, 27607, United States
Investigator Site 8006
Columbus Ohio, 43214, United States
Investigator Site 8015
Franklin Tennessee, 37064, United States
Investigator Site 8042
Orem Utah, 84058, United States
Investigator Site 3605
Grodno , 23001, Belarus
Investigator Site 3603
Minsk , 22002, Belarus
Investigator Site 3602
Minsk , 22011, Belarus
Investigator Site 3606
Vitebsk , 21002, Belarus
Investigator Site 3604
Vitebsk , 21003, Belarus
Investigator Site 9104
Sarajevo , 71000, Bosnia and Herzegovina
Investigator Site 2709
Plovdiv , 4002, Bulgaria
Investigator Site 2711
Sofia , 1113, Bulgaria
Investigator Site 2702
Sofia , 1309, Bulgaria
Investigator Site 2707
Sofia , 1407, Bulgaria
Investigator Site 2701
Sofia , 1431, Bulgaria
Investigator Site 2708
Sofia , 1431, Bulgaria
Investigator Site 2703
Sofia , 1606, Bulgaria
Investigator Site 8102
Edmonton Alberta, T6G 1, Canada
Investigator Site 8120
Victoria British Columbia, V8R 1, Canada
Investigator Site 8101
Ottawa Ontario, K1H 8, Canada
Investigator Site 8113
Greenfield Park Quebec, J4V 2, Canada
Investigator Site 2506
Osijek , 31000, Croatia
Investigator Site 2502
Zagreb , 10000, Croatia
Investigator Site 2508
Zagreb , 10000, Croatia
Investigator Site 2509
Zagreb , 10000, Croatia
Investigator Site 3009
Brno , 625 0, Czechia
Investigator Site 3003
Brno , 656 9, Czechia
Investigator Site 3010
Hradec Králové , 500 0, Czechia
Investigator Site 3006
Jihlava , 586 3, Czechia
Investigator Site 3002
Ostrava-Poruba , 708 5, Czechia
Investigator Site 3007
Pardubice , 532 0, Czechia
Investigator Site 3001
Praha 2 , 128 0, Czechia
Investigator Site 3008
Praha 5 , 150 0, Czechia
Investigator Site 3004
Teplice , 415 2, Czechia
Investigator Site 2212
Tampere , 33100, Finland
Investigator Site 2202
Turku , 20520, Finland
Investigator Site 1713
Bordeaux Cedex , 33076, France
Investigator Site 1703
Clermont Ferrand Cedex 1 , 63003, France
Investigator Site 1715
Nantes Cedex 1 , 44093, France
Investigator Site 1706
Nice Cedex 1 , 06002, France
Investigator Site 1705
Strasbourg Cedex , 67091, France
Investigator Site 3905
Tbilisi , 0112, Georgia
Investigator Site 3904
Tbilisi , 0160, Georgia
Investigator Site 3903
Tbilisi , 0179, Georgia
Investigator Site 3906
Tbilisi , 0179, Georgia
Investigator Site 3902
Tbilisi , 0194, Georgia
Investigator Site 1113
Dresden , 01307, Germany
Investigator Site 1107
Erfurt , 99089, Germany
Investigator Site 1109
Leipzig , 04107, Germany
Investigator Site 1104
Mainz , 55131, Germany
Investigator Site 1102
Ulm , 89081, Germany
Investigator Site 1303
Athens , 11521, Greece
Investigator Site 1301
Athens , 11525, Greece
Investigator Site 1307
Athens , 15125, Greece
Investigator Site 2903
Budapest , 1145, Hungary
Investigator Site 2905
Budapest , 1204, Hungary
Investigator Site 2910
Esztergom , 2500, Hungary
Investigator Site 2902
Gyor , 9023, Hungary
Investigator Site 2909
Kistarcsa , 2143, Hungary
Investigator Site 4005
Ashkelon , 78306, Israel
Investigator Site 4004
Haifa , 31096, Israel
Investigator Site 4006
Jerusalem , 91120, Israel
Investigator Site 4010
Zfat , 13100, Israel
Investigator Site 1403
Cefalu , 90015, Italy
Investigator Site 1409
Genova , 16132, Italy
Investigator Site 1413
L'Aquila , 67100, Italy
Investigator Site 1405
Roma , 00189, Italy
Investigator Site 3401
Riga , 1015, Latvia
Investigator Site 3402
Riga , LV-10, Latvia
Investigator Site 3403
Riga , LV-10, Latvia
Investigator Site 3502
Kaunas , 50161, Lithuania
Investigator Site 3503
Klaipeda , 92288, Lithuania
Investigator Site 3504
Siauliai , 76231, Lithuania
Investigator Site 7410
Chihuahua , 31203, Mexico
Investigator Site 7409
Monterrey , 64710, Mexico
Investigator Site 3219
Bialystok , 15-27, Poland
Investigator Site 3215
Bydgoszcz , 85-79, Poland
Investigator Site 3208
Gdansk , 80-80, Poland
Investigator Site 3217
Katowice , 40-59, Poland
Investigator Site 3203
Katowice , 40-75, Poland
Investigator Site 3205
Konstancin-Jeziorna , 05-51, Poland
Investigator Site 3216
Ksawerow , 95-05, Poland
Investigator Site 3220
Lublin , 20-01, Poland
Investigator Site 3202
Poznan , 60-35, Poland
Investigator Site 3214
Poznan , 60-84, Poland
Investigator Site 3207
Poznan , 61-85, Poland
Investigator Site 3213
Wroclaw , 51-68, Poland
Investigator Site 1602
Amadora , 2720 , Portugal
Investigator Site 1605
Braga , 4710-, Portugal
Investigator Site 1603
Coimbra , 3000-, Portugal
Investigator Site 1604
Porto , 4099-, Portugal
Investigator Site 2807
Bucuresti , 01082, Romania
Investigator Site 2811
Bucuresti , 02290, Romania
Investigator Site 2804
Bucuresti , 05009, Romania
Investigator Site 2802
Timisoara , 30072, Romania
Investigator Site 3821
Barnaul Altai Krai, 65602, Russian Federation
Investigator Site 3818
Belgorod , 30800, Russian Federation
Investigator Site 3837
Bryansk , 24103, Russian Federation
Investigator Site 3836
Ekaterinburg , 62010, Russian Federation
Investigator Site 3811
Kazan , 42002, Russian Federation
Investigator Site 3822
Kemerovo , 65006, Russian Federation
Investigator Site 3814
Krasnoyarsk , 66003, Russian Federation
Investigator Site 3823
Kursk , 30500, Russian Federation
Investigator Site 3831
Moscow , 11904, Russian Federation
Investigator Site 3803
Moscow , 12701, Russian Federation
Investigator Site 3840
Moscow , 12701, Russian Federation
Investigator Site 3810
Moscow , 12912, Russian Federation
Investigator Site 3802
Nizhniy Novgorod , 60315, Russian Federation
Investigator Site 3834
Nizhny Novgorod , 60307, Russian Federation
Investigator Site 3835
Novgorod , 17300, Russian Federation
Investigator Site 3829
Novosibirsk , 63000, Russian Federation
Investigator Site 3839
Perm , 61499, Russian Federation
Investigator Site 3812
Pyatigorsk , 35753, Russian Federation
Investigator Site 3813
Saint Petersburg , 19711, Russian Federation
Investigator Site 3805
Samara , 44309, Russian Federation
Investigator Site 3825
Smolensk , 21401, Russian Federation
Investigator Site 3808
St. Petersburg , 19435, Russian Federation
Investigator Site 3833
St. Petersburg , 19702, Russian Federation
Investigator Site 3807
St. Petersburg , 19737, Russian Federation
Investigator Site 3815
St. Petersburg , 19770, Russian Federation
Investigator Site 3801
Tomsk , 63405, Russian Federation
Investigator Site 3819
Tver , 17002, Russian Federation
Investigator Site 3842
Yaroslavl , 15003, Russian Federation
Investigator Site 2601
Belgrade , 11000, Serbia
Investigator Site 2606
Belgrade , 11000, Serbia
Investigator Site 2607
Belgrade , 11080, Serbia
Investigator Site 2603
Kragujevac , 34000, Serbia
Investigator Site 2602
Nis , 18000, Serbia
Investigator Site 1509
Barcelona , 08003, Spain
Investigator Site 1505
Barcelona , 08035, Spain
Investigator Site 1504
Barcelona , 08036, Spain
Investigator Site 1502
Madrid , 28006, Spain
Investigator Site 1501
Malaga , 29010, Spain
Investigator Site 1506
Sevilla , 41009, Spain
Investigator Site 2103
Goteborg , 413 4, Sweden
Investigator Site 2110
Stockholm , 141 8, Sweden
Investigator Site 2101
Stockholm , 171 7, Sweden
Investigator Site 9004
Trabzon , 61080, Turkey
Investigator Site 3714
Chernihiv , 14001, Ukraine
Investigator Site 3701
Chernihiv , 14029, Ukraine
Investigator Site 3713
Ivano-Frankivsk , 76008, Ukraine
Investigator Site 3711
Ivano-Frankivsk , 76018, Ukraine
Investigator Site 3723
Kharkiv , 61103, Ukraine
Investigator Site 3724
Kharkiv , 61176, Ukraine
Investigator Site 3716
Kyiv , 03115, Ukraine
Investigator Site 3715
Lviv , 79000, Ukraine
Investigator Site 3721
Lviv , 79010, Ukraine
Investigator Site 3703
Odessa , 65009, Ukraine
Investigator Site 3717
Poltava , 36011, Ukraine
Investigator Site 3730
Ternopil , 46027, Ukraine
Investigator Site 3718
Vinnytsia , 21005, Ukraine
Investigator Site 3722
Zaporizhia , 69000, Ukraine
Investigator Site 3725
Zhytomyr , 10008, Ukraine
Investigator Site 2015
Glasgow , G51 4, United Kingdom
Investigator Site 2021
Lancashire , PR2 9, United Kingdom
Investigator Site 2003
Salford , M6 8H, United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Multiple Sclerosis

Phase:

Phase 3

Estimated Enrollment:

1133

Study ID:

NCT02425644

Recruitment Status:

Completed

Sponsor:


Actelion

How clear is this clinincal trial information?

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