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This study will assess the efficacy, safety, and tolerability of ACT-128800 in patients with relapsing-remitting multiple sclerosis.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| ACT-128800 Dose 1 | Experimental | ACT-128800 Dose 1 |
|
| ACT-128800 Dose 2 | Experimental | ACT-128800 Dose 2 |
|
| ACT-128800 Dose 3 | Experimental | ACT-128800 Dose 3 |
|
| Placebo | Placebo Comparator | Matching placebo |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ACT-128800 Dose 1 | Drug | ACT-128800 (Dose 1) administered orally once daily |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Cumulative Number of New T1 Gadolinium-Enhancing (Gd+) Lesions on Magnetic Resonance Imaging (MRI) Scan From Week 12 to Week 24 | Cumulative Number of new T1 gadolinium-enhancing (Gd+) lesions per year on magnetic resonance imaging (MRI) scan from Week 12 to Week 24 were reported. Negative binomial (NB) regression analysis on Per protocol analysis set and imputation was applied for the missing data. Here, MS signifies multiple sclerosis. | From Week 12 to 24 |
| Measure | Description | Time Frame |
|---|---|---|
| Annualized Confirmed Relapse Rate | Relapse: occurrence of acute episode of one or more new symptoms or worsened symptoms of Multiple Sclerosis (MS), not associated with fever/infection and lasting 24 hours after stable 30 days period. Confirmed relapse: increase from baseline at least 0.5 point Expanded Disability Status Scale (EDSS) score or increase of one point in one, two or three Functional Systems (FS), excluding bowel/bladder and cerebral/mental FS. EDSS and FS scores are based on neurological examination for assessing its impairment in MS. Among eight FS, seven are ordinal clinical rating scales ranging from 0-5 or 6 with higher scale indicating overall functional impairment assessing Visual, Brain Stem, Pyramidal, Cerebellar, Sensory, Bowel/Bladder and Cerebral functions. Rating individual FS scores is used to rate EDSS with information concerning gait and use of assistance. EDSS is ordinal clinical scale ranges 0 (normal neurological examination) to 10(death due to MS) |
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Inclusion Criteria:
Exclusion Criteria:
Additional inclusion and exclusion criteria apply with respect to medical conditions and concomitant treatments which could affect patients' risk from participating in the study.
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| Name | Affiliation | Role |
|---|---|---|
| Actelion Pharmaceuticals | Actelion | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Clinical Investigative Site 3132 | Scottsdale | Arizona | 85259 | United States | ||
| Clinical Investigative Site 3100 |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 24659797 | Result | Olsson T, Boster A, Fernandez O, Freedman MS, Pozzilli C, Bach D, Berkani O, Mueller MS, Sidorenko T, Radue EW, Melanson M. Oral ponesimod in relapsing-remitting multiple sclerosis: a randomised phase II trial. J Neurol Neurosurg Psychiatry. 2014 Nov;85(11):1198-208. doi: 10.1136/jnnp-2013-307282. Epub 2014 Mar 21. | |
| 33914286 | Derived |
| Label | URL |
|---|---|
| A dose-finding study to evaluate the efficacy, safety, and tolerability of three doses of ACT-128800, an oral S1P1 receptor agonist, administered for twenty-four weeks in patients with relapsing-remitting multiple sclerosis | View source |
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| ID | Title | Description |
|---|---|---|
| FG000 | Ponesimod 40 mg | Participants received ponesimod capsules once daily as per up-titration schedule with an initial dose of 10 milligram (mg) ponesimod on Days 1 to 7 followed by first up-titration dose of 20 mg ponesimod on Days 8 to 14 and lastly received 40 mg ponesimod as second up-titration dose on Day 15 to Week 24. |
| FG001 |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
Not provided
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| Placebo |
| Drug |
Matching placebo administered orally once daily |
|
| ACT-128800 Dose 2 | Drug | ACT-128800 (Dose 2) administered orally once daily |
|
| ACT-128800 Dose 3 | Drug | ACT-128800 (Dose 3) administered orally once daily |
|
| Up to 24 weeks |
| Number of Participants With First Confirmed Relapse as Assessed by Kaplan-Meier Estimate From Baseline to Week 24 | Relapse: occurrence of acute episode of one or more new symptoms or worsened symptoms of MS, not associated with fever/infection and lasting 24 hours after stable 30 days period. Confirmed relapse: increase from baseline at least 0.5 point Expanded Disability Status Scale (EDSS) score or increase of one point in one, two or three Functional Systems (FS), excluding bowel/bladder and cerebral/mental FS. EDSS and FS scores are based on neurological examination for assessing its impairment in MS. Among eight FS, seven are ordinal clinical rating scales ranging from 0-5 or 6 with higher scale indicating overall functional impairment assessing Visual, Brain Stem, Pyramidal, Cerebellar, Sensory, Bowel/Bladder and Cerebral functions. Rating individual FS scores is used to rate EDSS with information concerning gait and use of assistance. EDSS is ordinal clinical scale ranges 0 (normal neurological examination) to 10(death due to MS). Kaplan-Meier estimate used for Outcome Measure analysis. | Baseline to Week 24 |
| Tucson |
| Arizona |
| 85741 |
| United States |
| Clinical Investigative Site 3115 | Sacramento | California | 95817 | United States |
| Clinical Investigative Site 3117 | Stanford | California | 94305 | United States |
| Clinical Invesigative Site 3116 | Sarasota | Florida | 34233 | United States |
| Clinical Investigative Site 3101 | Indianapolis | Indiana | 46202 | United States |
| Clinical Investigative Site 3105 | Kansas City | Kansas | 66160 | United States |
| Clinical Investigative Site 3107 | Lenexa | Kansas | 66214 | United States |
| Clinical Investigative Site 3118 | Baltimore | Maryland | 21201 | United States |
| Clinical Investigative Site 3133 | Worcester | Massachusetts | 01605 | United States |
| Clinical Investigator 3136 | St Louis | Missouri | 63100 | United States |
| Clinical Investigative Site # 3135 | Newark | New Jersey | 07103 | United States |
| Clinical Investigative Site 3129 | Latham | New York | 12110 | United States |
| Clinical Investigative Site # 3128 | New York | New York | 10032 | United States |
| Clinical Investigative Site 3127 | Schenectady | New York | 12308 | United States |
| Clinical Investigative Site 3120 | Stony Brook | New York | 11794 | United States |
| Clinical Investigative Site 3119 | Raleigh | North Carolina | 27607 | United States |
| Clinical Investigator 3126 | Akron | Ohio | 44320 | United States |
| Clinical Investigative Site 3113 | Cincinnati | Ohio | 45219 | United States |
| Clinical Investigative Site 3130 | Columbus | Ohio | 43221 | United States |
| Clinical Investigator 3104 | Portland | Oregon | 97225 | United States |
| Clinical Investigative Site 3125 | Philadelphia | Pennsylvania | 19107 | United States |
| Clinical Investigative Site 3112 | Burlington | Vermont | 05401 | United States |
| Clinical Investigative Site 3111 | Richmond | Virginia | 23298 | United States |
| Clinical Investigative Site 3102 | Kirkland | Washington | 98034 | United States |
| Clinical Investigative Site # 1001 | Fitzroy | 3065 | Australia |
| Clinical Investigative Site 1000 | Westmead | 2145 | Australia |
| Clinical Investigative Site 1102 | Amstetten | 3300 | Austria |
| Clinical Investigative Site 1100 | Sankt Pölten | 3100 | Austria |
| Clinical Investigative Site 1101 | Vienna | 1090 | Austria |
| Clinical Investigative Site 1201 | La Louvière | 7100 | Belgium |
| Clinical Investigative Site # 1205 | Liège | 4000 | Belgium |
| Clinical Investigative Site 1204 | Ottignies | 1340 | Belgium |
| Clinical Investigative Site 1203 | Sijsele-Damme | 8340 | Belgium |
| Clinical Investigative Site 1302 | Sofia | 1309 | Bulgaria |
| Clinical Investigative Site 1301 | Sofia | 1431 | Bulgaria |
| Clinical Investigative Site 1303 | Varna | 9010 | Bulgaria |
| Clinical Investigative Site 1304 | Varna | 9010 | Bulgaria |
| Clinical Investigative Site 1401 | Burbaby | British Columbia | V5G 2X6 | Canada |
| Clinical Investigative Site # 1401 | Burnaby | V5G 2X6 | Canada |
| Clinical Investigative Site 1400 | Ottawa | K1H 8L6 | Canada |
| Clinical Investigative Site 1502 | Brno | 656 91 | Czechia |
| Clinical Investigative Site 1506 | Jihlava | 586 33 | Czechia |
| Clinical Investigative Site 1504 | Olomouc | 775 20 | Czechia |
| Clinical Investigative Site 1501 | Ostrava-Poruba | 70852 | Czechia |
| Clinical Investigative Site 1500 | Prague | 128 08 | Czechia |
| Clinical Investigative Site 1503 | Teplice | Czechia |
| Clinical Investigative Site 1600 | Helsinki | 00100 | Finland |
| Clinical Investigative Site 1601 | Hyvinkää | 05800 | Finland |
| Clinical Investigative Site 1603 | Tampere | 33520 | Finland |
| Clinical Investigative Site 1602 | Turku | 20100 | Finland |
| Clinical Investigative Site 1701 | Montpellier | 34295 | France |
| Clinical Investigative Site # 1806 | Bayreuth | 95445 | Germany |
| Clinical Investigative 1807 | Berlin | 10117 | Germany |
| Clinical Investigative Site 1803 | Berlin | 13347 | Germany |
| Clinical Investigative site 1800 | Düsseldorf | 40225 | Germany |
| Clinical Investigative Site 1802 | Essen | 45147 | Germany |
| Clinical Investigative Site 1805 | Homburg/Saar | 66421 | Germany |
| Clinical Investigative Site 1804 | Ulm | 89081 | Germany |
| Clinical Investigative Site 1905 | Budapest | 1134 | Hungary |
| Clinical Investigative Site # 1904 | Budapest | H-1115 | Hungary |
| Clinical Investigative Site 1908 | Budapest | H-1145 | Hungary |
| Clinical Investigative Site 1902 | Győr | 11-9024 | Hungary |
| Clinical Investigative Site 1900 | Petofi | 2500 | Hungary |
| Clinical Investigative Site 1901 | Szentpeteri-Kapu | 3526 | Hungary |
| Clinical Investigative Site 2000 | Ashkelon | 78278 | Israel |
| Clinical Investigative Site 2003 | Tel Aviv | 64239 | Israel |
| Clinical Investigative Site 2001 | Tel Litwinsky | 52621 | Israel |
| Clinical Investigative Site 2002 | Ẕerifin | 70300 | Israel |
| Clinical Investigative Site 2101 | Gallarte | 21013 | Italy |
| Clinical Investigative Site 2104 | Genova | 16132 | Italy |
| Clinical Investigative Site # 2106 | Milan | 20132 | Italy |
| Clinical Investigative Site 2102 | Padova | 35128 | Italy |
| Clinical Investigative Site 2103 | Roma | 00189 | Italy |
| Clinical Investigative Site 2105 | Siena | 53100 | Italy |
| Clinical Investigative Site 2203 | Breda | 4818 | Netherlands |
| Clinical Investigative Site 2202 | Nijmegen | 6533 | Netherlands |
| Clinical Investigative Site 2201 | Sittard-Geleen | 6162 | Netherlands |
| Clinical Investigative Site 2305 | Katowice | 47-752 | Poland |
| Clinical Investigative Site 2303 | Poznan | 60-355 | Poland |
| Clinical Investigative Site 2304 | Warsaw | 02-957 | Poland |
| Clinical Investigative Site 2302 | Wroclaw | 50-044 | Poland |
| Clinical Investigative Site 2400 | Bucharest | 022903 | Romania |
| Clinical Investigative Site 2401 | Cluj-Napoca | 428063 | Romania |
| Clinical Investigative Site 2402 | Timișoara | 300736 | Romania |
| Clinical Investigative Site # 3202 | Moscow | 127018 | Russia |
| Clinical Investigative Site # 3203 | Nizhny Novgorod | 603155 | Russia |
| Clinical Investigative Site # 3206 | Pyatigorsk | 357538 | Russia |
| Clinical Investigative Site # 3204 | Saint Petersburg | 194354 | Russia |
| Clinical Investigative Site 3201 | Saint Petersburg | 197022 | Russia |
| Clinical Investigative Site 3200 | Saint Petersburg | 197376 | Russia |
| Clinical Investigative Site # 3201 | Samara | 443095 | Russia |
| Clinical Investigative Site 3209 | Saratov | 410030 | Russia |
| Clinical Investigative Site 3208 | Ufa | 450005 | Russia |
| Clinical Investigative Site 2501 | Belgrade | 11000 | Serbia |
| Clinical Investigative Site 2503 | Kragujevac | 34000 | Serbia |
| Clinical Investigative Site 2502 | Niš | 18000 | Serbia |
| Clinical Investigative Site 2706 | Barcelona | 08035 | Spain |
| Clinical Investigative Site 2702 | Madrid | 28040 | Spain |
| Clinical Investigative Site 2705 | Madrid | 28222 | Spain |
| Clinical Investigative Site 2701 | Málaga | 29010 | Spain |
| Clinical Investigative Site 2700 | Seville | 41009 | Spain |
| Clinical Investigative Site 2704 | Valencia | 46009 | Spain |
| Clinical Investigative Site 2802 | Gothenburg | 41345 | Sweden |
| Clinical Investigative Site 2800 | Stockholm | 17176 | Sweden |
| Clinical Investigative Site 2801 | Umed | 90185 | Sweden |
| Clinical Investigative Site 2901 | Lugano | CH-6900 | Switzerland |
| Clinical Investigative Site 2900 | Sankt Gallen | CH-9007 | Switzerland |
| Clinical Investigative Site 3302 | Chernihiv | 14029 | Ukraine |
| Clinical Investigative Site 3303 | Dnipropetrovsk | 49044 | Ukraine |
| Clinical Investigative Site 3300 | Kyiv | 03110 | Ukraine |
| Clinical Investigative Site 3304 | Odesa | 65000 | Ukraine |
| Clinical Investigative Site 3003 | Bristol | BS16 1LE | United Kingdom |
| Clinical Investigative Site 3004 | Devon | PL6 SBX | United Kingdom |
| Clinical Investigative Site 3002 | London | SE5 9RS | United Kingdom |
| Gisleskog PO, Valenzuela B, Scherz T, Burcklen M, Perez-Ruixo JJ, Poggesi I. An Exposure-Response Analysis of the Clinical Efficacy of Ponesimod in a Randomized Phase II Study in Patients with Multiple Sclerosis. Clin Pharmacokinet. 2021 Sep;60(9):1227-1237. doi: 10.1007/s40262-021-01020-2. Epub 2021 Apr 29. |
| Ponesimod 20 mg |
Participants received ponesimod capsules once daily as per up-titration schedule with an initial dose of 10 mg ponesimod on Days 1 to 7 followed by 20 mg ponesimod on Day 8 to Week 24. |
| FG002 | Ponesimod 10 mg | Participants received ponesimod capsules once daily as per up-titration schedule with a dose of 10 mg ponesimod on Day 1 to Week 24. |
| FG003 | Placebo | Participants received the ponesimod matching placebo tablets once daily for up to Week 24 as per up-titration schedule. |
| Treated |
|
| COMPLETED |
|
| NOT COMPLETED |
|
|
All-randomized analysis set included all randomized participants, whether or not they received study drug.
Not provided
| ID | Title | Description |
|---|---|---|
| BG000 | Ponesimod 40 mg | Participants received ponesimod capsules once daily as per up-titration schedule with an initial dose of 10 milligram (mg) ponesimod on Days 1 to 7 followed by first up-titration dose of 20 mg ponesimod on Days 8 to 14 and lastly received 40 mg ponesimod as second up-titration dose on Day 15 to Week 24. |
| BG001 | Ponesimod 20 mg | Participants received ponesimod capsules once daily as per up-titration schedule with an initial dose of 10 mg ponesimod on Days 1 to 7 followed by 20 mg ponesimod on Day 8 to Week 24. |
| BG002 | Ponesimod 10 mg | Participants received ponesimod capsules once daily as per up-titration schedule with a dose of 10 mg ponesimod on Day 1 to Week 24. |
| BG003 | Placebo | Participants received the ponesimod matching placebo tablets once daily for up to Week 24 as per up-titration schedule. |
| BG004 | Total | Total of all reporting groups |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean | Standard Deviation | years |
| |||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
| ||||||||||||||||
| Ethnicity (NIH/OMB) | Count of Participants | Participants |
| ||||||||||||||||
| Race (NIH/OMB) | Count of Participants | Participants |
| ||||||||||||||||
| Region of Enrollment | Count of Participants | Participants |
|
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Cumulative Number of New T1 Gadolinium-Enhancing (Gd+) Lesions on Magnetic Resonance Imaging (MRI) Scan From Week 12 to Week 24 | Cumulative Number of new T1 gadolinium-enhancing (Gd+) lesions per year on magnetic resonance imaging (MRI) scan from Week 12 to Week 24 were reported. Negative binomial (NB) regression analysis on Per protocol analysis set and imputation was applied for the missing data. Here, MS signifies multiple sclerosis. | Per protocol analysis set included participants of mITT set (randomized participants who received at least one dose of study drug, and had at least one valid post-baseline MRI) who met the criteria for evaluable participants for the analysis of MRI data (participants with Relapsing-remitting multiple sclerosis (RRMS) received study drug until 168 days, two post-baseline MRIs b/w Week 12-24, no forbidden treatment for MS). | Posted | Mean | Standard Deviation | Lesions | From Week 12 to 24 |
|
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Annualized Confirmed Relapse Rate | Relapse: occurrence of acute episode of one or more new symptoms or worsened symptoms of Multiple Sclerosis (MS), not associated with fever/infection and lasting 24 hours after stable 30 days period. Confirmed relapse: increase from baseline at least 0.5 point Expanded Disability Status Scale (EDSS) score or increase of one point in one, two or three Functional Systems (FS), excluding bowel/bladder and cerebral/mental FS. EDSS and FS scores are based on neurological examination for assessing its impairment in MS. Among eight FS, seven are ordinal clinical rating scales ranging from 0-5 or 6 with higher scale indicating overall functional impairment assessing Visual, Brain Stem, Pyramidal, Cerebellar, Sensory, Bowel/Bladder and Cerebral functions. Rating individual FS scores is used to rate EDSS with information concerning gait and use of assistance. EDSS is ordinal clinical scale ranges 0 (normal neurological examination) to 10(death due to MS) | All treated analysis set included all randomized participants who received at least one dose of study drug. | Posted | Mean | Standard Deviation | Relapse per year | Up to 24 weeks |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Secondary | Number of Participants With First Confirmed Relapse as Assessed by Kaplan-Meier Estimate From Baseline to Week 24 | Relapse: occurrence of acute episode of one or more new symptoms or worsened symptoms of MS, not associated with fever/infection and lasting 24 hours after stable 30 days period. Confirmed relapse: increase from baseline at least 0.5 point Expanded Disability Status Scale (EDSS) score or increase of one point in one, two or three Functional Systems (FS), excluding bowel/bladder and cerebral/mental FS. EDSS and FS scores are based on neurological examination for assessing its impairment in MS. Among eight FS, seven are ordinal clinical rating scales ranging from 0-5 or 6 with higher scale indicating overall functional impairment assessing Visual, Brain Stem, Pyramidal, Cerebellar, Sensory, Bowel/Bladder and Cerebral functions. Rating individual FS scores is used to rate EDSS with information concerning gait and use of assistance. EDSS is ordinal clinical scale ranges 0 (normal neurological examination) to 10(death due to MS). Kaplan-Meier estimate used for Outcome Measure analysis. | All treated analysis set included all randomized participants who received at least one dose of study drug. Here 'N' (number of participants analyzed) included all participants who were evaluated for this outcome measure. | Posted | Count of Participants | Participants | Baseline to Week 24 |
|
Up to 29 weeks (AEs for Treatment duration (24 weeks) and follow up (5 Weeks) on Day 7 and Day 30 after last dose)
All Treated Analysis set included all randomized participants who received at least one dose of study drug.
Not provided
| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Ponesimod 40 mg | Participants received ponesimod capsules once daily as per up-titration schedule with an initial dose of 10 milligram (mg) ponesimod on Days 1 to 7 followed by first up-titration dose of 20 mg ponesimod on Days 8 to 14 and lastly received 40 mg ponesimod as second up-titration dose on Day 15 to Week 24. | 0 | 119 | 3 | 119 | 83 | 119 |
| EG001 | Ponesimod 20 mg | Participants received ponesimod capsules once daily as per up-titration schedule with an initial dose of 10 mg ponesimod on Days 1 to 7 followed by 20 mg ponesimod on Day 8 to Week 24. | 0 | 114 | 7 | 114 | 73 | 114 |
| EG002 | Ponesimod 10 mg | Participants received ponesimod capsules once daily as per up-titration schedule with a dose of 10 mg ponesimod on Day 1 to Week 24. | 0 | 108 | 7 | 108 | 69 | 108 |
| EG003 | Placebo | Participants received the ponesimod matching placebo tablets once daily for up to Week 24 as per up-titration schedule. | 0 | 121 | 5 | 121 | 77 | 121 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Atrioventricular Block Second Degree | Cardiac disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Coronary Artery Disease | Cardiac disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Vertigo | Ear and labyrinth disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Macular Oedema | Eye disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Papilloedema | Eye disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Abdominal Pain Upper | Gastrointestinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Pyrexia | General disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Anaphylactoid Reaction | Immune system disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Appendicitis | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Cellulitis | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Measles | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Urinary Tract Infection Bacterial | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Alanine Aminotransferase Increased | Investigations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Aspartate Aminotransferase Increased | Investigations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Electrocardiogram QT Prolonged | Investigations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Nuclear Magnetic Resonance Imaging Abnormal | Investigations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Breast Cancer | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Cervix Carcinoma | Neoplasms benign, malignant and unspecified (incl cysts and polyps) | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Somnolence | Nervous system disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Postmenopausal Haemorrhage | Reproductive system and breast disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Dyspnoea | Respiratory, thoracic and mediastinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Pleural Effusion | Respiratory, thoracic and mediastinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Appendicectomy | Surgical and medical procedures | MedDRA Version 14.0 | Non-systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Lymphopenia | Blood and lymphatic system disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Bradycardia | Cardiac disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Palpitations | Cardiac disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Ear Pain | Ear and labyrinth disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Eye Pain | Eye disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Abdominal Pain | Gastrointestinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Abdominal Pain Upper | Gastrointestinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Diarrhoea | Gastrointestinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Dry Mouth | Gastrointestinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Dyspepsia | Gastrointestinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Nausea | Gastrointestinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Vomiting | Gastrointestinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Asthenia | General disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Chest Discomfort | General disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Disease Progression | General disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Fatigue | General disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Oedema Peripheral | General disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Pain | General disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Bronchitis | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Gastroenteritis | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Influenza | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Nasopharyngitis | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Oral Herpes | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Rhinitis | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Sinusitis | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Upper Respiratory Tract Infection | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Urinary Tract Infection | Infections and infestations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Contusion | Injury, poisoning and procedural complications | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Muscle Strain | Injury, poisoning and procedural complications | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Alanine Aminotransferase Increased | Investigations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Blood Cholesterol Increased | Investigations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Forced Expiratory Volume Decreased | Investigations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Hepatic Enzyme Increased | Investigations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Pulmonary Function Test Decreased | Investigations | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Hypercholesterolaemia | Metabolism and nutrition disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Arthralgia | Musculoskeletal and connective tissue disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Back Pain | Musculoskeletal and connective tissue disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Joint Swelling | Musculoskeletal and connective tissue disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Muscle Spasms | Musculoskeletal and connective tissue disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Musculoskeletal Chest Pain | Musculoskeletal and connective tissue disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Musculoskeletal Pain | Musculoskeletal and connective tissue disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Myalgia | Musculoskeletal and connective tissue disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Pain in Extremity | Musculoskeletal and connective tissue disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Dizziness | Nervous system disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Headache | Nervous system disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Hypoaesthesia | Nervous system disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Migraine | Nervous system disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Paraesthesia | Nervous system disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Affect Lability | Psychiatric disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Anxiety | Psychiatric disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Depression | Psychiatric disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Insomnia | Psychiatric disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Cough | Respiratory, thoracic and mediastinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Dyspnoea | Respiratory, thoracic and mediastinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
| |
| Oropharyngeal Pain | Respiratory, thoracic and mediastinal disorders | MedDRA Version 14.0 | Non-systematic Assessment |
|
No limitation was identified for this study.
If an investigator wishes to publish information from the study, a copy of the manuscript must be provided to the sponsor for review at least 60 days before submission for publication or presentation. If requested by the sponsor in writing, the investigator will withhold such publication for up to an additional 60 days.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Clinical Leader | Actelion Pharmaceuticals Ltd. | 844-434-4210 | ClinicalTrialDisclosure@its.jnj.com |
| ID | Term |
|---|---|
| D009103 | Multiple Sclerosis |
| ID | Term |
|---|---|
| D020278 | Demyelinating Autoimmune Diseases, CNS |
| D020274 | Autoimmune Diseases of the Nervous System |
| D009422 | Nervous System Diseases |
| D003711 | Demyelinating Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |
Not provided
Not provided
| Male |
|
| Not Hispanic or Latino |
|
| Unknown or Not Reported |
|
| Asian |
|
| Native Hawaiian or Other Pacific Islander |
|
| Black or African American |
|
| White |
|
| More than one race |
|
| Unknown or Not Reported |
|
| Austria |
|
| Belgium |
|
| Bulgaria |
|
| Canada |
|
| Finland |
|
| Czech Republic |
|
| France |
|
| Germany |
|
| Hungary |
|
| Israel |
|
| Italy |
|
| Netherlands |
|
| Poland |
|
| Romania |
|
| Russia |
|
| Spain |
|
| Serbia |
|
| Sweden |
|
| Switzerland |
|
| United Kingdom |
|
| Ukraine |
|
| United States |
|
| Treatment effect (rate ratio) |
| 0.170 |
| 2-Sided |
| 95 |
| 0.100 |
| 0.289 |
| Superiority |
| Negative binomial regression model | 0.0318 | Treatment effect (rate ratio) | 0.566 | 2-Sided | 95 | 0.337 | 0.952 | Superiority |
Participants received ponesimod capsules once daily as per up-titration schedule with an initial dose of 10 mg ponesimod on Days 1 to 7 followed by 20 mg ponesimod on Day 8 to Week 24. |
| OG002 | Ponesimod 10 mg | Participants received ponesimod capsules once daily as per up-titration schedule with a dose of 10 mg ponesimod on Day 1 to Week 24. |
| OG003 | Placebo | Participants received the ponesimod matching placebo tablets once daily for up to Week 24 as per up-titration schedule. |
|
|
| OG001 | Ponesimod 20 mg | Participants received ponesimod capsules once daily as per up-titration schedule with an initial dose of 10 mg ponesimod on Days 1 to 7 followed by 20 mg ponesimod on Day 8 to Week 24. |
| OG002 | Ponesimod 10 mg | Participants received ponesimod capsules once daily as per up-titration schedule with a dose of 10 mg ponesimod on Day 1 to Week 24. |
| OG003 | Placebo | Participants received the ponesimod matching placebo tablets once daily for up to Week 24 as per up-titration schedule. |
|
|