Efficacy and Safety of Fingolimod in Patients With Relaps... | NCT00340834 | Trialant
NCT00340834
Sponsor
Novartis
Status
Completed
Last Update Posted
Sep 21, 2017Actual
Enrollment
1,292Actual
Phase
Phase 3
Conditions
Multiple Sclerosis
Interventions
Fingolimod 1.25 mg
Fingolimod 0.5 mg
Interferon β-1a 30 µg
Countries
United States
Argentina
Australia
Austria
Belgium
Brazil
Canada
Egypt
France
Germany
Greece
Hungary
Italy
Portugal
South Korea
Spain
Switzerland
United Kingdom
Protocol Section
Identification Module
NCT ID
NCT00340834
Obsolete or Duplicate NCT IDs
Not provided
Organization Study
CFTY720D2302
Secondary IDs
ID
Type
Description
Link
CFTY720D2302E1
Other Identifier
Novartis
Brief Title
Efficacy and Safety of Fingolimod in Patients With Relapsing-remitting Multiple Sclerosis With Optional Extension Phase
Official Title
A 12-month Double-blind, Randomized, Multicenter, Active-controlled, Parallel-group Study Comparing the Efficacy and Safety of 0.5 mg and 1.25 mg Fingolimod (FTY720) Administered Orally Once Daily Versus Interferon ß-1a (Avonex) Administered im Once Weekly in Patients With Relapsing-remitting Multiple Sclerosis With Optional Extension Phase
Acronym
TRANSFORMS
Organization
NovartisINDUSTRY
Status Module
Record Verification Date
Aug 2017
Overall Recruitment Status or Expanded Access Status
Completed
Last Known Status
Not provided
Delayed Posting
Not provided
Why Stopped
Not provided
Expanded Access Info
No
Start Date
May 2006
Primary Completion Date
Jul 2011Actual
Completion Date
Jul 2011Actual
First Submitted Date
Jun 19, 2006
First Submission Date that Met QC Criteria
Jun 20, 2006
First Posted Date
Jun 21, 2006Estimated
Results Waived
Not provided
Results First Submitted Date
Jan 4, 2011
Results First Submitted that Met QC Criteria
Apr 20, 2011
Results First Posted Date
May 16, 2011Estimated
Certification/Extension (aka Delayed Results) First Submitted Date
Not provided
Certification/Extension First Submitted that Passed QC Review
Not provided
Certification/Extension First Posted Date
Not provided
Last Update Submitted Date
Aug 18, 2017
Last Update Posted Date
Sep 21, 2017Actual
Sponsor/Collaborators Module
Responsible Party, by Official Title
Sponsor
Lead Sponsor
NovartisINDUSTRY
Collaborators
Not provided
Oversight Module
No data available
No data is available for this block.
Description Module
Brief Summary
This study assessed the safety, tolerability, and efficacy of 2 doses of oral fingolimod versus interferon β-1a to reduce the frequency of relapses in patients with relapsing-remitting multiple sclerosis.
Detailed Description
Not provided
Conditions Module
Conditions
Multiple Sclerosis
Keywords
FTY720
Interferon
RRMS
Multiple Sclerosis
Efficacy
Design Module
Study Type
Interventional
Number of References to an Expanded Access Study
Not provided
Expanded Access Types
Not provided
Patient Registry
Not provided
Target Follow-Up Duration
Not provided
Phases
Phase 3
Interventional Study Design
Allocation
Biospecimen
No data available
No data is available for this block.
Enrollment
1,292Actual
Arms/Interventions Module
Arm Groups
Label
Type
Description
Intervention Names
Fingolimod 1.25 mg
Experimental
Drug: Fingolimod 1.25 mg
Fingolimod 0.5 mg
Experimental
Drug: Fingolimod 0.5 mg
Interferon β-1a 30 µg
Active Comparator
Drug: Interferon β-1a 30 µg
Interventions
Name
Type
Description
Arm Group Labels
Other Names
Fingolimod 1.25 mg
Drug
Core: Patients self-administered fingolimod 1.25 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
Extension: Patients self-administered fingolimod 1.25 mg capsules orally once daily until switched to 0.5 mg capsules upon study protocol amendment.
Outcomes Module
Primary Outcomes
Measure
Description
Time Frame
Estimated Annualized Aggregate Relapse Rate (ARR) in the Core Phase of the Study
The ARR is defined as the number of confirmed relapses in a year. A relapse is defined as the appearance of a new or worsening of a previously stable or improving pre existing neurological abnormality, separated by at least 30 days from onset of a preceding relapse. The abnormality must be present for at least 24 hours and occur in the absence of fever or infection. The annualized ARR for each treatment group was calculated using negative binomial regression adjusted by treatment, country, number of relapses in the previous 2 years, and the baseline Expanded Disability Status Scale score.
Baseline to Month 12
Secondary Outcomes
Measure
Description
Time Frame
Number of New or Newly Enlarged T2 Lesions in Comparison With Baseline in the Core Phase of the Study
The number of new or newly enlarged T2 lesions in comparison to baseline was assessed with T2-weighted magnetic resonance image (MRI) scans. A T2-weighted MRI scan utilizes particular values of the echo time (TE) and the repetition time (TR) parameters of image acquisition. Inflammation and tissue damage are seen as bright areas in T2 images and are often referred to as T2 lesions. T2-weighted MRI scans are a sensitive way to evaluate the brain for demyelinating diseases, such as multiple sclerosis.
Other Outcomes
Not provided
Eligibility Module
Eligibility Criteria
Inclusion Criteria:
Male and female patients between ages 18-55 with a diagnosis of multiple sclerosis (MS)
Patients with a relapsing-remitting disease course
Patients with Expanded Disability Status Scale (EDSS) score of 0-5.5
Exclusion Criteria:
Patients with other chronic disease of the immune system, malignancies, acute pulmonary disease, cardiac failure, etc
Pregnant or nursing women
Patients who cannot tolerate treatment with an interferon
Other protocol-defined inclusion/exclusion criteria applied to the study.
Accepts Healthy Volunteers
No
Sex
All
Sex/Gender Based
Not provided
Sex/Gender Description
Not provided
Minimum Age
18 Years
Maximum Age
55 Years
Standard Ages
Adult
Study Population
Not provided
Sampling Method
Not provided
Contacts/Locations Module
Central Contacts
Not provided
Overall Officials
Name
Affiliation
Role
Novartis Pharmaceuticals
Novartis Pharmacuticals
Study Director
Locations
Facility
Status
City
State
ZIP
Country
Contacts
North Central Neurology Associates, PC, 1809 Kress Street
Patients randomized in the Core Phase (CP) to receive 0.5 mg or 1.25 mg fingolimod received the same dose in the Extension Phase (EP). Patients randomized to receive interferon-β-1a in the CP were re-randomized to receive either 0.5 mg or 1.25 mg fingolimod in a 1:1 ratio in the EP. Upon protocol amendment, all patients received 0.5 mg fingolimod.
Type of Units Analyzed
Not provided
Arm/Group Information
ID
Title
Description
FG000
Fingolimod 1.25 mg
Patients self-administered fingolimod 1.25 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
FG001
Fingolimod 0.5 mg
Periods
Title
Milestones
Reasons Not Completed
Core Phase of Study
Type
Comment
Milestone Data
STARTED
Baseline Characteristics Module
Baseline Analysis Population Description
Not provided
Outcome Measures Module
Outcome Measures
Adverse Events Module
Frequency Threshold
5
More Info Module
Limitations and Caveats
Not provided
Annotation Section
No data available
No data is available for this block.
Document Section
No data available
No data is available for this block.
Derived Section
Miscellaneous Info Module
Version Holder
Jul 10, 2026
Removed Countries
Puerto Rico
Submission Tracking
No data available
No data is available for this block.
Condition Browse Module
MeSH Terms
Intervention Browse Module
MeSH Terms
Randomized
Intervention Model
Parallel Assignment
Intervention Model Description
Not provided
Primary Purpose
Treatment
Observational Model
Not provided
Time Perspective
Not provided
Masking Info
Masking
Triple
Masking Description
Not provided
Who Masked
ParticipantCare ProviderOutcomes Assessor
Fingolimod 1.25 mg
FTY720
Fingolimod 0.5 mg
Drug
Core: Patients self-administered fingolimod 0.5 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
Extension: Patients self-administered fingolimod 0.5 mg capsules orally once daily.
Fingolimod 0.5 mg
FTY720
Interferon β-1a 30 µg
Drug
Core: Patients self-administered interferon β-1a 30 μg in an intramuscular (im) injection once weekly. In addition, they self-administered a fingolimod placebo capsule orally once daily.
Extension: Patients self-administered either fingolimod 1.25 mg or 0.5 mg capsules orally once daily until switched to 0.5 mg capsules upon study protocol amendment.
Interferon β-1a 30 µg
Baseline to Month 12
Percentage of Participants Free of 3-month Disability Progression Assessed With the Expanded Disability Status Scale (EDSS) at the End of the Core Phase of the Study
The EDSS is a scale for assessing disability in 8 functional systems (visual, brain stem, pyramidal, cerebellar, sensory, bowel & bladder, cerebral, other functions). An overall score ranging from 0 (normal) to 10 (death due to MS) is calculated. Disability progression was determined by the EDSS score based on the following criteria: One point increase from baseline in patients with baseline EDSS score from 0 to 5.0; or half a point increase in patients with baseline EDSS score of 5.5 or above. Percent of patients free of disability progression was calculated using the Kaplan-Meier method.
Baseline to Month 12
Estimated Annualized Aggregate Relapse Rate (ARR) in the Core and Extension Phases of the Study
The ARR is defined as the number of confirmed relapses in a year. A relapse is defined as the appearance of a new or worsening of a previously stable or improving pre existing neurological abnormality, separated by at least 30 days from onset of a preceding relapse. The abnormality must be present for at least 24 hours and occur in the absence of fever or infection. The annualized ARR for each treatment group was calculated using negative binomial regression adjusted by treatment, country, number of relapses in the previous 2 years, and the baseline Expanded Disability Status Scale score.
Month 0 to end of study (up to approximately 4.5 years)
Number of New or Newly Enlarged T2 Lesions in the Extension Phase of the Study
The number of new or newly enlarged T2 lesions in comparison to baseline was assessed with T2-weighted magnetic resonance image (MRI) scans. A T2-weighted MRI scan utilizes particular values of the echo time (TE) and the repetition time (TR) parameters of image acquisition. Inflammation and tissue damage are seen as bright areas in T2 images and are often referred to as T2 lesions. T2-weighted MRI scans are a sensitive way to evaluate the brain for demyelinating diseases, such as multiple sclerosis.
Month 12 to end of study (up to approximately 3.5 years)
Percentage of Participants Free of 3-month and 6-month Disability Progression Assessed With the Expanded Disability Status Scale (EDSS) at the End of the Extension Phase of the Study
The EDSS is a scale for assessing disability in 8 functional systems (visual, brain stem, pyramidal, cerebellar, sensory, bowel & bladder, cerebral, other functions). An overall score ranging from 0 (normal) to 10 (death due to MS) is calculated. Disability progression was determined by the EDSS score based on the following criteria: One point increase from baseline in patients with baseline EDSS score from 0 to 5.0; or half a point increase in patients with baseline EDSS score of 5.5 or above. Percent of patients free of disability progression was calculated using the Kaplan-Meier method.
Baseline to end of study (up to approximately 4.5 years)
Phoenix
Arizona
85013
United States
The Neurology Center, 3907 Waring Road, Suite 3
Oceanside
California
92056
United States
Associated Neurologists, PC, 69 Sand Pit Road, Suite 300
Danbury
Connecticut
06810
United States
Associated Neurologists of Southern CT, PC, 75 Kings Highway Cutoff
Fairfield
Connecticut
06824
United States
Yale University Multiple Sclerosis Center
New Haven
Connecticut
06510
United States
University of Florida Health Science Center
Jacksonville
Florida
32209
United States
Neurology Associates, PA, 301 N. Maitland Avenue, Suite A1
Maitland
Florida
32751
United States
University of Miami, Department of Neurology
Miami
Florida
33136
United States
Neurological Associates
Pompano Beach
Florida
33060
United States
Roskamp Institute, 2040 Whitfield Ave.
Sarasota
Florida
34243
United States
AMO Corporation
Tallahassee
Florida
32308
United States
Axiom Clinical Research of Florida, 2919 Swann Avenue, Suite 401
Tampa
Florida
33609
United States
University of South Florida, Department of Neurology
Tampa
Florida
33612
United States
The MS Center of Vero Beach
Vero Beach
Florida
32960
United States
University of Kansas Medical Center
Kansas City
Kansas
66160
United States
Mid America Neuroscience Institute, 8550 Marshall Drive, Suite 100
Lenexa
Kansas
66214
United States
University Physician Group, #1 Barnes-Jewish Hospital Plaza, Suite 16304
St Louis
Missouri
63110
United States
Neuroscience and Spine Center
Charlotte
North Carolina
28207
United States
Raleigh Neurology Associates, 1540 Sunday Drive
Raleigh
North Carolina
27607
United States
Neurology & Neuroscience Associates, Inc
Akron
Ohio
44302
United States
Northern Ohio Neuroscience, LLC
Bellevue
Ohio
44811
United States
Cleveland Clinic
Cleveland
Ohio
44195
United States
Oregon Neurology
Tualatin
Oregon
97062
United States
University of Pittsburgh, Department of Neurology
Pittsburgh
Pennsylvania
15213
United States
Absher Neurology, 274-A Commonwealth Drive
Greenville
South Carolina
29615
United States
Mountain Empire Neurological Associates, PC, 3183 West State Street, Suite 1201
Bristol
Tennessee
37620
United States
Advanced Neurosciences Institute
Franklin
Tennessee
37064
United States
Baylor College of Medicine
Houston
Texas
77030
United States
Private Practice, 3815 23rd Street
Lubbock
Texas
79410
United States
Integra Clinical Research, 4242 Medical Drive, Suite 6100
San Antonio
Texas
78229
United States
Swedish Neuroscience Institute
Seattle
Washington
98122
United States
Rockwood Clinic, P.S.
Spokane
Washington
99202
United States
West Virginia University Health Associates
Morgantown
West Virginia
26506
United States
Center for Neurological Disorders - Aurora St. Luke's Med Center
Milwaukee
Wisconsin
53215
United States
Ineba
Guarda Vieja 4435, Capital Federal
Buenos Aires
1428
Argentina
Fundacion Rosarina de Neurorehabilitacion
Rosario
Santa Fe Province
2000
Argentina
Instituto de Neurociencias de Rosario
Rosario
Santa Fe Province
2000
Argentina
Hospital Italiano de Buenos Aires
Buenos Aires
C118ACK
Argentina
Fundacion Lenox Cordoba
Córdoba
5000
Argentina
Hospital J. M. Ramos Mejia
General Urquiza 609, Buenos Aires
C1221ADC
Argentina
FLENI
Montaneses 2325, Buenos Aires
C1428AQK
Argentina
Strategic Health Evaluators
Chatswood
New South Wales
2067
Australia
Royal Prince Alfred Hospital
Department of Medicine, Level, Missenden R, Camperdown
New South Wales
2050
Australia
Liverpool Hospital, Neurology Department, Health Services Building, 4th Floor, Goulburn and Campbell Street
Khatri BO, Pelletier J, Kappos L, Hartung HP, Comi G, Barkhof F, von Rosenstiel P, Meng X, Grinspan A, Hashmonay R, Cohen JA; TRANSFORMS Study Group. Effect of prior treatment status and reasons for discontinuation on the efficacy and safety of fingolimod vs. interferon beta-1a intramuscular: Subgroup analyses of the Trial Assessing Injectable Interferon vs. Fingolimod Oral in Relapsing-Remitting Multiple Sclerosis (TRANSFORMS). Mult Scler Relat Disord. 2014 May;3(3):355-63. doi: 10.1016/j.msard.2013.11.006. Epub 2013 Dec 12.
Twiss J, Doward LC, McKenna SP, Eckert B. Interpreting scores on multiple sclerosis-specific patient reported outcome measures (the PRIMUS and U-FIS). Health Qual Life Outcomes. 2010 Oct 11;8:117. doi: 10.1186/1477-7525-8-117.
Cohen JA, Barkhof F, Comi G, Hartung HP, Khatri BO, Montalban X, Pelletier J, Capra R, Gallo P, Izquierdo G, Tiel-Wilck K, de Vera A, Jin J, Stites T, Wu S, Aradhye S, Kappos L; TRANSFORMS Study Group. Oral fingolimod or intramuscular interferon for relapsing multiple sclerosis. N Engl J Med. 2010 Feb 4;362(5):402-15. doi: 10.1056/NEJMoa0907839. Epub 2010 Jan 20.
Patients self-administered fingolimod 0.5 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
FG002
Interferon β-1a 30 µg
Patients self-administered interferon β-1a 30 μg in an intramuscular (im) injection once weekly. In addition, they self-administered a fingolimod placebo capsule orally once daily.
FG003
Interferon β-1a/Fingolimod 1.25 mg
Patients who received Interferon β-1a 30 µg in the core phase of the study were randomized to receive self-administered fingolimod 1.25 mg capsules orally once daily.
FG004
Interferon β-1a/Fingolimod 0.5 mg
Patients who received Interferon β-1a 30 µg in the core phase of the study were randomized to receive self-administered fingolimod 0.5 mg capsules orally once daily.
FG000426 subjects
FG001431 subjects
FG002435 subjects
FG0030 subjectsThis group was formed at the beginning of the extension phase of the study.
FG0040 subjectsThis group was formed at the beginning of the extension phase of the study.
COMPLETED
FG000369 subjectsOn study drug: 358, Off study drug: 11
FG001398 subjectsOn study drug: 385, Off study drug: 13
FG002386 subjectsOn study drug: 380, Off study drug: 6
FG0030 subjects
FG0040 subjects
NOT COMPLETED
FG00057 subjects
FG00133 subjects
FG00249 subjects
FG0030 subjects
FG0040 subjects
Type
Comment
Reasons
Adverse Event
FG00026 subjects
FG0019 subjects
FG0029 subjects
FG0030 subjects
FG0040 subjects
Withdrawal by Subject
FG00011 subjects
FG0019 subjects
FG00216 subjects
FG0030 subjects
FG004
Administrative Problems
FG0006 subjects
FG0012 subjects
FG0027 subjects
FG0030 subjects
FG004
Lack of Efficacy
FG0003 subjects
FG0013 subjects
FG0027 subjects
FG0030 subjects
FG004
Abnormal laboratory value(s)
FG0004 subjects
FG0016 subjects
FG0021 subjects
FG0030 subjects
FG004
Abnormal test procedure result(s)
FG0004 subjects
FG0013 subjects
FG0023 subjects
FG0030 subjects
FG004
Lost to Follow-up
FG0001 subjects
FG0011 subjects
FG0024 subjects
FG0030 subjects
FG004
Death
FG0002 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG004
Protocol Violation
FG0000 subjects
FG0010 subjects
FG0022 subjects
FG0030 subjects
FG004
Extension Phase of Study
Type
Comment
Milestone Data
STARTED
FG000330 subjectsEntry into the extension phase of the study was optional.
FG001357 subjectsEntry into the extension phase of the study was optional.
FG0020 subjectsThis group did not exist in the extension phase of the study.
FG003176 subjectsEntry into the extension phase of the study was optional.
FG004167 subjectsEntry into the extension phase of the study was optional.
Received Study Drug
FG000330 subjects
FG001356 subjects
FG0020 subjects
FG003174 subjects
FG004
COMPLETED
FG000245 subjects
FG001281 subjects
FG0020 subjects
FG003123 subjects
FG004
NOT COMPLETED
FG00085 subjects
FG00176 subjects
FG0020 subjects
FG00353 subjects
FG004
Type
Comment
Reasons
Subject did not receive study drug
FG0000 subjects
FG0011 subjects
FG0020 subjects
FG003
Type of Units Analyzed
Not provided
Arm/Group Information
ID
Title
Description
BG000
Fingolimod 1.25 mg
Patients self-administered fingolimod 1.25 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
BG001
Fingolimod 0.5 mg
Patients self-administered fingolimod 0.5 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
BG002
Interferon β-1a 30 µg
Patients self-administered interferon β-1a 30 μg in an intramuscular (im) injection once weekly. In addition, they self-administered a fingolimod placebo capsule orally once daily.
BG003
Interferon β-1a/Fingolimod 1.25 mg
Patients who received Interferon β-1a 30 µg in the core phase of the study were randomized to receive self-administered fingolimod 1.25 mg capsules orally once daily.
BG004
Interferon β-1a/Fingolimod 0.5 mg
Patients who received Interferon β-1a 30 µg in the core phase of the study were randomized to receive self-administered fingolimod 0.5 mg capsules orally once daily.
BG005
Total
Total of all reporting groups
Denominators
Units
Counts
Participants
BG000426
BG001431
BG002435
BG003174
BG004167
BG0051633
Baseline Measures
Title
Description
Population Description
Parameter Type
Dispersion Type
Unit of Measure
Calculate Percentage
Denominator Units Selected
Denominators
Classes
Age, Continuous
Core phase of study. Total number of patients is 1292. Demographics are based on the randomized population.
Mean
Standard Deviation
years
Title
Denominators
Categories
Title
Measurements
BG00035.8± 8.39
BG00136.7± 8.81
BG00236.0± 8.29
BG003
Age, Continuous
Extension phase of study. The number of patients in the optional extension phase was less than the overall number of baseline participants who started the study. Total number of patients is 1027. Demographics are based on the intent-to-treat population.
Mean
Standard Deviation
Years
Title
Denominators
Categories
Title
Measurements
BG00035.5± 8.42
BG001
Age, Customized
Core phase of study. Total number of patients is 1292. Demographics are based on the randomized population.
Number
Participants
Title
Denominators
Categories
< 18
Title
Measurements
BG0000
BG0010
BG002
Age, Customized
Extension phase of study. The number of patients in the optional extension phase was less than the overall number of baseline participants who started the study. Total number of patients is 1027. Demographics are based on the intent-to-treat population.
Number
Participants
Title
Denominators
Categories
< 18
Title
Measurements
BG0000
BG001
Sex: Female, Male
Core phase of study. Total number of patients is 1292. Demographics are based on the randomized population.
Count of Participants
Participants
Title
Denominators
Categories
Title
Measurements
Female
BG000293
BG001282
BG002
Sex/Gender, Customized
Extension phase of study. The number of patients in the optional extension phase was less than the overall number of baseline participants who started the study. Total number of patients is 1027. Demographics are based on the intent-to-treat population.
Number
Participants
Title
Denominators
Categories
Female
Title
Measurements
BG000227
BG001
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
Estimated Annualized Aggregate Relapse Rate (ARR) in the Core Phase of the Study
The ARR is defined as the number of confirmed relapses in a year. A relapse is defined as the appearance of a new or worsening of a previously stable or improving pre existing neurological abnormality, separated by at least 30 days from onset of a preceding relapse. The abnormality must be present for at least 24 hours and occur in the absence of fever or infection. The annualized ARR for each treatment group was calculated using negative binomial regression adjusted by treatment, country, number of relapses in the previous 2 years, and the baseline Expanded Disability Status Scale score.
Intent-to-treat population (ITT): All patients who were randomized and received at least 1 dose of study medication.
Posted
Number
95% Confidence Interval
Estimate relapses per year
Baseline to Month 12
ID
Title
Description
OG000
Fingolimod 1.25 mg
Patients self-administered fingolimod 1.25 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
OG001
Fingolimod 0.5 mg
Patients self-administered fingolimod 0.5 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
OG002
Interferon β-1a µg/Fingolimod 1.25 or 0.5 mg
Patients received Interferon β-1a 30 µg in the core phase of the study (Baseline to Month 12) and were then randomized to receive self administered fingolimod capsules orally once daily, either 1.25 or 0.5 mg, for the remainder of the study.
Units
Counts
Participants
OG000420
OG001429
OG002431
Title
Denominators
Categories
Title
Measurements
OG0000.203(0.157 to 0.264)
OG0010.161(0.122 to 0.212)
OG0020.331(0.262 to 0.417)
Secondary
Number of New or Newly Enlarged T2 Lesions in Comparison With Baseline in the Core Phase of the Study
The number of new or newly enlarged T2 lesions in comparison to baseline was assessed with T2-weighted magnetic resonance image (MRI) scans. A T2-weighted MRI scan utilizes particular values of the echo time (TE) and the repetition time (TR) parameters of image acquisition. Inflammation and tissue damage are seen as bright areas in T2 images and are often referred to as T2 lesions. T2-weighted MRI scans are a sensitive way to evaluate the brain for demyelinating diseases, such as multiple sclerosis.
Intent-to-treat population (ITT): All randomized patients who received at least 1 dose of study medication.
Posted
Mean
Standard Deviation
T2 lesions
Baseline to Month 12
ID
Title
Description
OG000
Fingolimod 1.25 mg
Patients self-administered fingolimod 1.25 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
OG001
Fingolimod 0.5 mg
Patients self-administered fingolimod 0.5 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
OG002
Interferon β-1a µg/Fingolimod 1.25 or 0.5 mg
Secondary
Percentage of Participants Free of 3-month Disability Progression Assessed With the Expanded Disability Status Scale (EDSS) at the End of the Core Phase of the Study
The EDSS is a scale for assessing disability in 8 functional systems (visual, brain stem, pyramidal, cerebellar, sensory, bowel & bladder, cerebral, other functions). An overall score ranging from 0 (normal) to 10 (death due to MS) is calculated. Disability progression was determined by the EDSS score based on the following criteria: One point increase from baseline in patients with baseline EDSS score from 0 to 5.0; or half a point increase in patients with baseline EDSS score of 5.5 or above. Percent of patients free of disability progression was calculated using the Kaplan-Meier method.
Intent-to-treat population (ITT): All randomized patients who received at least 1 dose of study medication.
Posted
Number
95% Confidence Interval
Percentage of participants
Baseline to Month 12
ID
Title
Description
OG000
Fingolimod 1.25 mg
Patients self-administered fingolimod 1.25 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
OG001
Fingolimod 0.5 mg
Patients self-administered fingolimod 0.5 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
Secondary
Estimated Annualized Aggregate Relapse Rate (ARR) in the Core and Extension Phases of the Study
The ARR is defined as the number of confirmed relapses in a year. A relapse is defined as the appearance of a new or worsening of a previously stable or improving pre existing neurological abnormality, separated by at least 30 days from onset of a preceding relapse. The abnormality must be present for at least 24 hours and occur in the absence of fever or infection. The annualized ARR for each treatment group was calculated using negative binomial regression adjusted by treatment, country, number of relapses in the previous 2 years, and the baseline Expanded Disability Status Scale score.
Intent-to-treat population (ITT): All patients who were randomized and received at least 1 dose of study medication.
Posted
Number
95% Confidence Interval
Estimated relapses per year
Month 0 to end of study (up to approximately 4.5 years)
ID
Title
Description
OG000
Fingolimod 1.25 mg
Patients self-administered fingolimod 1.25 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
OG001
Fingolimod 0.5 mg
Patients self-administered fingolimod 0.5 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
Secondary
Number of New or Newly Enlarged T2 Lesions in the Extension Phase of the Study
The number of new or newly enlarged T2 lesions in comparison to baseline was assessed with T2-weighted magnetic resonance image (MRI) scans. A T2-weighted MRI scan utilizes particular values of the echo time (TE) and the repetition time (TR) parameters of image acquisition. Inflammation and tissue damage are seen as bright areas in T2 images and are often referred to as T2 lesions. T2-weighted MRI scans are a sensitive way to evaluate the brain for demyelinating diseases, such as multiple sclerosis.
Intent-to-treat population (ITT): All randomized patients who received at least 1 dose of study medication.
Posted
Mean
Standard Deviation
T2 lesions
Month 12 to end of study (up to approximately 3.5 years)
ID
Title
Description
OG000
Fingolimod 1.25 mg
Patients self-administered fingolimod 1.25 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
OG001
Fingolimod 0.5 mg
Patients self-administered fingolimod 0.5 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
OG002
Interferon β-1a µg/Fingolimod 1.25 or 0.5 mg
Secondary
Percentage of Participants Free of 3-month and 6-month Disability Progression Assessed With the Expanded Disability Status Scale (EDSS) at the End of the Extension Phase of the Study
The EDSS is a scale for assessing disability in 8 functional systems (visual, brain stem, pyramidal, cerebellar, sensory, bowel & bladder, cerebral, other functions). An overall score ranging from 0 (normal) to 10 (death due to MS) is calculated. Disability progression was determined by the EDSS score based on the following criteria: One point increase from baseline in patients with baseline EDSS score from 0 to 5.0; or half a point increase in patients with baseline EDSS score of 5.5 or above. Percent of patients free of disability progression was calculated using the Kaplan-Meier method.
Intent-to-treat population (ITT): All randomized patients who received at least 1 dose of study medication.
Posted
Number
95% Confidence Interval
Percentage of participants
Baseline to end of study (up to approximately 4.5 years)
ID
Title
Description
OG000
Fingolimod 1.25 mg
Patients self-administered fingolimod 1.25 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
OG001
Fingolimod 0.5 mg
Patients self-administered fingolimod 0.5 mg capsules orally once daily. In addition, they self-administered an interferon β-1a placebo intramuscular (im) injection once weekly.
Time Frame
Not provided
Description
Not provided
All-Cause Mortality Comment
Not provided
Arm/Groups
ID
Title
Description
Deaths (Affected)
Deaths (At Risk)
Serious Events (Affected)
Serious Events (At Risk)
Other Events (Affected)
Other Events (At Risk)
EG000
COR FTY720 1.25 mg
COR FTY720 1.25 mg
45
420
310
420
EG001
COR FTY720 0.5 mg
COR FTY720 0.5 mg
30
429
302
429
EG002
COR Interferon Beta-1a
COR Interferon beta-1a
25
431
359
431
EG003
EXT FTY720 1.25 mg
EXT FTY720 1.25 mg
77
504
446
504
EG004
EXT FTY720 0.5 mg
EXT FTY720 0.5 mg
76
523
439
523
Serious Adverse Events
Term
Organ System
Source Vocabulary
Assessment Type
Notes
Statistical Information
Autoimmune thrombocytopenia
Blood and lymphatic system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG0031 affected504 at risk
EG004
Iron deficiency anaemia
Blood and lymphatic system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Leukopenia
Blood and lymphatic system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Lymphadenopathy
Blood and lymphatic system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Lymphopenia
Blood and lymphatic system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Splenomegaly
Blood and lymphatic system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Angina unstable
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Arrhythmia
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Atrial fibrillation
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Atrioventricular block complete
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Atrioventricular block first degree
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0002 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Atrioventricular block second degree
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0003 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Bradycardia
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0008 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Cardiogenic shock
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Coronary artery disease
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Coronary artery occlusion
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Myocardial infarction
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Palpitations
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Sinus bradycardia
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0002 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Sinus tachycardia
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Supraventricular extrasystoles
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Ventricular extrasystoles
Cardiac disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Atrial septal defect
Congenital, familial and genetic disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Congenital absence of cranial vault
Congenital, familial and genetic disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Congenital anomaly in offspring
Congenital, familial and genetic disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Ear disorder
Ear and labyrinth disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Tinnitus
Ear and labyrinth disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Vertigo
Ear and labyrinth disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Goitre
Endocrine disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Cystoid macular oedema
Eye disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Diplopia
Eye disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Macular oedema
Eye disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Tolosa-Hunt syndrome
Eye disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Abdominal pain
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Abdominal pain lower
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Anal skin tags
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Colitis
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Constipation
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Crohn's disease
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Gastritis
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Haemorrhoidal haemorrhage
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Inguinal hernia
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Nausea
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Pancreatitis acute
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Peritonitis
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Rectal haemorrhage
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Sigmoiditis
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Vomiting
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Abasia
General disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Chest discomfort
General disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Complication of device insertion
General disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Influenza like illness
General disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Multi-organ failure
General disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Non-cardiac chest pain
General disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Pyrexia
General disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Biliary colic
Hepatobiliary disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Cholangitis acute
Hepatobiliary disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Cholecystitis acute
Hepatobiliary disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Cholelithiasis
Hepatobiliary disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0021 affected431 at risk
EG003
Jaundice
Hepatobiliary disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Abscess sweat gland
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Administration site infection
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Anal abscess
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Appendicitis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0002 affected420 at risk
EG0010 affected429 at risk
EG0022 affected431 at risk
EG003
Bartholin's abscess
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Cholecystitis infective
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Chronic tonsillitis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Cystitis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Encephalitis herpes
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Encephalitis viral
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Gastroenteritis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Gastrointestinal candidiasis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Helicobacter gastritis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Herpes ophthalmic
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Herpes virus infection
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Herpes zoster
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Herpes zoster disseminated
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Herpes zoster ophthalmic
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Incision site abscess
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Influenza
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Laryngitis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Lower respiratory tract infection
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Nasopharyngitis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Papilloma viral infection
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Perirectal abscess
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Pneumonia
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Pyelonephritis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Salpingitis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Septic encephalopathy
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Urinary tract infection
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Urosepsis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Varicella
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Viral infection
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Ankle fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Complicated fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Facial bones fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Fall
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Femoral neck fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Incisional hernia
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Jaw fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Laceration
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Ligament rupture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Lower limb fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Meniscus lesion
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Patella fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Radius fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Rib fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Road traffic accident
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0021 affected431 at risk
EG003
Skull fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Tendon rupture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Upper limb fracture
Injury, poisoning and procedural complications
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Electrocardiogram QT prolonged
Investigations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Electrocardiogram ST segment elevation
Investigations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Hepatic enzyme increased
Investigations
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Human papilloma virus test positive
Investigations
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Lymphocyte count decreased
Investigations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Weight decreased
Investigations
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Abnormal loss of weight
Metabolism and nutrition disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Decreased appetite
Metabolism and nutrition disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Diabetes mellitus
Metabolism and nutrition disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Arthralgia
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Back pain
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Foot deformity
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Intervertebral disc protrusion
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Lumbar spinal stenosis
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Muscle spasms
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Muscular weakness
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Musculoskeletal chest pain
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Osteoarthritis
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Osteonecrosis
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Plica syndrome
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Rotator cuff syndrome
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Sjogren's syndrome
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Spondylolisthesis
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Synovial cyst
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Basal cell carcinoma
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0002 affected420 at risk
EG0012 affected429 at risk
EG0020 affected431 at risk
EG003
Benign mediastinal neoplasm
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Benign neoplasm of thyroid gland
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Bone neoplasm malignant
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Breast cancer
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0002 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Breast cancer in situ
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Lymphoma
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Malignant melanoma
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0012 affected429 at risk
EG0020 affected431 at risk
EG003
Malignant melanoma in situ
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Neoplasm malignant
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Ovarian epithelial cancer
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Ovarian neoplasm
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Squamous cell carcinoma
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Squamous cell carcinoma of skin
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Testis cancer
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Thyroid cancer
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Transitional cell carcinoma
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Uterine leiomyoma
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0021 affected431 at risk
EG003
Ataxia
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Carotid artery occlusion
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Carotid artery stenosis
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Central nervous system lesion
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Cerebral ischaemia
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Cervicobrachial syndrome
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Cognitive disorder
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Coma
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Critical illness polyneuropathy
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Demyelination
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Dural fistula
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Facial neuralgia
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Grand mal convulsion
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Headache
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Migraine
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Multiple sclerosis relapse
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0021 affected431 at risk
EG003
Nerve root lesion
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Neuropathy peripheral
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Optic neuritis
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003
Paraesthesia
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Paraparesis
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Presyncope
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Progressive relapsing multiple sclerosis
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Radicular syndrome
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Radiculitis
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Sciatica
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Sensorimotor disorder
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Spinal cord ischaemia
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Status epilepticus
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Tension headache
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Transient ischaemic attack
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Abortion
Pregnancy, puerperium and perinatal conditions
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0021 affected431 at risk
EG003
Abortion spontaneous
Pregnancy, puerperium and perinatal conditions
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Complication of pregnancy
Pregnancy, puerperium and perinatal conditions
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Unintended pregnancy
Pregnancy, puerperium and perinatal conditions
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Completed suicide
Psychiatric disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Depression
Psychiatric disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Generalised anxiety disorder
Psychiatric disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Paranoia
Psychiatric disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Suicide attempt
Psychiatric disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Nephrolithiasis
Renal and urinary disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0021 affected431 at risk
EG003
Acquired hydrocele
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Adenomyosis
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Cervical dysplasia
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Epididymitis
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Haemorrhagic ovarian cyst
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Infertility
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Menometrorrhagia
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Menorrhagia
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Spermatocele
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Testicular pain
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Uterine polyp
Reproductive system and breast disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Asthma
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Dyspnoea
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG0002 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Hyperventilation
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Hypoxia
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Lung disorder
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Pleurisy
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Pneumonia aspiration
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Pneumothorax
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0011 affected429 at risk
EG0021 affected431 at risk
EG003
Pulmonary embolism
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Psoriasis
Skin and subcutaneous tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Skin lesion
Skin and subcutaneous tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Urticaria
Skin and subcutaneous tissue disorders
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Abortion induced
Surgical and medical procedures
MedDRA 11.1
Systematic Assessment
EG0000 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Arterial occlusive disease
Vascular disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Hypertensive crisis
Vascular disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Peripheral arterial occlusive disease
Vascular disorders
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0010 affected429 at risk
EG0020 affected431 at risk
EG003
Other Adverse Events
Term
Organ System
Source Vocabulary
Assessment Type
Notes
Statistical Information
Lymphopenia
Blood and lymphatic system disorders
MedDRA 11.1
Systematic Assessment
EG0003 affected420 at risk
EG0011 affected429 at risk
EG0020 affected431 at risk
EG003108 affected504 at risk
EG00477 affected523 at risk
Diarrhoea
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG00035 affected420 at risk
EG00132 affected429 at risk
EG00221 affected431 at risk
EG003
Nausea
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG00029 affected420 at risk
EG00140 affected429 at risk
EG00229 affected431 at risk
EG003
Toothache
Gastrointestinal disorders
MedDRA 11.1
Systematic Assessment
EG00018 affected420 at risk
EG00112 affected429 at risk
EG0029 affected431 at risk
EG003
Fatigue
General disorders
MedDRA 11.1
Systematic Assessment
EG00060 affected420 at risk
EG00144 affected429 at risk
EG00245 affected431 at risk
EG003
Influenza like illness
General disorders
MedDRA 11.1
Systematic Assessment
EG00015 affected420 at risk
EG00115 affected429 at risk
EG002158 affected431 at risk
EG003
Pyrexia
General disorders
MedDRA 11.1
Systematic Assessment
EG00014 affected420 at risk
EG00118 affected429 at risk
EG00276 affected431 at risk
EG003
Bronchitis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG00019 affected420 at risk
EG00120 affected429 at risk
EG00211 affected431 at risk
EG003
Gastroenteritis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG00012 affected420 at risk
EG00110 affected429 at risk
EG00211 affected431 at risk
EG003
Influenza
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG00028 affected420 at risk
EG00129 affected429 at risk
EG00232 affected431 at risk
EG003
Nasopharyngitis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG00093 affected420 at risk
EG00188 affected429 at risk
EG00288 affected431 at risk
EG003
Oral herpes
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG0009 affected420 at risk
EG0013 affected429 at risk
EG0027 affected431 at risk
EG003
Pharyngitis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG00019 affected420 at risk
EG00113 affected429 at risk
EG00213 affected431 at risk
EG003
Sinusitis
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG00018 affected420 at risk
EG00110 affected429 at risk
EG00211 affected431 at risk
EG003
Upper respiratory tract infection
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG00036 affected420 at risk
EG00131 affected429 at risk
EG00227 affected431 at risk
EG003
Urinary tract infection
Infections and infestations
MedDRA 11.1
Systematic Assessment
EG00024 affected420 at risk
EG00126 affected429 at risk
EG00221 affected431 at risk
EG003
Alanine aminotransferase increased
Investigations
MedDRA 11.1
Systematic Assessment
EG00024 affected420 at risk
EG00128 affected429 at risk
EG0028 affected431 at risk
EG003
Gamma-glutamyltransferase increased
Investigations
MedDRA 11.1
Systematic Assessment
EG00019 affected420 at risk
EG00114 affected429 at risk
EG0021 affected431 at risk
EG003
Lymphocyte count decreased
Investigations
MedDRA 11.1
Systematic Assessment
EG0001 affected420 at risk
EG0012 affected429 at risk
EG0020 affected431 at risk
EG003
Hypercholesterolaemia
Metabolism and nutrition disorders
MedDRA 11.1
Systematic Assessment
EG0009 affected420 at risk
EG00110 affected429 at risk
EG0023 affected431 at risk
EG003
Arthralgia
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG00017 affected420 at risk
EG00112 affected429 at risk
EG00224 affected431 at risk
EG003
Back pain
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG00027 affected420 at risk
EG00126 affected429 at risk
EG00223 affected431 at risk
EG003
Myalgia
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG00014 affected420 at risk
EG00114 affected429 at risk
EG00244 affected431 at risk
EG003
Pain in extremity
Musculoskeletal and connective tissue disorders
MedDRA 11.1
Systematic Assessment
EG00020 affected420 at risk
EG00121 affected429 at risk
EG00228 affected431 at risk
EG003
Melanocytic naevus
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA 11.1
Systematic Assessment
EG00042 affected420 at risk
EG00128 affected429 at risk
EG00224 affected431 at risk
EG003
Dizziness
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG00023 affected420 at risk
EG00126 affected429 at risk
EG00221 affected431 at risk
EG003
Headache
Nervous system disorders
MedDRA 11.1
Systematic Assessment
EG00096 affected420 at risk
EG00199 affected429 at risk
EG00288 affected431 at risk
EG003
Depression
Psychiatric disorders
MedDRA 11.1
Systematic Assessment
EG00018 affected420 at risk
EG00121 affected429 at risk
EG00232 affected431 at risk
EG003
Insomnia
Psychiatric disorders
MedDRA 11.1
Systematic Assessment
EG00019 affected420 at risk
EG00117 affected429 at risk
EG00213 affected431 at risk
EG003
Cough
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG00030 affected420 at risk
EG00120 affected429 at risk
EG00216 affected431 at risk
EG003
Dyspnoea
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG00021 affected420 at risk
EG0018 affected429 at risk
EG0027 affected431 at risk
EG003
Oropharyngeal pain
Respiratory, thoracic and mediastinal disorders
MedDRA 11.1
Systematic Assessment
EG00020 affected420 at risk
EG00117 affected429 at risk
EG00215 affected431 at risk
EG003
Hypertension
Vascular disorders
MedDRA 11.1
Systematic Assessment
EG00021 affected420 at risk
EG00116 affected429 at risk
EG0028 affected431 at risk
EG003
Certain Agreements
Are all PI(s) employees of the sponsor?
No
Restriction Type
OTHER
Results Disclosure Restriction on PI(s)?
Yes
Other Details
There IS an agreement between the Principal Investigator and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
The terms and conditions of Novartis' agreements with its investigators may vary. However, Novartis does not prohibit any investigator from publishing. Any publications from a single-site are postponed until the publication of the pooled data (ie, data from all sites) in the clinical trial.
Point of Contact
Title
Organization
Phone
Extension
Email
Study Director
Novartis Pharmaceuticals
862-778-8300
ID
Term
D009103
Multiple Sclerosis
Ancestor Terms
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
Browse Leaves
Not provided
Browse Branches
Not provided
ID
Term
D000068876
Fingolimod Hydrochloride
Ancestor Terms
ID
Term
D013110
Sphingosine
D000605
Amino Alcohols
D000438
Alcohols
D009930
Organic Chemicals
D011409
Propylene Glycols
D006018
Glycols
D000588
Amines
Browse Leaves
Not provided
Browse Branches
Not provided
0 subjects
0 subjects
0 subjects
0 subjects
0 subjects
0 subjects
0 subjects
0 subjects
167 subjects
123 subjects
44 subjects
2 subjects
FG0040 subjects
Subject withdrew consent
FG00026 subjects
FG00131 subjects
FG0020 subjects
FG00312 subjects
FG00415 subjects
Adverse Event
FG00021 subjects
FG00122 subjects
FG0020 subjects
FG00319 subjects
FG0047 subjects
Abnormal laboratory value(s)
FG00014 subjects
FG00113 subjects
FG0020 subjects
FG00313 subjects
FG0044 subjects
Unsatisfactory therapeutic effect
FG00013 subjects
FG0017 subjects
FG0020 subjects
FG0034 subjects
FG0049 subjects
Lost to Follow-up
FG0001 subjects
FG0011 subjects
FG0020 subjects
FG0032 subjects
FG0043 subjects
Subject no longer requires study drug
FG0004 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG0042 subjects
Administrative problems
FG0003 subjects
FG0010 subjects
FG0020 subjects
FG0031 subjects
FG0041 subjects
Abnormal test procedure result(s)
FG0000 subjects
FG0011 subjects
FG0020 subjects
FG0030 subjects
FG0042 subjects
Protocol Violation
FG0003 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG0040 subjects
Death
FG0000 subjects
FG0010 subjects
FG0020 subjects
FG0030 subjects
FG0041 subjects
NA
± NA
This group did not exist in the core phase of the study.
BG004NA± NAThis group did not exist in the core phase of the study.
BG00536.2± 8.50
36.5
± 8.67
BG002NA± NAThis group did not exist in the extension phase of the study.
BG00336.1± 8.11
BG00436.1± 8.59
BG00536.0± 8.48
0
BG003NAThis group did not exist in the core phase of the study.
BG004NAThis group did not exist in the core phase of the study.
BG0050
18-30
Title
Measurements
BG000125
BG001117
BG002113
BG003NAThis group did not exist in the core phase of the study.
BG004NAThis group did not exist in the core phase of the study.
BG005355
31-40
Title
Measurements
BG000160
BG001150
BG002185
BG003NAThis group did not exist in the core phase of the study.
BG004NAThis group did not exist in the core phase of the study.
BG005495
41-55
Title
Measurements
BG000141
BG001164
BG002137
BG003NAThis group did not exist in the core phase of the study.
BG004NAThis group did not exist in the core phase of the study.
BG005442
> 55
Title
Measurements
BG0000
BG0010
BG0020
BG003NAThis group did not exist in the core phase of the study.
BG004NAThis group did not exist in the core phase of the study.
BG0050
0
BG002NAThis group did not exist in the extension phase of the study.
BG0030
BG0040
BG0050
18-30
Title
Measurements
BG000100
BG00198
BG002NAThis group did not exist in the extension phase of the study.
BG00339
BG00448
BG005285
31-40
Title
Measurements
BG000122
BG001127
BG002NAThis group did not exist in the extension phase of the study.
BG00383
BG00462
BG005394
41-55
Title
Measurements
BG000108
BG001131
BG002NAThis group did not exist in the extension phase of the study.
BG00352
BG00457
BG005348
>55
Title
Measurements
BG0000
BG0010
BG002NAThis group did not exist in the extension phase of the study.
BG0030
BG0040
BG0050
295
BG003NAThis group did not exist in the core phase of the study.
BG004NAThis group did not exist in the core phase of the study.
BG005NATotal not calculated because data are not available (NA) in one or more arms.
Male
BG000133
BG001149
BG002140
BG003NAThis group did not exist in the core phase of the study.
BG004NAThis group did not exist in the core phase of the study.
BG005NATotal not calculated because data are not available (NA) in one or more arms.
235
BG002NAThis group did not exist in the extension phase of the study.
BG003114
BG004109
BG005685
Male
Title
Measurements
BG000103
BG001121
BG002NAThis group did not exist in the extension phase of the study.
BG00360
BG00458
BG005342
Patients received Interferon β-1a 30 µg in the core phase of the study (Baseline to Month 12) and were then randomized to receive self administered fingolimod capsules orally once daily, either 1.25 or 0.5 mg, for the remainder of the study.
Units
Counts
Participants
OG000420
OG001429
OG002431
Title
Denominators
Categories
Title
Measurements
OG0001.6± 3.23
OG0011.6± 3.16
OG0022.6± 5.50
OG002
Interferon β-1a µg/Fingolimod 1.25 or 0.5 mg
Patients received Interferon β-1a 30 µg in the core phase of the study (Baseline to Month 12) and were then randomized to receive self administered fingolimod capsules orally once daily, either 1.25 or 0.5 mg, for the remainder of the study.
Units
Counts
Participants
OG000420
OG001429
OG002431
Title
Denominators
Categories
Title
Measurements
OG00093.3(90.92 to 95.77)
OG00194.1(91.82 to 96.33)
OG00292.1(89.45 to 94.66)
OG002
Interferon β-1a µg/Fingolimod 1.25 or 0.5 mg
Patients received Interferon β-1a 30 µg in the core phase of the study (Baseline to Month 12) and were then randomized to receive self administered fingolimod capsules orally once daily, either 1.25 or 0.5 mg, for the remainder of the study.
Units
Counts
Participants
OG000420
OG001429
OG002431
Title
Denominators
Categories
Month 12 to Month 24, n=330, 356, 341
Title
Measurements
OG0000.156(0.114 to 0.214)
OG0010.182(0.138 to 0.242)
OG0020.266(0.207 to 0.341)
Month 24 to Month 36, n=287, 321, 293
Title
Measurements
OG0000.116(0.079 to 0.169)
OG0010.110(0.076 to 0.160)
OG0020.121(0.084 to 0.176)
Month 36 to Month 48, n=267, 303, 271
Title
Measurements
OG000NA(NA to NA)Not estimable due to sparse data.
OG001NA(NA to NA)Not estimable due to sparse data.
OG002NA(NA to NA)Not estimable due to sparse data.
Month 48 to end of study, n=36, 38, 29
Title
Measurements
OG000NA(NA to NA)Not estimable due to sparse data.
OG001NA(NA to NA)Not estimable due to sparse data.
OG002NA(NA to NA)Not estimable due to sparse data.
Month 0 to end of study, n=420, 429, 431
Title
Measurements
OG0000.192(0.160 to 0.229)
OG0010.166(0.139 to 0.199)
OG0020.271(0.230 to 0.318)
Patients received Interferon β-1a 30 µg in the core phase of the study (Baseline to Month 12) and were then randomized to receive self administered fingolimod capsules orally once daily, either 1.25 or 0.5 mg, for the remainder of the study.
Units
Counts
Participants
OG000279
OG001317
OG002288
Title
Denominators
Categories
Month 12 to Month 24
Title
Measurements
OG0001.08± 2.644
OG0010.87± 1.624
OG0020.97± 1.923
Month 24 to Month 36, n=255, 289, 258
Title
Measurements
OG0001.40± 3.418
OG0011.04± 4.408
OG0020.72± 1.733
Month 36 to Month 48, n=36, 34, 35
Title
Measurements
OG0000.97± 1.682
OG0010.59± 1.438
OG0020.49± 1.483
Last MRI scan to end of study, n=275, 309, 290
Title
Measurements
OG0001.75± 7.248
OG0010.86± 2.674
OG0021.03± 4.350
OG002
Interferon β-1a µg/Fingolimod 1.25 or 0.5 mg
Patients received Interferon β-1a 30 µg in the core phase of the study (Baseline to Month 12) and were then randomized to receive self administered fingolimod capsules orally once daily, either 1.25 or 0.5 mg, for the remainder of the study.