Comparison · NCT02373098-sae
Fingolimod 0.5 mg vs All Patients: serious adverse events
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Fingolimod 0.5 mg vs All Patients: serious adverse events. Trial comparisons, record NCT02373098-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02373098-sae
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0455 | 0.0156 | 0.125 | wilson | |
| Risk in group 2 | 0.0455 | 0.0156 | 0.125 | wilson | |
| Risk difference, group 1 minus group 2 | 0 | -0.0853 | 0.0853 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1 | 0.209 | 4.78 | log | |
| Odds ratio, group 1 over group 2 | 1 | 0.194 | 5.14 | log | |
| Number needed to harm | from the risk difference interval | the two groups' risks are equal |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Fingolimod 0.5 mg | Relapsing-remitting multiple sclerosis (RRMS) patients were treated with fingolimod 0.5 mg capsule od. | 3 | 66 | EG000 |
| Group 2 | All Patients | All patients in the trial | 3 | 66 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Adverse Events (AEs) are collected from First Patient First Visit (FPFV) until Last Patient Last Visit (LPLV). All AEs reported in this record are from date of First Patient First Visit until 30 days after Last Patient Last Visit) up to approximately 2 years.
Source ClinicalTrials.gov
Trial
- Title
- Fingolimod Effect on Cytokine and Chemokine Levels
- NCT number
- NCT02373098
- Phases
- PHASE4
- Conditions
- Relapsing Remitting Multiple Sclerosis
- Interventions
- Fingolimod 0.5 mg
- Lead sponsor
- Novartis Pharmaceuticals
- Results first posted
- 2019-09-30
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02373098?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
For software
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GET https://conductscience.org/api/comparisons/v1/NCT02373098-sae