ConductScience.org, home

Comparison · NCT00509145-sae

Laquinimod 0.6 mg vs Placebo: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. Laquinimod 0.6 mg vs Placebo: serious adverse events. Trial comparisons, record NCT00509145-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00509145-sae

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1110.08730.14wilson
Risk in group 20.09530.07360.123wilson
Risk difference, group 1 minus group 20.0156-0.02050.0518newcombe hybrid score
Risk ratio, group 1 over group 21.160.8211.65log
Odds ratio, group 1 over group 21.180.8031.75log
Number needed to harm, for one more participant with a serious adverse event on Laquinimod 0.6 mg than on Placebo64.2from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Laquinimod 0.6 mgLaquinimod 0.6 mg capsule taken orally once a day61550EG000
Group 2PlaceboMatching placebo capsule taken orally once a day53556EG001

Harm

What it counts
Total, serious adverse events
Time frame
Baseline to 24 months

Source ClinicalTrials.gov

Trial

Title
Safety and Efficacy of Orally Administered Laquinimod Versus Placebo for Treatment of Relapsing Remitting Multiple Sclerosis (RRMS)
NCT number
NCT00509145
Phases
PHASE3
Conditions
Multiple Sclerosis
Interventions
Laquinimod, Placebo
Lead sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
Results first posted
2021-11-02

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

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT00509145-sae