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Comparison · NCT01808144-sae

Lesinurad 200 mg + Febuxostat 80 mg vs Lesinurad 400 mg + Febuxostat 80 mg: serious adverse events

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

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

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ConductScience Library. Lesinurad 200 mg + Febuxostat 80 mg vs Lesinurad 400 mg + Febuxostat 80 mg: serious adverse events. Trial comparisons, record NCT01808144-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01808144-sae

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Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1650.1040.251wilson
Risk in group 20.1920.1260.28wilson
Risk difference, group 1 minus group 2-0.027-0.1340.0814newcombe hybrid score
Risk ratio, group 1 over group 20.8590.471.57log
Odds ratio, group 1 over group 20.8320.3991.73log
Number needed to treat, for one fewer participant with a serious adverse event on Lesinurad 200 mg + Febuxostat 80 mg than on Lesinurad 400 mg + Febuxostat 80 mg37.1from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Lesinurad 200 mg + Febuxostat 80 mg1697EG000
Group 2Lesinurad 400 mg + Febuxostat 80 mg1999EG001

Harm

What it counts
Total, serious adverse events
Time frame
Up to approximately 2.5 years (at Extension Month 12)

Source ClinicalTrials.gov

Trial

Title
Lesinurad and Febuxostat Combination Extension Study in Gout
NCT number
NCT01808144
Phases
PHASE3
Conditions
Gout
Interventions
lesinurad, lesinurad, febuxostat
Lead sponsor
Ardea Biosciences, Inc.
Results first posted
2018-01-30

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.

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