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Comparison · NCT02446899-22a460bd

Anifrolumab 300 mg vs Placebo: Number of Participants Who Achieved and Maintained an Oral Corticosteroids (OCS) Dose of ≤7.5 mg/Day at Week 52 in the Sub-Group of Participants With Baseline OCS ≥10 mg/Day

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. Anifrolumab 300 mg vs Placebo: Number of Participants Who Achieved and Maintained an Oral Corticosteroids (OCS) Dose of ≤7.5 mg/Day at Week 52 in the Sub-Group of Participants With Baseline OCS ≥10 mg/Day. Trial comparisons, record NCT02446899-22a460bd. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02446899-22a460bd

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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 10.5170.4140.619wilson
Risk in group 20.3010.2130.407wilson
Risk difference, group 1 minus group 20.2160.06810.351newcombe hybrid score
Risk ratio, group 1 over group 21.721.172.52log
Odds ratio, group 1 over group 22.491.324.67log
Number needed to treat, for one more participant with the outcome on Anifrolumab 300 mg than on Placebo4.632.8514.7from the risk difference interval

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Anifrolumab 300 mgAnifrolumab (300 mg) administered via an intravenous infusion (IV) every 4 weeks for up to 48 weeks (13 doses).4587OG000
Group 2PlaceboMatching placebo administered via an intravenous infusion (IV) every 4 weeks for up to 48 weeks (13 doses).2583OG001

Outcome

Type
SECONDARY
Title
Number of Participants Who Achieved and Maintained an Oral Corticosteroids (OCS) Dose of ≤7.5 mg/Day at Week 52 in the Sub-Group of Participants With Baseline OCS ≥10 mg/Day
Description
Maintained OCS reduction was defined by meeting all of the following criteria:~* Achieve an OCS dose of ≤7.5 mg/day prednisone or equivalent by Week 40~* Maintain an OCS dose ≤7.5 mg/day prednisone or equivalent from Week 40 to Week 52~* No discontinuation of investigational product~* No use of restricted medications beyond the protocol allowed threshold before assessment
Time frame
Week 40; Week 52
Population
Full Analysis Set: All participants who were randomized and received at least one dose of study drug, who had a baseline OCS dose of ≥10 mg/day.

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety of Anifrolumab Compared to Placebo in Adult Subjects With Active Systemic Lupus Erythematosus
NCT number
NCT02446899
Phases
PHASE3
Conditions
Active Systemic Lupus Erythematosus
Interventions
Anifrolumab, Placebo
Lead sponsor
AstraZeneca
Results first posted
2020-03-18

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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