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Comparison · NCT04008069-d3aa683a

Double-Blind Sarilumab (Post-randomization) vs Double-Blind Placebo (Post-randomization): Number of Participants Without Sarcoidosis Flare (Flare-Free Survival)

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. Double-Blind Sarilumab (Post-randomization) vs Double-Blind Placebo (Post-randomization): Number of Participants Without Sarcoidosis Flare (Flare-Free Survival). Trial comparisons, record NCT04008069-d3aa683a. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT04008069-d3aa683a

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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 110.3421wilson
Risk in group 20.8750.5290.978wilson
Risk difference, group 1 minus group 20.125-0.5410.471newcombe hybrid score
Risk ratio, group 1 over group 21.140.881.49log
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to treat, for one more participant with the outcome on Double-Blind Sarilumab (Post-randomization) than on Double-Blind Placebo (Post-randomization)8from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Double-Blind Sarilumab (Post-randomization)After completing the open-label period, participants are randomized to receive sarilumab every two weeks for 12 weeks.22OG000
Group 2Double-Blind Placebo (Post-randomization)After completing the open-label period, participants are randomized receive placebo every two weeks for 12 weeks.78OG001

Outcome

Type
PRIMARY
Title
Number of Participants Without Sarcoidosis Flare (Flare-Free Survival)
Description
The primary outcome was flare-free survival of sarilumab-treated patients compared to placebo-treated controls. Patients will be considered to have flared if they receive rescue medication including increased glucocorticoids, or if they discontinue the study treatment in order to start a different therapy.
Time frame
Week 16 to Week 28
Population
Assessed in participants in the randomized-withdrawal period

Source ClinicalTrials.gov

Trial

Title
Sarilumab in Patients With Glucocorticoid-Dependent Sarcoidosis
NCT number
NCT04008069
Phases
PHASE2
Conditions
Sarcoidosis
Interventions
Sarilumab, Placebo
Lead sponsor
Stanford University
Results first posted
2023-10-05

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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