ConductScience.org, home

Comparison · NCT01705977-87860c77

Belimumab 10 mg/kg vs Placebo: Number of Deaths Reported - On-study Period (Week 52)

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. Belimumab 10 mg/kg vs Placebo: Number of Deaths Reported - On-study Period (Week 52). Trial comparisons, record NCT01705977-87860c77. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01705977-87860c77

On this page

Measures6

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

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.006490.00380.0111wilson
Risk in group 20.0110.007270.0166wilson
Risk difference, group 1 minus group 2-0.0045-0.01070.0014newcombe hybrid score
Risk ratio, group 1 over group 20.5910.2981.17log
Odds ratio, group 1 over group 20.5880.2951.17log
Number needed to treat, for one fewer participant with the outcome on Belimumab 10 mg/kg than on Placebo222from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Belimumab 10 mg/kg
Participants received belimumab 10 milligrams per kilogram (mg/kg) on Days 0, 14, 28 and every 28 days through Week 48 with a final visit conducted at Week 52. Participants continued to receive standard SLE treatment and were followed up until end of study (up to 5 years).
132,002OG001
Group 2Placebo
Participants received placebo via the intravenous route on Days 0, 14, 28 and every 28 days through Week 48 with a final visit conducted at Week 52. Participants continued to receive standard SLE treatment and were followed up until end of study (up to 5 years).
222,001OG000

Outcome

Type
SECONDARY
Title
Number of Deaths Reported - On-study Period (Week 52)
Description
Number of participants who died during on-study period (Week 52) is reported. The on-study period (which includes on and off treatment data) was defined as first dose to the end of the Week 52 study follow-up (or death). The on-study period was a supportive analysis period for safety analysis.
Time frame
Up to Week 52 (On-study period)
Population
As-Treated Population. One participant in placebo group who received belimumab \>50% of the time was reported in the belimumab group.

Source ClinicalTrials.gov

Trial

Title
Belimumab Assessment of Safety in SLE
NCT number
NCT01705977
Phases
PHASE4
Conditions
Systemic Lupus Erythematosus
Interventions
Placebo plus standard therapy, Belimumab 10 mg/kg plus standard therapy, Standard therapy
Lead sponsor
GlaxoSmithKline
Results first posted
2019-11-29

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/NCT01705977-87860c77