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Albiglutide vs Placebo: Number of Participants With Adverse Events (AEs) Leading to Discontinuation of Investigational Product (AELD)

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.09050.08270.099wilsonClinicalTrials.gov
Risk in group 20.07080.06390.0785wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.01970.00870.0307newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.281.111.47logClinicalTrials.gov
Odds ratio, group 1 over group 21.311.121.52logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on Albiglutide than on Placebo50.832.6115from the risk difference intervalClinicalTrials.gov

Groups 2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1Albiglutide
Albiglutide was administered once weekly as subcutaneous injection in the abdomen, thigh or upper arm region. Participants were administered albiglutide at a dose of 30 milligrams (mg) or 50 mg once weekly in addition to the standard of care therapy for diabetes and cardiovascular health.
4274,717OG001ClinicalTrials.gov
Group 2Placebo
Albiglutide matching placebo was administered once weekly as subcutaneous injection in the abdomen, thigh or upper arm region in addition to the standard of care therapy for diabetes and cardiovascular health.
3344,715OG000ClinicalTrials.gov

Outcome 5

FieldValueSource
TypeSECONDARYClinicalTrials.gov
TitleNumber of Participants With Adverse Events (AEs) Leading to Discontinuation of Investigational Product (AELD)ClinicalTrials.gov
DescriptionThe number of participants with on-therapy AEs leading to discontinuation of investigational product is reported.ClinicalTrials.gov
Time frameUp to 2.7 yearsClinicalTrials.gov
PopulationSafety PopulationClinicalTrials.gov

Trial 8

FieldValueSource
TitleEffect of Albiglutide, When Added to Standard Blood Glucose Lowering Therapies, on Major Cardiovascular Events in Subjects With Type 2 Diabetes MellitusClinicalTrials.gov
NCT numberNCT02465515ClinicalTrials.gov
PhasesPHASE4ClinicalTrials.gov
ConditionsDiabetes MellitusClinicalTrials.gov
InterventionsAlbiglutide 30 mg, Albiglutide 50 mg, Albiglutide matching placeboClinicalTrials.gov
Lead sponsorGlaxoSmithKlineClinicalTrials.gov
Results first posted2019-03-06ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT02465515?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.