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Comparison · NCT00740051-sae

Linagliptin vs Placebo/Glimepiride: 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. Linagliptin vs Placebo/Glimepiride: serious adverse events. Trial comparisons, record NCT00740051-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00740051-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 10.006620.001170.0366wilson
Risk in group 20.03950.01350.11wilson
Risk difference, group 1 minus group 2-0.0329-0.1030.00677newcombe hybrid score
Risk ratio, group 1 over group 20.1680.01771.59log
Odds ratio, group 1 over group 20.1620.01661.59log
Number needed to treat, for one fewer participant with a serious adverse event on Linagliptin than on Placebo/Glimepiride30.4from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1LinagliptinPatients treated with Linagliptin 5mg once daily (up to 52 weeks)1151EG001
Group 2Placebo/GlimepiridePatients treated with matching placebo (up to 18 weeks) followed by Glimepiride (after 18 weeks to 52 weeks)376EG000

Harm

What it counts
Total, serious adverse events
Time frame
52 weeks + 7 days

Source ClinicalTrials.gov

Trial

Title
A Randomised, db, Placebo-controlled Study of BI 1356 for 18 Weeks Followed by a 34 Week Double-blind Extension Period (Placebo Patients Switched to Glimepiride) in Type 2 Diabetic Patients for Whom Treatment With Metformin is Inappropriate
NCT number
NCT00740051
Phases
PHASE3
Conditions
Diabetes Mellitus, Type 2
Interventions
Linagliptin, Linagliptin Placebo, Glimepiride
Lead sponsor
Boehringer Ingelheim
Results first posted
2011-10-26

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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