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Comparison · NCT01703208-e900985f

Omarigliptin 25 mg vs Placebo: Number of Participants With MACE-plus (Confirmed Cardiovascular [CV]-Related Death, Nonfatal Myocardial Infarction [MI], Nonfatal Stroke, or Hospitalization Due to Unstable Angina)

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. Omarigliptin 25 mg vs Placebo: Number of Participants With MACE-plus (Confirmed Cardiovascular [CV]-Related Death, Nonfatal Myocardial Infarction [MI], Nonfatal Stroke, or Hospitalization Due to Unstable Angina). Trial comparisons, record NCT01703208-e900985f. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01703208-e900985f

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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 10.03160.02490.04wilson
Risk in group 20.03330.02650.0419wilson
Risk difference, group 1 minus group 2-0.00175-0.01260.00909newcombe hybrid score
Risk ratio, group 1 over group 20.9470.6811.32log
Odds ratio, group 1 over group 20.9460.6721.33log
Number needed to treat, for one fewer participant with the outcome on Omarigliptin 25 mg than on Placebo570from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Omarigliptin 25 mgOmarigliptin (MK-3102) 25 mg capsule or tablet administered orally once weekly662,090OG000
Group 2PlaceboMatching placebo to omarigliptin capsule or tablet administered once weekly.702,100OG001

Outcome

Type
PRIMARY
Title
Number of Participants With MACE-plus (Confirmed Cardiovascular [CV]-Related Death, Nonfatal Myocardial Infarction [MI], Nonfatal Stroke, or Hospitalization Due to Unstable Angina)
Description
Participants with confirmed MACE-plus events (confirmed cardiovascular, CV-related death, nonfatal myocardial infarction \[MI\], nonfatal stroke, or hospitalization due to unstable angina). In the MK-3102-018 study, MACE plus events had a data cut-off date of April 15, 2015.
Time frame
Up to 156 weeks
Population
The analysis population included all randomized participants who took at least one dose of blinded study medication and were evaluated for MACE-plus events.

Source ClinicalTrials.gov

Trial

Title
A Study to Assess Cardiovascular Outcomes Following Treatment With Omarigliptin (MK-3102) in Participants With Type 2 Diabetes Mellitus (MK-3102-018)
NCT number
NCT01703208
Phases
PHASE3
Conditions
Type 2 Diabetes Mellitus
Interventions
Omarigliptin, Placebo
Lead sponsor
Merck Sharp & Dohme LLC
Results first posted
2017-12-12

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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