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Comparison · NCT05142722-sae

Obicetrapib 10mg vs Placebo: 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. Obicetrapib 10mg vs Placebo: serious adverse events. Trial comparisons, record NCT05142722-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05142722-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 10.1250.110.142wilson
Risk in group 20.1390.1170.164wilson
Risk difference, group 1 minus group 2-0.0136-0.04270.0138newcombe hybrid score
Risk ratio, group 1 over group 20.9020.7311.11log
Odds ratio, group 1 over group 20.8880.6971.13log
Number needed to treat, for one fewer participant with a serious adverse event on Obicetrapib 10mg than on Placebo73.7from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Obicetrapib 10mgone 10mg obicetrapib tablet once daily~Obicetrapib: 10mg obicetrapib tablet2111,685EG001
Group 2Placeboone placebo tablet once daily~Placebo: placebo tablet made to resemble active117843EG000

Harm

What it counts
Total, serious adverse events
Time frame
From first dose of study drug up to Week 54

Source ClinicalTrials.gov

Trial

Title
Randomized Study to Evaluate the Effect of Obicetrapib on Top of Maximum Tolerated Lipid-Modifying Therapies
NCT number
NCT05142722
Phases
PHASE3
Conditions
Dyslipidemias, High Cholesterol, Hypercholesterolemia, Familial Hypercholesterolemia, Atherosclerotic Cardiovascular Disease
Interventions
Placebo, Obicetrapib
Lead sponsor
NewAmsterdam Pharma
Results first posted
2025-09-19

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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