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Comparison · NCT05425745-sae

Obicetrapib 10 mg 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 10 mg vs Placebo: serious adverse events. Trial comparisons, record NCT05425745-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05425745-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 10.05560.03280.0927wilson
Risk in group 20.06780.03480.128wilson
Risk difference, group 1 minus group 2-0.0122-0.07670.0375newcombe hybrid score
Risk ratio, group 1 over group 20.8190.3491.92log
Odds ratio, group 1 over group 20.8090.3262.01log
Number needed to treat, for one fewer participant with a serious adverse event on Obicetrapib 10 mg than on Placebo81.7from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Obicetrapib 10 mgone 10 mg Obicetrapib tablet once daily~Obicetrapib: 10 mg Obicetrapib tablet13234EG001
Group 2Placeboone placebo tablet once daily~Placebo: placebo tablet made to resemble active8118EG000

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
Evaluate the Effect of Obicetrapib in Patients With HeFH on Top of Maximum Tolerated Lipid-Modifying Therapies.
NCT number
NCT05425745
Phases
PHASE3
Conditions
Dyslipidemias, High Cholesterol, Hypercholesterolemia, Familial Hypercholesterolemia, Lipid Metabolism Disorder, Metabolic Disease, Lipid Metabolism, Inborn Errors, Genetic Disease, Inborn, Hyperlipoproteinemias
Interventions
Obicetrapib, Placebo
Lead sponsor
NewAmsterdam Pharma
Results first posted
2025-06-11

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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