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Comparison · NCT03187769-sae

ALKS 3831 vs Olanzapine: 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. ALKS 3831 vs Olanzapine: serious adverse events. Trial comparisons, record NCT03187769-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03187769-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 10.03790.01930.073wilson
Risk in group 20.03720.0190.0717wilson
Risk difference, group 1 minus group 20.000705-0.03850.0403newcombe hybrid score
Risk ratio, group 1 over group 21.020.392.66log
Odds ratio, group 1 over group 21.020.3762.77log
Number needed to harm, for one more participant with a serious adverse event on ALKS 3831 than on Olanzapine1,420from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1ALKS 3831Coated bilayer tablet~ALKS 3831: Olanzapine + samidorphan, daily oral dosing8211EG000
Group 2OlanzapineCoated bilayer tablet~Olanzapine: Daily oral dosing8215EG001

Harm

What it counts
Total, serious adverse events
Time frame
16 Weeks

Source ClinicalTrials.gov

Trial

Title
Study to Evaluate the Efficacy of ALKS 3831 on Body Weight in Young Adults Who Have Been Recently Diagnosed With Schizophrenia, Schizophreniform, or Bipolar I Disorder
NCT number
NCT03187769
Phases
PHASE3
Conditions
Schizophrenia, Schizophreniform Disorders, Bipolar I Disorder
Interventions
ALKS 3831, Olanzapine
Lead sponsor
Alkermes, Inc.
Results first posted
2023-01-19

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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