ConductScience.org, home

Comparison · NCT02694328-98e25fbb

Olanzapine vs ALKS 3831: Number of Participants Experiencing of Adverse Events (AEs)

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. Olanzapine vs ALKS 3831: Number of Participants Experiencing of Adverse Events (AEs). Trial comparisons, record NCT02694328-98e25fbb. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02694328-98e25fbb

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.8220.7730.863wilson
Risk in group 20.7410.6860.789wilson
Risk difference, group 1 minus group 20.08160.01250.15newcombe hybrid score
Risk ratio, group 1 over group 21.111.021.21log
Odds ratio, group 1 over group 21.621.072.44log
Number needed to treat, for one more participant with the outcome on Olanzapine than on ALKS 383112.36.6780.1from the risk difference interval

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1OlanzapineAdministered as a coated bilayer tablet~Olanzapine: Daily dosing227276OG000
Group 2ALKS 3831Administered as a coated bilayer tablet~ALKS 3831: Daily dosing203274OG001

Outcome

Type
SECONDARY
Title
Number of Participants Experiencing of Adverse Events (AEs)
Description
Time frame
24 weeks
Population
The Safety Population includes all randomized subjects who received at least 1 dose of study drug.

Source ClinicalTrials.gov

Trial

Title
A Study of ALKS 3831 in Adults With Schizophrenia (The ENLIGHTEN-2 Study)
NCT number
NCT02694328
Phases
PHASE3
Conditions
Schizophrenia
Interventions
ALKS 3831, Olanzapine
Lead sponsor
Alkermes, Inc.
Results first posted
2020-02-10

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT02694328-98e25fbb