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Comparison · NCT02432703-sae

JNJ-42165279 25 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. JNJ-42165279 25 mg vs Placebo: serious adverse events. Trial comparisons, record NCT02432703-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02432703-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 10.0270.007440.0933wilson
Risk in group 200.000000000000000003470.0487wilson
Risk difference, group 1 minus group 20.027-0.02550.0933newcombe hybrid score
Risk ratio, group 1 over group 2loga group has no participants with the outcome
Odds ratio, group 1 over group 2loga cell of the two-by-two table is zero
Number needed to harm, for one more participant with a serious adverse event on JNJ-42165279 25 mg than on Placebo37from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1JNJ-42165279 25 mgParticipants with SAD received JNJ-42165279 25 milligrams (mg) orally once daily for 12 weeks.274EG001
Group 2PlaceboParticipants with social anxiety disorder (SAD) received matching placebo orally once daily for 12 weeks.075EG000

Harm

What it counts
Total, serious adverse events
Time frame
Up to 20 weeks

Source ClinicalTrials.gov

Trial

Title
A Safety and Efficacy Study of JNJ-42165279 in Participants With Social Anxiety Disorder
NCT number
NCT02432703
Phases
PHASE2
Conditions
Phobic Disorders
Interventions
JNJ-42165279, Placebo
Lead sponsor
Janssen Research & Development, LLC
Results first posted
2021-09-02

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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