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Comparison · NCT02424253-sae

ZPL-3893787 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. ZPL-3893787 vs Placebo: serious adverse events. Trial comparisons, record NCT02424253-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02424253-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 1000.0558wilson
Risk in group 20.03030.005370.153wilson
Risk difference, group 1 minus group 2-0.0303-0.1530.0308newcombe 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 treat, for one fewer participant with a serious adverse event on ZPL-3893787 than on Placebo33from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1ZPL-389378730 mg ZPL-3893787 orally once daily for 8 weeks.065EG000
Group 2Placebo1 capsule orally once daily for 8 weeks.133EG001

Harm

What it counts
Total, serious adverse events
Time frame
Adverse events were collected from Screening to up to 28 days post last dose, up to approximately 10 months.

Source ClinicalTrials.gov

Trial

Title
A Study to Determine the Efficacy of ZPL-3893787 in Subjects With Atopic Dermatitis
NCT number
NCT02424253
Phases
PHASE2
Conditions
Atopic Dermatitis
Interventions
ZPL-3893787, Placebo
Lead sponsor
Ziarco Pharma Ltd
Results first posted
2021-05-13

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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