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Comparison · NCT03285490-sae

KX2-391 Ointment 1% 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. KX2-391 Ointment 1% vs Placebo: serious adverse events. Trial comparisons, record NCT03285490-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03285490-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 10.005620.0009920.0311wilson
Risk in group 20.02310.009030.0579wilson
Risk difference, group 1 minus group 2-0.0175-0.05260.0116newcombe hybrid score
Risk ratio, group 1 over group 20.2430.02742.15log
Odds ratio, group 1 over group 20.2390.02642.16log
Number needed to treat, for one fewer participant with a serious adverse event on KX2-391 Ointment 1% than on Placebo57.1from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1KX2-391 Ointment 1%KX2-391 Ointment 1% was applied topically once daily for 5 consecutive days in a treatment area of 25 cm\^2 on face or scalp.1178EG001
Group 2PlaceboVehicle Ointment was applied topically once daily for 5 consecutive days in a treatment area of 25 cm\^2 on face or scalp.4173EG000

Harm

What it counts
Total, serious adverse events
Time frame
From Baseline (Day 1 predose) up to 15 months (12 months post-Day 57)

Source ClinicalTrials.gov

Trial

Title
A Multi-Center Study to Evaluate the Efficacy and Safety of KX2-391 Ointment 1% on Actinic Keratosis on Face or Scalp (AK004)
NCT number
NCT03285490
Phases
PHASE3
Conditions
Actinic Keratosis
Interventions
KX2-391 Ointment 1%, Placebo
Lead sponsor
Almirall, S.A.
Results first posted
2021-03-10

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.

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