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Trial · NCT03135548

Results by group15

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants With Palmoplantar (pp) Pustular Psoriasis Area and Severity Index 50 (PASI) (ppPASI50) at Week 16BI 655130 Low Dose31.6Percentage of participants (%)
Percentage of Participants With Palmoplantar (pp) Pustular Psoriasis Area and Severity Index 50 (PASI) (ppPASI50) at Week 16BI 655130 High Dose31.6Percentage of participants (%)
Percentage of Participants With Palmoplantar (pp) Pustular Psoriasis Area and Severity Index 50 (PASI) (ppPASI50) at Week 16Placebo Matching to BI 65513023.8Percentage of participants (%)
Number of Participants With Drug-related Adverse Events (AEs)BI 655130 Low Dose8Participants
Number of Participants With Drug-related Adverse Events (AEs)BI 655130 High Dose8Participants
Number of Participants With Drug-related Adverse Events (AEs)Placebo Matching to BI 6551309Participants
Percentage of Participants With Palmoplantar Pustular Psoriasis Area and Severity Index 75 (ppPASI75) at Week 16BI 655130 Low Dose0.0Percentage of participnats (%)
Percentage of Participants With Palmoplantar Pustular Psoriasis Area and Severity Index 75 (ppPASI75) at Week 16BI 655130 High Dose21.1Percentage of participnats (%)
Percentage of Participants With Palmoplantar Pustular Psoriasis Area and Severity Index 75 (ppPASI75) at Week 16Placebo Matching to BI 6551309.5Percentage of participnats (%)
Percent Change From Baseline in the ppPASI at Week 16BI 655130 Low Dose-32.74Standard Deviation 38.52Unit on scale
Percent Change From Baseline in the ppPASI at Week 16BI 655130 High Dose-45.80Standard Deviation 27.00Unit on scale
Percent Change From Baseline in the ppPASI at Week 16Placebo Matching to BI 655130-39.97Standard Deviation 32.94Unit on scale
Percentage of Participants Achieving Treatment Success (Treatment Success Defined as Achieving a Clinical Response of 0 or 1=Clear/Almost Clear) Via Palmoplantar Pustulosis Physicians Global Assessment (pppPGA) at Week 16
BI 655130 Low Dose0.0Percentage of participants (%)
Percentage of Participants Achieving Treatment Success (Treatment Success Defined as Achieving a Clinical Response of 0 or 1=Clear/Almost Clear) Via Palmoplantar Pustulosis Physicians Global Assessment (pppPGA) at Week 16
BI 655130 High Dose15.8Percentage of participants (%)
Percentage of Participants Achieving Treatment Success (Treatment Success Defined as Achieving a Clinical Response of 0 or 1=Clear/Almost Clear) Via Palmoplantar Pustulosis Physicians Global Assessment (pppPGA) at Week 16
Placebo Matching to BI 65513014.3Percentage of participants (%)

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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