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Trial · NCT06527404

Registered outcomes24

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryGlobal: Number of Participants Achieving Reduction from Baseline in Weekly Average of Daily Itch Score at Week 24Up to 24 weeks
PrimaryUS Only: Number of Participants Achieving Reduction from Baseline in Weekly Average of Daily Itch Score and Prurigo Nodularis Stage Assessment at Week 24Up to 24 weeks
SecondaryGlobal: Number of Participants Achieving Improvement in Prurigo Nodularis Stage Assessment Score at Week 24Week 24
SecondaryGlobal: Number of Participants Achieving Reduction from Baseline in Weekly Average of Daily Itch Score and Prurigo Nodularis Stage Assessment at Week 24Baseline and Week 24
SecondaryGlobal: Percentage Improvement from Baseline in Weekly Average of Daily Itch Score at Week 24Baseline and Week 24
SecondaryGlobal: Number of Participants Achieving Reduction in Weekly Average Daily Prurigo Nodularis Skin Pain Assessment at Week 24 in Those with Baseline NRS Above CutoffBaseline and Week 24
SecondaryUS Only: Number of Participants Achieving Reduction from Baseline in Weekly Average of Daily Itch Score at Week 24Baseline and Week 24
SecondaryUS Only: Number of Participants with Improvement in Prurigo Nodularis Stage Assessment at Week 24Week 24
SecondaryUS Only: Percent Improvement from Baseline in Weekly Average of Daily Itch Score at Week 24Week 24
SecondaryUS Only: Number of Participants Achieving Reduction from Baseline in Weekly Average of Daily Skin Pain Assessment at Week 24 in Participants With Baseline Score Greater Than or Equal to a Cutoff ScoreWeek 24
SecondaryChange from Baseline in Weekly Average of Daily Itch Score at Weeks 24, 36 and 52Baseline, Week 24, Week 36 and Week 52
SecondaryPercent Improvement from Baseline in Weekly Average of Daily Itch Score at Week 36 and 52Baseline, Week 36 and Week 52
SecondaryNumber of Participants Achieving Reduction from Baseline in Weekly Average of Daily Itch Score at Weeks 16, 36 and 52Baseline, Week 16, Week 36 and Week 52
SecondaryNumber of Participants Achieving Weekly Average of Daily Itch Score Less than a Cutoff Score at Week 36 and 52Week 36 and Week 52
SecondaryChange from Baseline in Prurigo Nodularis Stage Assessment Score at Week 24, 36, and 52Baseline, Week 24, Week 36 and Week 52
SecondaryNumber of Participants Achieving Improvement in Prurigo Nodularis Stage Assessment Score at Weeks 36 and 52Week 36 and Week 52
SecondaryNumber of Participants Achieving Improvement in Prurigo Nodularis Activity Assessment Score at Weeks 24, 36 and 52Week 24, Week 36 and Week 52
SecondaryChange from Baseline in Quality of Life Assessment Score at Weeks 24, 36 and 52Baseline, Week 24, Week 36 and Week 52
SecondaryNumber of Participants Achieving Reduction from Baseline in Quality of Life Assessment Score at Weeks 24, 36 and 52 in Participants with Baseline Score Greater Than or Equal to a Cutoff ScoreBaseline, Week 24, Week 36 and Week 52
SecondaryChange from Baseline in Weekly Average of Daily Skin Pain Assessment Score at Weeks 24, 36 and 52Baseline, Week 24, Week 36 and Week 52

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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GET https://conductscience.org/api/trials/v1/NCT06527404/registered