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Trial · NCT05075408

Results by group18

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Responders With an Improvement of Worst Itch Numeric Rating Scale (WI NRS) Greater Than and Equal to (>=) 4 From Baseline at Week 12Nemolizumab 30 mg38.5Percentage of Participants
Percentage of Responders With an Improvement of Worst Itch Numeric Rating Scale (WI NRS) Greater Than and Equal to (>=) 4 From Baseline at Week 12Nemolizumab 60 mg47.7Percentage of Participants
Percentage of Responders With an Improvement of Worst Itch Numeric Rating Scale (WI NRS) Greater Than and Equal to (>=) 4 From Baseline at Week 12Placebo32.4Percentage of Participants
Percentage of Responders With an Improvement of WI NRS >= 3 From Baseline at Week 12Nemolizumab 30 mg49.3Percentage of Participants
Percentage of Responders With an Improvement of WI NRS >= 3 From Baseline at Week 12Nemolizumab 60 mg60.6Percentage of Participants
Percentage of Responders With an Improvement of WI NRS >= 3 From Baseline at Week 12Placebo47.1Percentage of Participants
Percentage of Responders With an Improvement of WI NRS >= 4 From Baseline at Week 4Nemolizumab 30 mg24.3Percentage of Participants
Percentage of Responders With an Improvement of WI NRS >= 4 From Baseline at Week 4Nemolizumab 60 mg26.6Percentage of Participants
Percentage of Responders With an Improvement of WI NRS >= 4 From Baseline at Week 4Placebo7.4Percentage of Participants
Percentage of Responders With an Improvement of Sleep Disturbance Numerical Rating Scale (SD NRS) >= 4 From Baseline at Week 12Nemolizumab 30 mg27.7Percentage of Participants
Percentage of Responders With an Improvement of Sleep Disturbance Numerical Rating Scale (SD NRS) >= 4 From Baseline at Week 12Nemolizumab 60 mg42.6Percentage of Participants
Percentage of Responders With an Improvement of Sleep Disturbance Numerical Rating Scale (SD NRS) >= 4 From Baseline at Week 12Placebo25.3Percentage of Participants
Percentage of Responders With an Improvement of WI NRS >= 3 From Baseline at Week 4Nemolizumab 30 mg36.5Percentage of Participants
Percentage of Responders With an Improvement of WI NRS >= 3 From Baseline at Week 4Nemolizumab 60 mg35.0Percentage of Participants
Percentage of Responders With an Improvement of WI NRS >= 3 From Baseline at Week 4Placebo12.8Percentage of Participants
Percentage of Responders With an Improvement of SD NRS >= 4 From Baseline at Week 4Nemolizumab 30 mg16.1Percentage of Participants
Percentage of Responders With an Improvement of SD NRS >= 4 From Baseline at Week 4Nemolizumab 60 mg23.6Percentage of Participants
Percentage of Responders With an Improvement of SD NRS >= 4 From Baseline at Week 4Placebo2.8Percentage 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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