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Trial · NCT04501679

Results by group20

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With an Improvement of Greater Than or Equal to (>=) 4 From Baseline in Weekly Average Peak Pruritus Numeric Rating Scale (PP NRS) at Week 16Nemolizumab103Participants
Number of Participants With an Improvement of Greater Than or Equal to (>=) 4 From Baseline in Weekly Average Peak Pruritus Numeric Rating Scale (PP NRS) at Week 16Placebo19Participants
Number of Participants With an Investigator Global Assessment (IGA) Success at Week 16Nemolizumab69Participants
Number of Participants With an Investigator Global Assessment (IGA) Success at Week 16Placebo10Participants
Number of Participants With an Improvement of >= 4 From Baseline in Weekly Average PP NRS at Week 4Nemolizumab75Participants
Number of Participants With an Improvement of >= 4 From Baseline in Weekly Average PP NRS at Week 4Placebo7Participants
Number of Participants With PP NRS < 2 at Week 16Nemolizumab64Participants
Number of Participants With PP NRS < 2 at Week 16Placebo7Participants
Number of Participants With an Improvement of >=4 From Baseline in Sleep Disturbance Numeric Rating Scale (SD NRS) at Week 16Nemolizumab95Participants
Number of Participants With an Improvement of >=4 From Baseline in Sleep Disturbance Numeric Rating Scale (SD NRS) at Week 16Placebo19Participants
Number of Participants With an Improvement of >=4 From Baseline in SD NRS at Week 4Nemolizumab68Participants
Number of Participants With an Improvement of >=4 From Baseline in SD NRS at Week 4Placebo9Participants
Number of Participants With PP NRS < 2 at Week 4Nemolizumab36Participants
Number of Participants With PP NRS < 2 at Week 4Placebo2Participants
Number of Participants With Adverse Events, Treatment Emergent Adverse Events (TEAEs), Adverse Events of Special Interest (AESIs), and Serious Adverse Events (SAEs)NemolizumabTreatment Emergent Adverse Events (TEAEs)112Participants
Number of Participants With Adverse Events, Treatment Emergent Adverse Events (TEAEs), Adverse Events of Special Interest (AESIs), and Serious Adverse Events (SAEs)PlaceboTreatment Emergent Adverse Events (TEAEs)48Participants
Number of Participants With Adverse Events, Treatment Emergent Adverse Events (TEAEs), Adverse Events of Special Interest (AESIs), and Serious Adverse Events (SAEs)NemolizumabAdverse Events of Special Interest (AESIs)21Participants
Number of Participants With Adverse Events, Treatment Emergent Adverse Events (TEAEs), Adverse Events of Special Interest (AESIs), and Serious Adverse Events (SAEs)PlaceboAdverse Events of Special Interest (AESIs)9Participants
Number of Participants With Adverse Events, Treatment Emergent Adverse Events (TEAEs), Adverse Events of Special Interest (AESIs), and Serious Adverse Events (SAEs)NemolizumabSerious Adverse Events (SAEs)4Participants
Number of Participants With Adverse Events, Treatment Emergent Adverse Events (TEAEs), Adverse Events of Special Interest (AESIs), and Serious Adverse Events (SAEs)PlaceboSerious Adverse Events (SAEs)5Participants

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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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT04501679/results