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Trial · NCT03131648

Results by group50

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

OutcomeGroupCategoryValueSpreadUnits
Subjects With Investigator's Global Assessment (IGA) Score of 0 (Clear) or 1 (Almost Clear) at Week 16Tralokinumab 300 mg Q2W95Participants
Subjects With Investigator's Global Assessment (IGA) Score of 0 (Clear) or 1 (Almost Clear) at Week 16Placebo Q2W14Participants
Subjects Achieving at Least 75% Reduction in Eczema Area and Severity Index [EASI] at Week 16Tralokinumab 300 mg Q2W150Participants
Subjects Achieving at Least 75% Reduction in Eczema Area and Severity Index [EASI] at Week 16Placebo Q2W25Participants
Reduction of Worst Daily Pruritus Numeric Rating Scale (Weekly Average) of at Least 4 From Baseline to Week 16.Tralokinumab 300 mg Q2W119Participants
Reduction of Worst Daily Pruritus Numeric Rating Scale (Weekly Average) of at Least 4 From Baseline to Week 16.Placebo Q2W20Participants
Change in Scoring Atopic Dermatitis (SCORAD) From Baseline to Week 16Tralokinumab 300 mg Q2W-25.2Standard Error 0.94units on a scale
Change in Scoring Atopic Dermatitis (SCORAD) From Baseline to Week 16Placebo Q2W-14.7Standard Error 1.80units on a scale
Change in Dermatology Life Quality Index (DLQI) Score From Baseline to Week 16Tralokinumab 300 mg Q2W-7.1Standard Error 0.31units on a scale
Change in Dermatology Life Quality Index (DLQI) Score From Baseline to Week 16Placebo Q2W-5.0Standard Error 0.59units on a scale
Subjects With Investigator's Global Assessment (IGA) Score of 0 (Clear) or 1 (Almost Clear) at Week 52 Among Subjects With IGA of 0/1 at Week 16Tralokinumab 300 mg Q2W20Participants
Subjects With Investigator's Global Assessment (IGA) Score of 0 (Clear) or 1 (Almost Clear) at Week 52 Among Subjects With IGA of 0/1 at Week 16Tralokinumab 300 mg Q4W14Participants
Subjects With Investigator's Global Assessment (IGA) Score of 0 (Clear) or 1 (Almost Clear) at Week 52 Among Subjects With IGA of 0/1 at Week 16Placebo Q2W9Participants
Subjects With at Least 75% Reduction in Eczema Area and Severity Index [EASI] at Week 52 Among Subjects With EASI75 at Week 16Tralokinumab 300 mg Q2W28Participants
Subjects With at Least 75% Reduction in Eczema Area and Severity Index [EASI] at Week 52 Among Subjects With EASI75 at Week 16Tralokinumab 300 mg Q4W28Participants
Subjects With at Least 75% Reduction in Eczema Area and Severity Index [EASI] at Week 52 Among Subjects With EASI75 at Week 16Placebo Q2W10Participants
Safety and Tolerability: Adverse Event (AE) /Serious Adverse Event (SAE) FrequencyTralokinumab 300 mg Q2WAEs411Participants
Safety and Tolerability: Adverse Event (AE) /Serious Adverse Event (SAE) FrequencyPlacebo Q2WAEs133Participants
Safety and Tolerability: Adverse Event (AE) /Serious Adverse Event (SAE) FrequencyTralokinumab 300 mg Q2WSAEs23Participants
Safety and Tolerability: Adverse Event (AE) /Serious Adverse Event (SAE) FrequencyPlacebo Q2WSAEs8Participants

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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