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Trial · NCT02728752

Results by group89

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

OutcomeGroupCategoryValueSpreadUnits
Measure the Number of Patients Who Had an Increase of ≥20 Points on the Total Improvement Score (TIS)Placebo21Participants
Measure the Number of Patients Who Had an Increase of ≥20 Points on the Total Improvement Score (TIS)Octagam10%37Participants
Proportion of TIS Responders by Improvement Category at Week 16PlaceboPrimary21Participants
Proportion of TIS Responders by Improvement Category at Week 16Octagam10%Primary37Participants
Proportion of TIS Responders by Improvement Category at Week 16PlaceboAt least moderate improvement11Participants
Proportion of TIS Responders by Improvement Category at Week 16Octagam10%At least moderate improvement32Participants
Proportion of TIS Responders by Improvement Category at Week 16PlaceboAt least major improvement4Participants
Proportion of TIS Responders by Improvement Category at Week 16Octagam10%At least major improvement15Participants
Proportion of TIS Responders by Improvement Category at Week 40PlaceboAt least minimal improvement32Participants
Proportion of TIS Responders by Improvement Category at Week 40Octagam10%At least minimal improvement32Participants
Proportion of TIS Responders by Improvement Category at Week 40PlaceboAt least moderate improvement28Participants
Proportion of TIS Responders by Improvement Category at Week 40Octagam10%At least moderate improvement26Participants
Proportion of TIS Responders by Improvement Category at Week 40PlaceboAt least major improvement14Participants
Proportion of TIS Responders by Improvement Category at Week 40Octagam10%At least major improvement17Participants
Mean Change From Baseline (Week 0) to End of First Period (Week 16) in the Modified Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI)PlaceboTotal Activity Score-1.16Standard Deviation 7.000units on a scale
Mean Change From Baseline (Week 0) to End of First Period (Week 16) in the Modified Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI)Octagam10%Total Activity Score-9.36Standard Deviation 10.542units on a scale
Mean Change From Baseline (Week 0) to End of First Period (Week 16) in the Modified Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI)PlaceboTotal Damage Score-0.02Standard Deviation 0.771units on a scale
Mean Change From Baseline (Week 0) to End of First Period (Week 16) in the Modified Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI)Octagam10%Total Damage Score-0.67Standard Deviation 1.871units on a scale
Mean Change From End of First Period (Week 16) to End of Extension Period (Week 40) in the Modified Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI)PlaceboTotal Activity Score-8.52Standard Deviation 11.344units on a scale
Mean Change From End of First Period (Week 16) to End of Extension Period (Week 40) in the Modified Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI)Octagam10%Total Activity Score-1.79Standard Deviation 4.169units on a scale

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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