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Trial · NCT05918978

Results by group45

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With TEAEs, TESAEs and TEAESIsEfgartigimod-EfgartigimodTEAEs13Participants
Number of Participants With TEAEs, TESAEs and TEAESIsPlacebo-EfgartigimodTEAEs12Participants
Number of Participants With TEAEs, TESAEs and TEAESIsEfgartigimod-EfgartigimodTESAEs0Participants
Number of Participants With TEAEs, TESAEs and TEAESIsPlacebo-EfgartigimodTESAEs0Participants
Number of Participants With TEAEs, TESAEs and TEAESIsEfgartigimod-EfgartigimodTEAESIs7Participants
Number of Participants With TEAEs, TESAEs and TEAESIsPlacebo-EfgartigimodTEAESIs5Participants
Change From Baseline to Weeks 24 and 48 in the COMPASS 31 (2-week Recall Version)Efgartigimod-EfgartigimodWeek 2413.608Standard Deviation 29.7026score on a scale
Change From Baseline to Weeks 24 and 48 in the COMPASS 31 (2-week Recall Version)Placebo-EfgartigimodWeek 248.447Standard Deviation 18.1170score on a scale
Change From Baseline to Weeks 24 and 48 in the COMPASS 31 (2-week Recall Version)Efgartigimod-EfgartigimodWeek 481.780score on a scale
Change From Baseline to Weeks 24 and 48 in the MaPSEfgartigimod-EfgartigimodWeek 24-0.8Standard Deviation 22.02score on a scale
Change From Baseline to Weeks 24 and 48 in the MaPSPlacebo-EfgartigimodWeek 2410.3Standard Deviation 24.95score on a scale
Change From Baseline to Weeks 24 and 48 in the MaPSEfgartigimod-EfgartigimodWeek 48-17.0score on a scale
Percentage of Participants With Improved PGI-S at Weeks 24 and 48Efgartigimod-EfgartigimodWeek 24, 1-week recall12.5percentage of participants
Percentage of Participants With Improved PGI-S at Weeks 24 and 48Placebo-EfgartigimodWeek 24, 1-week recall0percentage of participants
Percentage of Participants With Improved PGI-S at Weeks 24 and 48Efgartigimod-EfgartigimodWeek 24, 2-week recall12.5percentage of participants
Percentage of Participants With Improved PGI-S at Weeks 24 and 48Placebo-EfgartigimodWeek 24, 2-week recall0percentage of participants
Percentage of Participants With Improved PGI-S at Weeks 24 and 48Efgartigimod-EfgartigimodWeek 48, 1-week recall25.0percentage of participants
Percentage of Participants With Improved PGI-S at Weeks 24 and 48Placebo-EfgartigimodWeek 48, 1-week recall0percentage of participants
Percentage of Participants With Improved PGI-S at Weeks 24 and 48Efgartigimod-EfgartigimodWeek 48, 2-week recall25.0percentage of participants
Percentage of Participants With Improved PGI-S at Weeks 24 and 48Placebo-EfgartigimodWeek 48, 2-week recall0percentage of participants

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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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