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Trial · NCT06072482

Registered outcomes20

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPercentage of Participants Experiencing Treatment-emergent Adverse Events (TEAEs)Up to Month 60
PrimaryPercentage of Participants Experiencing Adverse Events of Special InterestUp to Month 60
PrimaryPercentage of Participants Experiencing Serious Adverse EventsUp to Month 60
PrimaryPercentage of Participants Experiencing Adverse Events Leading to WithdrawalUp to Month 60
PrimaryPercentage of Participants Experiencing Adverse Events Leading to DeathUp to Month 60
PrimaryNumber of Participants Experiencing Clinical Significant Changes from Baseline in Vital Signs MeasurementsUp to Month 60
PrimaryNumber of Participants Experiencing Clinical Significant Changes from Baseline in Hematology AssessmentsUp to Month 60
PrimaryNumber of Participants Experiencing Clinical Significant Changes from Baseline in Serum Chemistry AssessmentsUp to Month 60
PrimaryNumber of Participants Experiencing Clinical Significant Changes from Baseline in Urinalysis AssessmentsUp to Month 60
SecondaryGroup A and B Participants who Achieved Remission at Month 12: Time to Relapse in AAV Between Month 12 and Month 60Month 12 to Month 60
SecondaryGroup A and B Participants who Achieved Remission at Month 12: Percentage of Participants who Relapse After Achieving Remission at Month 12Month 12 to Month 60
SecondaryGroups A and C: Percentage of Participants who Achieved Sustained Remission at Month 60Month 60
SecondaryGroup A and C Participants with Overt Renal Disease at Baseline: Change from Baseline to Month 60 in Estimated Glomerular Filtration Rate (eGFR)Baseline and Month 60
SecondaryGroups A and C: Change from Baseline to Month 60 in Short Form 36 Health Survey Version 2 (SF-36 v2) General Health Perception ScoreBaseline and Month 60
SecondaryGroups A and C: Change from Baseline to Month 60 in EuroQoL-5 Dimension 5 Levels (EQ-5D-5L) Visual Analogue Scale (VAS)Baseline and Month 60
SecondaryPercentage of Participants who Achieved Remission at Month 6Month 6
SecondaryGroups A and C: Change from Baseline to Month 60 in Vasculitis Damage Index (VDI)Baseline and Month 60
SecondaryGroups A and C: Percentage of Participants with Composite Outcome of Initiation of Maintenance Dialysis, Kidney Transplantation, or DeathUp to Month 60
SecondaryPercentage of Participants With Glucocorticoid UseUp to Month 60
SecondaryPercentage of Participants With Immunosuppressant UseUp to Month 60

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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