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Trial · NCT03131219

Results by group57

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

OutcomeGroupCategoryValueSpreadUnits
Percentage Of Complement Inhibitor Treatment-naïve Participants With Complete Thrombotic Microangiopathy (TMA) Response at Week 26Complement Inhibitor Treatment NaïveComplete TMA response77.895% Confidence Interval 52.4 to 93.6percentage of participants
Percentage Of Complement Inhibitor Treatment-naïve Participants With Complete Thrombotic Microangiopathy (TMA) Response at Week 26Complement Inhibitor Treatment NaïvePlatelet count normalization94.495% Confidence Interval 72.7 to 99.9percentage of participants
Percentage Of Complement Inhibitor Treatment-naïve Participants With Complete Thrombotic Microangiopathy (TMA) Response at Week 26Complement Inhibitor Treatment NaïveLDH normalization88.995% Confidence Interval 65.3 to 98.6percentage of participants
Percentage Of Complement Inhibitor Treatment-naïve Participants With Complete Thrombotic Microangiopathy (TMA) Response at Week 26Complement Inhibitor Treatment Naïve≥ 25% improvement in serum creatinine from baseline83.395% Confidence Interval 58.6 to 96.4percentage of participants
Time To Complete TMA Response In Complement Inhibitor Treatment-naïve ParticipantsComplement Inhibitor Treatment Naïve30.0Inter-Quartile Range 22.0 to 88.0days
Proportion Of Complement Inhibitor Treatment-naïve Participants With Complete TMA Response At Week 52Complement Inhibitor Treatment NaïveComplete TMA responder0.88295% Confidence Interval 0.636 to 0.985proportion of participants
Proportion Of Complement Inhibitor Treatment-naïve Participants With Complete TMA Response At Week 52Complement Inhibitor Treatment NaïvePlatelet count normalization0.88295% Confidence Interval 0.636 to 0.985proportion of participants
Proportion Of Complement Inhibitor Treatment-naïve Participants With Complete TMA Response At Week 52Complement Inhibitor Treatment NaïveLDH normalization1.00095% Confidence Interval 0.805 to 1.000proportion of participants
Proportion Of Complement Inhibitor Treatment-naïve Participants With Complete TMA Response At Week 52Complement Inhibitor Treatment Naïve≥25% improvement in serum creatinine from baseline1.00095% Confidence Interval 0.805 to 1.000proportion of participants
Participants Who Do Not Require Dialysis at Weeks 26 and 52Complement Inhibitor Treatment NaïveWeek 265Participants
Participants Who Do Not Require Dialysis at Weeks 26 and 52Eculizumab ExperiencedWeek 260Participants
Participants Who Do Not Require Dialysis at Weeks 26 and 52Complement Inhibitor Treatment NaïveWeek 526Participants
Participants Who Do Not Require Dialysis at Weeks 26 and 52Eculizumab ExperiencedWeek 520Participants
Change From Baseline In eGFR At Weeks 26 and 52Complement Inhibitor Treatment NaïveBaseline22.0Full Range 10 to 84mL/min/1.73 m^2
Change From Baseline In eGFR At Weeks 26 and 52Eculizumab ExperiencedBaseline99.75Full Range 54 to 136.5mL/min/1.73 m^2
Change From Baseline In eGFR At Weeks 26 and 52Complement Inhibitor Treatment NaïveChange From Baseline at Week 2680.0Full Range 0 to 222mL/min/1.73 m^2
Change From Baseline In eGFR At Weeks 26 and 52Eculizumab ExperiencedChange From Baseline at Week 26-2.00Full Range -94 to 18mL/min/1.73 m^2
Change From Baseline In eGFR At Weeks 26 and 52Complement Inhibitor Treatment NaïveChange From Baseline at Week 5294.0Full Range 10 to 230mL/min/1.73 m^2
Change From Baseline In eGFR At Weeks 26 and 52Eculizumab ExperiencedChange From Baseline at Week 52-3.00Full Range -20 to 9mL/min/1.73 m^2
Participants With Change From Baseline In CKD Stage At Weeks 26 and 52Complement Inhibitor Treatment NaïveWeek 26, Improved15Participants

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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