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Trial · NCT03703908

Outcomes14

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYThe Number of Subjects With a Reduction in Urine Protein to Creatinine Ratio (UPCR) of at Least 20%Baseline to week 12ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYAchievement of Partial or Complete Remission of UPCR Through Week 12 and Through the End of TreatmentBaseline to week 12ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYProportion of Subjects With Achievement of Complete Remission During the Treatment PeriodBaseline to week 52ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYTime Taken of Subjects to Achieve Complete Remission During the Treatment PeriodBaseline to week 52daysNUMBER
SECONDARYChange From Baseline in Urine Protein:Creatinine Ratio (UPCR) Over TimeBaseline to week 12 and week 52Data was not available for all patients at each timepointg protein/g creatinineMEAN
SECONDARYAssessment of Time to and Proportion of Subjects With Achievement of Partial Remission During the Treatment PeriodBaseline to week 52ParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYTime to Rescue TherapyBaseline to week 52Due to the small sample size and early termination of the study, no data could be collected
SECONDARYMean Change From Baseline for eGFR Using the CKD-EPI Cystatin C Equation Over TimeBaseline to Week 12 and Week 52Data was not available for all patients at each timepointmL/min/1.73m²MEAN
SECONDARYMean Change From Baseline for the eGFR CKD-EPI Creatinine Equation Over TimeBaseline to Week 12 and Week 52Data was not available for all patients at each timepointml/min/1.73 m²MEAN
SECONDARYMean Change From Baseline for eGFR CKD-EPI Creatinine-Cystatin C Equation Over TimeBaseline to Week 12 and Week 52Data was not available for all patients at each timepointml/min/1.73 m²MEAN
SECONDARYMean Change From Baseline for the MDRD Creatinine Equation Over TimeBaseline to Week 12 and Week 52Data was not available for all patients at each timepointml/min/1.73 m²MEAN
SECONDARYEffect of CCX140-B Treatment on Quality of Life Endpoint SF-36V2Baseline to Week 52Due to the small sample size and early termination of the study, no data could be collected
SECONDARYEffect of CCX140-B Treatment on Quality of Life Endpoint EQ-5D-5L for the Overall TrialBaseline to Week 12 and Week 52Data was not available for all patients at each timepoint.score on a scaleMEAN
SECONDARYChanges to Laboratory Parameters Related to Renal Function Including Serum Albumin, Creatinine, Cystatin C, Urinary Albumin:Creatinine Ratio, Total 24-hour Protein Excretion During the TrialBaseline to Day 57No data collected

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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