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Trial · NCT01613118

Results by group12

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

OutcomeGroupCategoryValueSpreadUnits
Percent Change in Urine Protein/Creatinine (Up/C)RE-021 (Sparsentan) 200, 400, 800 mg Pooled-44.895% Confidence Interval -52.7 to -35.7percent change
Percent Change in Urine Protein/Creatinine (Up/C)Irbesartan 300 mg Pooled-18.595% Confidence Interval -34.6 to 1.7percent change
Percent Change in Urine Protein/Creatinine (Up/C)RE-021 (Sparsentan) 400 and 800 mg Pooled-47.495% Confidence Interval -56.3 to -36.9percent change
Percent Change in Urine Protein/Creatinine (Up/C)RE-021 (Sparsentan) 200mg-33.195% Confidence Interval -49.3 to -11.6percent change
Percent Change in Urine Protein/Creatinine (Up/C)RE-021 (Sparsentan) 400mg-52.795% Confidence Interval -64.3 to -37.2percent change
Percent Change in Urine Protein/Creatinine (Up/C)RE-021 (Sparsentan) 800mg-41.395% Confidence Interval -54.4 to -24.4percent change
Percentage of Patients Achieving FSGS Partial Remission Endpoint (FPRE)RE-021 (Sparsentan) 200, 400, 800 mg Pooled28.13percentage of patients
Percentage of Patients Achieving FSGS Partial Remission Endpoint (FPRE)Irbesartan 300 mg Pooled9.38percentage of patients
Percentage of Patients Achieving FSGS Partial Remission Endpoint (FPRE)RE-021 (Sparsentan) 400 and 800 mg Pooled31.37percentage of patients
Percentage of Patients Achieving FSGS Partial Remission Endpoint (FPRE)RE-021 (Sparsentan) 200 mg15.38percentage of patients
Percentage of Patients Achieving FSGS Partial Remission Endpoint (FPRE)RE-021 (Sparsentan) 400 mg38.10percentage of patients
Percentage of Patients Achieving FSGS Partial Remission Endpoint (FPRE)RE-021 (Sparsentan) 800 mg26.67percentage of patients

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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