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Disease · MONDO_0005016

Comparisons in its trials44

Comparisons Trial comparisons calculated in the trials shown here, most participants first. A comparison in one of these trials does not always compare a treatment for the disease, so read the two groups.

ComparisonGroup 1, with the outcomeGroup 2, with the outcomeParticipantsTrialSource
Finerenone vs Placebo: The First Occurrence of the Composite Endpoint of Onset of Kidney Failure, a Sustained Decrease of eGFR ≥40% From Baseline Over at Least 4 Weeks, or Renal Death.350 of 3,686395 of 3,6667,352NCT02545049Trial comparisons
Finerenone vs Placebo: All-cause Hospitalization1,573 of 3,6861,605 of 3,6667,352NCT02545049Trial comparisons
Finerenone vs Placebo: deaths from any cause339 of 3,686383 of 3,6667,352NCT02545049Trial comparisons
Finerenone vs Placebo: All-cause Mortality333 of 3,686370 of 3,6667,352NCT02545049Trial comparisons
Finerenone vs Placebo: The First Occurrence of the Composite Endpoint of Onset of Kidney Failure, a Sustained Decrease in eGFR of ≥57% From Baseline Over at Least 4 Weeks, or Renal Death108 of 3,686139 of 3,6667,352NCT02545049Trial comparisons
Finerenone vs Placebo: The First Occurrence of the Composite Endpoint of Cardiovascular Death, Non-fatal Myocardial Infarction, Non Fatal Stroke, or Hospitalization for Heart Failure.458 of 3,686519 of 3,6667,352NCT02545049Trial comparisons
Finerenone vs Placebo: serious adverse events1,158 of 3,6831,215 of 3,6587,341NCT02545049Trial comparisons
Finerenone vs Placebo: All-cause Mortality219 of 2,833244 of 2,8415,674NCT02540993Trial comparisons
Finerenone vs Placebo: The First Occurrence of the Composite Endpoint of Onset of Kidney Failure, a Sustained Decrease of eGFR ≥40% From Baseline Over at Least 4 Weeks, or Renal Death504 of 2,833600 of 2,8415,674NCT02540993Trial comparisons
Finerenone vs Placebo: The First Occurrence of the Composite Endpoint of Cardiovascular Death, Non-fatal Myocardial Infarction, Non-fatal Stroke, or Hospitalization for Heart Failure367 of 2,833420 of 2,8415,674NCT02540993Trial comparisons
Finerenone vs Placebo: All-cause Hospitalization1,263 of 2,8331,321 of 2,8415,674NCT02540993Trial comparisons
Finerenone vs Placebo: The First Occurrence of the Composite Endpoint of Onset of Kidney Failure, a Sustained Decrease in eGFR of ≥57% From Baseline Over at Least 4 Weeks, or Renal Death252 of 2,833326 of 2,8415,674NCT02540993Trial comparisons
Finerenone vs Placebo: deaths from any cause222 of 2,833250 of 2,8415,674NCT02540993Trial comparisons
Finerenone vs Placebo: serious adverse events902 of 2,827971 of 2,8315,658NCT02540993Trial comparisons
Canagliflozin 100 mg vs Placebo: deaths from any cause164 of 2,200193 of 2,1974,397NCT02065791Trial comparisons
Canagliflozin 100 mg vs Placebo: serious adverse events737 of 2,200806 of 2,1974,397NCT02065791Trial comparisons
Intent-to-Treat (ITT) Atrasentan vs Intent-to-Treat Placebo: Time to First Occurrence of a Component of Composite Renal Endpoint for All Randomized Participants (Pooled)152 of 1,834192 of 1,8343,668NCT01858532Trial comparisons
Intent-to-Treat (ITT) Responder Atrasentan vs Intent-to-Treat (ITT) Responder Placebo: Time to the First Occurrence of a Component of the Composite Renal Endpoint in the Intent-to-Treat (ITT) Responder Set (as Randomized)
79 of 1,325105 of 1,3232,648NCT01858532Trial comparisons
Intent-to-Treat (ITT) Responder Atrasentan vs Intent-to-Treat (ITT) Responder Placebo: Time to a 50% Estimated Glomerular Filtration Rate Reduction in the Intent-to-Treat (ITT) Responder Set (as Randomized)
78 of 1,32588 of 1,3232,648NCT01858532Trial comparisons
Intent-to-Treat (ITT) Responder Atrasentan vs Intent-to-Treat (ITT) Responder Placebo: Time to Cardio-renal Composite Endpoint in the Intent-to-Treat (ITT) Responder Set (as Randomized)147 of 1,325172 of 1,3232,648NCT01858532Trial comparisons

diseases-2026-09-18-0.1.0

Sources 6

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • NLM's MeSHNLM's terms
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
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
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • NLM's MeSHNLM's
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PubMedNLM's terms

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/diseases/v1/MONDO_0005016/comparisons