An Observational Study to Learn More About How Safe Finerenone is and How Well it Works in Indian People With Chronic Kidney Disease and Type 2 Diabetes in Routine Medical Practice
NotablePrimary endpoints: details revised at 1 of 12 entriesShow 4 more changesShow less
Primary and study completion pushed from Sep 30, 2026 to Oct 31, 2026
Eligibility criteria expanded, about 6 words
Secondary endpoints: details revised at 3 of 7 entries
Study description expanded, about 10 words
MinorPrimary and study completion pushed from Jun 30, 2026 to Sep 30, 2026
Site details revised
v18
Minor3 versionsRe-verified since Apr 9, 2026, no change to tracked fieldsv15-v17
MinorPrimary and study completion dates: Apr 30, 2026 to Jun 30, 2026
Start date: Sep 23, 2025 to Sep 22, 2025
v14
MinorSite details revisedv13
Show 11 earlier versionsHide 11 earlier versions
MinorPrimary and study completion dates: Jan 31, 2026 to Apr 30, 2026
Site details revised
v12
MinorTrial status: Not Yet Recruiting to Active, Not Recruiting
Start date changed from estimate of Sep 19, 2025 to Sep 23, 2025
v11
MinorStart date: Aug 25, 2025 to Sep 19, 2025v10
MinorStart date: Aug 1, 2025 to Aug 25, 2025v9
MinorRe-verified, no change to tracked fieldsv8
NotableStart date: Jun 2, 2025 to Aug 1, 2025
Primary and study completion dates: Dec 1, 2025 to Jan 31, 2026
v7
MinorRe-verified, no change to tracked fieldsv6
NotableStart date: May 1, 2025 to Jun 2, 2025
Primary and study completion dates: Oct 31, 2025 to Dec 1, 2025
v5
NotableStart date: Feb 28, 2025 to May 1, 2025
Primary and study completion dates: Jun 30, 2025 to Oct 31, 2025
v4
MinorRe-verified, no change to tracked fieldsv3
NotableStart date: Jan 1, 2025 to Feb 28, 2025
Site details revised
v2
MinorStudy First Submitted
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Availability of this study's data will later be determined according to Bayer's commitment to the EFPIA/PhRMA "Principles for responsible clinical trial data sharing". This pertains to scope, timepoint and process of data access. As such, Bayer commits to sharing upon request from qualified researchers patient-level clinical trial data, study-level clinical trial data, and protocols from clinical trials in patients for medicines and indications approved in the US and EU as necessary for conducting legitimate research. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014.
Interested researchers can use www.vivli.org to request access to anonymized patient-level data and supporting documents from clinical studies to conduct research. Information on the Bayer criteria for listing studies and other relevant information is provided in the member section of the portal.