Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Phase 3 Study to Investigate the Efficacy and Safety of FInerenone, in Addition to Standard of Care, on the Progression of Kidney Disease in Patients With Non-Diabetic Chronic Kidney Disease

Trial Profile

A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Phase 3 Study to Investigate the Efficacy and Safety of FInerenone, in Addition to Standard of Care, on the Progression of Kidney Disease in Patients With Non-Diabetic Chronic Kidney Disease

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 27 Aug 2026

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Finerenone (Primary)
  • Indications Renal failure
  • Focus Registrational; Therapeutic Use
  • Acronyms FIND-CKD
  • Sponsors Bayer

Most Recent Events

  • 20 Aug 2026 According to Bayer media release, data from this trial will be presented at the European Society of Cardiology (ESC) Congress 2026 in Munich, Germany, from August 28-31, 2026.
  • 30 Jul 2026 According to a Bayer media release, company announced the submission of a New Drug Application to the Center of Drug Evaluation (CDE) of China's National Medical Products Administration (NMPA), seeking approval to extend the indication of finerenone in China to include adult patients with non-diabetic chronic kidney disease is based on positive data from the Phase III FIND-CKD study.
  • 05 Jun 2026 According to a Bayer media release, a prespecified subgroup analysis from this trial were simultaneously published in JAMA.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top