Phase 4 Type 2 Diabetes Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are 18 years of age or older.
- People who have been diagnosed with type 2 diabetes, based on World Health Organization criteria.
- People who are currently taking a medication called an SGLT2 inhibitor at the highest dose that is tolerable for them.
- People who are currently taking a blood pressure medication known as an ACE inhibitor or an ARB, at the highest dose that is tolerable for them.
- People whose blood potassium level was 4.8 mmol/L or lower at the time of their screening appointment.
- People who have chronic kidney disease, defined as having a certain level of kidney function (eGFR of 25 or above) and a certain level of protein in the urine (confirm with trial site for exact values).
- People who speak and understand Danish fluently.
Who may not be able to join:
- People who are unable to give informed consent to participate.
- People with severely reduced kidney function (eGFR below 25 ml/min/1.73m²).
- People with severe liver disease, as shown by certain blood test results.
- People with an active cancer diagnosis, other than a common type of skin cancer called basal cell carcinoma.
- People who are taking steroid medications affecting the whole body at the time they would be assigned to a treatment group.
- People who have had weight-loss (bariatric) surgery in the past 2 years, or other bowel or stomach surgeries that cause long-term problems with absorbing nutrients.
- People who have had issues with alcohol or drug use within the 3 months before giving consent, or who have any ongoing condition that may make it difficult to follow the trial procedures reliably.
- People with chronic or acute inflammation of the pancreas (pancreatitis).
- People who are pregnant or breastfeeding.
- People with a poorly controlled serious medical condition, such as severe heart failure, a stroke or heart attack within the past 3 months, or any other condition the trial investigator considers too risky for participation.
- People who are allergic to the trial drug (finerenone) or any of its ingredients.
- People currently taking certain medications that strongly interact with how the body processes the trial drug (confirm specific medication names with the trial site).
- People currently taking other medications in a class called mineralocorticoid receptor antagonists (MRAs), such as spironolactone or eplerenone.
- People with rare inherited conditions affecting how the body handles certain sugars, including galactose intolerance, total lactase deficiency, or glucose-galactose malabsorption.
- People with a condition called Addison's disease, which affects the adrenal glands.
- People who are unable to have an MRI scan.
- People who have previously had a kidney or heart transplant.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: +4528928399
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in left ventricular mass measured by non-contrast cardiac MRI of the heart; Change in albuminuria measured by a urinary albumin-to-creatinine ratio (UACR) in morning spot urine samples (first morning voids).
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.