Phase 3 Chronic Kidney Disease Trial, Recruiting NCT05679024 Sponsor: Region Stockholm Condition: Chronic Kidney Disease
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Phase 3 Chronic Kidney Disease Trial, Recruiting

NCT05679024
Recruiting Phase 3

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 aged 18 or older
  • People who have signed a written consent form to take part in the study
  • People who are currently on ongoing dialysis treatment, OR whose kidney function test results (called eGFR) show a reading below 20 on at least two separate occasions at least 3 months apart — with at least one of those readings below 15 — due to chronic kidney disease, within the past 12 months
  • People who have been diagnosed with a recurring, ongoing, or permanent irregular heart rhythm known as atrial fibrillation (AF) or atrial flutter (AFL)
  • People whose stroke risk score (called CHA2DS2-VASc) is 2 or higher for men, or 3 or higher for women, which indicates a need for blood-thinning medication
  • Women who could become pregnant must have a negative pregnancy test at the start of the study and must agree to use contraception throughout the treatment period

Who may not be able to join:

  • People whose AF or AFL is caused by a treatable, temporary condition (such as a thyroid problem or inflammation around the heart)
  • People who have a certain type of heart valve narrowing (mitral stenosis), whether caused by rheumatic disease at any level, or by other causes if it is moderate to severe
  • People who need long-term blood-thinning medication for a reason other than AF or AFL — for example, a mechanical heart valve or a condition called antiphospholipid syndrome
  • People who have any reason they cannot safely take blood-thinning medication, including: a heart infection (endocarditis), a known intolerance to the specific study medication (apixaban), a liver disease that affects blood clotting, or who are pregnant or breastfeeding
  • People who are currently bleeding actively, or who have had a serious bleeding episode within the past 3 months, or who have a blood disorder that causes bleeding, or who are currently taking two different types of blood-thinning platelet medications at the same time
  • People who are planned to have certain surgeries, including: a kidney transplant from a living donor within the next 3 months; a heart valve surgery; or people on a kidney transplant waiting list at a centre where the study medication (apixaban) is not permitted (confirm with trial site)
  • People who regularly take certain medications that are known to interact with the study drug apixaban — including specific strong-acting medications that affect how the body processes drugs, or regular use of anti-inflammatory pain medications such as NSAIDs or COX-2 inhibitors
  • People whom the study doctor believes should not take part, for any documented reason

Note: Being on a kidney transplant waiting list does not automatically prevent someone from joining, provided the transplant centre's current guidelines allow the use of apixaban. Any changes to waiting list status must be reported to the study team promptly (confirm with trial site).


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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 20 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Marie Evans, Ass Prof, Karolinska University Hospital

Phone: +46760520852

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

Status
Recruiting
Phase
Phase 3
Sponsor
Region Stockholm
Registry
ClinicalTrials.gov
Start date
17 February 2023
Est. completion
31 December 2027

Where this trial is recruiting

🇫🇮 Finland Iceland 🇳🇴 Norway 🇸🇪 Sweden

Primary endpoints

Ischemic stroke or systemic embolism (efficacy); Intracranial bleeding (including hemorrhagic stroke) and fatal bleeding (safety)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov