Compare Apixaban and Vitamin-K Antagonists in Patients With Atrial Fibrillation (AF) and End-Stage Kidney Disease (ESKD)

Atrial Fibrillation Clinical Trial

— AXADIA  

Official title:

A Safety Study Assessing Oral Anticoagulation With Apixaban Versus Vitamin-K Antagonists in Patients With Atrial Fibrillation (AF) and End-Stage Kidney Disease (ESKD) on Chronic Hemodialysis Treatment

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02933697
• Other study ID #: AXADIA - AFNET 8
• Status: Completed
• Phase: Phase 3
• Start date: June 20, 2017
• Est. completion date: July 31, 2022

Study information

• Verified date: September 2022
• Source: Atrial Fibrillation Network
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The Study is an open-labeled, randomized controlled trial, phase IIIb. Its objective is to assess the safety of the factor Xa inhibitor apixaban versus the vitamin-K antagonist (VKA) phenprocoumon in patients with NVAF and ESKD on hemodialysis. The safety will be assessed by means of the incidence of major and clinically relevant, non-major bleeding on anticoagulation.

Description:

AXADIA is an investigator-driven, prospective, parallel-group, single country, multi-center phase IIIb trial to assess the safety of apixaban versus the vitamin-K antagonist phenprocoumon in patients with NVAF and ESKD on hemodialysis treatment. The trial will be conducted in about 25-30 sites in Germany. The primary goal of this study is to assess the safety of two types of oral anticoagulants in patients with ESKD on hemodialysis with non-valvular atrial fibrillation (NVAF). The novel FXa inhibitor apixaban (at a reduced dose of 2x 2.5 mg/day) will be compared to the vitamin-K antagonist (VKA) phenprocoumon (target range: International Normalized Ratio (INR) 2.0-3.0) regarding bleeding rates during chronic administration for prevention of stroke or systemic embolism. The primary hypothesis of the study is that oral anticoagulation with apixaban will improve the safety by significantly reducing bleeding rates in patients with ESKD on hemodialysis and NVAF compared to the VKA phenprocoumon.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 108
• Est. completion date: July 31, 2022
• Est. primary completion date: July 31, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• End-stage kidney disease (ESKD) with chronic hemodialysis treatment 3 times per week (with about at least 3.5 hours per dialysis)
• Chronic (i.e. repeated) paroxysmal, persistent or permanent atrial fibrillation (AF) or atrial flutter (AFL) documented by standard or Holter ECG on at least 2 separate days before (or apart from) hemodialysis procedures
• Increased risk of stroke or systemic embolism identified by a CHA2DS2-VASc score of 2 or more as an indication for oral anticoagulation
• Patients with ischemic stroke that meet the above criteria, can be included after more than 3 months if not severely handicapped (modified Rankin scale 0 or 1 of 6, i.e. no symptoms or no significant disability and able to carry out all usual activities, despite some symptoms (Farrell, Godwin, Richards, and Warlow (1991))
• Males and females, aged 18 or older

Exclusion Criteria:

• AF or AFL due to reversible causes (e.g., thyrotoxicosis, pericarditis)
• Patients with a new onset of hemodialysis within the last 3 months
• Clinically significant (moderate or severe) aortic and mitral stenosis
• Conditions other than AF or AFL that require chronic anticoagulation (e.g., a prosthetic mechanical heart valve).
• Active infective endocarditis
• Any planned interventional or surgical AF or AFL ablation procedure
• Any active bleeding
• A serious bleeding event in the previous 6 months before screening
• Inadequately controlled (HbA1c levels >8.5%) or untreated diabetes
• History of malignant neoplasms at high risk of current bleeding (see summary of product characteristics (SmPC) of study drugs)
• Known indication for treatment with NSAIDs (see SmPC of study drugs) - acetylsalicylic acid (ASA) up to 100 mg per day is allowed
• Known Antiphospholipid Syndrome requiring anticoagulation
• Impaired liver function e.g., caused by active infection with HIV, HBV or HCV, hepatitis or other liver damage (No limits for ALT and AST values are defined in this study protocol, although mentioned in the SmPC because they are frequently elevated in dialysis patients. In case of clinically relevant increase of ALT or AST level, patient's eligibility is to be decided by the responsible investigator)
• Any type of stroke within 3 months prior to baseline
• Other indication for anticoagulation than AF or AFL
• Valvular heart disease requiring surgery
• A high risk of bleeding (e.g., active peptic ulcer disease, a platelet count of <100,000 per cubic millimeter or hemoglobin level of <8 g per deciliter)
• Documented hemorrhagic tendencies or blood dyscrasias
• Current alcohol or drug abuse
• Life expectancy of less than 1 year
• Indication for dual platelet inhibition at baseline (ASA = 100 mg/day is allowed, clopidrogel is excluded at any dose).
• Active infection or symptoms suggestive of COVID-19 infection.

Related Conditions & MeSH terms

• Atrial Fibrillation
• End-stage Kidney Disease
• Kidney Diseases
• Kidney Failure, Chronic

Intervention

Drug:
• Apixaban
Patients will be instructed to take one tablet of 2.5 mg twice daily: one tablet in the morning and one in the evening at approximately the same time every day (with about 12 hours gap) irrespective of the time of dialysis.
• Phenprocoumon
Subjects in phenprocoumon treatment group will receive phenprocoumon individually adjusted to an INR of 2.0-3.0 as recommended in the appropriate SmPC for AF patients.

Locations

Country	Name	City	State
Germany	Universitätsklinikum Münster	Münster

Sponsors (3)

Lead Sponsor	Collaborator
Atrial Fibrillation Network	Bristol-Myers Squibb, Pfizer

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Assess the safety of the factor Xa inhibitor apixaban versus a vitamin-K antagonist phenprocoumon in patients with NVAF and ESKD on hemodialysis.	The safety will be assessed by means of the incidence of major and clinically relevant, non-major bleeding as well as specific bleedings in dialysis patients (e.g., after shunt removal) on anticoagulation.	1-60 months
Secondary	Compare the efficacy of the factor Xa inhibitor apixaban with the VKA phenprocoumon regarding prevention of thromboembolic events in patients with ESKD on hemodialysis and AF	The efficacy of the factor Xa inhibitor apixaban with the VKA phenprocoumon regarding prevention of thromboembolic events in patients with ESKD on hemodialysis and AF	1-60 months