Pharmacokinetics of Apixaban in Nephrotic Syndrome

Proteinuria Clinical Trial

Official title:

Pharmacokinetics of Apixaban in Nephrotic Syndrome

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02599532
• Other study ID #: 14-1455
• Secondary ID: 550KR161709
• Status: Completed
• Phase: Phase 1
• Start date: April 30, 2017
• Est. completion date: June 28, 2019

Study information

• Verified date: July 2019
• Source: University of North Carolina, Chapel Hill
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is to investigate the pharmacokinetics and pharmacodynamics of apixaban in nephrotic syndrome.

Description:

Nephrotic syndrome (NS) is characterized by proteinuria and hypoalbuminemia, and patients with nephrotic syndrome are known to be hypercoaguable with increased incidence of venous thromboembolism necessitating anticoagulation. While classically warfarin has been used as an anticoagulant in NS, newer oral anticoagulants, such as apixaban, are increasingly used to treat venous thromboembolism (VTE) in the general population. It is unknown how hypoalbuminemia and proteinuria affect the pharmacokinetics and pharmacodynamics of apixaban.

This will be a parallel arm, single-dose pilot study of the pharmacokinetics of apixaban in adults with nephrotic syndrome. Goal enrollment of twenty subjects with non-diabetic nephropathy who have nephrotic-range proteinuria, defined as >3.5g/24 hours or UPC >3.5 and ten healthy control subjects without nephrotic syndrome. Each subject will be administered a single dose of apixaban 10 mg. Plasma drug concentration level and plasma anti-Xa activity levels will be measured at 0, 0.5, 1, 3, 4, 6, 8, 24 hours after drug administration in order to determine the maximum plasma concentration of apixaban, area under the curve, and half-life of apixaban in the setting of hypoalbuminemia and proteinuria due to nephrotic syndrome. Apixaban levels will be measured via liquid-chromatography spectrometry mass. Additionally, thrombin generation will be measured at 0, 3, 6, and 24 hours.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 21
• Est. completion date: June 28, 2019
• Est. primary completion date: June 28, 2019
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 79 Years

Eligibility

• Inclusion Criteria:

• Study subjects:

• Between 18 and 79 years old

• Confirmed diagnosis of Nephrotic Syndrome, with at least one of the following:

• 1. Nephrotic-range proteinuria, defined as >3.5 g/24 hours or UPC >3.5 (confirmed within 1 month prior to scheduled study visit)

• 2. Hypoalbuminemia, defined as <3 g/dL (confirmed within 1 month prior to scheduled study visit)

• Control subjects:

• Between 18 and 79 years old

• Normal albumin levels (=3.5 mg/dL)

• No proteinuria (UPC <0.15)

• Exclusion criteria:

• Age <18 or = 80 years old

• SCr = 1.5 AND weight = 60kg (these subjects would receive a reduce dose of apixaban, per drug labeling)

• On dialysis

• Baseline prolonged PT/INR, PTT (as defined by greater than the upper limit of normal)

• INR will be used as the primary lab value to evaluate bleeding risk (e.g. a patient presenting with an INR within normal limits, but prolonged PT or PTT, will not meet this exclusion criterion and will still be eligible for the study)

• Reference Ranges

• INR: >1.4

• PT: >13.3 sec

• aPTT: >37.7 sec

• Platelets <100

• History of GI bleed

• History of intracranial bleed

• History of stroke

• Use of (but not limited to) the following medications within the past 14 days:

• Inducers of CYP3A4 (e.g. rifampin, carbamazepine, phenytoin, St. John's wort, etc.)

• Strong inhibitors of CYP3A4 (e.g. ketoconazole, ritonavir, clarithromycin, etc.)

• Antiplatelet and/ or anticoagulant agents: heparin, aspirin* (see below), clopidogrel, prasugrel, NSAIDs, warfarin, rivaroxaban, dabigatran, edoxaban

• Selective serotonin reuptake inhibitor (SSRI) or serotonin-norepinephrine reuptake inhibitors (SNRI)

• Pregnancy/breastfeeding

• Liver disease with impaired synthetic function (INR >1.4, total bilirubin >1.2)

• Congestive heart failure

Special consideration for patients on aspirin: for patients on chronic low-dose aspirin therapy, we will allow a 7 day wash out period. This will only be allowed for patients who are taking aspirin as primary prophylaxis or for unclear indications. Patients who are on aspirin therapy for following indications will be excluded: primary prophylaxis of stroke due to atrial fibrillation, secondary prevention of stroke or myocardial infarction, history of coronary artery disease or peripheral vascular disease. For patients who meet the potential criteria for the 7-day wash out, their medical history will be reviewed by one of the clinician investigators to ensure that it is safe and appropriate to hold the agent.

Those subjects taking aspirin for the following reasons will be excluded:

• Primary stroke prevention from atrial fibrillation

• Secondary prevention due to prior stroke, heart attack or cardiac stent

• Existing heart disease or peripheral vascular disease.

Related Conditions & MeSH terms

• Nephrosis
• Nephrotic Syndrome
• Proteinuria
• Syndrome

Intervention

Drug:
• apixaban
Study subjects will be given a single-dose of apixaban 10 mg.

Locations

Country	Name	City	State
United States	University of North Carolina at Chapel Hill	Chapel Hill	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
University of North Carolina, Chapel Hill	North Carolina Translational and Clinical Sciences Institute

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Proportion of germline variants in genes involved in apixaban metabolism and clearance	Explore the relationship between variant genes responsible for apixaban metabolism and clearance (CYP3A4/5, CYP1A2, CYP2J2, ABCB1, and ABCG2) and drug exposure as measured by AUC. Genotyping analyses will be performed at conclusion of study and appropriate conventional statistical analyses will be employed to assess all genotype-phenotype associations.	DNA extracted from whole blood specimens will be genotyped at the conclusion of enrollment, approximately 12 months.
Primary	Area under the concentration versus time curve after single dose (AUC) of apixaban		Predose; 0.5, 1, 3, 4, 6, and 8 hours (hr) postdose on Day 1; 24 hours postdose on Day 2
Secondary	Mean terminal phase plasma half-life (t½)		Predose; 0.5, 1, 3, 4, 6, and 8 hours postdose on Day 1; 24 hours postdose on Day 2
Secondary	Apparent oral clearance (CL/F)		Predose; 0.5, 1, 3, 4, 6, and 8 hours postdose on Day 1; 24 hours postdose on Day 2
Secondary	Maximum observed drug concentration in plasma after single dose administration (Cmax)		Predose; 0.5, 1, 3, 4, 6, and 8 hours postdose on Day 1; 24 hours postdose on Day 2
Secondary	Thrombin Generation Assay		Predose; 3 and 6 hours postdose on Day 1; 24 hours postdose on Day 2
Secondary	Anti-Xa activity		Predose; 0.5, 1, 3, 4, 6, and 8 hours postdose on Day 1; 24 hours postdose on Day 2