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Inaxaplin in Subjects With Proteinuric APOL1-mediated Kidney Disease

This study is being done to learn more about the safety, effectiveness, and tolerability of Inaxaplin in participants with APOL1-mediated kidney disease (AMKD). People of African ancestry are more likely to have certain APOL1 variants and are more at risk for chronic kidney disease (CKD). Currently, treatment for CKD exists only to control some aspects of the disease, such as high blood pressure. However, it is important to also treat the worsening of the kidney function as well as the underlying cause of CKD. Inaxaplin is being studied to determine if it can slow or stop the worsening of kidney function and target the underlying cause of this disease. Inaxaplin is an investigational drug.

Age & Gender

  • 18 years ~ 67 years
  • Male, Female, Gender Inclusive

Visit Availability

  • Standard business hours (M-F, 8-5)

Location

North Carolina (Statewide), South Carolina, Virginia

What will be asked of you

Blood collection, height, weight, electrocardiogram (ecg), urine collection, physical exam, taking investigational drug.

Incentives

depends on visit $25-$250, parking paid

In-person visits:
7
Total length of participation:
5 months

Looking for Specific Volunteers

Able to participate:

  • APOL1-mediated Kidney Disease
  • African descent or american indian or Hispanic
  • Protein in urine

Not eligible if:

  • on dialysis or transplant
  • pregnant or breastfeeding

Contact the Team

Visit Location

Contact & Visit Location

Primary Contact

Visit Study Website

Primary Visit Location

Burnett-Womack Building (UNC-Chapel Hill)
160 Dental Cir, Chapel Hill, NC 27514, USA

Secondary Visit Location

UNC Eastowne Medical Office Building
100 Eastowne Dr, Chapel Hill, NC 27514, USA

Additional Study Information

Principal Investigator

Vimal Derebail
Medicine-Nephrology

Study Type

Clinical or Medical
Interventional

Study Topics

Blood Pressure
Diabetes
Kidneys and Liver

IRB Number

24-2946

ClinicalTrials.gov

NCT05312879

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