Post Approval Study of Liposorber LA-15 System for the Treatment of Focal Segmental Glomerulosclerosis in Children

Key facts

Sponsor

Kaneka Medical America LLC

Principal Investigator

Jeffrey I Silberzweig, MD

Weill Medical College of Cornell University

Intervention

LIPOSORBER® LA-15 System(device)

Enrollment

35 target

Eligibility

21 years · All sexes

Timeline

2015 – 2028

Study locations (12)

• Loma Linda University Children's Hospital, Loma Linda, California, United States
• Cedars Sinai Medical Center, Los Angeles, California, United States
• Nemours/A.I. duPont Hospital for Children, Wilmington, Delaware, United States
• Nemours Children's Health, Orlando, Florida, United States
• Helen DeVos Children's Hospital, Grand Rapids, Michigan, United States
• University of Minnesota, Minneapolis, Minnesota, United States
• Weill Cornell Medical Center / NewYork-Presbyterian, New York, New York, United States
• University of North Carolina, Chapel Hill, North Carolina, United States
• Akron Children's Hospital, Akron, Ohio, United States
• St. Christopher's Hospital for Children, Philadelphia, Pennsylvania, United States
• Medical University of South Carolina Children's Hospital, Charleston, South Carolina, United States
• Children's Hospital of Richmond at VCU, Richmond, Virginia, United States

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

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Additional recruiting or active studies for the same condition.

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• RECRUITINGPHASE3NCT07220083
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• RECRUITINGPHASE1, PHASE2NCT06090227
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• RECRUITINGNCT05650619
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• RECRUITINGNANCT04065438
  Post Approval Study for Treatment of Drug-resistant Adult and Pediatric Primary FSGS Using the LIPOSORBER® LA-15 System
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• ACTIVE NOT RECRUITINGPHASE3NCT03493685
  Study of Sparsentan in Patients With Primary Focal Segmental Glomerulosclerosis (FSGS)
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See all trials for Idiopathic multidrug-resistant nephrotic syndrome →