Treatment of Drug-resistant Pediatric Primary Focal Segmental Glomerulosclerosis Using the Liposorber® LA-15 System

Status: Recruiting
Location: See all (12) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Liposorber® LA-15 System is a blood purification therapy that selectively removes malignant lipoproteins including low density lipoprotein from circulating blood flow and rapidly reduces the plasma cholesterol level. The system was originally developed for the treatment of patients with serious dyslipidemia such as familial hypercholesterolemia and then applied to improve the dyslipidemia, a common complication of nephrotic syndrome and found to bring about improvement not only with the dyslipidemic condition but the nephrotic condition (e.g, proteinuria and hypoproteinemia). Although the definitive mechanism by which the system may relieve nephrotic syndrome is unknown, it has been recognized as one of alternative therapies for refractory nephrotic syndrome including focal segmental glomerulosclerosis (FSGS) in Japan and referred in the Guidelines for the Treatment of Nephrotic Syndrome endorsed by The Japanese Society of Nephrology. This study is conducted as a post approval study imposed by Humanitarian Device Exemption (HDE) order to confirm the safety and efficacy of the Liposorber® LA-15 System in the treatment of drug-resistant pediatric primary FSGS.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 21
Healthy Volunteers: f
View:

• A pediatric patient is deemed suitable for inclusion in the study if the patient has FSGS with a GFR ≥ 45 ml/min/1.73 m 2 and any of the following:

‣ Refractory nephrotic syndrome in which standard treatment options are unsuccessful (i.e., patient is unresponsive to standard corticosteroid and/or calcineurin inhibitor therapy for at least 8 weeks resulting in failure to achieve complete or partial remission);

⁃ Refractory nephrotic syndrome in which standard treatment options are not well tolerated (i.e., patients intolerant to standard therapies due to severe side effects that negatively affect quality of life without providing an acceptable level of clinical benefit);

⁃ Refractory or recurrent nephrotic syndrome in which standard therapy is contraindicated.

∙ or

∙ \- Pediatric post renal transplant patients with nephrotic syndrome associated with primary FSGS.

Locations
United States
California
Loma Linda University Children's Hospital
RECRUITING
Loma Linda
Cedars Sinai Medical Center
RECRUITING
Los Angeles
Delaware
Nemours/A.I. duPont Hospital for Children
RECRUITING
Wilmington
Florida
Nemours Children's Health
TERMINATED
Orlando
Michigan
Helen DeVos Children's Hospital
RECRUITING
Grand Rapids
Minnesota
University of Minnesota
RECRUITING
Minneapolis
North Carolina
University of North Carolina
RECRUITING
Chapel Hill
New York
Weill Cornell Medical Center / NewYork-Presbyterian
RECRUITING
New York
Ohio
Akron Children's Hospital
RECRUITING
Akron
Pennsylvania
St. Christopher's Hospital for Children
RECRUITING
Philadelphia
South Carolina
Medical University of South Carolina Children's Hospital
RECRUITING
Charleston
Virginia
Children's Hospital of Richmond at VCU
WITHDRAWN
Richmond
Contact Information
Primary
Ayaka Kitamura
Ayaka.Kitamura1@kaneka.co.jp
+81-74431813933
Time Frame
Start Date: 2015-05-03
Estimated Completion Date: 2028-07-03
Participants
Target number of participants: 35
Treatments
Experimental: Liposorber® LA-15 System
All study patients who meet the study eligibility criteria will undergo the extracorporeal treatment using Liposorber® LA-15 System. The participants are to be treated with the system twice weekly for the 3weeks and then once weekly for the following 6 weeks.
Sponsors
Leads: Kaneka Medical America LLC

This content was sourced from clinicaltrials.gov

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