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Extracorporeal Blood Treatment
LIPOSORBER® LA-15 System for Focal Segmental Glomerulosclerosis (FSGSALLAGE Trial)
N/A
Recruiting
Research Sponsored by Kaneka Medical America LLC
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
A patient has nephrotic syndrome associated with primary FSGS when standard treatment options are unsuccessful or not well tolerated and the patient's glomerular filtration rate (GFR) ≥ 45 ml/min/1.73 m2
A patient is post renal transplantation
Must not have
Cardiac impairments such as uncontrolled arrhythmia, unstable angina, decompensated congestive heart failure, or valvular disease
Body weight < 15 kg (33.1 lbs)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 month after the final apheresis treatment.
Awards & highlights
No Placebo-Only Group
Summary
This trial tests a blood-filtering device called the LIPOSORBER® LA-15 System in adults with kidney issues from FSGS who haven't had success with other treatments or have had severe side effects. The device helps by cleaning the blood to protect the kidneys.
Who is the study for?
This trial is for adults and children with a kidney disease called primary FSGS who haven't improved on standard treatments or can't handle their side effects. Participants need to have a certain level of kidney function (GFR ≥ 45 ml/min/1.73m2) and can be post-kidney transplant patients. It's not for those over 75, under 22, with severe health issues that could affect the study, or women who are pregnant.
What is being tested?
The LIPOSORBER® LA-15 System is being tested in this study. It's designed for people whose focal segmental glomerulosclerosis hasn't responded to usual treatments like steroids or calcineurin inhibitors, or if these treatments caused severe side effects.
What are the potential side effects?
Possible side effects of using the LIPOSORBER® LA-15 System may include reactions related to blood filtering process such as low blood pressure, bleeding due to heparin (a drug used during the procedure), allergic reactions to materials used in the device like dextran sulfate, and complications from having tubes placed in the body.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have FSGS with unsuccessful standard treatments and my kidney function is still okay.
Select...
I have had a kidney transplant.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I do not have serious heart problems like uncontrolled irregular heartbeat or severe heart failure.
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My body weight is less than 33.1 lbs.
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I am taking blood pressure medicine that isn't an ACE inhibitor and can't stop it for apheresis.
Select...
I am unable or unwilling to sign the consent form.
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I cannot undergo LIPOSORBER® treatment due to severe heart or blood pressure issues.
Select...
I cannot take blood thinners due to severe bleeding disorders or stomach ulcers.
Select...
I do not have any ongoing infections that could interfere with the study.
Select...
I cannot or do not want to follow the study's visit schedule.
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I am either over 75 or under 22 years old.
Select...
I have thyroid or liver problems.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 1 month after the final apheresis treatment.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 month after the final apheresis treatment.
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Evaluate the safety and probable benefit of the LIPOSORBER® LA-15 System in relieving nephrotic syndrome associated with primary FSGS at 1 month after the final apheresis treatment. partial remission at 1 month after the final apheresis treatment.
Secondary study objectives
Nephrotic condition at 1, 3, 6, 12, and 24 months after the final apheresis treatment, including the percentage of patients who obtain complete or partial remission at 3, 6, 12, and 24 months.
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: LIPOSORBER® LA-15 SystemExperimental Treatment1 Intervention
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.
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for Focal Segmental Glomerulosclerosis (FSGS) include corticosteroids, calcineurin inhibitors, and lipid apheresis systems like the LIPOSORBER® LA-15. Corticosteroids work by reducing inflammation and suppressing the immune system, which helps to decrease proteinuria and preserve kidney function.
Calcineurin inhibitors also suppress the immune system but specifically target T-cell activation, reducing the immune response that contributes to kidney damage. The LIPOSORBER® LA-15 system removes lipoproteins and immune complexes from the blood, which can help reduce the levels of circulating factors that contribute to kidney injury.
These treatments are crucial for FSGS patients as they aim to reduce proteinuria, slow disease progression, and improve overall kidney function, thereby enhancing the patient's quality of life and long-term prognosis.
[Case of a focal segmental glomerulosclerosis collapsing variant associated with a hypertrophic column of Bertin].
[Case of a focal segmental glomerulosclerosis collapsing variant associated with a hypertrophic column of Bertin].
Find a Location
Who is running the clinical trial?
Kaneka Medical America LLCLead Sponsor
12 Previous Clinical Trials
682 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I do not have serious heart problems like uncontrolled irregular heartbeat or severe heart failure.I have FSGS with unsuccessful standard treatments and my kidney function is still okay.You are pregnant, breastfeeding, or planning to get pregnant before the study is finished. If you have the potential to become pregnant, you should avoid getting pregnant while using the LIPOSORBER device and during the study.I have had a kidney transplant.My body weight is less than 33.1 lbs.I am taking blood pressure medicine that isn't an ACE inhibitor and can't stop it for apheresis.I am unable or unwilling to sign the consent form.I cannot undergo LIPOSORBER® treatment due to severe heart or blood pressure issues.I cannot take blood thinners due to severe bleeding disorders or stomach ulcers.I do not have any ongoing infections that could interfere with the study.I cannot or do not want to follow the study's visit schedule.I am either over 75 or under 22 years old.You are allergic to dextran sulfate, heparin, or ethylene oxide.I have thyroid or liver problems.I cannot stop my ACE inhibitor medication for 24 hours before apheresis.
Research Study Groups:
This trial has the following groups:- Group 1: LIPOSORBER® LA-15 System
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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