Immunoadsorption
DeviceFresenius Globaffin
NCT Number: NCT03255447
Autoimmune Membranous Nephropathy is now understood to be a condition caused by the immune system although the exact mechanism is not completely known. This study aims to remove the offending part of the immune system using immunoadsorption to not only treat the disease but also use the opportunity to better understand the mechanism of disease. This will allow more targeted treatment in the future with less complications and side effects.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Central Manchester University Hospital Foundation Trust, Manchester, Greater Manchester, United Kingdom
Membranous nephropathy (MN) is among the most common causes of nephrotic syndrome in adults worldwide. The majority of patients will remain stable with either complete remission or partial remission but approximately 20% will progress slowly to end stage renal disease necessitating the need for renal replacement therapy (RRT).
Current standard therapy for primary (or autoimmune) membranous nephropathy is a regime of rotating high dose steroids and immunosuppression was first described in the mid-nineties and has been the mainstay of treatment since but comes with a high side effect burden.
Idiopathic membranous nephropathy is now understood to be an autoimmune disease characterised by the presence of IgG autoantibodies to M-Type Phospholipase A2 Receptor (anti-PLA2R). Immunoadsorption is a method of removing specific circulating immunoglobulins and has been shown to remove over 80% of circulating IgG with a single session immunoadsorption of 2.5 plasma volumes, with albumin and antithrombin III almost unaffected. With multiple sessions this can rise to over 98%.
Immunoadsorption therapy has been in use for a number of years and this study will use Peptide GAM Immunoadsorption therapy developed by Fresenius Healthcare. This uses two systems, the Art Universal and ADAsorb. The Art Universal became commercially available in 2005 and the ADAsorb in 2002.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Fresenius Globaffin
Time frame: 14 days
Reduction in serum anti-PLA2R titres to normal range
Time frame: Day 14, 28, 56, 84, 168 and 365
To assess the safety and tolerability of Immunoadosorption therapy
Time frame: Day 14, 28, 56, 84, 168 and 365
Assessment of reduction in proteinuria level and change in eGFR from baseline
Time frame: Day 14, 28, 56, 84, 168 and 365
Kinetic modelling of serum anti-PLA2R levels
Time frame: Day 14, 28, 56, 84, 168 and 365
To determine the effect on Quality of life measures (EQ5D)
Time frame: Day 14, 28, 56, 84, 168 and 365
Cost-effectiveness of treatment (Incremental cost-effectiveness ratio)
Manchester University NHS Foundation Trust
Other Gov
Phase II Trial Investigating the Safety and Feasibility of Peptide GAM Immunoadsorption in Anti-PLA2R Positive Autoimmune Membranous Nephropathy
Acronym: PRISM
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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