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NCT Number: NCT03255447

Peptide GAM Immunoadsorption Therapy in Autoimmune Membranous Nephropathy

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Central Manchester University Hospital Foundation Trust, Manchester, Greater Manchester, United Kingdom

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Biopsy confirmed Primary Membranous Nephropathy within the last 3 years
  • Active disease despite 6 months of supportive care including ACEi or ARB (Active disease defined as uPCR > 300mg/mmol or 24 hour urinary protein >3.5g/1.73m2)
  • Disease severity that in the physicians view warrants treatment prior to completion of 6 months supportive care
  • Anti-PLA2R titre > 170 u/ml
  • Haemophilus and Pneumococcal vaccinations up to date
  • Above the age of 18
  • Able to provide informed consent

Exclusion criteria

  • Evidence of causes of secondary membranous nephropathy
  • eGFR < 20ml/min
  • Treatment with steroids or immunosuppression (including but not limited to cyclophosphamide, MMF or azathioprine) and Biologics (including but limited to Rituximab or belimumab) within 6 months of screening
  • Therapeutic Plasma Exchange within 28 days of screening
  • Previous renal transplantation
  • Co-morbidity, which in physicians' view, would preclude patient from treatment with immunoadsorption.
  • Pregnant at time of screening

Treatment and study plan

Immunoadsorption

Device

Fresenius Globaffin

Primary outcomes

  1. Serum anti-PLA2R titres

    Time frame: 14 days

    Reduction in serum anti-PLA2R titres to normal range

Secondary outcomes

  1. The incidence of treatment related adverse events as defined by CTCAE v4.0

    Time frame: Day 14, 28, 56, 84, 168 and 365

    To assess the safety and tolerability of Immunoadosorption therapy

  2. To determine the effect on disease activity (efficacy)

    Time frame: Day 14, 28, 56, 84, 168 and 365

    Assessment of reduction in proteinuria level and change in eGFR from baseline

  3. Serum anti-PLA2R titres

    Time frame: Day 14, 28, 56, 84, 168 and 365

    Kinetic modelling of serum anti-PLA2R levels

  4. To determine the effect on Quality of life measures (EQ5D)

    Time frame: Day 14, 28, 56, 84, 168 and 365

    To determine the effect on Quality of life measures (EQ5D)

  5. Cost-effectiveness

    Time frame: Day 14, 28, 56, 84, 168 and 365

    Cost-effectiveness of treatment (Incremental cost-effectiveness ratio)

Sponsors and collaborators

Lead sponsor

Manchester University NHS Foundation Trust

Other Gov

Collaborators

  • Fresenius AG

Registry information

Official study title

Phase II Trial Investigating the Safety and Feasibility of Peptide GAM Immunoadsorption in Anti-PLA2R Positive Autoimmune Membranous Nephropathy

Acronym: PRISM

Important dates

Study start
2016
Primary completion
2019
Study completion
2019
First posted
Aug 21, 2017
Registry last updated
Jun 8, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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