Endopeptidase Cleavage of Anti-Glomerular Basement Membrane Antibodies in vivo in Severe Kidney Disease: An Open-Label Phase 2a StudyShow others and affiliations
2022 (English)In: Journal of the American Society of Nephrology, ISSN 1046-6673, E-ISSN 1533-3450, Vol. 33, no 4, p. 829-838Article in journal (Refereed) Published
Abstract [en]
Background The prognosis for kidney survival is poor in patients presenting with circulating anti-glomerular basement membrane (GBM) antibodies and severe kidney injury. It is unknown if treat-ment with an endopeptidase that cleaves circulating and kidney bound IgG can alter the prognosis.& nbsp;Methods An investigator-driven phase 2a one-arm study (EudraCT 2016-004082-39) was performed in 17 hospitals in five European countries. A single dose of 0.25 mg/kg of imlifidase was given to 15 adults with circulating anti-GBM antibodies and an eGFR < 15 ml/min per 1.73m(2). All patients received standard treatment with cyclophosphamide and corticosteroids, but plasma exchange only if autoantibodies rebounded. The primary outcomes were safety and dialysis independency at 6 months.& nbsp;Results At inclusion, ten patients were dialysis dependent and the other five had eGFR levels between 7 and 14 ml/min per 1.73m(2). The median age was 61 years (range 19-77), six were women, and six were also positive for anti-neutrophil cytoplasmic antibodies. Then 6 hours after imlifidase infusion, all patients had anti-GBM antibodies levels below the reference range of a prespecified assay. At 6 months 67% (ten out of 15) were dialysis independent. This is significantly higher compared with 18% (nine out of 50) in a historical control cohort (P < 0.001, Fishers exact test). Eight serious adverse events (including one death) were reported, none assessed as probably or possibly related to the study drug.& nbsp;Conclusions In this pilot study, the use of imlifidase was associated with a better outcome compared with earlier publications, without major safety issues, but the findings need to be confirmed in a randomized controlled trial.
Place, publisher, year, edition, pages
AMER SOC NEPHROLOGY , 2022. Vol. 33, no 4, p. 829-838
Keywords [en]
anti-GBM disease; endopeptidases; clinical trial; glomerulonephritis; Goodpasture syndrome
National Category
Urology and Nephrology
Identifiers
URN: urn:nbn:se:liu:diva-183877DOI: 10.1681/ASN.2021111460ISI: 000767598900001PubMedID: 35260419Scopus ID: 2-s2.0-85128001625OAI: oai:DiVA.org:liu-183877DiVA, id: diva2:1648200
Note
Funding Agencies|Region Skane [2020-O000028]; Region Ostergotland [LIO-755 381]; Ingrid Asp Foundation [991602]; Hansa Biopharma [IMH-2016-00286]
2022-03-302022-03-302023-04-04Bibliographically approved