1. Endopeptidase Cleavage of Anti-Glomerular Basement Membrane Antibodies in vivo in Severe Kidney Disease: An Open-Label Phase 2a Study
- Author
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Uhlin, Fredrik, Szpirt, Wladimir, Kronbichler, Andreas, Bruchfeld, Annette, Soveri, Inga, Rostaing, Lionel, Daugas, Eric, Lionet, Arnaud, Kamar, Nassim, Rafat, Cedric, Myslivecek, Marek, Tesar, Vladimir, Fernström, Anders, Kjellman, Christian, Elfving, Charlotte, McAdoo, Stephen, Molne, Johan, Bajema, Ingeborg, Sonesson, Elisabeth, Segelmark, Mårten, Uhlin, Fredrik, Szpirt, Wladimir, Kronbichler, Andreas, Bruchfeld, Annette, Soveri, Inga, Rostaing, Lionel, Daugas, Eric, Lionet, Arnaud, Kamar, Nassim, Rafat, Cedric, Myslivecek, Marek, Tesar, Vladimir, Fernström, Anders, Kjellman, Christian, Elfving, Charlotte, McAdoo, Stephen, Molne, Johan, Bajema, Ingeborg, Sonesson, Elisabeth, and Segelmark, Mårten
- Abstract
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., Funding Agencies|Region Skane [2020-O000028]; Region Ostergotland [LIO-755 381]; Ingrid Asp Foundation [991602]; Hansa Biopharma [IMH-2016-00286]
- Published
- 2022
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