Head-to-head trial of pegunigalsidase alfa versus agalsidase beta in patients with Fabry disease and deteriorating renal function: results from the 2-year randomised phase III BALANCE study
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Published:2023-11-08
Issue:
Volume:
Page:jmg-2023-109445
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ISSN:0022-2593
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Container-title:Journal of Medical Genetics
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language:en
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Short-container-title:J Med Genet
Author:
Wallace Eric L, Goker-Alpan Ozlem, Wilcox William R, Holida Myrl, Bernat John, Longo Nicola, Linhart AlešORCID, Hughes Derralynn AORCID, Hopkin Robert J, Tøndel Camilla, Langeveld Mirjam, Giraldo Pilar, Pisani Antonio, Germain Dominique PaulORCID, Mehta Ankit, Deegan Patrick B, Molnar Maria Judit, Ortiz Damara, Jovanovic Ana, Muriello Michael, Barshop Bruce A, Kimonis Virginia, Vujkovac Bojan, Nowak AlbinaORCID, Geberhiwot Tarekegn, Kantola Ilkka, Knoll Jasmine, Waldek Stephen, Nedd Khan, Karaa Amel, Brill-Almon Einat, Alon Sari, Chertkoff Raul, Rocco Rossana, Sakov Anat, Warnock David GORCID
Abstract
BackgroundPegunigalsidase alfa is a PEGylated α-galactosidase A enzyme replacement therapy. BALANCE (NCT02795676) assessed non-inferiority of pegunigalsidase alfa versus agalsidase beta in adults with Fabry disease with an annualised estimated glomerular filtration rate (eGFR) slope more negative than −2 mL/min/1.73 m2/year who had received agalsidase beta for ≥1 year.MethodsPatients were randomly assigned 2:1 to receive 1 mg/kg pegunigalsidase alfa or agalsidase beta every 2 weeks for 2 years. The primary efficacy analysis assessed non-inferiority based on median annualised eGFR slope differences between treatment arms.ResultsSeventy-seven patients received either pegunigalsidase alfa (n=52) or agalsidase beta (n=25). At baseline, mean (range) age was 44 (18–60) years, 47 (61%) patients were male, median eGFR was 74.5 mL/min/1.73 m2and median (range) eGFR slope was −7.3 (−30.5, 6.3) mL/min/1.73 m2/year. At 2 years, the difference between median eGFR slopes was −0.36 mL/min/1.73 m2/year, meeting the prespecified non-inferiority margin. Minimal changes were observed in lyso-Gb3 concentrations in both treatment arms at 2 years. Proportions of patients experiencing treatment-related adverse events and mild or moderate infusion-related reactions were similar in both groups, yet exposure-adjusted rates were 3.6-fold and 7.8-fold higher, respectively, with agalsidase beta than pegunigalsidase alfa. At the end of the study, neutralising antibodies were detected in 7 out of 47 (15%) pegunigalsidase alfa-treated patients and 6 out of 23 (26%) agalsidase beta-treated patients. There were no deaths.ConclusionsBased on rate of eGFR decline over 2 years, pegunigalsidase alfa was non-inferior to agalsidase beta. Pegunigalsidase alfa had lower rates of treatment-emergent adverse events and mild or moderate infusion-related reactions.Trial registration numberNCT02795676.
Funder
Chiesi USA, Inc Protalix Biotherapeutics, Inc.
Subject
Genetics (clinical),Genetics
Cited by
13 articles.
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