Long-Term Results from an Open-Label Extension Study of Atacicept for the Treatment of IgA Nephropathy

• Published in: Journal of the American Society of Nephrology Vol. 36; no. 4; pp. 679 - 687
• Main Authors: Barratt, Jonathan, Barbour, Sean J., Brenner, Robert M., Cooper, Kerry, Wei, Xuelian, Eren, Necmi, Floege, Jürgen, Jha, Vivekanand, Kim, Sung Gyun, Maes, Bart, Phoon, Richard K.S., Singh, Harmeet, Tesař, Vladimír, Lafayette, Richard
• Format: Journal Article
• Language: English
• Published: United States American Society of Nephrology 01.04.2025
• Subjects: kidney disease; IgA nephropathy
• ISSN: 1046-6673; 1533-3450; 1533-3450
• DOI: 10.1681/ASN.0000000541

Visual Abstract Key PointsParticipants who completed a 36-week double-blind study of atacicept were eligible for a 60-week, open-label extension study.Atacicept 96-week treatment resulted in sustained reductions in galactose-deficient IgA1, hematuria, and urine protein-creatinine ratio.The slope of the eGFR was similar to that observed in the general population without kidney disease.BackgroundB-cell activating factor (BAFF) and A proliferation-inducing ligand (APRIL) play key roles in the pathogenesis of IgA nephropathy. Atacicept is a novel fully humanized fusion protein, self-administered at home by subcutaneous injection, that binds and inhibits BAFF and APRIL. By inhibiting BAFF and APRIL, atacicept targets the underlying B-cell-mediated pathogenesis driving disease progression. This study evaluated the long-term efficacy and safety of atacicept in patients with IgA nephropathy over 96 weeks.MethodsParticipants with IgA nephropathy who received atacicept (25, 75, or 150 mg) or placebo in a 36-week phase 2b, randomized, blinded trial were enrolled in an open-label extension study and received atacicept 150 mg for an additional 60 weeks. Key efficacy outcomes were changes in galactose-deficient IgA1 (Gd-IgA1), percentage of participants with hematuria, urine protein-creatinine ratio (UPCR), and eGFR over 96 weeks. Long-term safety data were also evaluated.ResultsThere were 113 participants (67 [59%] male; 46 [41%] female) who ranged in age from 18 to 67 years who received ≥1 atacicept dose. Over 96 weeks, safety data demonstrated that atacicept was generally well tolerated. There were also sustained reductions (mean±SEM) in Gd-IgA1 (−66%±2%), percentage of participants with hematuria (−75%; 95% confidence intervals, −87 to −59; in participants with baseline hematuria), and UPCR (−52%±5%). The mean annualized slope of eGFR was −0.6±0.5 ml/min per 1.73 m2 through 96 weeks.ConclusionsAtacicept was well tolerated over the duration of the study. Atacicept treatment reduced Gd-IgA1, hematuria, and UPCR with stabilization of eGFR through 96 weeks.Clinical Trial registry name and registration number:Atacicept in Subjects with IgA Nephropathy (ORIGIN 2), NCT04716231.PodcastThis article contains a podcast at https://dts.podtrac.com/redirect.mp3/www.asn-online.org/media/podcast/JASN/2024_10_26_KTS_October2024.mp3