| Literature DB >> 30205177 |
Anu Cherukuri1, Heather Cahan2, Greg de Hart3, Andrea Van Tuyl3, Peter Slasor4, Laurie Bray4, Joshua Henshaw3, Temitayo Ajayi4, Dave Jacoby4, Charles A O'Neill5, Becky Schweighardt3.
Abstract
Treatment with intracerebroventricular (ICV)-delivered cerliponase alfa enzyme replacement therapy (ERT) in a Phase 1/2 study of 24 subjects with CLN2 disease resulted in a meaningful preservation of motor and language (ML) function and was well tolerated. Treatment was associated with anti-drug antibody (ADA) production in the cerebrospinal fluid (CSF) of 6/24 (25%) and in the serum of 19/24 (79%) of clinical trial subjects, respectively, over a mean exposure of 96.4 weeks (range 0.1-129 weeks). Neutralizing antibodies (NAb) were not detected in the CSF of any of the subjects. No events of anaphylaxis were reported. Neither the presence of serum ADA nor drug-specific immunoglobulin E was associated with the incidence or severity of hypersensitivity adverse events. Serum and CSF ADA titers did not correlate with change in ML score. Therefore, the development of an ADA response to cerliponase alfa is not predictive of an adverse safety profile or poor treatment outcome.Entities:
Keywords: Anti-drug antibodies; CLN2; Cerliponase alfa; Enzyme replacement therapy; Hypersensitivity; Immunogenicity; Neuronal ceroid lipofuscinosis
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Year: 2018 PMID: 30205177 DOI: 10.1016/j.clim.2018.09.003
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969