Literature DB >> 31884868

Review of Cerliponase Alfa: Recombinant Human Enzyme Replacement Therapy for Late-Infantile Neuronal Ceroid Lipofuscinosis Type 2.

Grace Lewis1,2, Amanda M Morrill1, Stephanie L Conway-Allen1, Bernard Kim1,2.   

Abstract

The objective of this review is to summarize the pharmacology, efficacy, and safety of cerliponase alfa for the treatment of late infantile neuronal ceroid lipofuscinosis type 2 (CLN2). Cerliponase alfa is recombinant human tripeptidyl peptidase 1 enzyme replacement therapy. A phase 1/2 trial established the efficacy and safety of cerliponase alfa for treatment of neuronal ceroid lipofuscinosis type 2. Treatment with intracerebroventricular cerliponase alfa resulted in slower decline of motor and language functions compared with natural history controls. Common adverse events include convulsions, electrocardiography abnormalities, pyrexia, vomiting, and upper respiratory tract infections. Intracerebroventricular device-related adverse events also occur. Cerliponase alfa is the first therapy for neuronal ceroid lipofuscinosis type 2 that targets the disease etiology. Cerliponase alfa is effective in delaying the progression of motor language decline for patients with neuronal ceroid lipofuscinosis type 2.

Entities:  

Keywords:  BMN 190; batten disease; cerliponase; enzyme replacement therapy; neuronal ceroid lipofuscinosis

Year:  2019        PMID: 31884868     DOI: 10.1177/0883073819895694

Source DB:  PubMed          Journal:  J Child Neurol        ISSN: 0883-0738            Impact factor:   1.987


  6 in total

1.  Neuronal ceroid lipofuscinosis: genetic and phenotypic spectrum of 14 patients from Turkey.

Authors:  Melis Kose; Engin Kose; Aycan Ünalp; Ünsal Yılmaz; Selvinaz Edizer; Hande Gazeteci Tekin; Pakize Karaoğlu; Taha Reşid Özdemir; Esra Er; Hüseyin Onay; Eser Sozmen Yildirim
Journal:  Neurol Sci       Date:  2021-01-23       Impact factor: 3.307

2.  Presymptomatic treatment of classic late-infantile neuronal ceroid lipofuscinosis with cerliponase alfa.

Authors:  J Schaefers; L J van der Giessen; C Klees; E H Jacobs; S Sieverdink; M H G Dremmen; J K H Spoor; A T van der Ploeg; J M P van den Hout; H H Huidekoper
Journal:  Orphanet J Rare Dis       Date:  2021-05-14       Impact factor: 4.123

3.  Characterization of neurological disease progression in a canine model of CLN5 neuronal ceroid lipofuscinosis.

Authors:  Elizabeth J Meiman; Grace Robinson Kick; Cheryl A Jensen; Joan R Coates; Martin L Katz
Journal:  Dev Neurobiol       Date:  2022-04-28       Impact factor: 3.102

Review 4.  Molecular networking in the neuronal ceroid lipofuscinoses: insights from mammalian models and the social amoeba Dictyostelium discoideum.

Authors:  Robert J Huber
Journal:  J Biomed Sci       Date:  2020-05-20       Impact factor: 8.410

5.  Intracranial delivery of AAV9 gene therapy partially prevents retinal degeneration and visual deficits in CLN6-Batten disease mice.

Authors:  Katherine A White; Hemanth R Nelvagal; Timothy A Poole; Bin Lu; Tyler B Johnson; Samantha Davis; Melissa A Pratt; Jon Brudvig; Ana B Assis; Shibi Likhite; Kathrin Meyer; Brian K Kaspar; Jonathan D Cooper; Shaomei Wang; Jill M Weimer
Journal:  Mol Ther Methods Clin Dev       Date:  2021-01-05       Impact factor: 6.698

6.  The LINCE Project: A Pathway for Diagnosing NCL2 Disease.

Authors:  Daniel Rodrigues; Maria José de Castro; Pablo Crujeiras; Anna Duat-Rodriguez; Ana Victoria Marco; Mireia Del Toro; María L Couce; Cristóbal Colón
Journal:  Front Pediatr       Date:  2022-03-29       Impact factor: 3.418

  6 in total

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