Literature DB >> 27839981

Long-term safety and efficacy of taliglucerase alfa in pediatric Gaucher disease patients who were treatment-naïve or previously treated with imiglucerase.

Ari Zimran1, Derlis Emilio Gonzalez-Rodriguez2, Aya Abrahamov3, Peter A Cooper4, Sheeba Varughese4, Pilar Giraldo5, Milan Petakov6, Ee Shien Tan7, Raul Chertkoff8.   

Abstract

Taliglucerase alfa is an enzyme replacement therapy approved for treatment of Gaucher disease (GD) in children and adults in several countries. This multicenter extension study assessed the efficacy and safety of taliglucerase alfa in pediatric patients with GD who were treatment-naïve (n=10) or switched from imiglucerase (n=5). Patients received taliglucerase alfa 30 or 60U/kg (treatment-naïve) or the same dose as previously treated with imiglucerase every other week. In treatment-naïve patients, taliglucerase alfa 30 and 60U/kg, respectively, reduced mean spleen volume (-18.6 multiples of normal [MN] and -26.0MN), liver volume (-0.8MN and -0.9MN), and chitotriosidase activity (-72.7% and -84.4%), and increased mean Hb concentration (+2.0g/dL and +2.3g/dL) and mean platelet count (+38,200/mm3 and +138,250/mm3) from baseline through 36 total months of treatment. In patients previously treated with imiglucerase, these disease parameters remained stable through 33 total months of treatment with taliglucerase alfa. Most adverse events were mild/moderate; treatment was well tolerated. These findings extend the taliglucerase alfa safety and efficacy profile and demonstrate long-term clinical improvement in treatment-naïve children receiving taliglucerase alfa and maintenance of disease stability in children switched to taliglucerase alfa. Treatment was well-tolerated, with no new safety signals. This study is registered at www.clinicaltrials.gov as NCT01411228.
Copyright © 2016 Shire Human Genetic Therapies, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Enzyme replacement therapy; Gaucher disease; Imiglucerase; Pediatrics; Taliglucerase alfa

Mesh:

Substances:

Year:  2016        PMID: 27839981     DOI: 10.1016/j.bcmd.2016.10.005

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  5 in total

1.  Safety and effectiveness of taliglucerase alfa in patients with Gaucher disease: an interim analysis of real-world data from a multinational drug registry (TALIAS).

Authors:  Lina Titievsky; Tilman Schuster; Ronnie Wang; Muhammad Younus; Andrew Palladino; Kabir Quazi; Michael P Wajnrajch; Betina Hernandez; Pamela S Becker; Neal J Weinreb; Christina Chambers; Roy Mansfield; Louise Taylor; Li-Jung Tseng; Paige Kaplan
Journal:  Orphanet J Rare Dis       Date:  2022-04-01       Impact factor: 4.123

2.  Switching between Enzyme Replacement Therapies and Substrate Reduction Therapies in Patients with Gaucher Disease: Data from the Gaucher Outcome Survey (GOS).

Authors:  Derralynn A Hughes; Patrick Deegan; Pilar Giraldo; Özlem Göker-Alpan; Heather Lau; Elena Lukina; Shoshana Revel-Vilk; Maurizio Scarpa; Jaco Botha; Noga Gadir; Ari Zimran
Journal:  J Clin Med       Date:  2022-08-31       Impact factor: 4.964

Review 3.  Spotlight on taliglucerase alfa in the treatment of pediatric patients with type 1 Gaucher disease.

Authors:  Punita Gupta; Gregory M Pastores
Journal:  Pediatric Health Med Ther       Date:  2017-06-16

Review 4.  Taliglucerase alfa: safety and efficacy across 6 clinical studies in adults and children with Gaucher disease.

Authors:  Ari Zimran; Michael Wajnrajch; Betina Hernandez; Gregory M Pastores
Journal:  Orphanet J Rare Dis       Date:  2018-02-23       Impact factor: 4.123

Review 5.  Compendium on Food Crop Plants as a Platform for Pharmaceutical Protein Production.

Authors:  Aneta Gerszberg; Katarzyna Hnatuszko-Konka
Journal:  Int J Mol Sci       Date:  2022-03-17       Impact factor: 5.923

  5 in total

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