Literature DB >> 30022433

Pegvaliase: First Global Approval.

Anthony Markham1.   

Abstract

BioMarin Pharmaceutical is developing pegvaliase (PALYNZIQ™) as a treatment for phenylketonuria, a genetic disorder caused by deficiency of phenylalanine hydroxylase which leads to neurotoxic accumulation of phenylalanine. Data from the phase III PRISM clinical trial program indicate treatment with pegvaliase is associated with sustained reductions in blood phenylalanine levels and sustained improvements in neurological sequelae in patients with phenylketonuria. Based on these positive results pegvaliase was recently approved in the US for adults with phenylketonuria who have uncontrolled blood phenylalanine concentrations on current treatment. This article summarizes the milestones in the development of pegvaliase leading to this first approval.

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Year:  2018        PMID: 30022433     DOI: 10.1007/s40259-018-0292-3

Source DB:  PubMed          Journal:  BioDrugs        ISSN: 1173-8804            Impact factor:   5.807


  4 in total

1.  Phenylalanine Monitoring via Aptamer-Field-Effect Transistor Sensors.

Authors:  Kevin M Cheung; Kyung-Ae Yang; Nako Nakatsuka; Chuanzhen Zhao; Mao Ye; Michael E Jung; Hongyan Yang; Paul S Weiss; Milan N Stojanović; Anne M Andrews
Journal:  ACS Sens       Date:  2019-11-01       Impact factor: 7.711

2.  A microparticulate based formulation to protect therapeutic enzymes from proteolytic digestion: phenylalanine ammonia lyase as case study.

Authors:  Irene Pereira de Sousa; Charlotte Gourmel; Olena Berkovska; Michael Burger; Jean-Christophe Leroux
Journal:  Sci Rep       Date:  2020-02-27       Impact factor: 4.379

3.  Expression of phenylalanine ammonia lyase as an intracellularly free and extracellularly cell surface-immobilized enzyme on a gut microbe as a live biotherapeutic for phenylketonuria.

Authors:  Yu Jiang; Bingbing Sun; Fenghui Qian; Feng Dong; Chongmao Xu; Wuling Zhong; Rui Huang; Qiwei Zhai; Yu Jiang; Sheng Yang
Journal:  Sci China Life Sci       Date:  2022-07-28       Impact factor: 10.372

Review 4.  Protein Degradation and the Pathologic Basis of Phenylketonuria and Hereditary Tyrosinemia.

Authors:  Neha Sarodaya; Bharathi Suresh; Kye-Seong Kim; Suresh Ramakrishna
Journal:  Int J Mol Sci       Date:  2020-07-15       Impact factor: 5.923

  4 in total

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