Literature DB >> 35639287

Olipudase Alfa: First Approval.

Susan J Keam1.   

Abstract

Olipudase alfa (XENPOZYME®) is a recombinant human acid sphingomyelinase that has been developed by Sanofi, for the treatment of acid sphingomyelinase deficiency (ASMD). Olipudase alfa catalyses the hydrolysis of sphingomyelin accumulated in hepatocytes and in mononuclear-macrophage cells, such as the lungs, liver, spleen, kidneys and bone marrow. Olipudase alfa was approved in Japan under the SAKIGAKE designation on 28 March 2022 for use in adult and paediatric patients with non-CNS manifestations of ASMD and has received a positive Committee for Medicinal Products for Human Use opinion in the EU. Regulatory review in the USA is underway. This article summarizes the milestones in the development of olipudase alfa leading to this first approval for the treatment of patients with ASMD.
© 2022. The Author(s), under exclusive licence to Springer Nature Switzerland AG.

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Year:  2022        PMID: 35639287     DOI: 10.1007/s40265-022-01727-x

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  1 in total

1.  A randomized, placebo-controlled clinical trial evaluating olipudase alfa enzyme replacement therapy for chronic acid sphingomyelinase deficiency (ASMD) in adults: One-year results.

Authors:  Melissa Wasserstein; Robin Lachmann; Carla Hollak; Laila Arash-Kaps; Antonio Barbato; Renata C Gallagher; Roberto Giugliani; Norberto Bernardo Guelbert; Takayuki Ikezoe; Olivier Lidove; Paulina Mabe; Eugen Mengel; Maurizio Scarpa; Eubekir Senates; Michel Tchan; Jesus Villarrubia; Yixin Chen; Sandy Furey; Beth L Thurberg; Atef Zaher; Monica Kumar
Journal:  Genet Med       Date:  2022-04-26       Impact factor: 8.864

  1 in total

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