Results of a prospective observational study of imiglucerase biosimilar in adults with type I Gaucher disease

Long-term therapy with the imiglucerase biosimilar was associated with a stable course of GD without progression. It was characterized by a good safety profile and low immunogenicity.

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Publication Details

Journal
Terapevticheskii arkhiv
Published
2025-03-26
DOI
https://doi.org/10.26442/00403660.2025.02.203194
Citations
1
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
1.16
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article

Results of a prospective observational study of imiglucerase biosimilar in adults with type I Gaucher disease

Rais K. Khayretdinov, Vadim Bezrukikh, Е. В. Сайфуллина, О. А. Markova et al.
1 citations
Terapevticheskii arkhiv
Lysosomal Storage Disorders Research
1.16
article

Results of a prospective observational study of imiglucerase biosimilar in adults with type I Gaucher disease

Rais K. Khayretdinov, Vadim Bezrukikh, Е. В. Сайфуллина, О. А. Markova, Elena Lukina, С. А. Волкова, Evgeniy V. Vasiliev, Tatiana Shelekhova, A.Yu. Borozinets, Е. Г. Кириллова, О. Е. Данилова, Marina Kosinova, Р. В. Пономарев, И. Л. Давыдкин, E. V. Zuev, Galina N. Salogub
article en
1 citations

Abstract

Long-term therapy with the imiglucerase biosimilar was associated with a stable course of GD without progression. It was characterized by a good safety profile and low immunogenicity.

Terapevticheskii arkhivVol. 97(2)
Privolzhsky Research Medical University (RU), Federal Almazov North-West Medical Research Centre (RU), Medical Genetics Center (DE), Saratov State Medical University (RU), Bashkir State Medical University (RU), Krasnoyarsk Regional Clinical Hospital (RU), Samara State Medical University (RU)
Openalex Percentile: Top 24%
Lysosomal Storage Disorders Research
1.16
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