WO2026138489 - CAPSID-MODIFIED ADENO-ASSOCIATED VIRUS, PREPARATION THEREFOR AND USE THEREOF

National phase entry is expected:
Publication Number WO/2026/138489
Publication Date 02.07.2026
International Application No. PCT/CN2025/141126
International Filing Date 09.12.2025
Title **
[English] CAPSID-MODIFIED ADENO-ASSOCIATED VIRUS, PREPARATION THEREFOR AND USE THEREOF
[French] VIRUS ADÉNO-ASSOCIÉ MODIFIÉ PAR CAPSIDE, SA PRÉPARATION ET SON UTILISATION
[Chinese] 一种衣壳修饰的腺相关病毒及其制备和应用
Applicants **
QILU PHARMACEUTICAL CO., LTD.
Inventors
WANG, Zhenhua
LUO, Youguang
AN, Zhenming
XIAO, Tongqian
XU, Xianggang
SUN, Zhen
ZHAO, Peilu
ZHANG, Qun
ZHANG, Min
Priority Data
202411906949.8   23.12.2024   CN
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译文

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Quotation for National Phase entry

Country StagesTotal
China Filing, Examination, Granting1703
EPO Filing, Examination, Granting11446
Japan Filing, Examination, Granting2182
South Korea Filing, Examination, Granting2130
USA Filing, Examination, Granting4740
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Total: 22,201
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Abstract[English] Provided are a capsid-modified adeno-associated virus (AAV), preparation therefor and a use thereof. Specifically, provided are an AAV capsid protein variant, a preparation method for recombinant AAV particles comprising a variant capsid protein, and compared with an AAV containing an unmodified parental AAV capsid protein, increased infectivity and gene product expression thereof in target cells such as retinal cells.[French] L'invention concerne un virus adéno-associé (VAA) modifié par capside, sa préparation et son utilisation. En particulier, l'invention concerne un variant de protéine capsidique de VAA, un procédé de préparation de particules de VAA recombinantes comprenant une protéine capsidique de variant, et par comparaison avec un VAA contenant une protéine capsidique de VAA parental non modifiée, une infectivité accrue et une expression de produit génique de celle-ci dans des cellules cibles telles que des cellules rétiniennes.[Chinese] 提供一种衣壳修饰的腺相关病毒(AAV)及其制备和应用。具体地,提供了AAV衣壳蛋白变体、含有所述变体衣壳蛋白的重组AAV病毒颗粒的制备方法,以及与包含未修饰的亲本AAV衣壳蛋白的AAV病毒相比,其对靶细胞(例如视网膜细胞)具有增加的感染性及基因产物表达。