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    • 4. 发明申请
    • EBOLAVIRUS AND MARBURGVIRUS VACCINES
    • EBOLAVIRUS和MARBURGVIRUS疫苗
    • WO2016097065A1
    • 2016-06-23
    • PCT/EP2015/080108
    • 2015-12-16
    • CUREVAC AG
    • RAUCH, SusanneJASNY, Edith
    • A61K39/00A61K39/12C12N15/67
    • A61K39/12A61K2039/53A61K2039/54A61K2039/575A61K2039/70C07K14/005C12N7/00C12N2760/14134C12N2760/14234C12N2830/50
    • The present invention relates to an mRNA sequence, comprising a coding region, encoding at least one antigenic peptide or protein derived from the glycoprotein (GP) and/or the matrix protein 40 (VP40) and/or the nucleoprotein (NP) of a virus of the genus Ebolavirus or Marburgvirus or a fragment, variant or derivative thereof. Additionally, the present invention relates to a composition comprising a plurality of mRNA sequences comprising a coding region, encoding at least one antigenic peptide or protein derived from the glycoprotein (GP) and/or the matrix protein 40 (VP40) and/or the nucleoprotein (NP) of a virus of the genus Ebolavirus or Marburgvirus or a fragment, variant or derivative thereof. Furthermore it also discloses the use of the mRNA sequence or the composition comprising a plurality of mRNA sequences for the preparation of a pharmaceutical composition, especially a vaccine, e.g. for use in the prophylaxis or treatment of Ebolavirus or Marburgvirus infections. The present invention further describes a method of treatment or prophylaxis of Ebolavirus or Marburgvirus infections using the mRNA sequence.
    • 本发明涉及一种mRNA序列,其包含编码来自病毒的糖蛋白(GP)和/或基质蛋白40(VP40)和/或核蛋白(NP)的至少一种抗原肽或蛋白质的编码区 的埃博病毒属或马尔堡病毒或其片段,变体或衍生物。 另外,本发明涉及包含多个mRNA序列的组合物,所述mRNA序列包含编​​码区,编码至少一种衍生自糖蛋白(GP)的抗原肽或蛋白质和/或基质蛋白40(VP40)和/或核蛋白 (NP)或其片段,变体或衍生物。 此外,它还公开了使用mRNA序列或包含多个mRNA序列的组合物用于制备药物组合物,特别是疫苗,例如疫苗。 用于预防或治疗埃博病毒或马尔堡病毒感染。 本发明还描述了使用mRNA序列治疗或预防埃博病毒或马尔堡病毒感染的方法。
    • 7. 发明申请
    • OPTIMIZED NUCLEIC ACID MOLECULES
    • 优化的核酸分子
    • WO2017081082A2
    • 2017-05-18
    • PCT/EP2016/077145
    • 2016-11-09
    • CUREVAC AG
    • BAUMHOF, PatrickRAUCH, SusanneKOWALCZYK, AleksandraLUTZ, JohannesJASNY, EdithPETSCH, BenjaminTHESS, AndreasSCHLAKE, ThomasFOTIN-MLECZEK, MariolaHEIDENREICH, ReginaLAZZARO, SandraDÖNER, FatmaGROßE, Wolfgang
    • C12N15/00A61K48/00
    • C12N15/00A61K48/00A61K2039/53C07K2319/00
    • The present invention provides optimized nucleic acid molecules, methods for optimization of nucleic acid molecules and uses of optimized nucleic acid molecules. A modular design principle is provided that is suitable to generate a nucleic acid, particularly mRNA, which is tailored for a respective application. The nucleic acid molecules of the present invention can be obtained by the versatile combination of multiple modules on nucleic acid level. Such nucleic acid, e.g. mRNA, can be tailored by combining one or more modules, comprising (i) a nucleic acid moiety encoding a polypeptide of interest (e.g. a protein potentially producing a therapeutic outcome) and (ii) at least one further coding or non-coding nucleic acid moiety, e.g. selected among nucleic acid moieties encoding a polypeptide element, such as a secretory signal peptide (SSP), a multimerization element (dimerization, trimerization, tetramerization and oligomerization), a virus like particle (VLP) forming element, a transmembrane element, a dendritic cell targeting element, an immunological adjuvant element, an element promoting antigen presentation; a 2A peptide; a peptide linker element, elements that extend protein half-life, and/or any other polypeptide or protein. Non-coding nucleic acid moieties may be selected e.g. from the group comprising 3'-UTR, 5'-UTR, IRES element, miRNA moiety, histone stem loop, poly(C) sequence, polyadenylation signal, polyA-sequence. The optimized nucleic acid molecule can further be characterized by the presence of at least one modified nucleoside. The versatility of the present invention allows for rational design of a large variety of different nucleic acid molecules with desired properties.
    • 本发明提供了优化的核酸分子,用于优化核酸分子的方法和优化的核酸分子的用途。 提供了模块化设计原理,其适合于产生针对相应应用定制的核酸,特别是mRNA。 本发明的核酸分子可以通过在核酸水平上多种组件的多种组合来获得。 这样的核酸,例如 可以通过组合一种或多种模块来定制mRNA,所述模块包含(i)编码感兴趣的多肽(例如可能产生治疗结果的蛋白质)的核酸部分和(ii)至少一种另外的编码或非编码核酸 部分,例如 (SSP),多聚化元件(二聚化,三聚化,四聚化和低聚化),病毒样颗粒(VLP)形成元件,跨膜元件,树突状细胞等的编码多肽元件的核酸部分 靶向元件,免疫佐剂元件,促进抗原呈递的元件; 2A肽; 肽接头元件,延长蛋白质半衰期的元件,和/或任何其他多肽或蛋白质。 可以选择例如非编码核酸部分。 来自包含3'-UTR,5'-UTR,IRES元件,miRNA部分,组蛋白茎环,聚(C)序列,聚腺苷酸化信号,聚A序列的组。 优化的核酸分子可以进一步通过存在至少一种修饰的核苷来表征。 本发明的多功能性允许合理设计具有期望特性的多种不同核酸分子。
    • 9. 发明申请
    • BUNYAVIRALES VACCINE
    • WO2019038332A1
    • 2019-02-28
    • PCT/EP2018/072675
    • 2018-08-22
    • CUREVAC AG
    • PETSCH, BenjaminJASNY, Edith
    • C12N15/67C12N15/85
    • The present invention is directed to an artificial nucleic acid, particularly to an artificial RNA, and to polypeptides suitable for use in treatment or prophylaxis of an infection with a virus of the order Bunyavirales, particularly Severe fever with thrombocytopenia syndrome virus (SFTSV), Rift Valley fever virus (RVFV), or Crimean-Congo hemorrhagic fever virus (CCHFV), or a disorder related to such an infection. The present invention further concerns a Bunyavirales vaccine, particularly a SFTSV, RVFV, or CCHFV vaccine. The present invention is directed to an artificial nucleic acid, polypeptides, compositions and vaccines comprising the artificial nucleic acid or the polypeptides. The invention further concerns a method of treating or preventing a disorder or a disease, first and second medical uses of the artificial nucleic acid, polypeptides, compositions and vaccines. Further, the invention is directed to a kit, particularly to a kit of parts, comprising the artificial nucleic acid, polypeptides, compositions and vaccines.