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    • 3. 发明申请
    • Microparticles with adsorbed polynucleotide-containing species
    • 具有吸附的含多核苷酸物质的微粒
    • US20150072016A1
    • 2015-03-12
    • US14543221
    • 2014-11-17
    • Novartis Vaccines and Diagnostics, Inc.
    • Derek O'HAGANManmohan SINGH
    • A61K47/34A61K9/14C12N7/00A61K39/21
    • A61K47/34A61K9/14A61K9/1647A61K9/167A61K31/7088A61K39/21A61K2039/55511C12N7/00C12N2740/16022C12N2740/16371
    • Microparticles with adsorbed polynucleotide-containing species, compositions containing the same, methods of making such microparticles, and uses thereof are disclosed. The microparticles comprise (a) a biodegradable polymer, such as a polyhydroxy butyric acid, a polycaprolactone, a polyorthoester, a polyanhydride, or a polycyanoacrylate, (b) a cationic surfactant such as cetyltrimethylammonium bromide, (c) and a polynucleotide-containing species adsorbed on the surface of the microparticles, wherein the polynucleotide-containing species constitutes at least 5 percent of the total weight of said microparticles. Examples of polynucleotide-containing species include polynucleotide-containing immunological adjuvants, such as CpG oligonucleotides, and polynucleotide-containing species that encode polypeptide-containing antigens, such as RNA and DNA vector constructs. Methods of delivering a therapeutic amount of a polynucleotide-containing species to a host animal, methods of stimulating an immune response, methods of treating a host animal having a pathogenic organism infection, methods of immunizing a host animal against infection by a pathogenic organism, and uses of the microparticle compositions for vaccines are also provided.
    • 公开了具有吸附的含多核苷酸的微粒,含有它们的组合物,制备这种微粒的方法及其用途。 微粒包括(a)可生物降解的聚合物,例如多羟基丁酸,聚己内酯,聚原酸酯,聚酐或聚氰基丙烯酸酯,(b)阳离子表面活性剂如十六烷基三甲基溴化铵,(c)和含多核苷酸的物质 吸附在微粒表面上,其中含多核苷酸的物质占所述微粒总重量的至少5%。 含多核苷酸的物质的实例包括含多核苷酸的免疫佐剂,例如CpG寡核苷酸,以及编码含多肽的抗原的含多核苷酸的物种,例如RNA和DNA载体构建体。 将治疗量的含多核苷酸的物质递送至宿主动物的方法,刺激免疫应答的方法,治疗具有致病性生物体感染的宿主动物的方法,免疫宿主动物免受病原体感染的方法,以及 还提供了微粒组合物用于疫苗的用途。
    • 4. 发明申请
    • ANGIOGENICALLY EFFECTIVE UNIT DOSE OF FGF-2 AND METHOD OF USE
    • FGF-2的有效单位剂量及其使用方法
    • US20140349932A1
    • 2014-11-27
    • US14311523
    • 2014-06-23
    • Novartis Vaccines and Diagnostics, Inc.
    • Martha Jo Whitehouse
    • A61K38/18
    • A61K38/1825A61K2300/00
    • The present invention provides a unit dose composition comprising 0.2 μg/kg to 48 μg/kg of an FGF-2 of SEQ ID NO:2, or an angiogenically active fragment or mutein thereof in a pharmaceutically acceptable carrier. Also provided is a method for treating a human patient for coronary artery disease, comprising administering into one or more coronary vessels or a peripheral vein of said patient a safe and angiogenically effective dose of a recombinant FGF-2, or an angiogenically active fragment or mutein thereof. Also provided is a pharmaceutical composition comprising a therapeutically effective amount of FGF-2, alone or in combination with heparin, in a therapeutically effective carrier.
    • 本发明提供在药学上可接受的载体中包含0.2μg/ kg至48μg/ kg的SEQ ID NO:2的FGF-2或其血管生成活性片段或突变蛋白的单位剂量组合物。 还提供了一种用于治疗人类患者冠状动脉疾病的方法,包括向所述患者的一个或多个冠状动脉血管或外周静脉施用安全和血管生成有效剂量的重组FGF-2或血管生成活性片段或突变蛋白 其中。 还提供了药物组合物,其在治疗有效的载体中包含治疗有效量的单独或与肝素组合的FGF-2。
    • 10. 发明申请
    • NOROVIRUS AND SAPOVIRUS ANTIGENS
    • NOROVIRUS和SAPOVIRUS抗原
    • US20130095552A1
    • 2013-04-18
    • US13686837
    • 2012-11-27
    • Novartis Vaccines and Diagnostics, Inc.
    • Doris CoitMichael HoughtonColin McCoinAngelica Medina-SelbyMichael Vajdy
    • C12N9/14
    • C12N9/14A61K39/00A61K39/12A61K2039/5258A61K2039/53A61K2039/545A61K2039/55544A61K2039/55555C07K14/005C07K2319/00C07K2319/40C12N2770/16022C12N2770/16034
    • Immunogenic compositions that elicit immune responses against Norovirus and Sapovirus antigens are described. In particular, the invention relates to polynucleotides encoding one or more capsid proteins or other immunogenic viral polypeptides from one or more strains of Norovirus and/or Sapovirus, coexpression of such immunogenic viral polypeptides with adjuvants, and methods of using the polynucleotides in applications including immunization and production of immunogenic viral polypeptides and viral-like particles (VLPs). Methods for producing Norovirus- or Sapovirus-derived multiple epitope fusion antigens or polyproteins and immunogenic compositions comprising one or more immunogenic polypeptides, polynucleotides, VLPs, and/or adjuvants are also described. The immunogenic compositions of the invention may also contain antigens other than Norovirus or Sapovirus antigens, including antigens that can be used in immunization against pathogens that cause diarrheal diseases, such as antigens derived from rotavirus.
    • 描述了引起针对诺如病毒和曙红病毒抗原的免疫应答的免疫原性组合物。 特别地,本发明涉及编码来自一种或多种诺如病毒和/或札幌病毒株的一种或多种衣壳蛋白或其它免疫原性病毒多肽的多核苷酸,这种免疫原性病毒多肽与佐剂的共表达,以及在包括免疫的应用中使用多核苷酸的方法 以及产生免疫原性病毒多肽和病毒样颗粒(VLP)。 还描述了用于生产包含一种或多种免疫原性多肽,多核苷酸,VLP和/或佐剂的诺如病毒或札幌病毒衍生的多表位融合抗原或多蛋白的免疫原性组合物的方法。 本发明的免疫原性组合物还可以含有除诺如病毒或札幌病毒抗原以外的抗原,包括可用于免疫引起腹泻疾病的病原体的抗原,例如来源于轮状病毒的抗原。