会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明申请
    • SYNTHETIC HYPERGLYCOSYLATED, AND HYPERGLYCOSYLATED PROTEASE-RESISTANT POLYPEPTIDE VARIANTS, ORAL FORMULATIONS AND METHODS OF USING THE SAME
    • 合成高效液相色谱法和超高效抗菌多肽变体,口服制剂及其使用方法
    • WO2007092537A2
    • 2007-08-16
    • PCT/US2007/003333
    • 2007-02-07
    • ALIOS BIOPHARMA, INC.BLATT, Lawrence M.SEIWERT, Scott D.HONG, Jin
    • BLATT, Lawrence M.SEIWERT, Scott D.HONG, Jin
    • C07K14/555C07K14/56C07K14/565C07K14/57A61K38/21
    • C07K14/555A61K38/00C07K14/56C07K14/565C07K14/57Y02A50/385Y02A50/387Y02A50/393
    • The present invention provides synthetic Type I interferon receptor polypeptide agonists comprising consensus or hybrid Type I interferon receptor polypeptide agonists, containing one or more native or non-native glycosylation sites. The present invention provides synthetic Type I interferon receptor polypeptide agonists comprising consensus or hybrid Type I interferon receptor polypeptide agonists, containing one or more native or non-native glycosylation sites, as well as erythropoietin and darbepoetin alfa, each of which are linked to a penetrating peptide that facilitates translocation of a substance across a biological barrier as well as pharmaceutical compositions, including oral formulations, of the same. The present invention further provides oral formulations of hyperglycosylated or protease-resistant, hyperglycosylated polypeptide variants, which polypeptide variants lack at least one protease cleavage site found in a parent polypeptide, and thus exhibit increased protease resistance compared to the parent polypeptide, which polypeptide variants further include (1) a carbohydrate moiety covalently linked to at least one non-native glycosylation site not found in the parent protein therapeutic or (2) a carbohydrate moiety covalently linked to at least one native glycosylation site found but not glycosylated in the parent protein therapeutic. The present invention further provides compositions, including oral pharmaceutical compositions, comprising the synthetic Type I interferon receptor polypeptide agonist, the hyperglycosylated polypeptide variant, or the hyperglycosylated, protease-resistant polypeptide variant. The present invention further provides containers, devices, and kits comprising the synthetic Type I interferon receptor polypeptide agonist, the hyperglycosylated polypeptide variant, or the hyperglycosylated, protease-resistant polypeptide variant. The present invention further provides therapeutic methods involving administering an effective amount of an oral pharmaceutical composition comprising a synthetic Type I interferon receptor polypeptide agonist, a hyperglycosylated polypeptide variant, or a hyperglycosylated, protease-resistant polypeptide variant to an individual in need thereof.
    • 本发明提供含有一个或多个天然或非天然糖基化位点的含有共有或混合型I型干扰素受体多肽激动剂的合成的I型干扰素受体多肽激动剂。 本发明提供合成的I型干扰素受体多肽激动剂,其包含含有一个或多个天然或非天然糖基化位点的共有或混合型I型干扰素受体多肽激动剂,以及红细胞生成素和达比泊汀α,其各自与渗透性 促进物质穿过生物屏障移位的肽以及包含口服制剂的药物组合物。 本发明进一步提供高糖基化或蛋白酶抗性,高糖基化多肽变体的口服制剂,该多肽变体在母体多肽中缺少至少一个蛋白酶切割位点,因此与亲本多肽相比表现出增加的蛋白酶抗性,该多肽变体进一步 包括(1)与亲本蛋白质治疗剂中未发现的至少一个非天然糖基化位点共价连接的碳水化合物部分,或(2)与母体蛋白质治疗中发现但未糖基化的至少一个天然糖基化位点共价连接的碳水化合物部分 。 本发明还提供包含口服药物组合物的组合物,其包含合成的I型干扰素受体多肽激动剂,高糖基化多肽变体或高糖基化的,蛋白酶抗性多肽变体。 本发明还提供了包含合成的I型干扰素受体多肽激动剂,高糖基化多肽变体或高糖基化的蛋白酶抗性多肽变体的容器,装置和试剂盒。 本发明进一步提供治疗方法,其涉及向有需要的个体施用有效量的包含合成的I型干扰素受体多肽激动剂,高糖基化多肽变体或高糖基化的,蛋白酶抗性多肽变体的口服药物组合物。
    • 8. 发明申请
    • SYNTHETIC HYPERGLYCOSYLATED, PROTEASE-RESISTANT POLYPEPTIDE VARIANTS, ORAL FORMULATIONS AND METHODS OF USING THE SAME
    • 合成的低聚肽,抗蛋白酶的多肽变体,口服制剂和使用它们的方法
    • WO2006020580A2
    • 2006-02-23
    • PCT/US2005/028165
    • 2005-08-08
    • INTERMUNE, INC.
    • HONG, JinSEIWERT, Scott D.BLATT, Lawrence M.
    • A61K38/14A61K38/17
    • A61K38/212
    • The present invention provides synthetic Type I interferon receptor polypeptide agonists comprising consensus or hybrid Type I interferon receptor polypeptide agonists, containing one or more native or non-native glycosylation sites. The present invention further provides oral formulations of protease-resistant or protease-resistant, hyperglycosylated polypeptide variants, which polypeptide variants lack at least one protease cleavage site found in a parent polypeptide, and thus exhibit increased protease resistance compared to the parent polypeptide, which polypeptide variants further include (1) a carbohydrate moiety covalently linked to at least one non-native glycosylation site not found in the parent protein therapeutic or (2) a carbohydrate moiety covalently linked to at least one native glycosylation site found but not glycosylated in the parent protein therapeutic. The present invention further provides compositions, including oral pharmaceutical compositions, comprising the synthetic Type I interferon receptor polypeptide agonist, the hyperglycosylated polypeptide variant, the protease-resistant polypeptide variant, or the hyperglycosylated, protease-resistant polypeptide variant. The present invention further provides containers, devices, and kits comprising the synthetic Type I interferon receptor polypeptide agonist, the hyperglycosylated polypeptide variant, the protease-resistant polypeptide variant, or the hyperglycosylated, protease-resistant polypeptide variant. The present invention further provides therapeutic methods involving administering an effective amount of an oral pharmaceutical composition comprising a synthetic Type I interferon receptor polypeptide agonist, a hyperglycosylated polypeptide variant, a protease-resistant polypeptide variant, or a hyperglycosylated, protease-resistant polypeptide variant to an individual in need thereof.
    • 本发明提供了包含共有或杂合I型干扰素受体多肽激动剂的合成I型干扰素受体多肽激动剂,其含有一个或多个天然或非天然糖基化位点。 本发明进一步提供了蛋白酶抗性或蛋白酶抗性的高糖基化多肽变体的口服制剂,所述多肽变体缺少在亲本多肽中发现的至少一个蛋白酶切割位点,并因此表现出与亲本多肽相比增加的蛋白酶抗性,所述多肽 变体还包括(1)共价连接至亲本蛋白质治疗剂中未发现的至少一个非天然糖基化位点的碳水化合物部分,或(2)共价连接至在亲本蛋白质中发现但未糖基化的至少一个天然糖基化位点的碳水化合物部分 蛋白质治疗。 本发明进一步提供包含合成的I型干扰素受体多肽激动剂,高糖基化的多肽变体,蛋白酶抗性多肽变体或高糖基化的蛋白酶抗性多肽变体的组合物,包括口服药物组合物。 本发明进一步提供了包含合成的I型干扰素受体多肽激动剂,高糖基化的多肽变体,蛋白酶抗性多肽变体或高糖基化的蛋白酶抗性多肽变体的容器,装置和试剂盒。 本发明进一步提供了治疗方法,其包括将有效量的包含合成的I型干扰素受体多肽激动剂,高糖基化的多肽变体,蛋白酶抗性多肽变体或高糖基化的蛋白酶抗性多肽变体的口服药物组合物施用于 有需要的个人。