ORAL ADMINISTRATION OF A CALCITONIN
    14.
    发明申请
    ORAL ADMINISTRATION OF A CALCITONIN 有权
    钙激素的口服制剂

    公开(公告)号:US20100210526A1

    公开(公告)日:2010-08-19

    申请号:US12529371

    申请日:2008-02-29

    申请人: Yatindra Joshi

    发明人: Yatindra Joshi

    IPC分类号: A61K38/23 A61P19/02 A61P19/10

    摘要: The invention is directed to a method of administering pharmaceutical compositions comprising peptide drugs such as a calcitonin in combination with one or more oral delivery agents, together with an amount of a liquid, and method of treatment of disorders responsive to the action of peptide drugs such as a calcitonin employing such method of administration so as to enhance the oral bioavailability of a calcitonin. The methods of the invention increase the oral absorption and systemic bioavailability of peptide drugs, such as a calcitonin.

    摘要翻译: 本发明涉及一种给药药物组合物的方法,所述药物组合物包含多种药物如降钙素与一种或多种口服递送剂的组合以及一定量的液体,以及治疗响应于肽药物作用的病症的方法, 作为使用这种施用方法的降钙素,以提高降钙素的口服生物利用度。 本发明的方法增加了肽药物如降钙素的口服吸收和全身生物利用度。

    PHARMACEUTICAL COMPOSITION WHICH REDUCES OR ELIMINATES DRUG ABUSE POTENTIAL
    15.
    发明申请
    PHARMACEUTICAL COMPOSITION WHICH REDUCES OR ELIMINATES DRUG ABUSE POTENTIAL 审中-公开
    减少或消除药物滥用潜力的药物组合物

    公开(公告)号:US20090060848A1

    公开(公告)日:2009-03-05

    申请号:US12263790

    申请日:2008-11-03

    IPC分类号: A61K31/137 A61K31/445

    摘要: A pharmaceutical composition which reduces or eliminates the drug abuse potential of central nervous system stimulant comprising: (a) a drug selected from the group consisting of methylphenidate, amphetamine, methamphetamine, and combinations thereof; and (b) a gel forming polymer wherein the gel forming polymer is a polymer that forms a gel when contacted with moisture or placed in an aqueous solution. The present invention is based on the discovery that a central nervous system stimulant such as methylphenidate in combination with a gel forming polymer reduces or eliminates drug abuse potential by swelling in the presence of moisture, and thus, preventing nasal absorption and injectability of the drug.

    摘要翻译: 一种降低或消除中枢神经系统兴奋剂的药物滥用潜力的药物组合物,其包含:(a)选自哌甲酯,苯丙胺,甲基苯丙胺及其组合的药物; 和(b)凝胶形成聚合物,其中凝胶形成聚合物是当与水分接触或置于水溶液中时形成凝胶的聚合物。 本发明基于以下发现:中枢神经系统兴奋剂如哌甲酯与凝胶形成聚合物的组合通过在水分存在下溶胀而降低或消除药物滥用的潜力,从而防止药物的鼻吸收和注射。

    Oral administration of a calcitonin
    20.
    发明授权
    Oral administration of a calcitonin 有权
    口服降钙素

    公开(公告)号:US08410052B2

    公开(公告)日:2013-04-02

    申请号:US12529371

    申请日:2008-02-29

    申请人: Yatindra Joshi

    发明人: Yatindra Joshi

    摘要: The invention is directed to a method of administering pharmaceutical compositions comprising peptide drugs such as a calcitonin in combination with one or more oral delivery agents, together with an amount of a liquid, and method of treatment of disorders responsive to the action of peptide drugs such as a calcitonin employing such method of administration so as to enhance the oral bioavailability of a calcitonin. The methods of the invention increase the oral absorption and systemic bioavailability of peptide drugs, such as a calcitonin.

    摘要翻译: 本发明涉及一种给药药物组合物的方法,所述药物组合物包含多种药物如降钙素与一种或多种口服递送剂的组合以及一定量的液体,以及治疗响应于肽药物作用的病症的方法, 作为使用这种施用方法的降钙素,以提高降钙素的口服生物利用度。 本发明的方法增加了肽药物如降钙素的口服吸收和全身生物利用度。