Prostaglandin derivative for treating gastrointestinal disorder
    2.
    发明专利
    Prostaglandin derivative for treating gastrointestinal disorder 审中-公开
    用于治疗胃肠疾病的PROSTAGLANDIN衍生物

    公开(公告)号:JP2013049688A

    公开(公告)日:2013-03-14

    申请号:JP2012232180

    申请日:2012-10-19

    发明人: UENO TAKASHI

    IPC分类号: A61K31/558 A61P1/10

    摘要: PROBLEM TO BE SOLVED: To provide a method for long term treatment of gastrointestinal disorders in a human subject.SOLUTION: The invention relates to a method for the long term treatment of gastrointestinal disorders in a human subject, which comprises administering an effective amount of a halogenated prostaglandin compound and/or its tautomer to the subject. The method induces substantially no electrolyte shifting during the term of the treatment. The compound can improve quality of life in the human subjects with gastrointestinal disorders, is similarly effective in treating male and female human subjects, and also effective in a human subject aged even 65 years and older.

    摘要翻译: 待解决的问题:提供一种在人类受试者中长期治疗胃肠道疾病的方法。 解决方案:本发明涉及一种用于长期治疗人类受试者胃肠道疾病的方法,其包括对受试者施用有效量的卤化前列腺素化合物和/或其互变异构体。 该方法在治疗期间基本上不引起电解质移动。 该化合物可以改善患有胃肠道疾病的人类受试者的生活质量,同样有效地治疗男性和女性人类受试者,并且在65岁及以上的人类受试者中也是有效的。 版权所有(C)2013,JPO&INPIT

    Pharmaceutical composition for long term use of nsaid
    6.
    发明专利
    Pharmaceutical composition for long term use of nsaid 审中-公开
    长期使用NSAID的药物组合物

    公开(公告)号:JP2011032262A

    公开(公告)日:2011-02-17

    申请号:JP2010149382

    申请日:2010-06-30

    发明人: UENO TAKASHI

    摘要: PROBLEM TO BE SOLVED: To provide a method able to perform long term NSAID (non-steroidal anti-inflammatory drug) treatment.
    SOLUTION: The use of a pharmaceutical composition containing cobiprostone or a pharmaceutically acceptable salt, ester, ether or amide thereof together with an NSAID in the long term treatment of a disease or condition which is one of indications for NSAID use in a human patient is provided. In the use, cobiprostone is administered at least 36 mcg/day to the patient who is taking the NSAID. The patient can take the NSAID for a long period of time by administering cobiprostone or the pharmaceutically acceptable salt, ester, ether or amide thereof in combination with the NSAID.
    COPYRIGHT: (C)2011,JPO&INPIT

    摘要翻译: 待解决的问题:提供能够进行长期NSAID(非甾体抗炎药)治疗的方法。 解决方案:在长期治疗作为人类NSAID使用的适应症的疾病或病症中使用含有cobiprostone或其药学上可接受的盐,酯,醚或酰胺与NSAID的药物组合物的应用 提供病人 在使用中,对于服用NSAID的患者,cobiprostone至少每天施用36mcg。 患者可以长时间服用NSAID,通过与NSAID联合给药cobiprostone或其药学上可接受的盐,酯,醚或酰胺。 版权所有(C)2011,JPO&INPIT

    Method for diagnosing or predicting sensitivity to mental disorder
    7.
    发明专利
    Method for diagnosing or predicting sensitivity to mental disorder 有权
    用于诊断或预测精神障碍的灵敏度的方法

    公开(公告)号:JP2005245437A

    公开(公告)日:2005-09-15

    申请号:JP2005021515

    申请日:2005-01-28

    发明人: SAWA AKIRA

    摘要: PROBLEM TO BE SOLVED: To provide a method for diagnosing or predicting sensitivity to a mental disorder, by which the participation of disrupted-in schizophrenia-1 (DISC1) in the mental disorder can be elucidated. SOLUTION: This method for diagnosing or predicting fragility to a mental disorder such as bipolar disorder in an individual comprises confirming the molecular diversity and/or intracellular distribution of the DISC1 in a cell from the individual. In addition, the risk haplotype of the DISC1 for the mental disorder is also provided. Thereby, the method can be utilized for screening a medicine for treating the mental disorder. COPYRIGHT: (C)2005,JPO&NCIPI

    摘要翻译: 要解决的问题:提供用于诊断或预测精神障碍敏感性的方法,通过该方法可以阐明精神障碍中的精神分裂症-1(DISC1)的参与。 解决方案:用于诊断或预测个体精神障碍如双相性精神障碍的脆弱性的方法包括确认来自个体的细胞中DISC1的分子多样性和/或细胞内分布。 此外,还提供了精神障碍的DISC1风险单倍型。 因此,该方法可用于筛选用于治疗精神障碍的药物。 版权所有(C)2005,JPO&NCIPI

    Aqueous composition
    10.
    发明专利
    Aqueous composition 有权
    水分组合物

    公开(公告)号:JP2012167095A

    公开(公告)日:2012-09-06

    申请号:JP2012077406

    申请日:2012-03-29

    摘要: PROBLEM TO BE SOLVED: To provide an aqueous composition for topical administration using a 15-keto-prostaglandin compound superior in preparation stability as an active ingredient.SOLUTION: The aqueous composition for topical administration comprises a 15-keto-prostaglandin compound as an active ingredient and contains a polyoxyethylene castor oil derivative as a solubilizing agent. Preferably, the prostaglandin compound is a 15-keto-20-ethyl-prostaglandin compound, a 15-keto-16,16-difluoro-prostaglandin compound, a 15-keto-prostaglandin E compound, or a 15-keto-prostaglandin F compound. Preferably, the polyoxyethylene castor oil derivative is polyoxyethylene 40 hydrogenated castor oil or polyoxyethylene 60 hydrogenated castor oil. The aqueous composition preferably further contains a quaternary ammonium-type cationic surfactant, in particular benzalkonium chloride or benzethonium chloride.

    摘要翻译: 待解决的问题:提供一种使用制剂稳定性优异的15-酮 - 前列腺素化合物作为活性成分的局部给药用水性组合物。 解决方案:用于局部给药的水性组合物包含作为活性成分的15-酮 - 前列腺素化合物,并含有作为增溶剂的聚氧乙烯蓖麻油衍生物。 优选地,前列腺素化合物是15-酮-20-乙基 - 前列腺素化合物,15-酮-16,16-二氟 - 前列腺素化合物,15-酮前列腺素E化合物或15-酮前列腺素F化合物 。 优选地,聚氧乙烯蓖麻油衍生物是聚氧乙烯40氢化蓖麻油或聚氧乙烯60氢化蓖麻油。 水性组合物优选还含有季铵型阳离子表面活性剂,特别是苯扎氯铵或苄索氯铵。 版权所有(C)2012,JPO&INPIT