LAQUINIMOD FORMULATIONS WITHOUT ALKALIZING AGENT
    7.
    发明申请
    LAQUINIMOD FORMULATIONS WITHOUT ALKALIZING AGENT 审中-公开
    没有碱化剂的LAQUINIMOD配方

    公开(公告)号:US20140018386A1

    公开(公告)日:2014-01-16

    申请号:US13938733

    申请日:2013-07-10

    IPC分类号: A61K31/4704

    摘要: The subject invention provides a stable pharmaceutical composition comprising a therapeutically effective amount of laquinimod, an amount of a filler, and an amount of a lubricant, wherein the stable pharmaceutical composition is free of an alkalizing agent or an oxidation reducing agent. Also provided are processes for making the stable pharmaceutical composition and sealed packages comprising the stable pharmaceutical composition. Also provided is a method for treating a subject afflicted with a form of multiple sclerosis (MS) or for alleviating a symptom of MS in a subject afflicted with a form of MS comprising administering to the subject a stable pharmaceutical composition as described herein. Also provided is use of a stable pharmaceutical composition as described herein for treating a subject afflicted with a form of MS or for alleviating a symptom of MS in a subject afflicted with a form of multiple MS.

    摘要翻译: 本发明提供了稳定的药物组合物,其包含治疗有效量的拉喹莫德,一定量的填充剂和一定量的润滑剂,其中稳定的药物组合物不含碱化剂或氧化还原剂。 还提供了制备稳定的药物组合物和包含稳定的药物组合物的密封包装的方法。 还提供了治疗患有多发性硬化症(MS)形式的受试者或用于减轻患有MS形式的受试者中的MS症状的方法,包括向受试者施用如本文所述的稳定的药物组合物。 还提供了本文所述的稳定药物组合物的用途,用于治疗患有MS形式的受试者或用于减轻患有多发性MS形式的受试者的MS症状。

    Stable laquinimod preparations
    10.
    发明授权
    Stable laquinimod preparations 有权
    稳定的laquinimod制剂

    公开(公告)号:US08178127B2

    公开(公告)日:2012-05-15

    申请号:US12317104

    申请日:2008-12-19

    IPC分类号: A61K9/20

    摘要: The subject invention provides a pharmaceutical composition comprising N-ethyl-N-phenyl-1,2,-dihydro-4-hydroxy-5-chloro-1-methyl-2-oxoquinoline-3-carboxamide or the salt thereof; a pharmaceutically acceptable carrier; and not more than 0.5% w/w relative to N-ethyl-N-phenyl-1,2,-dihydro-4-hydroxy-5-chloro-1-methyl-2-oxoquinoline-3-carboxamide of 2-Chloro-6-(1-ethyl-N-methyl-2-oxoindoline-3-carboxamido)benzoic acid, 1H,3H-spiro[5-chloro-1-methylquinoline-2,4-dione-3,3′-[1]ethylindolin-[2]-one], or 5-Chloro-N-ethyl-3-hydroxy-1-methyl-2,4-dioxo-N-phenyl-1,2,3,4-tetrahydro-quinoline-3-carboxamide.

    摘要翻译: 本发明提供了包含N-乙基-N-苯基-1,2-二氢-4-羟基-5-氯-1-甲基-2-氧代喹啉-3-甲酰胺或其盐的药物组合物; 药学上可接受的载体; 并且相对于2-氯 - 苯基-1,2-二氢-4-羟基-5-氯-1-甲基-2-氧代喹啉-3-甲酰胺,相对于N-乙基-N-苯基-1,2-二氢-4-羟基-5-氯-1-甲基-2-氧代喹啉-3-甲酰胺为0.5%w / 6-(1-乙基-N-甲基-2-氧代二氢吲哚-3-甲酰氨基)苯甲酸,1H,3H-螺[5-氯-1-甲基喹啉-2,4-二酮-3,3' - [1] 乙醛基 - [2] - 酮]或5-氯-N-乙基-3-羟基-1-甲基-2,4-二氧代-N-苯基-1,2,3,4-四氢 - 甲酰胺。