首页> 外国专利> The solid oral pharmaceutical compositions containing S1P-agonist or pharmaceutically acceptable salts thereof, process for its preparation and method of treatment and reduce the frequency of clinical exacerbations MULTIPLE SCLEROSIS

The solid oral pharmaceutical compositions containing S1P-agonist or pharmaceutically acceptable salts thereof, process for its preparation and method of treatment and reduce the frequency of clinical exacerbations MULTIPLE SCLEROSIS

机译:包含S1P-激动剂或其药学上可接受的盐的固体口服药物组合物,其制备方法和治疗方法以及减少临床加重的频率

摘要

1. A solid oral pharmaceutical composition (solid oral dosage form) for the treatment of relapsing-remitting multiple sclerosis and to decrease the frequency of clinical exacerbations of disease and reduce the risk of the progression of disability in relapsing-remitting multiple sclerosis, suitable for oral administration comprising a therapeutically effective amount of a receptor agonist S1P (sphingosine-1-phosphate) and a pharmaceutically acceptable carrier, wherein the pharmaceutically acceptable my medium does not contain microcrystalline cellulose, sugar alcohol and croscarmellose (carboxymethylcellulose), or pharmaceutically acceptable derivatives kroskarmellozy.2. Solid oral pharmaceutical formulation (solid oral dosage form) according to claim 1, wherein the S1P receptor agonist is 2-amino-2- (2- (4-octylphenyl) ethyl) propane-1,3-diol (fingolimod ) of formula (I) or a pharmaceutically acceptable sol.3. Solid oral pharmaceutical formulation (solid oral dosage form) according to claim 2, characterized in that the pharmaceutically acceptable salt of 2-amino-2- (2- (4-octylphenyl) ethyl) proian-1,3-diol (fingolimod) is a gidrohlorid.4 fingolimod. Solid oral pharmaceutical formulation (solid oral dosage form) according to claim 1, characterized in that the pharmaceutically acceptable carrier comprises starch or a pharmaceutically acceptable proizvodnye.5. Solid oral pharmaceutical formulation (solid oral dosage form) according to claim 4, distinguished
机译:1.用于治疗复发-缓解型多发性硬化症并减少疾病的临床加重的频率并降低残疾-复发-缓解型多发性硬化症的固体口服药物组合物(固体口服剂型),适用于口服给药,包含治疗有效量的受体激动剂S1P(1-磷酸鞘氨醇)和药学上可接受的载体,其中药学上可接受的介质不含微晶纤维素,糖醇和交联羧甲基纤维素(羧甲基纤维素)或药学上可接受的衍生物.2。 2.根据权利要求1所述的固体口服药物制剂(固体口服剂型),其中所述S1P受体激动剂是式(2)的2-氨基-2-(2-(4-辛基苯基)乙基)丙烷-1,3-二醇(芬戈莫德)。 I)或药学上可接受的溶胶3。 3.根据权利要求2所述的固体口服药物制剂(固体口服剂型),其特征在于,2-氨基-2-(2-(4-辛基苯基)乙基)proian-1,3-二醇(芬戈莫德)的药学上可接受的盐是gidrohlorid。4芬戈莫德。 2.根据权利要求1所述的固体口服药物制剂(固体口服剂型),其特征在于,所述药学上可接受的载体包括淀粉或药学上可接受的proizvodnye。 5.根据权利要求4的固体口服药物制剂(固体口服剂型),

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