首页> 外国专利> PHARMACEUTICAL COMPOSITIONS OF DUAL ACTION ON THE BASIS OF NADMOLECULAR STRUCTURES OF ANTAGONISTS / ANGIOTENZINE (ARB) RECEPTOR BLOCK AND NEUTRAL ENDEPEPTIDASE (NEP) INHIBITOR (NEP)

PHARMACEUTICAL COMPOSITIONS OF DUAL ACTION ON THE BASIS OF NADMOLECULAR STRUCTURES OF ANTAGONISTS / ANGIOTENZINE (ARB) RECEPTOR BLOCK AND NEUTRAL ENDEPEPTIDASE (NEP) INHIBITOR (NEP)

机译:拮抗药/血管紧张素(ARB)受体区和神经内啡肽酶(NEP)抑制剂的分子结构基础上的双重作用的药物成分

摘要

1. A solid oral dosage form comprising:! (a) a double acting compound in an amount of from about 4 to about 90% based on the weight of the composition and! (b) at least one pharmaceutically acceptable excipient. ! 2. A solid oral dosage form comprising:! (a) a double acting compound in an amount of 100, 200 or 400 mg in one unit dosage form and! (b) at least one pharmaceutically acceptable excipient. ! 3. The solid oral dosage form according to claim 1 or 3, wherein said double acting compound is a supramolecular complex. ! 4. The solid oral dosage form according to claim 3, wherein said supramolecular complex is the trisodium salt semi-pentahydrate [3 - ((1S, 3R) -1-biphenyl-4-ylmethyl-3-ethoxycarbonyl-1-butylcarbamoyl) propionate- (S ) -3'-methyl-2 '- (pentanoyl {2' '- (tetrazol-5-ylate) biphenyl-4'-ylmethyl} amino) butyric acid]. ! 5. The solid oral dosage form according to claim 4, wherein said solid oral dosage form is a tablet. ! 6. The solid oral dosage form according to claim 5, wherein said tablet is an immediate release formulation. ! 7. A method for preparing a solid oral dosage form comprising the steps of:! (A) mixing a double-acting compound with at least one pharmaceutically acceptable excipient to form a mixture! (b) directly compressing said mixture into a solid oral dosage form! and optionally compressing the final mixture into a solid oral dosage form. ! 8. A method of obtaining a solid oral dosage form comprising a herd
机译:1.一种固体口服剂型,包括: (a)以组合物的重量计,约4至约90%的量的双作用化合物和! (b)至少一种药学上可接受的赋形剂。 ! 2.一种固体口服剂型,包括: (a)一种单位剂型中100、200或400毫克的双效化合物,以及! (b)至少一种药学上可接受的赋形剂。 ! 3.根据权利要求1或3的固体口服剂型,其中所述双作用化合物是超分子复合物。 ! 4.根据权利要求3的固体口服剂型,其中所述超分子复合物是三钠盐半五水合物[3-((1S,3R)-1-联苯基-4-基甲基-3-乙氧基羰基-1-丁基氨基甲酰基)丙酸酯]。 -(S)-3′-甲基-2′-(戊酰基{2′′-(四唑-5-基酸酯)联苯基-4′-甲基甲基}氨基)丁酸]。 ! 5.根据权利要求4的固体口服剂型,其中所述固体口服剂型是片剂。 ! 6.根据权利要求5的固体口服剂型,其中所述片剂是速释制剂。 ! 7.一种制备固体口服剂型的方法,其包括以下步骤: (A)将双效化合物与至少一种可药用赋形剂混合以形成混合物! (b)直接将所述混合物压制成固体口服剂型!以及任选地将最终混合物压制成固体口服剂型。 ! 8.一种获得包含牛群的固体口服剂型的方法

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