首页> 外国专利> METHOD FOR MANUFACTURING A PHARMACEUTICAL COMPOSITION IN THE FORM OF EXTENDED RELEASE TABLETS CONTAINING PIRFENIDONE AND USE THEREOF IN THE REGRESSION OF CHRONIC RENAL INSUFFICIENCY BREAST CAPSULAR CONTRACTURE AND HEPATIC FIBROSIS IN HUMANS

METHOD FOR MANUFACTURING A PHARMACEUTICAL COMPOSITION IN THE FORM OF EXTENDED RELEASE TABLETS CONTAINING PIRFENIDONE AND USE THEREOF IN THE REGRESSION OF CHRONIC RENAL INSUFFICIENCY BREAST CAPSULAR CONTRACTURE AND HEPATIC FIBROSIS IN HUMANS

机译:制造包含吡非尼酮的延长释放片剂形式的药物组合物的方法,并在慢性肾功能不全,男性,男性,男性,男性,男性,男性,男性,女性,男性,男性,女性,男性,女性,男性,女性患者中使用。

摘要

The present invention relates to a method for manufacturing a pharmaceutical composition in the form of extended release tablets that include from 600 milligrams to 2400 milligrams of Pirfenidone (PFD) such that the drug containing same is bioavailable during an extended period of 12 hours from the administration thereof. This optimizes the anti fibrotic and anti inflammatory action of the Pirfenidone. Additionally the present invention offers advantages and better therapeutic effectiveness over other pharmaceutical forms of Pirfenidone for oral administration and the therapeutic use thereof in the regression of chronic secondary renal insufficiency to primary glomerulosclerosis; it shows greater activity in the decrease and/or regression of the toxic effects on the breast capsular contracture observed after surgical implantation of breast implants in humans and exercises a significant anti TNF a and anti TGF ß? action in the treatment of hepatic fibrosis.
机译:本发明涉及一种用于制备包含600毫克至2400毫克吡非尼酮(PFD)的缓释片剂形式的药物组合物的方法,从而使得含有该药物的药物在给药后的12小时内可被生物利用其。这优化了吡非尼酮的抗纤维化和抗炎作用。另外,本发明相对于口服吡非尼酮的其他药物形式及其在慢性继发性肾功能不全向原发性肾小球硬化的消退中的治疗用途提供了优于吡非尼酮的其他优点和更好的治疗效果。它显示出更大的活性,可以降低人体内植入乳房假体后对乳房荚膜挛缩的毒性作用的减少和/或消退,并具有显着的抗TNFα和抗TGFβ活性。在治疗肝纤维化中的作用。

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