首页> 外国专利> Use of a Taxane derivative for the preparation of a Pharmaceutical composition.Use of a biodicponibilidad Improver of the derivative set afrmaceutico oral dosage form and understands it, and Method for forming an active Agent bioavailable.

Use of a Taxane derivative for the preparation of a Pharmaceutical composition.Use of a biodicponibilidad Improver of the derivative set afrmaceutico oral dosage form and understands it, and Method for forming an active Agent bioavailable.

机译:紫杉烷衍生物在制备药物组合物中的用途。衍生物的非生物药口服剂型的生物可生物改进剂的用途,并理解其,以及可生物利用的形成活性剂的方法。

摘要

The use of a taxonomic derivative to prepare a useful pharmaceutical ingredient for a therapeutic method, including oral presentation to a human patient with a disease related to the derivative Therefore, the derivative was effectively removed to treat the disease. The derivatives of taxano are Paclitaxel; docetaxel;A notorious derivative similar to plactitaxel or doeaxel and a prediction derivative called esplaclitaxel-2-mpm or docetaxel-2-mpm. The effective dose of placliftaxel is about 2-30 mg / kg of basic weight or 20-1000 mg / m2 of patient's body area. In addition, the aim of this method is to make steroid derivatives orally available to human patients in sufficient quantities to treat diseases associated with such derivatives.This includes the combination of oral administration of patients, the number of classified animals for effective treatment, plus the effective amount of biocompatible enhancers selected from the CYCLOPROPYLENE glycol to Z (me-ile-4) - CYCLOPROPYLENE, dihydrocyclopropane and propylene ceclosporina a groups. Based on the patient's Alpine ratio, the dosage of enhancer is between 0.1 and 20 mg / kg. The administration of this enhancer is as follows: (a) the prediction time is about 0.5-72 hours; and (b) the time of death is less than 0.5 hours.At the same time, or within the next 0.5 hours; or (c) two, about 0.5-72 hours in advance, plus less than 0.5 hormone, to be managed by the tax bureau. And enhancers are managed in an independent dose form
机译:使用分类学衍生物来制备用于治疗方法的有用药物成分,包括向患有与该衍生物有关的疾病的人类患者口服给药。因此,该衍生物被有效地去除以治疗该疾病。紫杉醇的衍生物为紫杉醇;紫杉醇为紫杉醇。 docetaxel;多西他赛;一种与普拉克他赛或doaaxel类似的臭名昭著的衍生物,以及称为esplaclitaxel-2-mpm或docetaxel-2-mpm的预测衍生物。 Placliftaxel的有效剂量约为患者体重的2-30 mg / kg体重或20-1000 mg / m2。此外,该方法的目的是使人类患者口服足够量的类固醇衍生物,以治疗与此类衍生物有关的疾病,包括患者口服给药,有效治疗的分类动物数量以及有效量的生物相容性增强剂,选自环丙二醇至Z(me-ile-4)-环丙烯,二氢环丙烷和丙稀头孢菌素a组。根据患者的高山比例,增强剂的剂量在0.1至20 mg / kg之间。该增强剂的施用如下:(a)预测时间为约0.5-72小时; (b)死亡时间少于0.5小时。在同一时间或接下来的0.5小时内; (c)提前两小时,约0.5-72小时,加上少于0.5的激素,由税务局管理。增强剂以独立的剂型进行管理

著录项

  • 公开/公告号AR012731A1

    专利类型

  • 公开/公告日2000-11-08

    原文格式PDF

  • 申请/专利权人 BAKER NORTON PHARMACEUTICALS INC.;

    申请/专利号AR1998P102356

  • 发明设计人

    申请日1998-05-21

  • 分类号A61K31/335;A61K38/13;

  • 国家 AR

  • 入库时间 2022-08-22 01:57:30

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