首页> 外国专利> Controlled release pharmaceutical composition for oral use containing midodrine and/or active metabolite, desglymidodrine

Controlled release pharmaceutical composition for oral use containing midodrine and/or active metabolite, desglymidodrine

机译:含有米多君和/或活性代谢产物地塞米多君的口服控释药物组合物

摘要

Novel controlled release pharmaceutical compositions for oral use containing midodrine and/or its active metabolite desglymidodrine. The novel compositions are designed to release midodrine and/or desglymidodrine after oral intake in a manner which enables absorption to take place in the gastrointestinal tract so that a relatively fast peak plasma concentration of the active metabolite desglymidodrine is obtained followed by a prolonged and relatively constant plasma concentration of desglymidodrine.;The novel compositions may be designed for administration once or twice daily, i.e. a therapeutically effective concentration of desglymidodrine is maintained for a period of at least 10-16 hours followed by a wash out period of about 8-12 hours in order to avoid the well-known midodrine related side effect with respect to supine hypertension. The therapeutically effective concentration of desglymidodrine is regarded as a plasma concentration of desglymidodrine of at least about 3 ng/ml. A composition is designed to release midodrine and/or desglymidodrine in at least the following consecutive steps: i) an initial relatively fast release of midodrine and/or desglymidodrine (in order to obtain a relatively fast onset of action), ii) a steady release or a slower release than in step 1 of midodrine and/or desglymidodrine (in order to maintain a plasma concentration of desglymidodrine which is prolonged and relatively constant), iii) a second rise in release of midodrine and/or desglymidodrine (in order to take advantage of absorption from the colon, i.e. such a second rise release is designed to take place when the composition (or the disintegrated parts of the composition) reaches the colon; normally this is regarded to take about 8 hours after oral intake, and iv) a decline in release rate corresponding to that essentially all midodrine and/or desglymidodrine have been released from the composition.;Also disclosed is a method for treating orthostatic hypotension and/or urinary incontinence, the method comprising administration to a patient in need thereof of an effective amount of midodrine and/or desglymidodrine in a composition according to the invention.
机译:含有米多君和/或其活性代谢产物desglymidodrine的新型口服控释药物组合物。新颖的组合物被设计成在口服后以能够在胃肠道中发生吸收的方式释放米多君和/或去糖基米多君,从而获得活性代谢产物去糖基米多君的相对较快的峰值血浆浓度,随后是较长且相对恒定的。可以设计每日一次或两次的新颖组合物的血浆浓度,即将治疗有效浓度的desglymidodrine维持至少10-16小时的时间,然后进行约8-12小时的冲洗时间为了避免关于仰卧位高血压的众所周知的米多君相关副作用。地塞米多君的治疗有效浓度被认为是至少约3ng / ml的地塞米多君的血浆浓度。设计组合物以至少在以下连续步骤中释放米多君和/或desglymidodrine:i)米多君和/或desglymidodrine的初始相对较快的释放(以便获得相对较快的起效),ii)稳定释放或比米多君和/或desglymidodrine的第1步释放缓慢(以维持desglymidodrine的血浆浓度延长且相对恒定),iii)米多君和/或desglymidodrine的释放第二次上升(以服用从结肠吸收的好处,即设计成当组合物(或组合物的崩解部分)到达结肠时发生第二次上升释放;通常认为这是在口服后约8个小时,和释放速率的下降对应于基本上所有米多君和/或去糖基米多君已经从组合物中释放。;还公开了一种治疗体位性低血压和/或方法。尿失禁,该方法包括在根据本发明的组合物中向需要其的患者施用有效量的米多君和/或去糖基米多君。

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