发明申请
US20130095180A1 TIME-DELAYED SUSTAINED RELEASE PHARMACEUTICAL COMPOSITION COMPRISING DAPOXETINE FOR ORAL ADMINISTRATION 审中-公开
延迟持续释放包含DAPOXETINE用于口服管理的药物组合物

  • 专利标题: TIME-DELAYED SUSTAINED RELEASE PHARMACEUTICAL COMPOSITION COMPRISING DAPOXETINE FOR ORAL ADMINISTRATION
  • 专利标题(中): 延迟持续释放包含DAPOXETINE用于口服管理的药物组合物
  • 申请号: US13805028
    申请日: 2011-07-05
  • 公开(公告)号: US20130095180A1
    公开(公告)日: 2013-04-18
  • 发明人: Chang-Kyoo LeeSang-Geun Park
  • 申请人: Chang-Kyoo LeeSang-Geun Park
  • 申请人地址: KR Suwon-si
  • 专利权人: NAVIPHARM. CO., LTD.
  • 当前专利权人: NAVIPHARM. CO., LTD.
  • 当前专利权人地址: KR Suwon-si
  • 优先权: KR10-2010-0064988 20100706
  • 国际申请: PCT/KR2011/004919 WO 20110705
  • 主分类号: A61K31/522
  • IPC分类号: A61K31/522 A61K31/4985 A61K31/138
TIME-DELAYED SUSTAINED RELEASE PHARMACEUTICAL COMPOSITION COMPRISING DAPOXETINE FOR ORAL ADMINISTRATION
摘要:
The present invention relates to a time-delayed sustained release pharmaceutical composition for oral administration, which comprises an immediate release phase and a prolonged sustained release phase, wherein said immediate release phase and prolonged sustained release phase respectively comprise Dapoxetine therein as an active ingredient. The pharmaceutical composition of the present invention comprises Dapoxetine, which is an agent for treating premature ejaculation, in both the immediate release phase and the prolonged sustained release phase thereof, to thereby immediately exhibit the effectiveness of the pharmaceutical composition of the present invention in order to enable a patient to achieve sexual satisfaction during the early stage of administration, as well as to reduce side effects by means of the time-delayed sustained release of the prolonged sustained release phase during the early stage of administration and enable a continuous in vivo absorption of Dapoxetines, to thereby lengthen the duration of the effectiveness of the pharmaceutical composition of the present invention. Further, agents for treating erectile dysfunction, such as sildenafil, tadalifil or the like can be added to the immediate release phase so as to allow for a coincidence of the durations of the effectiveness of a premature ejaculation treatment agent and erectile dysfunction treatment agents, even though a half-life difference exists between the two types of treatment agents, thus maximizing patient satisfaction.
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