Mesoprogrestins (progesterone receptor modulations) as a component of compositions for hormone replacement therapy (HRT)
    1.
    发明授权
    Mesoprogrestins (progesterone receptor modulations) as a component of compositions for hormone replacement therapy (HRT) 有权
    作为激素替代疗法(HRT)组合物组分的Mesoprogrestins(孕酮受体调节)

    公开(公告)号:US07629334B1

    公开(公告)日:2009-12-08

    申请号:US10433984

    申请日:2000-08-31

    IPC分类号: A61K31/56 C07J1/00 C07J6/00

    CPC分类号: A61K31/56

    摘要: The use of mesoprogestins as pharmaceutical components for the manufacture of a medicament for hormone replacement therapy (HRT) and as components for the combined use together with an estrogen for the manufacture of a medicament for HRT as well as in respective HRT-methods and methods of treating hormone deficiency and hormone irregularity symptoms. Mesoprogestins are defined as compounds possessing both agonistic and antagonistic activities at the progesterone receptor (PR) in vivo. They stabilize the function of PR at an intermediate level of agonistic and antagonistic. Corresponding functional states cannot be achieved with progestins or antiprogestins. J867, J912, J956 and J1042 are the mesoprogestins preferred herein.

    摘要翻译: 使用中孕烯素作为药物组分用于制造用于激素替代疗法(HRT)的药物,以及作为与雌激素联合使用以用于制备用于HRT的药物的组合以及相应的HRT方法和方法 治疗激素缺乏和激素不规则症状。 中孕烯孕素被定义为在体内孕酮受体(PR)具有激动作用和拮抗活性的化合物。 他们将PR的功能稳定在激进和对抗的中间水平。 孕激素或抗孕激素不能达到相应的功能状态。 J867,J912,J956和J1042是本文优选的中孕酮。

    Mesoprogestins (progesterone receptor modulators) for the treatment and prevention of benign hormone dependent gynecological disorders
    2.
    发明授权
    Mesoprogestins (progesterone receptor modulators) for the treatment and prevention of benign hormone dependent gynecological disorders 有权
    美孕激素(孕激素受体调节剂)用于治疗和预防良性激素依赖性妇科疾病

    公开(公告)号:US08193252B1

    公开(公告)日:2012-06-05

    申请号:US10450029

    申请日:2000-08-31

    IPC分类号: A61K31/56

    摘要: This present invention disclosed the use of mesoprogestins, a new class of progesterone receptor modulators (PRMs), for the treatment and prevention of benign hormone dependent gynecological disorders: a) for the treatment of gynecological disorder such as endometriosis, uterine fibroids, postoperative peritoneal adhesions, dysfunctional bleeding (metrorrhagia, menorrhagia) and dysmenorrhea; b) for the prevention of gynecological disorders such as postoperative, peritoneal adhesions, dysfunctional uterine bleeding (metrorrhagia, menorrhagia) and dysmenorrhea; and c) a method of treatment and prevention of the above mentioned disorders in a female, preferably in a human female, in need of treatment or prevention of one or more of these disorders, with an effective amount of a mesoprogestin. Mesoprogestins are defined as compounds possessing both agonistic and antagonistic activities at the progesterone receptor (PR) in vivo. They stabilize the function of PR at an intermediate level of agonistic and antagonistic. Corresponding functional states cannot be achieved with progestins or antiprogestins. The daily dose of mesoprogestin is 0.5 to 100 mg, preferably 5.0 to 50 mg and most preferably 10 to 25 mg. J867, J912, J956 and J1042 are the mesoprogestins preferred according to the invention.

    摘要翻译: 本发明公开了用于治疗和预防良性激素依赖性妇科疾病的新型孕激素受体调节剂(PRM)的使用:a)用于治疗妇科疾病如子宫内膜异位症,子宫肌瘤,术后腹膜粘连 功能障碍性出血(metrorrhagia,月经过多)和痛经; b)用于预防妇科疾病如术后,腹膜粘连,功能障碍性子宫出血(metrorrhagia,月经过多)和痛经; 和c)有效量的中孕酮治疗和预防女性,优选在人类女性中需要治疗或预防这些疾病中的一种或多种的上述病症的方法。 中孕烯孕素被定义为在体内孕酮受体(PR)具有激动作用和拮抗活性的化合物。 他们将PR的功能稳定在激进和对抗的中间水平。 孕激素或抗孕激素不能达到相应的功能状态。 中孕酮的日剂量为0.5〜100mg,优选为5.0〜50mg,最优选为10〜25mg。 J867,J912,J956和J1042是根据本发明优选的中孕妇。

    Combination of progesterone antagonists and antiestrogens with partial
agonistic action for hormone substitution therapy for perimenopausal
and postmenopausal women
    3.
    发明授权
    Combination of progesterone antagonists and antiestrogens with partial agonistic action for hormone substitution therapy for perimenopausal and postmenopausal women 失效
    孕激素拮抗剂和抗雌激素与绝经后和绝经后妇女的激素替代疗法部分激动作用的组合

    公开(公告)号:US5719136A

    公开(公告)日:1998-02-17

    申请号:US628702

    申请日:1996-07-05

    摘要: This invention describes the use of at least one compound having a progesterone-antagonistic (PA) action and at least one compound having an antiestrogenic (AO) action with a simultaneous partial agonistic action for the production of pharmaceutical agents for hormone substitution therapy (HRT) for perimenopausal and postmenopausal women. In the case of combined use of progesterone antagonist and antiestrogen, the stimulation of the endometrium by the progesterone antagonist that is caused by its partial agonistic action when an antiestrogen is used by itself is inhibited. For example, a pharmaceutical agent according to the invention contains onapristone (progesterone antagonist) and tamoxifen (antiestrogen).

    摘要翻译: PCT No.PCT / EP94 / 03408 Sec。 371日期:1996年7月5日第 102(e)日期1996年7月5日PCT 1994年10月17日PCT PCT。 公开号WO95 / 11013 日期1995年4月27日本发明描述了至少一种具有孕酮拮抗作用(PA)作用的化合物和至少一种具有抗雌激素(AOE)作用的化合物与同时部分激动作用用于产生激素药物的用途 围绝经期和绝经后妇女的替代疗法(HRT)。 在组合使用孕酮拮抗剂和抗雌激素的情况下,由抗雌激素本身使用时由其部分激动作用引起的孕激素拮抗剂对子宫内膜的刺激被抑制。 例如,根据本发明的药剂含有onapristone(孕酮拮抗剂)和他莫昔芬(antestrogen)。

    Sequential SPRM/ progestin treatment
    4.
    发明申请
    Sequential SPRM/ progestin treatment 审中-公开
    顺序SPRM /孕激素治疗

    公开(公告)号:US20050215536A1

    公开(公告)日:2005-09-29

    申请号:US11089275

    申请日:2005-03-24

    申请人: Kristof Chwalisz

    发明人: Kristof Chwalisz

    IPC分类号: A61K31/56

    摘要: The methods provided herein comprise administering a selective progesterone receptor modulator (SPRM) during a first dosing period and at least one progestogen during a second dosing period. The dosing periods can run concomitantly or sequentially with or without a period where neither the SPRM nor the progestogen is administered.

    摘要翻译: 本文提供的方法包括在第一给药期间施用选择性孕酮受体调节剂(SPRM)和在第二给药期间施用至少一种孕激素。 给药期可以伴随或顺序地伴随或不伴有施用SPRM和孕激素的期间。

    Combination contraceptive, kits that contain the latter, and a method that uses the latter
    10.
    发明申请
    Combination contraceptive, kits that contain the latter, and a method that uses the latter 审中-公开
    组合避孕药,含有后者的试剂盒,以及使用后者的方法

    公开(公告)号:US20050064031A1

    公开(公告)日:2005-03-24

    申请号:US10982799

    申请日:2004-11-08

    摘要: This invention relates to a multi-phase combination preparation that contains at least 28 daily dosage units: with a first phase of at least 21 initial daily dosage units, containing a competitive progesterone antagonist in a dosage which inhibits ovulation during the first above-named phase; and a second phase of 5 to 28 daily dosage units, in which each dosage unit of this second phase contains a gestagen, as well as a corresponding package (contraceptive kit) that contains this combination preparation and a contraceptive method which uses the combination preparation above.

    摘要翻译: 本发明涉及含有至少28个日剂量单位的多相组合制剂:第一阶段为至少21个初始日剂量单位,其中含有竞争性孕酮拮抗剂,其剂量在第一个上述阶段期间抑制排卵 ; 第二阶段为5〜28日剂量单位,其中第二阶段的每个剂量单位含有孕激素,以及含有该组合制剂的相应包装(避孕药盒)和使用上述组合制剂的避孕方法 。