PHARMAZEUTISCHE ZUBEREITUNG ZUR VERMINDERUNG DER ENDOMETRIOSE
    1.
    发明公开
    PHARMAZEUTISCHE ZUBEREITUNG ZUR VERMINDERUNG DER ENDOMETRIOSE 审中-公开
    药物制剂,减少子宫内膜异位症

    公开(公告)号:EP2059248A1

    公开(公告)日:2009-05-20

    申请号:EP08707797.0

    申请日:2008-02-23

    CPC分类号: A61K31/57 A61K31/573

    摘要: A pharmaceutical composition for the treatment of endometriosis without loss of bone density comprises a gestagenic having an antiandrogenic effect, preferably 17α-cyanomethyl-17ß-hydroxy-estra-4,9-diene-3-one (Dienogest), cyproteronacetate or chlormadinonacetate at a daily dosage which is no more than two times the dosage required to suppress ovulation, together with one or a plurality of pharmaceutically acceptable adjuvants/carriers. The pharmaceutical composition according to the invention provides both the alleviation of endometriosis and the lack of a negative affect on bone metabolism and bone density, and is simultaneously able to keep the side effects known from conventional pharmaceuticals (such as hot flashes, acne, negative affects on the lipid profile) within tolerable limits. The pharmaceutical composition is thus suitable for long-term application.

    VERWENDUNG VON ESTRADIOLVALERAT ODER ESTRADIOL IN KOMBINATION MIT DIENOGEST ZUR ORALEN THERAPIE DER DYSFUNKTIONELLEN UTERINEN BLUTUNG IN EINHEIT MIT EINER ORALEN KONTRAZEPTION
    5.
    发明授权
    VERWENDUNG VON ESTRADIOLVALERAT ODER ESTRADIOL IN KOMBINATION MIT DIENOGEST ZUR ORALEN THERAPIE DER DYSFUNKTIONELLEN UTERINEN BLUTUNG IN EINHEIT MIT EINER ORALEN KONTRAZEPTION 有权
    使用或雌激素雌二醇结合诺孕素FOR出血的功能失调性子宫出血单元口服避孕药口服治疗

    公开(公告)号:EP1933843B1

    公开(公告)日:2011-02-02

    申请号:EP06806225.6

    申请日:2006-10-12

    摘要: The invention relates to the use of estradiol valerate or estradiol combined with 17a- cyanomethyl-17-ß-hydroxyestra-4,9-diene-3on (dienogest) for producing a multi-phase combination preparation for the oral therapy of the dysfunctional uterine bleeding in the form of oral contraceptives. Said combination of estradiol valerate or estradiol with dienogest comprises a first phase consisting of 2 daily dose units of estradiol valerate at 3 mg or estradiol of less than 3mg, a second phase consisting of 2 groups of daily dose units, whereby the first group contains 5 daily dose units of a combination of 2 mg estradiol valerate or estradiol of less than 2mg and 2 mg of dienogest and the second group contains 17 daily dose units consisting of a combination of 2 mg of estradiol valerate or estradiol of less than 2mg and 3 mg dienogest, a third phase consisting of 2 daily dose units having 1 mg estradiol valerate or estradiol of less than 2mg and an additional phase consisting of 2 daily dose units on a pharmaceutically harmless placebo. All of the daily dose units of the multi-phase combination and the pharmaceutically harmless placebo correspond to 28 days. The duration of application comprises at least one menstruation cycle and is dependent on individual wishes of the woman with respect to contraception.

    VERWENDUNG VON ESTRADIOLVALERAT ODER ESTRADIOL IN KOMBINATION MIT DIENOGEST ZUR ORALEN THERAPIE DER DYSFUNKTIONELLEN UTERINEN BLUTUNG IN EINHEIT MIT EINER ORALEN KONTRAZEPTION
    6.
    发明公开
    VERWENDUNG VON ESTRADIOLVALERAT ODER ESTRADIOL IN KOMBINATION MIT DIENOGEST ZUR ORALEN THERAPIE DER DYSFUNKTIONELLEN UTERINEN BLUTUNG IN EINHEIT MIT EINER ORALEN KONTRAZEPTION 有权
    使用或雌激素雌二醇结合诺孕素FOR出血的功能失调性子宫出血单元口服避孕药口服治疗

    公开(公告)号:EP1933843A1

    公开(公告)日:2008-06-25

    申请号:EP06806225.6

    申请日:2006-10-12

    摘要: The invention relates to the use of estradiol valerate or estradiol combined with 17a- cyanomethyl-17-ß-hydroxyestra-4,9-diene-3on (dienogest) for producing a multi-phase combination preparation for the oral therapy of the dysfunctional uterine bleeding in the form of oral contraceptives. Said combination of estradiol valerate or estradiol with dienogest comprises a first phase consisting of 2 daily dose units of estradiol valerate at 3 mg or estradiol of less than 3mg, a second phase consisting of 2 groups of daily dose units, whereby the first group contains 5 daily dose units of a combination of 2 mg estradiol valerate or estradiol of less than 2mg and 2 mg of dienogest and the second group contains 17 daily dose units consisting of a combination of 2 mg of estradiol valerate or estradiol of less than 2mg and 3 mg dienogest, a third phase consisting of 2 daily dose units having 1 mg estradiol valerate or estradiol of less than 2mg and an additional phase consisting of 2 daily dose units on a pharmaceutically harmless placebo. All of the daily dose units of the multi-phase combination and the pharmaceutically harmless placebo correspond to 28 days. The duration of application comprises at least one menstruation cycle and is dependent on individual wishes of the woman with respect to contraception.