摘要:
The present invention relates to non-steroidal progesterone receptor modulators of the general formula (I), a process for their preparation, the use of the progesterone receptor modulators for producing medicaments, and pharmaceutical compositions comprising these compounds. The compounds according to the invention are suitable for the therapy and prophylaxis of gynaecological disorders such as endometriosis, leiomyomas of the uterus, dysfunctional (bleeding )and dysmenorrhoea, and for the therapy and prophylaxis of hormone-dependent tumours and for use for female fertility control and for hormone replacement therapy.
摘要:
The invention relates to a treatment regime and to combination preparations of 20,20,21,21,21 -pentafluoro-17-hydroxy-11 ß-[4- (hydroxyacetyl)phenyl]-19-nor-17α-pregna-4,9-diene-3-one of formula (I). Said invention relates to, in particular, a sequential regime for treating gynaecological diseases in which, in a first phase, the above-mentioned progesterone antagonist is administered and, in a second phase, a progestational hormone is administered.
摘要:
The present invention relates to progesterone receptor antagonists of general formula I: in which R1 can be a hydrogen atom and R2 a hydroxyl group or R1 and R2 together can be an oxo group.
摘要:
The aim of the present invention is the use of mineralcorticoid receptor antagonists for the production of a drug for the treatment of endometriosis. The present invention particularly relates to an improved therapeutic agent against endometriosis, which has a more favorable effectiveness profile and/or profile of side effects than previously available treatment therapies. With a mineralcorticoid receptor antagonist, endometriosis can be lastingly treated without resulting in a loss of bone mass.