CN101045155A - Method for the therapeutic management of extrauterine proliferation of endometrial tissue, chronic pelvic pain and fallopian tube obstruction - Google Patents
Method for the therapeutic management of extrauterine proliferation of endometrial tissue, chronic pelvic pain and fallopian tube obstruction Download PDFInfo
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- CN101045155A CN101045155A CNA2007100789192A CN200710078919A CN101045155A CN 101045155 A CN101045155 A CN 101045155A CN A2007100789192 A CNA2007100789192 A CN A2007100789192A CN 200710078919 A CN200710078919 A CN 200710078919A CN 101045155 A CN101045155 A CN 101045155A
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Abstract
本发明提供了通过用LH－RH拮抗剂短期诱导治疗4至12周来治疗子宫内膜组织子宫外增生、慢性骨盆疼痛和输卵管梗阻的方法。按照本发明的另一方面，短期LH－RH治疗之后，联合或单独给予一种或多种选自避孕药、优选口服避孕药、非甾族抗风湿剂、止痛剂、除17－α－烷基取代的睾酮外的雄激素或它们的任意组合的活性剂。按照本发明进一步的方面，提供了含有LHRH拮抗剂和一种或多种选自避孕药、优选口服避孕药、非甾族抗风湿剂、止痛剂、除17－α－烷基取代的睾酮外的雄激素或它们的任意组合的活性剂的药物组合物。The present invention provides a method for treating extrauterine hyperplasia of endometrial tissue, chronic pelvic pain and tubal obstruction by short-term induction therapy with LH-RH antagonists for 4 to 12 weeks. According to another aspect of the present invention, after short-term LH-RH treatment, one or more drugs selected from the group consisting of contraceptives, preferably oral contraceptives, non-steroidal antirheumatic agents, analgesics, 17-alpha-alkanes Active agents of androgens other than substituted testosterone or any combination thereof. According to a further aspect of the present invention there is provided a drug comprising an LHRH antagonist and one or more drugs selected from the group consisting of contraceptives, preferably oral contraceptives, non-steroidal antirheumatic agents, analgesics, 17-alpha-alkyl substituted testosterone A pharmaceutical composition of active agents of androgens or any combination thereof.
Description
The present invention is to be dividing an application of 20 days Chinese patent application of JIUYUE in 2000 00813196.1 applying date, and the denomination of invention of original application is " method that is used for the treatment of hypertrophy, chronic pelvic pain and obstruction of fallopian tube outside the endometrial tissue uterus ".
TECHNICAL FIELD OF THE INVENTION
Endometriosis is one of modal pathology in the gynecologic patient diagnosis.For example, 10% to 25% the women who has gynecological's symptom in Britain and the U.S. suffers from this disease.Usually by the laparoscopic visualization of the hemorrhage of pelvic organ or fibre modification focus is carried out clinical diagnosis.Ectopic endometrial tissue is along with the variation of ovarian hormone generating period.Come from the sedimentary cyclic hemorrhage of endometrium and help partial inflammatory reaction.Endometriosis betides the women of child-bearing age usually, sickness rate be at least 1% (referring to Shaw, R.W. (1993), endometriosis atlas (An Atlas ofEndometriosis, The Parthenon Publishing Group).
Endometriosis is divided into the outer endometriosis of adenomyosis interna (adenomyosis), external endometriosis and genitals usually.
Chronic pelvic pain can related generation with endometriosis, perhaps takes place with a kind of independently disease.
Obstruction of fallopian tube (FTO) is a kind of more common disease, can reach fallopian tube infertility situation 20% (referring to Winfield, A.C. etc., tangible angle obturation in the hysterosalpingography: rise the plain counter-rotating of sugar (Apparent cornual occlusion inhysterosalpingography:Reversal by glucagon) by pancreas, U.S. X line magazine (AJRAm J Roentgenol) 1982; 139:525-527).
Background information and prior art
Sampson proposes: the anti-stream of menstruation and endometrial tissue subsequently cause endometriosis [Sampson in the implantation of peritoneum face, J.A. (1927), the endometriosis (Peritoneal endometriosis due tomenstrual dissemination of the endometrial tissue into theperitoneal cavitiy) that enters peritoneum due to the peritoneal cavity is sent out in the menstruation of endometrial tissue. U.S.'s obstetrics and gynecology magazine (Am.J.Obstet.Gyneol.), 14,422].
The pathogeny of endometriosis can be relevant with several nosetiology factors:
Propositions such as Dmowski: heredity and immune factor cause endometriosis [Dmowski, W.P., Steele, R.W. and Baker, G.F. (1981), the cellular immunity deficiency in the endometriosis (Deficient cellular immunity in endometriosis), U.S.'s obstetrics and gynecology magazine (Am.J.Obstet.Gyneol.), 141,377].
Blood vessel and vasculolymphatic amphi position thromboembolism have proved and have explained (rare) discovery of the outer for example endometriosis of skin, lung and kidney of peritoneal cavity.
The cell of arranging on the Miller pipe results from germinal cell, and they are divided into peritoneal cell and are positioned at the cell on ovary surface.Someone proposes: these mature cell experience are dedifferented (de-differentiation) and are returned their original origin and be converted into endometrial cell [Levander then, G. (1941), by inductive osteogenesis (Bone formation byinduction), An.experimental study.Arch.Klin.Chir., 202,497].
Someone reports: dysmenorrhea, acute or chronic pelvic pain, dyspareunia and infertility are modal clinical symptoms.
The FTO representative derives from the preliminary inner closure of estrogen-sensitive disease or pathological one group of xenogenesis group on outside basis of oppressing, for example endometriosis, adenomyosis, adenomyosis tubae and muscular tumor.Except peritoneoscope, also often diagnose FTO by hysterosalpingography.
The first-selection of treatment comprises removes the endometrium infringement under the peritoneoscope.Can be with danazol or LHRH agonist treatment (6 months) after this step.The women who accepts danazol treatment may suffer the side effect of gastrointestinal tract and hepatic disease and serious generation male characteristic.
The somebody proposes from the viewpoint of theory: use by giving the endometriosis of suppression therapy immediately and the hysteromyoma of lhrh antagonist, improve subjective symptoms [Th.Reissmann etc. to shorten treatment time and quickening, human body reproduction magazine (Human Reprodution), the 10th volume, the 8th phase, the 1974-1981 page or leaf, (1995)].
And, Hodgen is at United States Patent (USP) 5,658, lectured a kind of in 884 by reducing the scheme of estrogen supply treatment gonad dependence disease, this scheme is by not stopping the dosage that endogenous estrogen produces with a kind of effective inhibition endometrial tissue hypertrophy basically, giving GnRH antagonist 6 months or longer time for a long time.For this purpose, Hodgen has lectured the dosage of a kind of like this scheme or GnRH antagonist, and in about 25 to 50pg/ml scopes, preferably approximately 35 to 45pg/ml with the level that obtains 24 hours serum estradiols.But Hodgen does not describe the estradiol serum levels and fluctuates between 50 to 75pg/ml.And Hodgen is at United States Patent (USP) 5,658, only lectured in 884 a kind of successive long-term treatment (based on every day or periodically, the latter's connotation be weekly or administration in every month), do not have the only short-term inductive treatment in 4 to 12 weeks of instruction.And Hodgen is not described in any combined therapy that has comprised the GnRH antagonist in the treatment endometriosis.This treatment only is described on the monkey, attacks experiment but also the costliness and the multiple progesterone that provide 30 to 50pg/ml 24 hourly average serum estradiol levels to be carried out are provided.
The symptom aggravation may take place in some sky in the result that LHRH-competition therapy plays a role suddenly.Needs extended treatment subsequently is to avoid the endometrial tissue generation of hypertrophy, hormone withdrawal symptom and skeleton demineraliting again.
Therefore, effectively pharmacotherapy should reduce the residual extra-uterine endometrial tissue that exists behind the laparoscopically surgical operation immediately.Treatment time should only be 4 to 12 weeks, occurred or ovarian cyst formation without any main hormone withdrawal symptom.
Lhrh antagonist produces the hormone that begins immediately to be suppressed, and therefore optimum at short notice gynecological tumor, for example fibroma uteri reduce [human body reproduction magazine (HumanReprodution) 1998,13].
The object of the invention
The present invention relates to the improvement of outgrowth Drug therapy outside the endometrial tissue uterus, promptly give lhrh antagonist to the patient with endometriosis clinical symptoms, its improvement is made up of following: reduce ectopic endometrial tissue immediately
Stop symptom for example serious pain, chronic pelvic pain and dysmenorrhea immediately
Any progress that wards off disease
Avoid occurring the hormone withdrawal symptom
The formation of prevention ovarian cyst, skeleton demineraliting and gastrointestinal tract or hepatic disease
Pharmacotherapy of the present invention can follicular phase in early days to mid-term, preferably the 1st to 3 day of cycle.During treating, the serum level of estradiol remains between 35 to 80pg/ml, preferably approximately between 45 to 75pg/ml, especially preferably approximately between 50 to 75pg/ml.Lhrh antagonist only gives 4 to 12 weeks (short-term inductive treatment), can pass through every day, weekly or by administration in every month.According to the present invention, after the short-term inductive treatment, give contraceptive, on-steroidal rheumatism, analgesic, the androgen except that the testosterone that the 17-alpha-alkyl replaces or their combination in any.
The present invention's general introduction
In the intrauterine membrane tissue, treatment is in beginning in the 1st to 3 day of menstrual cycle outside using lhrh antagonist treatment uterus.Before the treatment of beginning lhrh antagonist, diagnose by peritoneoscope.
Under the situation of serious pain, can not carry out laparoscopy earlier and begin the lhrh antagonist treatment.
Treatment will continue until clinical symptom disappearance and till can't see endometrial hyperplasia.Because endometrial further hypertrophy does not take place in the promoting sexual gland hormone LH that begins immediately and the inhibition of FSH and property steroid estradiol and progesterone.In the treatment in 4 to 12 weeks, benign tumor or the infringement of other property steroid dependency reduce to some extent as endometriosis.Owing to be not to play a role suddenly, therefore do not form ovarian cyst.
And, when the value of estradiol remain on follicular phase early 35 to 80pg/ml, preferably approximately 45 to 75pg/ml, between preferred especially about scope of 50 to 75pg/ml, and when further not increasing or reducing, do not see the hormone withdrawal symptom.The dosage that does not need the titration lhrh antagonist is for example attacked experiment by carrying out expensive progesterone.
Outgrowth method outside the treatment endometrial tissue uterus comprises according to its improvement of the present invention:
Reduce ectopic endometrial tissue immediately
Any progress that wards off disease
Avoid occurring the hormone withdrawal symptom
The formation of prevention ovarian cyst, skeleton demineraliting and gastrointestinal tract or hepatic disease
The the 1st to 3 day beginning Drug therapy in the cycle, and in whole treatment time, remain on the early numerical value of follicular phase, the wherein preferred cetrorelix of antagonist, teverelix, ganirelix, antide or abarelix by giving the level that lhrh antagonist makes estradiol.This antagonist can also be the lhrh antagonist D-63153 (Ac-D-Nal-D-pCl-Phe-D-Pal-Ser-N-Me-Tyr-D-Hci-Nle-Arg-Pro-D-Ala-NH2) described in the German patent application description the 19,911 771.3 of applying on March 11st, 1999.
Can give lhrh antagonist 4 to 12 weeks with the weekly dose in 3 to 10mg/ weeks, perhaps the daily dose with 0.25 to 0.5mg/ day gives lhrh antagonist 4 to 12 weeks.
Can also give lhrh antagonist 4 to 12 weeks with the moon dosage of 12 to the 40mg/ months.
In a multiple treatment, lhrh antagonist can give for 4 to 12 weeks, and this treatment repeated 2 or 3 times in 1 year, therefore can not directly follow a repetitive therapy after the short-term inductive treatment.Usually before the short-term inductive treatment finishes back and repetitive therapy and begins, there is a period of time of a few weeks or months, do not give lhrh antagonist during this period.
In order to prove that the estradiol secretion that keeps low under the LHRH-antagonist for treating of adjusting does not have the feasibility of withdrawal symptom so that therapeutic suppresses to occur, have endometriotic 9 patients to being proved, continue to treat in 8 weeks with the subcutaneous administration weekly of 3mg cetrorelix acetate.Patient's compliance is fabulous, thereby any hectic fever or other withdrawal symptom have been avoided, and confirm disease without any development by laparoscopy for the second time, average estradiol serum-concentration is between 37pg/ml to 64pg/ml, between the preferred 45-75pg/ml, especially preferably approximately fluctuate between the 50-75pg/ml.Histology's biopsy shows: when treatment finishes, do not have endometrial hyperplasia.Do not find that ovarian cyst forms.
Fig. 1 has shown that the successive estradiol level that reaches numerical value follicular phase early (35pg/ml to 80pg/ml, preferred 45-75pg/ml, especially preferably approximately 50-75pg/ml) that obtains suppresses from the endometriosis patient who accepts 8 weeks of 3mg weekly dose cetrorelix (lhrh antagonist) treatment.When treatment finishes, obtained instant suppressing, without any the sign and the endometrial hyperplasia of estradiol withdrawal symptom with successive estradiol level.
Fig. 2 has shown that respectively the weekly dose with weekly 1mg and 3mg gives the serum levels of the estradiol behind the cetrorelix.The serum levels of estradiol is approximately between the 35pg/ml to 80pg/ml, preferably approximately between the 45-75pg/ml, between about 50-75pg/ml.
Endometriosis patient with unique symptom pain is just suffering from a kind of chronic disease.The surgical method and the excretory Drug therapy of inhibition patient's property steroid of curing on the therapy meaning can only be brought temporary transient improvement usually.Uncomfortable relapse rate is very high, treats in 5 years in end and is approximately 70% (Schweppe, 1999).
Simultaneously, the basic surgical treatment and the inhibition of estrogen secretion have brought sizable side effect.The basic surgical treatment that has on the uterectomy meaning of both sides adnexectomy is unfavorable therapy for young, premenopausal women.Estrogenic chronic deficiency will cause following autonomous (vegetative) symptom: hectic fever, perspiration, vagina drying, sensation depression and the danger of suffering from osteoporosis.Owing to produce the effect of male characteristic, can cause manlike symptom with the alternative medicine of synthesizing the steroid danazol.
Drug therapy purpose to endometriosis patient with symptom pain is the negative influence that has obtained to be free from side effects, particularly to have avoided estrogen to suppress, and finishes the treatment of the long-time continuous and effective in back in treatment.The special pharmacology pattern of this lhrh antagonist effect provides new probability for the treatment of endometriosis.
With suitable dosage 3mg Cetrotide for example
Subcutaneous/as to give lhrh antagonist weekly, weekly, continued for 8 weeks, can cause the inhibition of estrogen secretion control, so that the serum-concentration that obtains is approximately between the 35pg/ml to 80pg/ml, preferably about 45-75pg/ml, especially preferably about 50-75pg/ml.In this serum-concentration scope, the autonomy symptom does not appear.Can also avoid the development of osteoporosis.In all stages of this disease (rAFS I-IV), symptomatic pain all will suppress effectively.In the rAFS I-II stage, can notice and implant clinical the disappearing (Felberbaum etc., 2000) that area reduces the disease on the meaning.
In a preferred embodiment of the invention, carry out these 8 to 12 weeks of treatment after, unless wish gestation, the patient can take contraceptive, the preferred oral contraceptive more preferably has the oral contraceptive of gestagen composition.In these associatings, must mention the associating of lynestrenol 2mg and 0.04mg ethinylestradiol or lynestrenol 2.5mg and 0.05mg ethinylestradiol (for example Yermonil, Lyn-ratiopharm-Sequenz).
After using lhrh antagonist separately or uniting use steroid rheumatism and/or analgesic short-term inductive treatment, can also use androgen, for example danazol the testosterone that replaces except that the 17-alpha-alkyl to carry out therapeutic alliance.Suitable androgenic example is halotestin
TM(fluoxymesterone).
With contraceptive, preferred oral contraceptive, preferably wherein contain the treatment that gestagen carries out and should continue to individuation up to the typical pain perception of appearance.Because the effect of the gestagen composition of this contraceptive, preferred oral contraceptive, in this stage, the patient will have fewer menstrual bleeding.And, for before the menstruation that overcomes especially severe and the pain perception of intermenstrual period, in this stage, can have for example concomitant drugs of diclofenac, ibuprofen, indomethacin, oxicam derivant or aspirin of the suitable moist medicine of on-steroidal wind resistance.Can also give for example flupirtinmaleat (Katadolon) of analgesic.
If during with the treatment of gestagen contraceptive, preferred oral contraceptive, further pain symptom also occurring, can repeat the every day of the lhrh antagonist of the suitable dosage of aforesaid usefulness, weekly or every month treatment.The particulars of selecting about corresponding treatment provides below.If the patient does not have pain fully, treatment can become gestagen contraceptive, preferred oral contraceptive and suitable on-steroidal rheumatism or analgesic administering drug combinations as concomitant drugs.
This interruption gives the therapy of lhrh antagonist and has brought new and unrestricted treatment rich innovation, and is free from side effects, and this treatment has reduced patient's medical expense significantly.
The pharmaceutical preparation that is suitable for treating
The pharmaceutical preparation that is suitable for treating the lhrh antagonist of hypertrophy, chronic pelvic pain and obstruction of fallopian tube (FTO) outside the endometrial tissue uterus can for example be
A) concentration is 1mg/1ml or lower acetate preparation, and wherein powder can be dissolved in water for injection (Wfl) or the gluconic acid (GA);
B) concentration is the acetate preparation of 1.5mg/1ml to 5.0mg/1ml, preferred 2.5mg/1ml, and wherein powder can be dissolved in water for injection (Wfl) or the gluconic acid (GA);
C) concentration is the acetate preparation of 10mg/1ml to 30mg/1ml, preferred 15mg/1ml, and wherein freeze-dried powder can be dissolved in gluconic acid (GA) or the water for injection (Wfl).
According to one aspect of the present invention, outside treatment endometrial tissue uterus in the method for hypertrophy, chronic pelvic pain and/or obstruction of fallopian tube (FTO), the improvement that provides is: need about 4 to 12 weeks of patient's lhrh antagonist of this treatment with the form of short-term inductive treatment, stop to give this lhrh antagonist then.
The time of short-term inductive treatment is that the connotation in about 4 to 12 weeks is: treatment time is between about 28 to about 84 days, or from about 1 month to about 3 months.
According to another aspect of the present invention, in aforesaid method, improvement is provided, wherein give lhrh antagonist and make estrogenic serum level approximately between the 35pg/ml to 80pg/ml, preferably approximately 45-75pg/ml, especially preferably approximately 50-75pg/ml.
According to another aspect of the present invention, in aforesaid method, provide improvement, it is characterized in that: after lhrh antagonist short-term inductive treatment, give contraceptive, the preferred oral contraceptive.
According to another aspect of the present invention, in aforesaid method, provide improvement, it is characterized in that: after lhrh antagonist short-term inductive treatment, give a kind of on-steroidal rheumatism.
According to another aspect of the present invention, in the aforesaid method, provide improvement, it is characterized in that: wherein use after the lhrh antagonist short-term inductive treatment, give analgesic.
According to another aspect of the present invention, in aforesaid method, provide improvement, it is characterized in that: after lhrh antagonist short-term inductive treatment, the androgen except that the testosterone that the 17-alpha-alkyl replaces.
According to another aspect of the present invention, in aforesaid method, improvement is provided, it is characterized in that: after lhrh antagonist short-term inductive treatment, associating or give one or more separately and be selected from contraceptive, preferred oral contraceptive, on-steroidal rheumatism, analgesic, the androgen except that the testosterone that the 17-alpha-alkyl replaces or the activating agent of their combination in any.
According to another aspect of the present invention, in aforesaid method, provide improvement, it is characterized in that: follicular phase begin to give lhrh antagonist in early days to mid-term, preferably the 1st to 3 day of cycle.
According to another aspect of the present invention, in aforesaid method, provide improvement, it is characterized in that: lhrh antagonist is selected from cetrorelix, teverelix, ganirelix, antide, abarelix and D-63153.
According to another aspect of the present invention,, it is characterized in that: in during 4 to 12 weeks of short-term inductive treatment, give lhrh antagonist with the weekly dose in 3 to 10mmg/ weeks in aforesaid improved method.
According to another aspect of the present invention, in aforesaid method, provide to improve it is characterized in that: in during 4 to 12 weeks of short-term inductive treatment, give lhrh antagonist with the daily dose of 0.25 to 0.5mg/ day.
According to another aspect of the present invention, in aforesaid method, provide improvement, it is characterized in that: in during 4 to 12 weeks of short-term inductive treatment, with 12 to the 40mg/ months the moon dosage give lhrh antagonist.
According to another aspect of the present invention, in aforesaid method, provide improvement, it is characterized in that: give lhrh antagonist and be used for 4 to 12 weeks of inductive treatment, and this treatment repeated 2 or 3 times in 1 year.
According to a further aspect of the present invention, provide and be used for the treatment of hypertrophy outside the endometrial tissue uterus, the pharmaceutical composition of chronic pelvic pain and/or obstruction of fallopian tube (FTO), it contains lhrh antagonist and optional one or more are selected from contraceptive preferred oral contraceptive, the on-steroidal rheumatism, analgesic, the androgen except that the testosterone that the 17-alpha-alkyl replaces or the composition of their combination in any, and optional pharmaceutically acceptable excipient, thus, the patient LH-RH antagonist that needs in about 4 to 12 weeks at the short-term inductive treatment, stop to give this LH-RH antagonist then, and randomly give together or individually the patient one or more be selected from contraceptive, the preferred oral contraceptive, the on-steroidal rheumatism, analgesic, the androgen except that the testosterone that the 17-alpha-alkyl replaces or the composition of their combination in any.
Suitable excipient and dosage form are for example by K.H.Bauer, K.H.Fr mming and C.F hrer, be described in Lehrbuch der Pharmazeutischen Technologie, the 6th edition, Stuttgart 1999, in 163-186 page or leaf (excipient) and the 227-386 page or leaf (dosage form), comprise the list of references of quoting as proof in the there.
The LH-RH antagonist can be for example through subcutaneous (s.c.), intramuscular (i.m.) or inhalation.The composition that is selected from contraceptive, preferred oral contraceptive, on-steroidal rheumatism, analgesic, the androgen except that the testosterone that the 17-alpha-alkyl replaces or their combination in any can be with mode administration as known in the art (referring to for example Germany, Europe or American Pharmacopeia), preferred oral or suction.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein give lhrh antagonist and make estrogenic serum level between about 35pg/ml to 80pg/ml, preferably approximately 45-75pg/ml, especially preferably approximately 50-75pg/ml.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein use after the lhrh antagonist short-term inductive treatment, give contraceptive, the preferred oral contraceptive.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein use after the lhrh antagonist short-term inductive treatment, give the on-steroidal rheumatism.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein use after the lhrh antagonist short-term inductive treatment, give analgesic.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein use after the lhrh antagonist short-term inductive treatment androgen the testosterone that gives to replace except that the 17-alpha-alkyl.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein use after the lhrh antagonist short-term inductive treatment associating or give one or more separately and be selected from contraceptive, preferred oral contraceptive, on-steroidal rheumatism, analgesic, the androgen except that the testosterone that the 17-alpha-alkyl replaces or the activating agent of their combination in any.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein follicular phase begin to give lhrh antagonist in early days to mid-term, preferably the 1st to 3 day of cycle.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein lhrh antagonist is selected from cetrorelix, teverelix, ganirelix, antide, abarelix and D-63153.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein during 4 to 12 weeks of short-term inductive treatment in, give lhrh antagonist with the weekly dose in 3 to 10mg/ weeks.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein during 4 to 12 weeks of short-term inductive treatment in, give lhrh antagonist with the daily dose of 0.25 to 0.5mg/ day.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein during 4 to 12 weeks of short-term inductive treatment in, with 12 to the 40mg/ months the moon dosage give lhrh antagonist.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, wherein give lhrh antagonist and be used for 4 to 12 weeks of inductive treatment, and this treatment repeated 2 or 3 times in 1 year.
According to another aspect of the present invention, aforesaid pharmaceutical composition is provided, and wherein one or more are selected from contraceptive, preferred oral contraceptive, on-steroidal rheumatism, analgesic, the androgen except that the testosterone that the 17-alpha-alkyl replaces or the activating agent of their combination in any and are dosage form identical or separately.
According to another aspect of the present invention, provide the LH-RH antagonist to be used for the purposes of the medicine of hypertrophy, chronic pelvic pain and/or obstruction of fallopian tube (FTO) outside the preparation treatment endometrial tissue uterus, wherein need patient's lhrh antagonist of this treatment, stop to give lhrh antagonist then with the form in about 4 to 12 weeks of short-term inductive treatment.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein give lhrh antagonist and make estrogenic serum level between the extremely about 80pg/ml of about 35pg/ml, preferably approximately 45-75pg/ml, especially preferably approximately 50-75pg/ml.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein use after the lhrh antagonist short-term inductive treatment, give contraceptive, the preferred oral contraceptive.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein use after the lhrh antagonist short-term inductive treatment, give the on-steroidal rheumatism.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein use after the lhrh antagonist short-term inductive treatment, give analgesic.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein use after the lhrh antagonist short-term inductive treatment, give the testosterone that replaces except that the 17-alpha-alkyl androgen.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein use after the lhrh antagonist short-term inductive treatment associating or give one or more separately and be selected from contraceptive, preferred oral contraceptive, on-steroidal rheumatism, analgesic, the androgen except that the testosterone that the 17-alpha-alkyl replaces or the activating agent of their combination in any.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein follicular phase begin to give lhrh antagonist in early days to mid-term, preferably the 1st to 3 day of cycle.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein lhrh antagonist is selected from cetrorelix, teverelix, ganirelix, antide, abarelix and D-63153.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein during 4 to 12 weeks of short-term inductive treatment in, give lhrh antagonist with the weekly dose in 3 to 10mg/ weeks.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein during 4 to 12 weeks of short-term inductive treatment in, give lhrh antagonist with the daily dose of 0.25 to 0.5mg/ day.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein during 4 to 12 weeks of short-term inductive treatment in, with 12 to the 40mg/ months the moon dosage give lhrh antagonist.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist is provided, wherein give lhrh antagonist and be used for 4 to 12 weeks of inductive treatment, and this treatment repeated 2 or 3 times in 1 year.
According to another aspect of the present invention, provide LH-RH antagonist and one or more to be selected from a kind of contraceptive preferred oral contraceptive, the on-steroidal rheumatism, analgesic, the androgen except that the testosterone that the 17-alpha-alkyl replaces or the activating agent of their combination in any are used for hypertrophy outside the preparation treatment endometrial tissue uterus, the purposes of the medicine of chronic pelvic pain and/or obstruction of fallopian tube (FTO), about 4 to 12 weeks of patient's lhrh antagonist that wherein need this treatment with the form of short-term inductive treatment, stop then giving this lhrh antagonist, and one or more are selected from contraceptive, the preferred oral contraceptive, the on-steroidal rheumatism, analgesic, the androgen that the testosterone that replaces except that the 17-alpha-alkyl is or the activating agent of their combination in any are together or independent patient.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein giving lhrh antagonist makes estrogenic serum level approximately between the extremely about 80pg/ml of 35pg/ml, preferred about 45-75pg/ml, especially preferably approximately 50-75pg/ml.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein use after the lhrh antagonist short-term inductive treatment, give contraceptive, the preferred oral contraceptive.
According to another aspect of the present invention, the purposes of a kind of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein use after the lhrh antagonist short-term inductive treatment, give the on-steroidal rheumatism.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein use after the lhrh antagonist short-term inductive treatment, give analgesic.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein use after the lhrh antagonist short-term inductive treatment androgen the testosterone that gives to replace except that the 17-alpha-alkyl.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein use after the lhrh antagonist short-term inductive treatment associating or give one or more separately and be selected from contraceptive, preferred oral contraceptive, on-steroidal rheumatism, analgesic, the androgen except that the testosterone that the 17-alpha-alkyl replaces or the activating agent of their combination in any.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein follicular phase begin to give lhrh antagonist in early days to mid-term, preferably the 1st to 3 day of cycle.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein lhrh antagonist is selected from cetrorelix, teverelix, ganirelix, antide, abarelix and D-63153.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein during 4 to 12 weeks of short-term inductive treatment in, give lhrh antagonist with the weekly dose in 3 to 10mg/ weeks.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein during 4 to 12 weeks of short-term inductive treatment in, give lhrh antagonist with the daily dose of 0.25 to 0.5mg/ day.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein during 4 to 12 weeks of short-term inductive treatment in, give lhrh antagonist with the moon dosage of 12 to the 40mg/ months.
According to another aspect of the present invention, the purposes of aforesaid LH-RH antagonist and one or more activating agents is provided, wherein give lhrh antagonist and be used for 4 to 12 weeks of short-term inductive treatment, and this treatment repeated 2 or 3 times in 1 year.
Claims (10)
1.LHRH the antagonist cetrorelix is used to prepare the purposes of the medicine of hypertrophy, chronic pelvic pain and/or obstruction of fallopian tube outside the treatment endometrial tissue uterus, medicine wherein is the form of amount that is provided for the cetrorelix of following short-term inductive treatment phase: (a) 4-12 week, (b) 28-84 days, or (c) 1-3 month, it is characterized in that cetrorelix with daily dose, weekly dose or month dosage provide.
2. the purposes of claim 1 wherein repeats described short-term inductive treatment behind the time durations of several weeks that do not give cetrorelix or several months.
3. the purposes of claim 1 wherein gives cetrorelix with the weekly dose form of 3-10mg weekly.
4. the purposes of claim 1, wherein with every day 0.25-0.5mg the daily dose form give cetrorelix.
5. the purposes of claim 1, wherein the moon dosage form with every month 12-40mg gives cetrorelix.
6. the purposes of claim 1, wherein repeat following short-term inductive treatment annual 2 or 3 times: (a) 4-12 week, (b) 28-84 days, or (c) 1-3 month.
7. the pharmaceutical composition that is used for the treatment of hypertrophy, chronic pelvic pain and/or obstruction of fallopian tube outside the endometrial tissue uterus, it comprises cetrorelix optional and pharmaceutically acceptable mixed with excipients, it is characterized in that pharmaceutical composition provides cetrorelix with the amount that is used for the following short-term inductive treatment phase: (a) 4-12 week, (b) 28-84 days, or (c) 1-3 month, wherein, cetrorelix provides with daily dose, weekly dose or month dosage.
8. the pharmaceutical composition of claim 7 wherein gives cetrorelix with the weekly dose form of 3-10mg weekly.
9. the pharmaceutical composition of claim 7, wherein with every day 0.25-0.5mg the daily dose form give cetrorelix.
10. the pharmaceutical composition of claim 7, wherein the moon dosage form with every month 12-40mg gives cetrorelix.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15547899P | 1999-09-23 | 1999-09-23 | |
| US60/155,478 | 1999-09-23 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN00813196A Division CN1376070A (en) | 1999-09-23 | 2000-09-20 | Method for treating extrauterine hyperplasia of endometrial tissue, chronic pelvic pain and tubal obstruction |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN101045155A true CN101045155A (en) | 2007-10-03 |
Family
ID=22555601
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN00813196A Pending CN1376070A (en) | 1999-09-23 | 2000-09-20 | Method for treating extrauterine hyperplasia of endometrial tissue, chronic pelvic pain and tubal obstruction |
| CNA2007100789192A Pending CN101045155A (en) | 1999-09-23 | 2000-09-20 | Method for the therapeutic management of extrauterine proliferation of endometrial tissue, chronic pelvic pain and fallopian tube obstruction |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN00813196A Pending CN1376070A (en) | 1999-09-23 | 2000-09-20 | Method for treating extrauterine hyperplasia of endometrial tissue, chronic pelvic pain and tubal obstruction |
Country Status (22)
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| EP (1) | EP1214086A2 (en) |
| JP (2) | JP2003509467A (en) |
| KR (1) | KR100772852B1 (en) |
| CN (2) | CN1376070A (en) |
| AU (1) | AU769482B2 (en) |
| BG (1) | BG66128B1 (en) |
| BR (1) | BR0014198A (en) |
| CA (1) | CA2383510A1 (en) |
| HK (1) | HK1049117A1 (en) |
| HU (1) | HUP0202741A3 (en) |
| IL (1) | IL148185A0 (en) |
| MX (1) | MXPA02002436A (en) |
| NO (1) | NO331198B1 (en) |
| NZ (1) | NZ534836A (en) |
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| RU (1) | RU2255759C2 (en) |
| SK (1) | SK3752002A3 (en) |
| TR (1) | TR200200738T2 (en) |
| TW (1) | TWI267373B (en) |
| UA (1) | UA73956C2 (en) |
| WO (1) | WO2001021194A2 (en) |
| ZA (1) | ZA200201374B (en) |
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|---|---|---|---|---|
| DE10157628A1 (en) * | 2001-11-26 | 2003-06-12 | Zentaris Ag | Solution for injection of an LHRH antagonist |
| US7214662B2 (en) | 2001-11-27 | 2007-05-08 | Zentaris Gmbh | Injectable solution of an LHRH antagonist |
| WO2009094634A1 (en) | 2008-01-24 | 2009-07-30 | Esperance Pharmaceuticals | Lytic domain fusion constructs and methods of making and using same |
| CA2750582A1 (en) * | 2009-01-22 | 2010-07-29 | Maatschap Interne Geneeskunde Rijnstate | Method for the prophylaxis or treatment of flushing |
| KR20210090298A (en) | 2012-10-30 | 2021-07-19 | 에스퍼란스 파마슈티컬스, 인코포레이티드 | Antibody/drug conjugates and methods of use |
| EP4223298A3 (en) | 2013-03-15 | 2023-08-16 | AbbVie Inc. | Compositions for use in treating heavy menstrual bleeding |
| SG11202001436YA (en) | 2017-08-18 | 2020-03-30 | Abbvie Inc | Pharmaceutical formulations for treating endometriosis, uterine fibroids, polycystic ovary syndrome or adenomyosis |
| TW201912157A (en) | 2017-08-18 | 2019-04-01 | 美商艾伯維有限公司 | Solid pharmaceutical formulation for the treatment of endometriosis, uterine fibroids, polycystic ovary syndrome and adenomyosis |
| US11690854B2 (en) | 2018-04-19 | 2023-07-04 | Abbvie Inc. | Methods of treating heavy menstrual bleeding |
| EP3560555A1 (en) | 2018-04-26 | 2019-10-30 | LifeArc | A composition for treating one or more estrogen related diseases |
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| US5064939A (en) * | 1990-02-06 | 1991-11-12 | The Salk Institute For Biological Studies | Cyclic gnrh antagonists |
| SE9301606D0 (en) * | 1993-05-07 | 1993-05-07 | Per-Christer Oden | COMPOSITION FOR THE TREATMENT OF IMPAIRED HAIR GROWTH |
| US5658884A (en) * | 1994-07-22 | 1997-08-19 | The Medical College Of Hampton Roads | Establishment of tonic ovarian estrogen secretion for extended therapeutic regimens |
| WO1996003138A1 (en) * | 1994-07-22 | 1996-02-08 | The Medical College Of Hampton Roads | Establishment of tonic ovarian estrogen secretion for extended therapeutic regimens |
| DE19513662A1 (en) * | 1995-04-08 | 1996-10-10 | Schering Ag | Combined pharmaceutical preparation for hormonal contraception |
| DE19604231A1 (en) * | 1996-01-29 | 1997-07-31 | Schering Ag | Combined pharmaceutical preparation and its use for the treatment of gynecological disorders |
| RU2108583C1 (en) * | 1996-07-29 | 1998-04-10 | Николай Владимирович Рымашевский | Method for determining indications to applying hormone therapy in genital endometriosis patients |
| CN1228708A (en) * | 1996-09-04 | 1999-09-15 | 有限会社多特 | Peptide-containing drug compositions for oral administration |
| EP0986550A1 (en) * | 1997-06-05 | 2000-03-22 | Merck & Co., Inc. | Antagonists of gonadotropin releasing hormone |
| DE19911771B4 (en) * | 1999-03-17 | 2006-03-30 | Zentaris Gmbh | LHRH antagonist, process for its preparation and its use |
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- 2000-09-20 HU HU0202741A patent/HUP0202741A3/en unknown
- 2000-09-20 KR KR1020027003740A patent/KR100772852B1/en not_active Expired - Fee Related
- 2000-09-20 HK HK03101215.4A patent/HK1049117A1/en unknown
- 2000-09-20 EP EP00967722A patent/EP1214086A2/en not_active Withdrawn
- 2000-09-20 UA UA2002043346A patent/UA73956C2/en unknown
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- 2000-09-20 CN CN00813196A patent/CN1376070A/en active Pending
- 2000-09-20 CA CA002383510A patent/CA2383510A1/en not_active Abandoned
- 2000-09-20 WO PCT/EP2000/009212 patent/WO2001021194A2/en not_active Ceased
- 2000-09-20 NZ NZ534836A patent/NZ534836A/en not_active IP Right Cessation
- 2000-09-20 SK SK375-2002A patent/SK3752002A3/en not_active Application Discontinuation
- 2000-09-20 IL IL14818500A patent/IL148185A0/en not_active IP Right Cessation
- 2000-09-20 AU AU77792/00A patent/AU769482B2/en not_active Ceased
- 2000-09-20 CN CNA2007100789192A patent/CN101045155A/en active Pending
- 2000-09-20 TR TR2002/00738T patent/TR200200738T2/en unknown
- 2000-09-20 BR BR0014198-4A patent/BR0014198A/en not_active Application Discontinuation
- 2000-09-20 RU RU2002111000/14A patent/RU2255759C2/en not_active IP Right Cessation
- 2000-09-22 TW TW089119671A patent/TWI267373B/en not_active IP Right Cessation
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2002
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- 2002-03-21 NO NO20021430A patent/NO331198B1/en not_active IP Right Cessation
- 2002-04-05 BG BG106584A patent/BG66128B1/en unknown
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Also Published As
| Publication number | Publication date |
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| KR100772852B1 (en) | 2007-11-02 |
| CA2383510A1 (en) | 2001-03-29 |
| NO331198B1 (en) | 2011-10-31 |
| JP2012051920A (en) | 2012-03-15 |
| NZ534836A (en) | 2007-07-27 |
| HUP0202741A3 (en) | 2003-12-29 |
| PL201898B1 (en) | 2009-05-29 |
| KR20020035879A (en) | 2002-05-15 |
| JP2003509467A (en) | 2003-03-11 |
| IL148185A0 (en) | 2002-09-12 |
| AU7779200A (en) | 2001-04-24 |
| NO20021430D0 (en) | 2002-03-21 |
| PL353244A1 (en) | 2003-11-03 |
| BG106584A (en) | 2003-02-28 |
| CN1376070A (en) | 2002-10-23 |
| SK3752002A3 (en) | 2003-06-03 |
| WO2001021194A3 (en) | 2002-03-14 |
| EP1214086A2 (en) | 2002-06-19 |
| TR200200738T2 (en) | 2002-08-21 |
| TWI267373B (en) | 2006-12-01 |
| ZA200201374B (en) | 2002-10-30 |
| WO2001021194A2 (en) | 2001-03-29 |
| BR0014198A (en) | 2002-05-21 |
| MXPA02002436A (en) | 2003-02-12 |
| UA73956C2 (en) | 2005-10-17 |
| BG66128B1 (en) | 2011-06-30 |
| AU769482B2 (en) | 2004-01-29 |
| HK1049117A1 (en) | 2003-05-02 |
| NO20021430L (en) | 2002-05-07 |
| RU2255759C2 (en) | 2005-07-10 |
| HUP0202741A2 (en) | 2003-01-28 |
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