CA2412864C - Methods of making, using and pharmaceutical formulations comprising 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one and 17 esters thereof - Google Patents

Abstract

Methods of using 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one (III) 7.alpha.-methyl-17.beta. hydroxyestra-4,14-dien-3-one, and 17 esters thereof for various hormonal therapies, oral and parenteral dosage forms comprising these actives, and processes for their preparation.

Description

METHODS OF MAKING, USING ANA PHARMACEUTICAL
FORMULATIONS COMPRISING 7a,11(3-DIMETHYL-17~
IiYDROXYESTRA-4,14-DIEN-3-ONE AND 17 ESTERS THEREOF AND
17 ESTERS OF 7a-METHYL-17~-HYDROXYESTRA-4,i4-DIEN-3-ONE
RELATED APPLICATIONS
[0001] 'This application is a continuation-in-part of, and claims priority to, PCT Application No. PCTIL1S01110293, filed March 30, 2001, which claims priority to U.S. Provisional Patent Application Nos. 60/193,530, filed March 31, 2000, and 60/194,440, filed April 4, 2000, each of which is incorporated by reference.
FIELD OF T)lIE INVENTION

[0002] The present invention generally relates to methods of making and using androgenic steriods and esters of androgenic steroids.
BACKGROUND OF THE INVENTION

[0003] Androgen is a term used to identify the human male sex hormones.
These hormones, which are chemically classified as steroids, are produced in the body by the testis, the cortex of the adrenal gland and, to a much lesser extent, by the ovaries. Testosterone is perhaps the most widely recognized androgen, and is responsible for the development of male characteristics in a human, including secondary sexual characteristics, libido and the ability to produce sperm.

[0004] When a person is unable to synthesize testosterone, therapy directed at replacing the missing hormone is commonly undertaken. In practice, however, this therapy can be problematic. For example, testosterone exhibits only weak activity when administered orally. While parenteral administration is possible, it is impractical because testosterone remains active in the body for only a short time.
Research has therefore focused on identifying so-called synthetic androgens that are acceptable substitutes for natural testosterone.

[0005] A number of oral and injectable synthetic androgens have been developed over the years, including esters of various androgens. While these esters are hydrolyzed in the body into their corresponding biologically-active alcohols, they are nonetheless administered because they slow the rapid degradation of the synthetic androgen by the body. This maximizes the amount of the biologically active alcohol that reaches the bloodstream.

[0006] Uizfortunately, the activity of these androgen esters is unpredictable.
Different androgens sharing the same ester group exhibit varying and unpredictable levels of activity, as do androgens having the same basic chemical structure, but different ester groups.

(0007] One of the esters that has emerged as a viable injectable synthetic androgen is testosterone enanthate. This enanthate is presently used extensively via intramuscular (IM) injection for hormone replacement therapy in hypogonadal men, and as the androgenic component of several experimental male contraceptives.
One drawback of this active is that it is not exceptionally long-acting-it must be administered IM every two weeks to maintain testosterone levels within a normal (therapeutic) range in hypogonadal men.

(0008] More specifically, testosterone enanthate is presently administered IM for the treatment of hypogonadism at a dose of 200 mg every two or three weeks.
If this enanthate is used for male contraception, it may be administered parenterally at from about 200-400 mg every week, and if used as the androgenic component with estrogen or progestins for contraception, it may be administered at about mg every two weeks. Testosterone bueyclate is another synthetic androgen disclosed in, e.g., U.S. Patent 4,948,790. If administered parenterally for the treatment of hypogonadism, this bucyclate would require a doss of about 1200 mg (given as 3 injections of 1 ml each due to its solubility) to retain activity for about 2-3 months.

[0009] The development of androgens that exhibit activity after oral administration has been less successful. At present, the most widely used effective oral formulation includes methyltcstosterone as the active ingredient, administered at 10~50 mg methyltestosterone/day. However, this active cannot be administered on a Long-term basis, as is required in androgen replacement therapy, because of its associated liver toxicity. It is well known that androgens alkyiated at the C,?
position, such as methyltestosterone, exhibit such toxicity. While removal of the C,~
alkyl group nnay appear at first glance to be an obvious solution to this problem, alkylation at this position is believed to be necessary to prevent degradation of the active by the liver after oral administration.

[0010] Illustrative of the development efforts relating to synthetic androgens is U.S. Patent 5,952,319. While this patent identifies a number of potentially-active synthetic androgens, including 7a,11[i-dimethyl-17(3-hydroxy-4-estren~3-one 17[i-trarts-4-n-butylcyclohexane carboxylate (referred to herein as 7a, t 1 (3~dimethyl-17(3-.. ~. -~':_ ;_ ~~"l'~.'~; ~',: _.'_. __ .: °?~ _3.~;~ .._ hydroxy-4-estren-3-one bucyclate), it provides no data regarding the biological activity of 7ae,1 I (3-dimethyl-17p-hydroxy-4-estreti-3-one bucyclate. There is similarly no data available concerning the biological activity of another synthetic androgen, 7cc,11[3-dimethyl-17[3-hydroxyestr-4-en-3-ozie 17-undecanoate.

[0011) A need therefore exists for a means of overcoming the foregoing and other problems associated with androgen replacement and other therapies that requite the administration of androgens.
BRIEF 5U'1~MARY OF TIDE INVENT'ION

(0012] The present invention meets the aforesaid and other needs by providing, in one aspect, a method for providing hormonal therapy to a patient comprising the oral adm;nistration of an amount sufficient to provide such therapy (advantageously from about I mg/day to about 25 mglday) of 7x,11 [i-dimethyl-1'~~-hydroxy-4-estren-3-one bucyelate, 7a,11(3-dimethyl-17(3-hydroxyestr-4-en-3-one 17~undecanoate, or a mixture thereof, to a patient in need thereof.

(0013] A related aspect of the present invention contemplates praviding hormonal therapy to a patient comprising the oral administration of an androgen selected from the group consisting of 7a,11 [3-dimethyl-17(i-hydroxyestra-4,14-dien-3-one, 1? esters of 7a,11~-di~methyl-17(i-hydmxyestra-4,14-dien-3-one, 17 esters of 7a-methyl..l7~-hydroxyestra-4,I4-dien-3-one or mixtures thereof in an amount effective to provide hormonal therapy to a patient in need thereof.
[00X4] The foregoing aspects ofthe invention arc predicated in significant part on the unexpected discoveries that 7a,11[i-dimethyl-17[i-hydroxy-a-estren-one bucyclate (also referred to herein as "the bucyclate"), 7cr" 11 [i-dimethyl-17(i-hydroxyestr 4-en-3-one 17-undecanoate (also referred to herein as "the undecanoate"), 7a,11 Q-dimethyl-17~-hydroxyestra-4,14-diem-3-one (also referred to herein as "14-dehydromethandrolone"), 17 esters of 7a,I I [i-dimethyl-17(i-hydroxyestra-4,14-lien-3-one (also referred to herein as "17 esters of 14-dehydromethandrolone"), and 17 esters of 7a-methyl-17[3-hydroxyestra-4,14-dien-one, and do not degrade after oral administration even though each lacks an alkyl group at the C» position, and exhibit actiYity far in excess of the current oral standard, methyltestosterone. These surprising discoveries permit hormonal therapies requiring the administration of a~n androgen to be conducted utilizing oral dosages of the foregoing androgens that are significantly lower than those required ":,.,, _ ' -;.~ - ___ when administering oral methyltestosterone to effect the same therapy. A
further expected benefit of using these compounds is that liver toxicity, if any, should be ~
minimal because these compounds are not alkylated at the C» position.
[0015] In another aspect, the present invention comprises a method for providing hormonal treatment comprising the paremeral administration of an effective amount, advantageously from about I mg up to about 1 OOmg, of the bucyclate and/or the undecanoate at intervals of at least about two weeks, and preferably up to about 600 mg at much longer intervals, e.g., a single administration of 600 mg providing effective therapy for up to about three months.
(0016) A related aspect contemplates a method for providing hormonal treatment comprising administering parenterally an androgen selected from the group consisting of 7a,11 ~-dimethyl-17(i-hydroxyestra-4,14-dien-3-one, 17 esters of 7a,1 I(3-dimethyi-17[i-hydroxyestra-4,14-lien-3-one, 17 esters of7amethyl-17(3-hydroxyestra-4,14-dien-3-one or mixtures thereaf in an amount effective to provide hormonal therapy to a patient in need thereof.
[001 ~) The aspects of the invention are predicated in part on the surprising relatively high potency, and unexpected long term activity, of the bucyclate and undecanoate when administered parenterally, which potency is higher and activity longer-lasting than esters of other potent androgcnic steroids, even bucyclic esters thereof. This activity was unexpected in view of the preparation and evaluation of several bucyciic esters of potent androgenic steroids other than 7a,11 [i-dimethyl-17~i-hydroxy-4-estren-3-one bucyclate, the former group of esters yielding disappointing results.
[0018] Another aspect of the present invention includes separate processes for preparing the bucyclate, undecanoate, 14-dehydromethandrolone and 17 esters of

14-dehydromethandrolone which provide these actives in relatively high yield, and advantageously in a solid form, preferably crystalline, at room temperature.
As each can be produced in solid form, the preparation of aqueous microcrystalline suspensions for parenteral administration (with the exception of the 17 undecanoate ester of 14-dehydromethandrolone which would not crystallize) is possible.
Moreover, because these actives are solid at room temperature, one is able to control the average particle size and particle size distribution of the solids, thereby positively affecting the duration of activity after parenteral administration of the respective suspensions.
[0019] Related aspects of the present invention include certain intermediates, in amorphous or, preferably, crystalline form, as well as one or more steps used in the aforementioned preferred process for preparing the bucyclate, undecanoate, 14.
dehydromethandrolone and 17 esters of 14-dehydromethandrolone.
[0020] Further aspects of the present invention include various formulations of these actives, including tablets, caplets, extended release tablets, soft gelcaps containing the actives in an oily carrier, transdermal patches, pre-filled syringes, vials and the like, in which the amount of the actives) included therein may be determined in view of their unexpected relatively high potency and long term activity.
[002Z] It is contemplated that the hormonal therapy of the present inve~ion includes, but is not limited to, hormone replacement therapy in males and females, male contraception, and the treatment of certain cancers, such as breast cancer.
[0022) These and other aspects and features of the present invention may best be understood with reference to the accompanying figures and in the following.
description of the preferred embodiments.
BRIEF DESCRI~'TI4N OF THE DRAWINGS
[0023] Figure 1 illustrates the chemical structure of 7x,11/3-dimethyl-17a-hydroxy-4-estren-3-one bucyclate, with numerals identifying the various carbon atom positions, including the non-alkylated C1~ position.
[0024] F'ig_ 2A illustrates the chemical structure of methyltestosterone.
[0025] Fig. 2B illustrates the chemical structure of testosterone cnanthate.
[0026] Fig. 3 is a graph comparing the androgenic potency of 7x,11 ~i-dimethyl-17(3-hydroxy-4-estren-3-one bucyclate and that of other compounds after oral administration.
j002'7] Fig. 4 is a graph comparing the androgenic potency of 7x,11 [3-dimethyl-17[3-hydroxy-4-estren-3-one bucyclate and that of other compounds after oral administration.
[0028) Fig. 5 is a graph comparing the duration of activity of 7x,11 ~-dimethyl-17p-hydroxy-4-estren-3-one bucyclate and that of other compounds after subcutaneous injection.
_ C _ ~ ~ 3 ~ J L~ ~ ~ ~'~ . ~ I _ . ~ . l a ._ ~ _ '_~~ ~ L .. . J '- ~~ ~
~~I~~ ~~ v " _ _ [0029] Fig. 5 is a ,graph comparing the androgenic potency of 7x,11 ø-dimethyl-17[i-hydroxy-~-estren-3-one bucyclate and that of other compounds after oral administration and subcutaneous injection.
[0030] Fig. 7 is a graph comparing the androgenie potency of 7x,1 t ø-dimethyl-17[3-hydroxy-4-estren-3-one bucyclate and that of other compounds after subcutaneous injection.
[0031) Fig. 8 is a graph comparing the duration of activity of 7a,11ø-dimethyl-17ø-hydroxy-4-estren-3-one bucyclate and that of other compounds after subcutaneous injection.
[0032] Fig. 9 is a graph comparing the duration of activity of 7x,11 ø-dimethyl-17ø-hydroxy-4-estrea-3-one bucyclate and that of other compounds after subcutaneous injection.
[0033] Fig. 10 is a graph comparing testosterone serum levels (pg/ml) after subcutaneous injection of 7x,11 ø-dimethy!-17[i-hydroxy-4-estren-3-one bucyclate and other compounds.
[0034] Fig. 11 is a description of a preferred method for preparing 7x,11 [i-dimethyl-17p-hydroxy-4-estren-3-one bucyclate.
[0035] Fig. 12 illustrates the chemical structure of 7x,11[3-dimethyl-17ø-hydroxyestr-4-en-3-one 17-undecanoate, with numerals iden'fying the various carbon atom positions, including the non-alkylated C,~ position.
[0036] Fig. 13 is a graph comparing the androgenic potency of 7x,11 ø-dimethyl-17[3-hydroxyestr-4-en-3-one 17-undecanoate and testosterone after subcutaneous injection.
[003] Fig. 14 is a graph comparing the androgenic potency of 7x,11 [3-dimethyl-17ø-hydroxyestr-4-en-3-one 17-undecanoate and methyitestosterone after oral administration.
[0038) Fig. 15 is a graph comparing the duration of activity of 7x,11 (3-dimethyl-17ø-hydmxyestr-4-en-3-one 17-undecanoate and that of testosterone enanthate (CDB-112F) after subcutaneous injection.
[0039] Fig. 16 is a description of a preferred method for preparing 7x,11 [i-dimethyl-17ø-hydroxyestr-4-en-3-one 17-undecanoatc.

(0040] Fig. 1? illustrates the chemical structure of 7x,11 (3-dirnethyl-17(3-hydroxyestra-4,14-dien-3-one, with numerals identifying the various carbon atom positions, including the non-alkylated C~~ position.
(0041] Fig. 18 illustrates the chemical structure of 7a,1 lp-dimethyl-17(i-hydroxyestra-4,14-then-3-one 17-undecanoate.
(p042] Fig. 19 illustrates the chemical structure of 7x,11 [i-dimethyl-17ø-hydroxyestra-4,14-dien-3-one 1?(i-4-n-butylcyclohexanecarboxyiate.
(0043] Fig. 20 is a graph comparing the androgenic potency of 7x,11 ~i-dimethyl-17(i-hydroxytstra-4,14-lien-3-one 17-undecanoate, 7a,11[i-dimethyl-17(3-hydmxyesrTa-4,14-dien-3-one 17~-4-n-butylcyclohexaneearboxylate, and testosterone after oral administration.
(0044] Fig. 21 is a graph comparing the androgenic potex~cy of 7a,11 (i-dimethyl-17a-hydroxyestra-4,14-dien-3-one 17-undecanoate, 7a,11ø-dimethyl-17j3-hydroxyestra-4,14-dien-3-one 17(i-4-n-butylcyclohexanecarboxylate, and testosterone after subcutaneous injection.
[Q04S] Fig. 22 is a graph comparing the duration of activity of 7a,11 (i-dimethyl-17p-hydroxyestra-4,14-diem-3-one 17-undecanoate, 7a,11[3-dimethyl-17p-hydroxyestra-4,14-dien-3-one 17ø-4-n-butylcyclohexanecarboxylate and that of other compounds after subcutaneous injection.
(0046] Fig. 23 is a graph comparing the androgenic potency of 7x,11 ø-dimethyl-17[3-hydroxyestra-4,I4-dien-3-one, 7a-methyl-17(i-hydroxyestra-4,14-dien-3-one 17ø-4-n-butylcyclohexanecarboxylate and 7a-methyl-17(3-hydroxyestra-4,14-dien-3-one after oral administration.
]0047) Fig. 24 is a graph comparing the duration of activity of 7x,11 p-ditnethyl-17[i-hydmxyestra-4,14-dien-3-one and 7a-methyl-17[3-hydroxyestra-4,14-dien-3-one after subcutaneous injection.
[0048] The various aspects of the present invention described in the following paragraphs are set forth with an emphasis on preferred embodiments.
However, it will be obvious to those of ordinary skill in the art that variations of the preferred embodiments may be successfully used, and that it is intended that the invention may be practiced otherwise than as specifically described herein.
The inventive methods, processes and formulations should therefore not lx construed as being limited to the preferred embodiments described herein.

g DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0049] The present invention provides a variety of methods for providing hormonal therapy to a patient (male or female} in need thereof. 1=ach method requires the administration of particular actives, 7a,11 [i-dimethyl-17[i-hydroxy-4-estren-3-one bucyclate, 7a,11(3~dimethyl-17[3-hydroxyestr-4-en-3-one I7-undecanoate, 7a,11 [i-dimethyl-17[i-hydroxyestrx4,14-diem-3-one, 17 esters of 7a,I Iii-dimethyl-17[3-hydroxyestra-4,14-lien-3-one, and 17 esters of 7a-methyl-17[3-hydroxyestra-4,14-diet-3-one either in combination or, preferably, alone.
The chemical structures of certain of the actives are set forth in Figs. 1, 12, I'7-19 and 23.
[0050] In significant part, the present invention rests upon the discovery that 7a,11/3-dimethyl-17[3-hydroxy-4-estren-3-one bucyclate, 7a,1 i~-dimethyl~17p-hydroxyestr-4-en~3-one 17-undecanoate, 7a,il[3-dictlethyl-173-hydroxyestra-4,14-dien-3-one, 17 esters of 7oc,11 [i-dimethyl-173-hydroxyestrs~,14-lien-3-one and 17 esters of 7a-methyl-17[i-hydroxyestra-4,14-dien~3-one (also referred to herein as "actives" or "the actives"), exhibit surprising and unexpected properties in vivo.
These properties permit these actives to be administered either orally or parenterally, in relatively lower amounts, at longer time intervals (at least with respect to those actives that can be provided as a solid), and with less side effects, as compared to existing alterngtive synthetic androgens, e.g., methyltestosterone, testosterone enanthate. "I"he chemical structures of these two well-known compounds (methyltestosterone, testosterone enanthate) are set forth in Figs. 2a and 2B, respectively.
[0051] The surprising properties of 7a,11 [i-dimethyl-1'7[i-hydroxy-4-estren-3-one bucyclate, 7a,11~-dimethyl-17[3-hydroxyestr-jt-en-3-one 17-undecanoate, '7x,11 ~3-dimethyl-17[~-hydroxyestra-4,14-lien-3-one, 17 esters of 7a,11 p-dimethyl-17[i-hydroxyestra-4,14-lien-3-one and 17 esters of 7a-methyl-17J3-hydroxyestra~
4,14-dien-3-one, render these actives well suited for any hormonal therapy in which an androgen is required, or desired. By way of example only, and without intending to limit the therapeutic uses of the actives, the actives tztay be used in the treatment of hypogonadal males, e.g., hypogonadatropic eunuehoidism (complete, incomplete, delayed puberty}, fertile eunuch, prepubertal panhypopituitarism, postpubettal pituitary failure (selective, panhypopituitarism). The actives may also be administered (either alone or, more effectively, in combination with one or more steroidal progestins or estrogens) to induce and maintain fertility suppression in male animals, or as an androgenic component for feedback. Further, and due to their anabolic properties, the actives may be administered to promote and maintain muscle growth and maintenance. These properties can be particularly important in persons afflicted with muscle wasting diseases such as AIDS, but are more generally applicable to the elderly who typically have relatively low muscle mass. In addition, the actives may be used for the treatment of cancer, e.g., the pilliative treatment of breast cancer in men and women, the treatment of osteoporosis, anemia, anabolism, hormonal replacement therapy (in males and females) and hypergonadotropic conditions (e.g., Klinefelter's, Reifenstein's, functional prepubertal castration syndrome, male Turner's syndrome, serotoli cell-only syndrome, adult seminiferous tubule failure (e.g., mumps orchids, irradiation, idiopathic, myotonia dystrophica), adult Leydig cell failure).
[005Z] The unexpected properties of 7a,11 [3-dimethyl-17(3-hydroxy-4-estren-3-one bucyclate, 7a,ll~i-dimethyl-17(3-hydroxyestr-4-en-3-one 17-undecanoate, 7x,11 ~i-dimethyl-17~i-hydroxyestra-4,14-then-3-one, 17 esters of 7a, I I ~-dimethyl-17[3-hydroxyestra-4,14-dien-3-one and 17 esters of 7a-methyl-17p-hydroxyestra-4,14-dien-3-one, were discovered after a series of in vivo animal studies undertaken in Sprague-Dawley rats. For example, based upon these experiments, it was unexpectedly found that the foregoing actives, despite their lack of alkylation at the C1~ position, not only do not degrade after oral administration, but exhibit activity far in excess of the current oral standard, methyltestosterone.
Moreover, this lack of alkylation is expected to minimize, or eliminate, any attendant liver toxicity. Thus, the foregoing and other therapies may be conducted utilizi.ag dosages of the actives that are significantly lower than those expected, and less than that required when administering methyltestosterone, to effect the same therapy. This is accomplished without the attendant concern of liver toxicity associated with existing synthetic androgens.
[0853] More specifically, it was found that the oral activity of 7a,11 [i-dimethyl-17[3-hydroxy-4-estren-3-one bucyclate was about four times greater than methyltestosterone (thereby providing what may be referred to as a potency ratio of about 4 relative to the standard, in this case, methyltestosterone). The oral activity of the undecanoate, 7a,I1~3-dimethyl-17(3-hydroxyestr-4-en-3-one 17-undecanoate, ., , ; : ~ ~ . _ ~ 3'' _. ~ _ .. . . ~. _. 1~ ~~ _ _ was found to be about twice that of methyltestosterone. V~lith regard to certain of the other actives, the oral activity of 7x,11 ~i-dimethyl-17(3-hydroxyestra-4,14-dien-3-one was found to be about twice ( 1.96), ?a, l l (3-dimethyl-17[3-hydroxyestra 4,14-dien-3-one 17-undecanoate was found to be at least about twice, 7x,11(3-dimethyl-17~3-hydroxyesua-4,14-dien-3-one 17~-4-n-butylcyclohexanecarboxylate was found to be at least about six times, and a 17 ester of 7a-methyl-17[i-hydroxyestra-4,14-dien-3-one was found to be at least about 18 ( 18.77) times, relative to the activity of methyltestosterone. Moreover, and with respect to bath the bucyclate and undecanoate, it was found that this oral activity was maximized when the actives were formulated with an oily carrier. Llnexpeetedly high levels of activity were also discovered in connection with the parenteral administration of the actives. In contrast to the oral formulation, activity was maximized when the parenteral formulation comprised the actives in an aqueous carrier.
[0054] As a general statement, it was found that the effective oral dosage of any of the actives for any hormone replacement therapy which requires an androgen, e.g., the treatment of hypogonadism, will be the inverse of its potency ratio relative to the amount of the standard required to provide the same effect, e.g., the amount of methyltestosterone administered orally required to provide the same effect.
[0055] For example, and in the case of hypogonadism, 7x,,11 ~i-dimethyl-17(3-hydmxy-4-estren-3-one bucyclate may be orally administered in therapeutically effective amounts. More specifically, the oral dosage may range from about 1 mg/day to about 25 mg/day, advantageously from about 2 rng/day to about 20 nng/day, and preferably up to about 15 rnglday. Administration of the undecanoate to effect this therapy may be undertaken within the foregoing bucyclate therapeutic dosage ranges, but is preferably undertaken at relatively greater levels relative to that of the bucyclate due to the undecanoate's slightly lower oral activity. For example, the undecanoate may be administered at from about 1 mg/day to about 75 mglday, advantageously from about 2 mglday to about 50 mg/day, and preferably up to about 25 mglday.
[0056] More generally, the actives, including the 17-undecanoate, may be administered at an average dosage of from about 1 mg to about 50 mg per day, and advantageously from about 5 mg to about 40 mg per day. The average daily dosage of the relatively potent actives may range from about 1 mg to about 25 mg.
,. ~ ~. ~~i:i_ifi~~_,.,,,i ~,, _ '_~ _'.'_. ~__. . ~ ~_,, (0057] The oral dosage regimens described herein, set forth on the basis of miliigramslday, includes any dosage regimen that is able to provide that dosage level to a patient per day. For example, an extended release formulation of an active may not need to be administered each day, yet would pmvide the required daily dosage.
However, administration of the therapeutic dosage on a daily basis is the preferred method of treatment.
[0458] 'The effective oral dosage of the actives, for example, the bucyclate, the 17~i-4-n-butylcy~lahexanecarboxylate ester of 7x,11 (3-dimethyl-17~i-hydroxyestra-4,14-diem-3-one or the 17~-4-n-butylcyclahexanecarboxylate ester of 7oc-methyl-17p-hydroxyestra-4,14-lien-3-one for the treatment of cancer, e.g., breast cancer in women can vary, but will range from at Least about 10 mglday, advantageously at letLSt about 25 mg/day, and preferably at least about 50 mglday.
Administration of the undecanoate or the 17 undecanoate ester of 7x,11 (3-dimethyl-17~i-hydroxyestrx4,14-dien-3-one to effect this therapy may, as before, be undertaken within the foregoing bucyelate therapeutic dosage ranges, but is preferably undertaken at relatively greater levels relative to that of the bucyciate.
For example, the undecanoate may be administered in an amount of at least about 20 mglday, advantageously at least about 50 mglday, and preferably at least about mglday.
[0059] In the use of the actives for male coatraceptivn, amounts effective to provide such therapy may be administered. Generally, the effective oral doses may vary, but can range from about 1 to about 50 mg per day. 4f course, the greater the relative gotetlcy, the lesser the dose. For example, for 7x,,1113-dimethyl-i7[3-hydroxy-4-estren-3-one bucyclate and the 17~-4-n-butylcyclohexanecarboxylate esters of 7x,11 [i-dimethyi-17(i-hydroxyestra-4,14.dien-3-one and 7a-methyl-17(3-hydmxyestra-4,14-diem-3-one, when administered for male contraception, an effective anal dose may range fiom about 1 mglday to about 25 mg/day, advantageously from about 2 mg/day to about 20 mgfday, and up to about 15 mglday. Administration of the undeeanoate and the 17 undecanoate ester to effect this therapy rnay, as before, be undertaken within the foregoing bucyclate therapeutic dosage ranges, but is preferably undertaken at relatively greater levels relative to that of the bucyclate. For example, these actives may be administered in iVn .~

an amount ranging from about 1 mg/day to about 50 mg/day, advantageously from about 2 mg/day to about 40 mglday, and up to about 30 mglday.
[0U60] In the case of conditions requiring chronic hormonal therapy, such as hypogonadism, an injectable bucyclate, undecanoate, 7a,11(3-dimethyl-17[3-hydroxyestra-4,14-dien-3-one, and/or 17 esters of 7a,1 I[3-dimethyl-17p-hydroxyestra-4,14-dies-3-one formulation is preferably administered. This preference is based upon the unexpected discovery that these actives are surprisingly potent and long-acting when dispersed (preferably as a suspension) in an aqueous formulation (with the exception of the 17 undecanoate esters of 7a,11 [3-dimethyl-17[3-hydroxyestra-4,14-dien-3-one, 7a-methyl-17[3-hydroxyestra-4,14-dien-3-one and 17 esters thereof, which exhibit relatively high potency and thus may be parenterally administered ~or any hormonal therapy, but are not longacting relative to other actives provided herein). Given these properties, and by way of example, the bucyclate and undecanoate may be administered in an aqueous formulation at lower doses compared to both testosterone enanthate (in an oily carrier) and testosterone bucyclate, and at relatively long intervals. More specifically, and by further way of comparative example, doses of the bucyclate and undecanoate, when dispersed in an aqueous formulation, may generally range from about one-third to about three-quarters the dose of testosterone enanthate (provided in a sesame oil carrier) required to provide substantially equivalent therapeutic results, with between about one-half and about two-thirds of that latter dose being preferred. With respect to testosterone enanthate, the bucyclate, undecanoate, when dispersed in an aqueous carrier, may be administered at between about one-quarter and about one-half of the dose of testosterone enanthate to provide substantially equivalent therapeutic effects.
With respect to testosterone bucyclate, the crystalline 17 esters of 7a,11 [i-dimethyl-17(3-hydroxyestra-4,14-dien-3-one (e.g., the 17[i-4-a-butylcyclohexanecarboxylate ester thereof), when dispersed in an aqueous earner, may be administered at between about one-quarter and about one-half of the dose of testosterone bucyclate in the same aqueous carrier to provide substantially equivalent therapeutic effects.
However, if any of the actives are formulated in a non-aqueous carrier, e.g., an oily carrier comprised of sesame or other vegetable oils, it was discovered that its potency over long periods remained, but that it was substantiahy equivalent to that of testosterone enanthate in a sesame oil carrier.

[0061] Because of its long-acting androgenie activity, particularly when administered parenterally in an aqueous carrier in effective amounts, the bucyclate, undecanoate, 7a,11 (i-dimethyl-17[1-hydroxyestra 4,14~dien-3-one and the crystalline 17 esters thereof (c.g., the 17(3-4-n-butylcyclohexanecarboxylate ester thereof), may be administered at intervals equal to, or in excess of, about two weeks.
More specifically, they may be administered at intervals of about one month, preferably about two months, more preferably once about every three months or about every two to four months. This provides a significant advantage to a patient relative to existing regimens that require therapeutic injections on a more frequent basis.
(0062] Again, the dosage of any of the actives administered parentecglly (particularly those able to be administered in an aqueous formulation) in an aqueous formulation at any interval will be significantly less than the amount of testosterone enanthate used to achieve substantially similar therapeutic results. For example, in treating hypogonadism, those actives able to be formulated in an aqueous carrier and provide therapeutic benefits over an extended time period may be administered in amounts ranging from about I mg up to about 100 mg about every two weeks, and advantageously from about 25 to about 75 mg during that period; up to about mg about every month, and advantageously from about 50 mg to about 150 mg during that time period; up to about 400 mg about every 2 months, and advantageously from about 100 to about 300 mg during that time period; and up to about 600 m~ about every 3 months, and advantageously from about 150 mg to about 450.tng during that lima period. These dosages, advantageously provided by a single injection at the begiruring of each time period, are less than the dosages of testosterone enanthate and testosterone bucyclace that may be uscd to provide similar therapeutic effects over the same pcr~iods.
[0063] By way of further example, dosages of the bucyclate, undecanoate, fa,l 1(3-dimethyl-17(i-hydroxyestra-4,14-diem-3-one and crystalline 17 esters thereof effective for male contraception via parenteral administration, if used alone, may range from about 25 mg/week up to about 200 snglweek, advantageously up to about 150 mg/week, and preferably from about 50 mglweek to about 100 mglweek. If used in a more typical manner, 1.e., combined with estrogen and/or progestins, parenteral dosages of the foregoing actives may range from about 1 mg up to about n. _ _ =;~rnnr~_~ ~;~i-~i:~~. ~~ ~.:_. ..._ ;. ~~~a:a?~~~
''Jr~

100 mg every about two weeks, advantpgeously from about 2 mg up to about 75 mg, and preferably up to about 50 mg, every two weeks. Of course, because of the long-acting activity of these actives, these dosages may be administered on a substantially linear basis if activity beyond the periods set forth above is desired.
[0064] The enhanced potency of the bucyclate, undecanoate, 7x,11 [3-dimethyl-17[i-hydroxyestra-4,14-dien-3-one and crystalline 17 esters thereof actives advantageously permits a further advantage in that effective amounts may be administered via a single injection, w'ch is desirable from a patient comfort and cast perspective. Equivalent therapeutic results using testosterone enanthate would require multiple injections. Of course, multiple injections of relatively lower doses of the inventive actives may be administered if required or desired. For example, actives formulated into an oily carrier, despite relatively high potency, need to be administered more frequently to obtain the desired therapy, with the dose being adjusted based upon the particular active's potency in that carrier. This is the situation, for example, with 7a-methyl-1'7(i-hydroacyestra-4,14.:dien-3-one.
[~(5) While the actives may be adrnmistered alone in the treatment of cancer, it is preferably administered in coordination with ane or more anti-cancer agents, e.g., therapeutically-effective amounts of chemotherapeutic agents, such as, cisplatin, carboplatin, doxorubicin, paclitaxel, taxatere, methotrexate, fluomuracil, camptothecin, cyclophosphamide and mixtures thereof, as well as therapeutically-effective amounts of anti-angiogenesis agents, either alone or in combination.
The identity of suitable anti-tumor and anti-angiogenesis agents and associated dosage regimens are well known, and as such will not be repeated herein. The timing of administration of the foregoing agents may occur at any time so long as the administration does not interfere with the inventive therapeutic methods.
[0066] While the actives may be prepared using any suitable process, a further aspect of the present invention is the discovery of the preferred synthesis routes described below, which provide these actives in relatively high yield, and in solid form, preferably in crystalline form, at room temperature. The preparation of these actives in solid form at room temperature was significant, as it led to the further discovery that the long-acting effect of these actives are enhanced when included in an injectable formulation at an average particle diameter of from about 1-50 pm, and preferably from about 3-30 pm. The average particle diameter of the ... _ ,,_, ..V~.~,:J~;Lylc =. _. ~__. ,. _. =?~' ~,~n~~

actives, and particularly the crystalline actives, when formulated as an injectable is thus preferably within the foregoing ranges.
[0067] As a solid at room temperature, the actives stand in marked contrast to testosterone enanthate. The latter exists as a liquid at room temperature, adversely affecting its activity over long periods of time. Further, the enanthate is precluded from commercialization as a lyophilizate or powder for reconstitution, or as a tablet, caplet or other solid dosage form.
[0468] Turning to Fig. l l, the preferred synthesis of 7a,11 ~3-dimethyl-17~i-hydroxy-4-estren-3-one bucyclate is depicted. Generally, this synthesis comprises the steps of:
{a) converting the ether group of Compound 1 Me0 (b) ketalizing the carbonyl group of Compound 2 to provide Compound 4 to a carbonyl group, providing Compound 2 is (c) epoxidizang Compound 4 to provide the epoxide of Compound 5 (d) opening the epoxide ring in Compound 5 and substituting an alkyl group at C" #o provide Compound 6 (comprising a mixture of 1 loc- and i 1 ~i-methyl isomers, Compounds 6a and 6b, respectively) by use of a Cxri,gnard reagent 6a: R ~ alpha Me 6b: R = beta-Me (e) deketalizing and dehydrating Compound 6 to provide Compound 7 (comprising a mixture of 1 la.- and 11 ~i-methyl isomers, Compounds 7a and 7b, respectively) OH

7a: R ~ alpha-Me 7b: R -- beta-Me (fj converting Compound 7a to Compound 9 i0 and (h) esterifying Compound 10 to provide Compound I (7x,11 (i-dimethyl-17(3-hydroxy-4-estren-3-one bucyclate).
(g) converting Compound 9 to Compound 10 [0069] Step (a) may also yield an undesirable by-product, Compound 3 O

[0070] If desired, before step (fj, one may ketalize the 1 la- and 11 (3-methyl isomers of Compound 7 to provide Compound 8 and then deketalize and epimerize Compound 8, thereby enhancing the ratio of the desirable 11 a-methyl isomer to 11 [;-methyl isomer.
[0071] Turning to F'ig. 16, a preferred synthesis mute for the preparation of the undecanoate is set forth. This synthesis comprises steps (a~(g) used in the bucyclate synthesis as set forth above. Thereafter, however, Compound 10 is estetified to provide Compound II (the undecanoate).
[0072] The preferred synthesis of 7x,,11 (3-dimethyl-1'7[3-hydroxyestrar4,14-diene-3-one (Compound III) is also provided as a further aspect of the present invention. Genezally, this synthesis comprises the steps of:
[0073] A method for preparing 7x,11 (i-dimethyl-17[i-hydroxyestra 4,14-dien-3-one (III) comprising the steps of (a) acetylating, aromatizing and hydrolyzing Compound 101 _, .. '- ;~bL'~'~'l_'. _.'_,'~. _.'-. ,___ .', _ .! ~~~"' C~H
(101) (102) (b) methylating the phenolic functionality of Compound 102 and oxidizing the hydroxyl group to provide Compound 103;
(103) {c) dehydrogenating Compound 103 to provide Compound 104;
to provide Compound 102;

{104) (d) enolacetylating Compound 104 to provide Compound 105;
(105) {e) reducing and hydrolysing Compound 1 p5 to provide Compound l Ob;
and (106) (~ reducing Compound 106 to provide 7x,11 ~-dimethyl-17~-hydroxyestra..4, i 4-dien-3-one (Compound III).

(III) [0074) The foregoing process may further comprise the step of esterifying Compound III by any suitable means to provide 17 esters thereof, preferably 7x,11 [i-dimethyl-17(3-hydroxyestra-4,14-dien-3-one 17-undecanoate (Compound IV) and 7a,ll~i-dimethyl-17~i-hydroxyestra 4,14-dien-3-one 17[3-4-n-butylcyclohexanecarboxylate (Compound V).
[0075] One or more of the intermediates formed during the foregoing synthesis routes are also contemplated as part of the present invention, and particularly the preferred crystalline forms of those intermediates. In addition, certain of the process steps, and combinations thereof, which provide advantages such as relatively high yields and/or parities of intermediates, constitute further aspects of the present invention. Other aspects of the present invention contemplate crystalline forms of the actives.
[0076] A pharmaceutically acceptable carrier is advantageously combined with each active to ease the administration of the active to a patient in need.
Suitable carriers for oral and buccal dosage farms, such as tablets, capsules, caplets and soft gelcaps (having an oily carrier), are well known, and may be used in connection with the actives. Preferably, oral dosage formulations of the actives include an oily carrier, and are provided in the farm of a soft gelcap, as this formulation was found to enhance the beneficial properties of the actives upon oral administration. illustrative of oily substances that may be used to provide an oily carrier include, but are not limited to, vegetable oils, e.g. olive oil, saftlower oil, corn oil, sunflower oil, cotton seed oil, tsubaki oil, rice bran oil, soybean oil, sesame oil, wheat germ oil, coconut oil, peanut oil, rape seed oil and the like, fish ails, e.g., cuttlefish oil, cod oil, and the like, liver oils, e.g., shark liver oil, cod liver oil and the ,~~~~

like, blubber oils, e.g., seal ail, blue whale oil, etc.), conchiferas oils, e.g., abalone oil, oyster oil, and the like, medicinal oily substances, e.g., castor oil, fatty acid glycerides, vitamin E, vitamin A, vitamin K, and the like, polyethylene glycol and the like, and mixtures thereof.
[0077] For parenteral administration, any type of carrier that maintains the benefits of the invention as described herein may be used. Preferably, however, and as previously mentioned, the bucyclate, undecanoate, 7oc,11ø-dimethyl-17~i-hydroxyestt~a-4, I4..dien-3-one andlor crystalline 17 esters thereof, is suspended in an aqueous carrier suitable for injection. The water component of the aqueous carrier should constitute at least half thereof, on a weight percent basis, preferably at least about 80 wt.%, and more preferably at least about 90 wt.% of the aqueous carrier.
Illustrative of a preferred parenteral formulation is one that includes up to 300 mg of the active suspended in about 1 ml of an aqueous carnet. An illustrative aqueous carrier may be prepared by combining: 1 g benzyl alcohol, 0.5 g sodium carboxylethyl cellulose 50, 0.376 g disodium hydmgen phosphate dehydrate, 1.495 g sodium dihydrogen phosphate dehydrate, with water for injection (WFi) being added to bring volume of the aqueous carrier up to 100 tnl.
(0078] When formulated as an injectable, the active may be provided in any suitable form, e.g., lyophilizate, dry powder for reconstitution, a ready-to-use liquid, and in any suitable container, e.g., vial, pre-filled syringe, or the like.
[0079] The actives may also be administered transdermally. Transderrnal delivery devices are well known. Illustrative transdermal devices are described in U.S. Patents S,b35,203 and 6,024,976. When a transdermal delivery device is used, the amount of the active included in the device for therapy should range from about 5% to about 25% of the parenteral dose, and preferably from about 10% to about 20% of that dose, as set forth herein.
(0080] The following examples are provided as further illustration of the present invention, but should not be construed as limiting the invention in any respect.

[0081] 'xhis example provides data on the androgenic potency of 7a,11 [i-demethyl-17(3-hydroxy-4-esuen-3-one bucyclate {CDB-43$6A), its free alcohol (CDB-1321D), testosterone bucyclate (CDB~1781V-1), methyltestosterone (CDB-_~_ _ _;~''_ ra _. _. _, _. _. _v v _, ,. ~''~_ __ 110}, testosterone (CDB-I 11C) and testosterone enanthate (CDB-112a) when administered orally.
[0082] Immature {about 21-day-old) Sprague-Dawley rats were orchidectomized under anesthesia, and randomly assignee to groups of ten animals for each dose level of the active undergoing testing. Each active was dissolved in 10% ethanoUsesame oil and administered by gavage (oral) each day for seven days beginning on the date of the orchidectomy. The animals were sacrificed 24 hours after the last dose, and the ventral prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0.1 mg. See, e.g., Hershberger, L. et al, Myotrophic Activity of 19-nortestosterone And Other Steroids Determined By Modified Levator And Muscle Method, Proc. Soc. Exptl. Biol. Med 83 175-180 (1953). Regression analysis was performed by conventional methods using a PROPHET data management system.
See, e.g., Bliss, C., The Statistics of Bioassay (Academic Press, New York, 1952);
Hollister, C., Nucleic Acids ReS. 16 1873-75 {1988). Ventral prostate weight was used as the endpoint because it is the sensitive organ to androgenic stimulation.
[0083] The data obtained from this study is presented in graphic form in Figs. 3 and 4. This data indicates that the oral androgenic activity of 7a,11 [3-dimethyl-17[3-hydroxy-4-estren-3-one bucyclate is about 4 times (3.77 times, at a 95% confidence interval 2.25-6.33) as potent as methyltestosterone and at least 4 times as potent as the free alcohol ( 1321 D), and testosterone bucyclate {
1781 V-1 ).
7x,11 (3-dimethyl-17[i-hydroxy-4-estron-3-one bucyclate is also about 10-100 times more potent than testosterone itself (111-C} or testosterone enanthate (112x) administered orally.

[0084] This example provides data that demonstrates the duration of activity of 7or.,113-dimethy!-17~-hydroxy-4-estren-3-one bucyclate (CDB-438&A) compared to its free alcohol (CDB-1321D), the 1 la-methyl analog of 7x,113-dimethyl-17~i-hydroxy-4-estren-3-one bucyclate (CDB-4386), testosterone bucyclate (CD$-17$la, -1781 V2), and testosterone enanthate (CDB-112E) when administered parenterally (by subcutaneous injection).
[0085] Immature (about 21-day-old) Sprague-Dawley rats were orchidectomized under anesthesia, and randomly assignee to groups of ten animals for each dose level of the active undergoing testing. Each active was administered by subcutaneous injection each day for seven days beginning on the date of the orchidectomy. The animals were sacrif ced 24 hours after the last dose, and the ventral prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0.1 mg.
Regression analysis was performed by conventional methods using a PROPHET data management system. Ventral prostate weight was used as the endpoint because it is the sensitive organ to androgenic stimulation.
[00$6] Except for testosterone enanthate, each active was formulated in two different carriers: (1) an aqueous suspension and (2) in sesame oil.
Testosterone enanthate was formulated using the sesame oil earner only, because it exists as a liquid at room temperature and could not therefore be formulated as an aqueous suspension.
[0087] The carrier used to provide the aqueous suspension was formulated as follows: 1 g benzyl alcohol, 0.5 g sodium carboxylethyl cellulose 50, 0.376 g disodium hydrogen phosphate dehydrate, 1.495 g sodium dihydrogen phosphate dehydrate, with water for injection (WFI} being added to bring volume of the carrier up to 100 nnl.
[0088] Each formulation was prepared at a concentration of 0.6 mgI0.2 mI.
To obtain further comparative data, testosterone bucyclate was formulated in the aqueous suspension at a higher dose ( 1.0 mg10.2 ml).
[0089] The results, shown graphically in Fig. 5, substantiate the unexpected activity of 7a,11p-dimethyl-17[i-hydroxy-4-estren-3-one bucyclate (CDB-4386A) as compared to other androgenic esters. The former exhibits activity in both potency and duration that far exceeds the activity exhibited by the comparative esters when administered in the same amounts, and particularly when 7a,11ø-dimethyl-17ø-hydraxy-4-estren-3-one bucyclate is formulated as an aqueous suspension. The activity of even CDB-43$6, which may be referred to as "close" to 7x,11 ø-dimethyl-17ø-hydroxy-4-estren-3-one bucyclate from a chemical structure perspective, nevertheless exhibits relatively low activity as compared to 7ct,11 ø-dimethyl-17ø-hydroxy-4-estren-3-one bucyclate.
X0090] Further, both the potency and long-term activity of the higher dosage of testosterone bucyclate (1.0 mg) was significantly less than that provided by the _ .;3rijiilfir=:'~, _. _. ~_ _.'_ __.. L. _ .~~~~~ p~~~~~a lower dosage of 7a,11 (3-dimethyl-17[3-hydroxy-4-estren-3-one bucyclate (0.6 mg) in an aqueous suspension.

[0091] This example illusuates the relative androgenic activity of testosterone and its derivatives.
[009Z] Immature (about 21-day-old) Sprague-Dawley rats were archidectomized under anesthesia, and randomly assignee to groups of ten animals for each dose levei of the active undergoing testing. Each active was dissolved in 10% ethanol/sesame oil and administered by gavage (oral) or subcutaneous injection each day for seven days beginning on the date of the orchidectomy. The animals wcrt sacrificed 24 hours after the last dose, and the ventral prostate and sezxiinal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0.1 mg. Regression analysis was performed by conventional methods using a PROPHET data management system. Ventral prostate weight was used as the endpoint because it is the sensitive organ to androgenic stimulation.
[0093] Figs. 6 and 7 are graphic representations of the andmgenic assays of the actives. Each data point represents the mean {n=10) and standard error of the mean (SEIvn for each prostate weight for each dose Level.
[0094] From the data, 7a.,11(i-dimethyl-I7(3-hydroxy-4-estren-3-one bucyciate (CDB-4386A) exhibited almost four times the oral activity of methyltestasterone (CDB-1 i0) (3.77 times, at 95% C.I. 2.3-6.3), the current oral standard. However, 7a, l I ]i-dimethyl-17[i-hydroxy-4-estren-3-one bucyclate demonstrated only 0.4 times the activity of testosterone (CDB-111 C) following subcutaneous administration {0.4 times, at 95% C.I. 0.2-0.6). The oral findings were unexpected because testosterone and its esters exhibit low activity upon oral administration.
[0095] The relatively weak activity upon subcutaneous administration was also unexpected in view of the results on the long-acting activity of 7x,11 (i-dimethyl-17[i-hydroxy-4-estren-3-one bucyclate in Example 5. Testosterone, on the other hand, exhibited the expected level of activity after subcutaneous injection.
The weak activity ofthe l la-methyl analog of 7a,11[i-dimethyl-17[3-hydroxy-4-estren-3-one bucyclate (CDB-4386, CDB-4415) after subcutaneous administration j, d _ .~finiir~''_~ .. _. -. ~.~~ '.. .~ ,--i.' ,. , ~ ~~~' i"
_ _ !~ ~ ~ ~. ~ J , indicates the importance of the stereoconftguration of the 7x,11 [i-dimethyl-17~3-hydroxy-4-estren-3-one bucyclate (CDB-4386A) molecule.
[009b] Although not desiring to be bound to any particular theory, the oral activity of 7at,11 (3-dimethyi-173-hydroxy-4-estren-3-one bucyclate may be due to its resistance to degradation in the gastrointestinal tract aadlor rapid metabolism by the liver. it is also possible that the lipophilic nature of 7a,ll~i-dimethyl-l7(3-hydroxy-4-estren-3-one bucyclate permits absorption of the active into the thoracic lymph, thereby avoiding direct entrance into the portal system and metabolism by the liver.
[0097] Further, the Iaek of activity experienced by 7x,11 ~i-dimethyl-17(3-hydroxy-4-estren-3-one bucyciate under subcutaneous administration may reflect the slow release, and possibly metabolism, of the active from the injection site over the relatively brief 7-day administration period. This same property, however, conveys long-acting activity on 7a,1 lei-dimethyl-1'7p-hydroxy 4-estren-3-one bucyclate after parenter~al administration in an aqueous vehicle.
[0098j In addition to the foregoing, the androgenic potency and relative binding affinity to the androgea receptor of several free alcohols ai~.er subcutaneous administration of their corresponding esters was also determined. The results are presented in the following Table.
Activity of Ester Com Cor_res ondin ound - Alcohol Relative :findingAndrogenie Com ound ID Meltin Point ' Potenc 2 C AfFtu 1 A 68-69 91 8.1 B 129-130 no data 1.2 C oil 148 61.1 D 108 no data 36.4-61.7 E 99-100 1 no data F 130-132 82 19.3 G 134-136 28 1.0 assi ed lFrom rat prostate; relative to methyltrienolone = 100 % {androgenic potency =
S.0) ZVentrai prostate weight assay following subcutaneous administration.
Did not pass one or more significance tests (p<0.05) 'Reference compound i ~_i- , ",~.~,,.s L'.IC
. _ _ __..

A: 7a-Methyl-19-nortestosterone-I7(i-bucyclate B : 7a-Methy 1-5 a-dihydro-19-nortestosterone-17 ~3-bucyc late C: 7a-Methyl-I 4-dehydro-testosterone- I 7~i-bucyciate D: 7a-Methyl-D-homo-testosterone-17 p-bucyclate E: 7a, lla-Dimethyl-19-nortestosterone-173-bucyclate F: 7a,I1~3-dimethyl-17~i-hydroxy-4-estren-3-one bucyclate (CDB-4386A) G: 'testosterone bucyclate [0(199] The foregoing data demonstrates that the activity of a particular androgenic bucyciate ester (such as 7a,t 1 ~-dimethy!-17[i-hydroxy-4-estren-3-one bucyclate, CD13-4386A) cannot be predicted on the basis of the androgenic activity of its corresponding &ee alcohol. More specifically, the superior activity of 7x,11 ~3-dimethyl-17p-hydroxy-4-estren-3-one bueyclate could not have been predicted from this data.

[00100] This example further illustrates the relative activity of various testosterone esters, including 7a,llp-dimethyl-17/3-hydroxy-4-estren-3-one bucyclate, over relatively long periods of time.
[00141) Tmmature (about 21-day-old) Sprague-Dawley rats were orchidectomized under anesthesia, and randomly assignee to groups of 40 or more.
Animals received a single subcutaneous injection of 0.6 mg of each ester in 0.2 ml of an aqueous suspending carrier andlor oily carrier (I0% ethanoU90% sesame oil or ethyl oleate) on the date of the orchidectomy. In cases whtre the ester was not solid at room temperature, 10% ethanollsesame oil or ethyl oleate was used as the carrier.
In this example, the carrier used to provide the aqueous suspension was formulated as follows: 1g benryl alcohol, 0.5 g sodium carboxylethyl cellulose 50, 0.376 g disvdium hydrogen phosphate dihydrate, I .495 g sodium dihydrogen phosphate dihydrate, with water for injection (WFI} being added to bring volume of the earner up to 100 ml.
[00102] Five animals from each group were sacrificed at weekly or biweekly intervals, and the ventral prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0. I
mg.
[00103] Ventral prostate weight was used as tht endpoint because it is the sensitive organ to androgeruc stimulation. Regression analysis was performed by -,.~ .". ~ " - ~, , ",a conventional methods using the laR4PHET data management system previously identified.
[00104] Figs. 8 and 9 are graphic representations of the androgenic assays of the actives. Each data point represents the mean (n=10) and standard error of the mean (SEM) for each prostate weight for each dose level.
[00105] Fig. 8 is a graph of the ventral prostate weights at weekly intervals over a 1 p week period aii~er the subcutaneous administration of 7a,1 I ø-dimethyl-17[i-hydmxy-4-estren-3-one bucyclatc (CDH-4386A) in both oily and aqueous carriers, its l la-methyl analog (CDB-4386) in both carriers, and testosterone enanthate (CDB-112E) in an oily carrier. 7a,ll[3-dimethyl-17~i-hydroxy-4-estren-3-one bucyclate in the aqueous vehicle exhibited the most dramatic increase and maintenance of ventral prostate weight. The area under the curve (AUC, calculated by the trapezoidal rule), was about 3 times greater for 7a,11[3-dimethyi-17~i-hydroxy-4-estren-3-one bucyclate than for testosterone enanthatc in sesame oil. The 11 a-methyl analog was inactive in this experiment, with evaluation being discontinued $ weeks after administration. This experiment highlights the significance of the ability to provide 7oc,11ø-dimethyl-17ø-hydroxy-4-estren-3-one bucyclate in the form of an aqueous suspension, which provides unexpected and desirable long-term androgetvc activity. This experiment also underscores the importance of the stereoco~guration of the C1, substituent.
[00106] Fig. 9 is a graph of the ventral prostate weights at various time intervals up to 20 weeks after administration of several different bucyclate esters:
7x,11 p-dimethyl-1"lø-hydroxy-4-estren-3-one bucyclate (CD$-4386A), 7a-Methyl-14-dehydro-19-nortestosterone-17ø-bucyciate (CDB-4327A), 7a-Methyl-19-nortestosterone-17ø-bucyctate (CDB-4288), 7a-Methyl-Ib-dehydro-D-homo-19-nortestosterone-17ø-bucyclate (CDB-4318) and 7a-Methyl-Sa-dihydro-19-nortestosterone-17ø-bucyclate (CDB-42$9). All esters other than 7x,11ø-dimethyl-17ø-hydroxy-4-estren-3-one bucyelate were administered in the oily carrier because they do not exist as solids at room temperature, or possess low melting points. ' 7a,11 [i-dimethyl-17(3-hydroxy-4-esuen-3-one bucyclate, suspended in the aqueous carrier, exhibited the greatest AUC over the 10-week period for which this parameter was calculated. CDB-4327A demonstrated surprising stimulation of ventral prostate size over the entire 20»week observation period, hawever, this is one ., ~ ; ' n ' = = i'~: ~-'_l _~~ .__ 3 ~;s IuCc~

of the most active synthetic androgens presently known. 'The remaining actives showed relatively weak activity. This experiment can be said to demonstrate that the prediction of activity cannot be based on the structure of the active, or on the carrier used in connection with the administration of the active.
(00107] Serum samples taken from the animals at autopsy showed the presence of the free alcohol (7x,11 (i-dimethyl-19-nortestosterone) which decreased with time over the 10 week observation period. The results are provided in Fig. 10.
7a,1 lei-dimethyl-I7[i-hydroxy-4-estren-3-one bucyclate, suspended in the aqueous carrier, provided the highest levels of the free alcohol, and maintained these relatively high levels over the 10-week observation period.
EXAMkLE 6 [00108] This example describes a preferred process for synthesizing 7a,11 ~i-dirnethyl-17p-hydroxy-4-estren-3-one bucyclste (Compound I). Reference may be made to Fig. I 1.
A. Preparation of 7a,-Me viestra-4 9-diene-3 17-dione (Compound 2) [00I09] Under a nitrogen flush through an inverted plastic funnel the antimony pentafluoride (110 mL, 5.79 mol) was weighed into a Teflon jar.
Hydrogen fluoride (436 nL, 21.8 t11o1), chilled to 4°C, was first collected in a Teflon separatory funnel, then added with extreme care to the reaction vessel under a nitrogen flush. Failure to assure ragid mixing can result in an eruption. As the mixture was stirred, it was cooled to 0°C for 20 min. 7a-methylestxone methyl ether (Compound 1, 25.0 g, 83.8 mmoi) was carefully added under nitrogen. The reaction was stirred at 0°C for 2.5 hr, after which it was slowly poured into a plastic beaker containing a mixture of saturated potassium carbonate {300 mL, 900 g/1000 mL}
and ice. Additional potassium carbonate was used to adjust the pH to ca. 8.
This mixture was then extracted with methylene chloride (3x) and the organic portions were washed with water and brine. After drying over sodium sulfate, the solvent was removed in vacuo to give 24.8 g of crude oil. This crude material contains Compound 2 and as isomeric by-product, 4,6-diene-dione-3,20 (Compound 3) in a 2:1 ratio. Therefore, the crude material was subjected to dry column chromatography on silica gel (63 - 200 mesh) eluted with 3% acetone in CH2ClZ.
This gave a segment which contained 15 g of the desired product (Compound 2).
ARer extraction, evaporation of the solvent followed by trituration with ether :~ T ~ ~ [, ~ r.~ ~ I_ '- '~ -~ . [. ~ _ ~ . ~ I rv _~ .. ~ - L : _ _! ~~. r r .:

afforded 9.24 g ,of Compound 2 in 38.8% yield. The mother liquor from this material was eombined.with the other principle portion of the column, and was rechromatographed using the same conditions. Trituration of the segments provided an additional 0.19 g of the desired product (Compound 2). Total amount was 9.43 g in 39.6% yield; m.p. 204-205°C. (Lit. m.p.~ (8). FRJR (KBr, diffuse reflectance):
vm",~ 3454, 3282, 3030, 296$, 2928, 2902, 1737, 1652, 1600, and 1580 Cm ~. NUR
('H, CDCI3) 8 0.859 (d, 3 H, J--3.5 Hz), C7a-CH3), 1.001 (s, 3 H, C18-CH3) and 5.726 (s, 1 H, C4-CH). NMR ('3C, CDC13) 8 12.641, 21.835, 24.885, 25.57b, 28.021, 30.62b, 35, 621, 36.893, 39.416, 42.4779, 45.966, 123.259 (C-4), 126.081 (C-10)m 140.295 (C-9), 154.572 (C-S), 199.052 (C-3) and 219.b33 (C-17).
B. The Preparation of 3,3-Ethylenedioxy-7a-mechyl-17,~-hvdroxvestra-Sf 10).901 -diene Compound 4?
[00110] A THF (500 mL) solution of the dione (Compound 2, 10.0 g, 35.16 mmol) was chilled to 0°C and treated dropwise with a THF solution of lithium tri-rert-butoxyaluminum hydride (1.0 MfIHF, 40.0 mL. 8.9 mmol). The mixture was stirred at 0°C for 2 hr. EtOAc (10.0 mL) was added and most of the solvent was removed in vacuo. The residue was diluted with cold 0.1 N HCl and the aqueous mixture was extracted with Et~Ac (3x). The Et4Ac layers were washed with water and brine, Combined, and dried over sodium sulfate. Evaporation of the solvent gave 10.61 g of a stable foam. The material was then dissolved in benzene ( 1 L).
Ethylene glycol (10.0 ml.) was added, followed byp-toluenesulfonic acid (500 mg).
The resulting mixture was heattd to reflux while draining off approximately 500 mL
of benzene from the Dean-Stark trap. The nuxture was cooled and diluted with saturated sodium bicarbonate solution. The benzene solution was washed with water and brine. The aqueous washes were extracted with EtOAc (2x). The combined organic extracts were dried over sodium sulfate. Evaporation of the solvent gave the f 2.b I g of a stable foam. The material was chromatographed (5%
acetone in CHZCIZ) to afford 10.05 g of the ketal (Compound 4) in 87% yield NMR
(CDC13) 8 0.725 (s,3 H, C 1$-CH3), 0.727 (d,3 H, J=7.2H~ C7a-CH3), 3.777{t ,l H, 3=8.7Hz, Cl7a-CIA, 3.979 (rn, 4 H, 3-ketal) and 5.638 (m, 1 H, C11=CEi}. MS
(El) mlz: relative intensity: 330 (M~.
C. Preparation of 3,3-ethylenedioxy-7a,-methyl-Sa l0a-~oxx-17~i-hydroxYestra-911 -ene Comtaound 5) a7 . .'~~ 1 ~7~~"~,l y':
"n1 [00111] A solution of hexafluoroacetone (30.0 g, 136.2 mmol) in CH2Clx, (150 mL) was chilled to 0°C. With vigorous stirring, 30% hydrogen peroxide (14.0 mL, 136.2 mmol) and solid disodium hydrogen phasphate (5.86 g, 41.30 mmol) was added. The resulting mixture was stirred at 0°C for '/z hr. A solution of the ketal (Compound 4, 1 S.0 g 45.39 mmol) in CHZC12 (300 mL) was added and the mixture was stirred at 4°C for 24 hr. The mixture was then diluted with 10%
sodium sulfite solution, and subsequently extracted with CHZCIZ (3x). The extracts were washed with water and brine, combined and dried over sodium sulfate. Evaporation of the solvent gave 16.26 g. of Compound 5. This material was used without further purification in the subsequent reaction. NMIt (CDC13) 8 0.725 (s, 3 H, C18-CH3), 0.762 (d, 3 H, J=7.2 Hz, C7a-CH3), 3.758 (t, 1 H, d= 8.7 Hz, Cl7a-CH), 3.895 (d, 4 H, 3-ketal) and 6.00 {m, 1 H, C11~CH).
D. Preparation of 3,3-ethylenedioxy-7x,11 p-dime vl-Sa.17~3-dihyrdoxYestra-9-ene lComnound 6) [00112] A solution of methylmagnesiumbromide (I:4 M THF/toluene, 210 mL, 295 mmol) was added to THF (150 mL) and copper (I) chloride (2.92 g, 29.5 mmol) was added. After stirring at room temperature for'/s hr, a solution of the epoxide (Compound 5, 16.26 g 46.99 mmol) in THF (450 mL) was added dropwise over 5 min. The mixture was stirred at roora temperature for 3 hr. The mixture was diluted with saturated ammonium chloride solution and air was bubbled through the mixture for %z hr to oxidize Cu(I) to Cu(II). The aqueous mixture was extracted with ether {3x). The ether extracts were washed with water and brine, combined, and dried over sodium sulfate. Evaporation of the solvent gave I6.70 g of a yellow semi-solid. The material was triturated with ether and the solid was filtered to afford 8.86 g o:f a mixture of Grignard products (7a,11 a-dimethyl and 7a,11 p-dimethyl, referred to as Compounds 6a and 6b, respectively). Evaporation of the filtrate gave 7.4 g of a stable foam. Total amount was 16.26 g in quantitative yield.
E. Hydrolysis of a Mixture of Compounds 6a and 6b to Isom rid c Compounds 7b and 7a (as a ca. 317 mixture) (00113] The solid (containing Compounds 6a and 6b) from Step D above {16.26 g, 54.2 mmol) was dissolved in acetic acidl"fHFlwater (3:1:1, 500 tnL) and heated to reflux for 2 hr. The solvent was evaporated in vacuo and the mixture was diluted with saturated sodium bicarbonate solution. The mixture was then extracted with CHZCIz. The CH2C12 extracts were washed with water, brine, combined, and dried over sodium sulfate. Evaporation of the solvent gave 7.45 g. The material was chromatographed ( 10% acetone/methylene chloride) to afford 5.12 g of Compounds 7a and 7b (7a,1 la-dimethyl and 7a,11ø-dirnethyl, respectively). The foam obtained in Step D was treated in the same manner to afford an additional 2.73 g of Compounds 7a and 7b aRer chromatography. Total amount was 7.85 g in 45.9% yield. NMR (CDGl3) s 0.747 (d, 3 H, J=7 Hz, C7a-CH3), 0.780 {s, 3 H, C18-CH3of Compound 6b), 0.963 (s, 3 H, C18-CH3 of Compound 6a), I .077 (d, 3 H, J=7 Hz, Clla~CH3), 1.173 (d, 3 H, J--7 Hz, C11 [i-CH3), and 3.770 (t, 1 H, J=8.?
Hz, C 17a-CH.
F. Preparation of3,3-Bthyleniedioxy-7cx,11-dimethyl-1713-hydroxvestra-5(107 9(111-diene ( ompound 8) [04114] A solution of Compounds ~al7b (2.0 g 6.65 mxnol) in benzene {500 mL) was treated with ethylene glycol (5.0 mL) andp-toluenesulfonic acid (250 mg).
The mixture was heated at reflux with azeotropic removal of water.
Approximately 254 mL of solvent was distilled off. The mixture was cooled to mom temperature and diluted with saturated sodiurri bicarbonate solution. The mixture was extracted wish Et4Ac. The EtOAc extracts were washed with water and brine, combined and dried over sodium sulfate. Evaporation of the solvent gave 2.15 g of stable foam in 93.9 % yield. The material was homogeneous by TLC and less polar than the starting material. NNM (CDC13) ~ 0.716 {s, 3 H, C 18-CH3), 0.725 (d, 3 H, J=7.2 Hz, C7a-CH3), 1.801 (br s, 3 H, C11-CH3), 3.755 (t, 1 H, J=8.7, Cl7a-CH) and 4.003 (m, 4 H, 3-ketal).
G. Preparation of 7a.,11/3-Dimethyl-17~-hydroxyestra-4,9-diene-3-one (Compounds 7b/7a. ca. 1011 via Hvdtolvsis of Compound 8 [001151 The ketal (Compound 8, 2.15 g 6.24 mmol) was dissolved in methanol (200 mL) and 10.0 mL of 10% HCl was added. The solution was heated at reflex for 18 hr. The solvent was evaporated in vacuo and the residue was diluted with saturated sodium bicarbonate solution. The aqueous mixture was extracted with CH2Cl2. The methylene chloride extracts were washed with water and brine, combined and dried over sodium sulfate. Evaporation of the solvent gave 1.89 g of a stable foam. The material was chromatographed (10% acetone in CH2C12) to afford 950 mg, of the 7x,11 [i-dimethyl corapound (Compound 7b) in 50.8%
yield.
Also isolated 703 mg of a Compound 7a/7b mixture in which was resubjected to the ketalization and equilibrium process to yield additional material. Compound 7b:
NMR (CDCI3) S 0.790 {d, 3 H, J=7.2 Hz, C7oc-CH3), 0.9b3 (s, 3 H, C18-CH3), 1.172(d, 3 H, C 11 [3-CH3), 3.186 (m, 5-lines, 1 H, C 11 a-CH), 3.661 (t, 1 H, J=8.7 Hz, Cl7oc-CH) and 5.702 (s, I H, C4-CIA.
H. Preparation of 7a,11 [i-Dimethyl-17[3- .
hvdrox'y-4-~g~ren-3-one fComyound 10) [00116] Lithium wire (253 mg, 36.45 txtmol), cut into small pieces, was added to redistilled (from sodium) ammonia (300 mL) and the mixture was stirred at ammonia reflex (-35°C) for'/ hr. The mixture was chilled to -78°C and a solution of the dienone (Compound 7b, 3.65 g 12.15 mmol) in THF (300 mL} and t-butanol (1.16 mL, 12.15 mmol) was added dropwise. Upon completion of the addition, the reaction was stirred for 15 min before any excess lithium was destroyed with the addition of isoprene (ca. 1.0 mL) and finally, quenched with the addition of solid ammonium chloride ( I 5 g). The ammonia was evaporated under argon gas and the mixture was diluted with 4.1 N phosphate buffer, pH=7Ø The mixture was extracted with ether. The ether extracts were washed with water and brine, combined, and dried over sodium sulfate. Evaporation of the solvent gave 3.83 g of Compound 9 as a light yellow solid in quantitative yield. The material was homogeneous by TLC sad was used without further purification in the following reaction. NMR (CDCI~) 8 0.812 (d, 3 H, J=7.2 Hz, C7cc-CH3)m 0.877 (s, 3 H, C

CH3), 0.903 (d, 3 H,1=7.2 Hz, C 11 (3-CHI), 2.754 (br q, 2 H, C4-CH2-), and 3.6b0 (t, 1 H, J=8.8 Hz, C 17oc-CI-I}.
[00117] The material prepared about was dissolved in methanol (400 mL) and 10% I-ICl (20 mL) was added aad the mixture was heated at reflex for 3 hr.
The solvent was evaporated and the residue was diluted with saturated sodium bicarbonate solution. The mixture was extracted with CHZCIz. The methylene chloride extracts were washed with water and brine, combined and dried over sodium sulfate. Evaporation of the solvent gave 3.81 ,g of a stable foam. The material was chromatographed {10% acetone in CHZC12) to afford 3.54 g of Compound 10 in 96.5% yield. The material was recrystallized from etherJhexane to give 3.14 g of Compound 10 as fine white needles in 86% yield: m.p.=1 SS-I57°C.
1'r c _ .n'i:ln'r~n'~rJ ~l'.. ~~ ,. _ I.:~_ , ~3~ ~'°.' I.:.~j Analysis by reverse phase HPLC on a NovaPak C1g column eluted with SO%
aqueous CH3CN at a flow rate of I mL per min and at ~,=240 nm indicated this material to have a purity in excess of 99% FTIR (KBr, dif~"use reflectance):
vm"~
3470, 2950, 1663 and 1622 cm's. NMR (CDCl3) s a.77o (d, 3 H, J=7.2 Hz, C7a-CH3), 0.886 (s, 3 H, C 18-CI i3), 1.075 (d, 3 H, J=7.2 Hz, C11 ~3-CH3), 3.626 (t, I H, J=8.7 Hz, C 17a-CH) and 5.849 (br s, 1 H, C4-CH). M$ (EI) m/z relative intensity:
302 (M'~. Analysis calculated for CZOH3oU2: C, 79.42; H, I0.00. Found: C, 79.18;
H, 10.00.
H. Preparation of 7a,11 ~i-Dimethyl-17~-hydroxy-4-esxren-3-one I?~i-trans-4-n-butvlr~ycloh~xane cartZoxyi t~ a (Cor~p~und I~
[U0118] Trans-4-n-Butylcyclohexanecarboxylic acid chloride {Compound 11, 2.25 g 110 mmol), dissolved in benzene ( 10 tnL), was added to a solution of 7a,11 [3-Dimethyl-17[3-hydroxy-4-estren-3-one (Compound 10, 608 mg, 2 mmol) in a mixture of benzene (100 tnL) sad pyridine (5.0 mL). The mixture was stirred overnight at room temperature. The mixture was chilled in an ice bath and diluted with 1.0 N sodium hydroxide solution. The aqueous mixture was extracted with ether. The ether extracts were washed with 1.0 N sodium hydroxide solution (2x), water and brine. The combined organic extracts were dried over sodium sulfate and evaporation of the solvent gave 1.72 g of a semi-solid. Recrystallization of the material (Compound I) from hexanes gave 765 mg of white powder in 82% yield:
m.p.=I30-132°C. Analysis by reverse Phase HPLC on a NovaPak C~g column eluted with CH3CN at a flow rate of 1.25 mL per minute and at ~.=240 nm showed the Compound I to be pure greater than 99%. FTIR (KBr, di;tTuse reflectance) vm"r 2933, 1726, 1669 and 1621 cm''. MR (CDCl3) 8 0.779 (d, 3 H, J=7.2 Hz, C7a-CH3), 0.886 {t, 3 H, n-butyl CH3), 0.923 (s, 3 H, C 18-CH3), 1.057 (d, 3 H, J=7.2 I-Iz, CI 1 [3-CH3), 4.545 (t, 1 H, J=8.7 Hz, Cl7a-CiT) and 5,84$ (br s, 1 H, C4-CH}, MS
(EI) m!z relative intensity: 468 (M'+, 6.9), 358 (65.3), 302(12.5), 284 {20.8), 269 (6.9}, 259 (12.5), 174 (62.5), 159 {26.5), I47 (19.4), 139 (25.0), 119 (18.1), (75.0}, 105 (8.1), 97 (36.1), 83 (100), 69 (38.9) and 55 (58.3).

[00119] This example provides data on the andmgenic potency of the undecanoate (CDH~521A) relative to methyltestosterone (CDB-111C) when administered via subcutaneous injection.
,_, , (00120] Immature (about 21-day-old) Sprague-Dawley rats were orchidectomi7xd under anesthesia, and randomly assignee to groups of ten animals for each dose level of the active undergoing testing. Each active was dissolved in 10% ethanoUsesame oil and administered by subcutaneous injection each day for seven days beginning on the date of the orchidectomy. The animals were sact~ficed 24 hours after the last dose, and the ventral prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0.1 mg. See, e.g., Hershberger, L. et al, Myotrophic Activity of 19-nortestosterone And Other Steroids Determined By Modified Levator And Muscle Method, Proc. Soc. Fxptl. Biol. Med 83 175-180 (1953). Regression analysis was performed by conventional methods using a PROPHET data management system. See, e.g., Bliss, C., The Statistics of Bioassay (Academic Press, New York, 1952); Hollister, C., Nucleic Acids Res. 16 1873-75 (1988).
Ventral prostate weight was used as the endpoint because it is the sensitive organ to androgenic stimulation.
[00121] The data obtained from this study is presented in graphic form in Fig.
13. This data indicates that the subcutaneous androgenic activity of the undecanoate (CDB-4521 A) is about half that of testosterone (0.52 times, at a 95°/d confidence interval, 0.29-0.93) when administered in the oily carrier. This data was surprising when compared to the results obtained when the undeeanoate was administered in an aqueous carrier.

[00122] This example provides data on the androgenic potency of the undecanoate (CDH-4521) and methyltestosterone (CDB-110) when orally administered in oily or aqueous carriers.
[00123] Immature (about 21-day-old) SpraguerDawley rats were orchidectomized under anesthesia, and randomly assignee to groups of ten animals for each dose loves of the active undergoing testing. Four dosage forms were prepared. The first two forms constituted a solution of each active in 10%
ethanol/sesame oil. The third and fourth dosage forms constituted a suspension of each active in an aqueous carrier (as described in Exannple 2, supra). These dosage forms were then administered by gavage {oral) to separate animal groups each day for seven days beginning on the date of the orchidectomy. Each corner was also administered (alone) to separate groups of animals as a control. The animals were sacrificed 24 hours after the last dose, and the ventral prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0.1 mg. See, e_g., Hershberger, L. et al, Myotrophic Activity of 19-nortestosterone And Other Steroids Determined By Modified lrevator And Muscle Method, Proc. Soc. Exptl. Biol. Med 83 175-i80 (1953). Regression analysis was performed by conventional methods using a PROPHET data management system. See, e.g., Bliss, C., The Statistics of Bioassay (Academic Press, New York, 1952); Hollister, C., Nucleic Acids Res. 16 1873~75 (1988).
Ventral prostate weight was used as the endpoint because it is the sensitive organ to androgenic stimulation.
[00124] The data obtained from this study is presented in graphic form in Fig.
14 and 4. This data indicates that the oral androgenic activity of the undecanoate (CDB-4521A) in the oily carrier is about 2 times (2.36 times, at a 95%
co~dence interval) as potent as methyltestosterone in the same oily carrier. In contrast, oral administration of the undecanoate in the aqueous carrier described in Example 2, supra, revealed a potency about the same (0.95 times, at a 95% confidence interval, 0.36-2.5) as that of methyltestostemne in the same aqutous carrier.

[00125] This example further illus~ates the relative activity of 7a,11 ~-dirnethyl-17(3-hydroxycstr-4-en-3-one 17-undecanoate (Compound II) compared to that of testosterone enanthate (CDH-112F) over relatively long periods of time.
[OO1Z6~ Immature (about 21-day-old) Sprague-Dawley rats were orchidectomized under anesthesia, and randomly assignee to groups of 40 or more.
Animals received a single subcutaneous injection of 0.6 mg of the undecanoate in 0.2 ml of an aqueous suspending carrier andlor oily carrier (10% ethano1/90%
sesame oil containing 5 mg/ml chlorobutanol as a preservative, or ethyloleate) an the date of the orchidectomy. The enanthate ester was formulated using the 10%
ethanollsesame oil or ethyloleate carrier as a first standard, with the i0°/a ethanoUsesame oil carrier used as a second standard.
[00127] ?n this example, the carrier used to provide the aqueous suspension was formulated as follows: 1g benzyl alcohol, 0.5 g sodium carboxylethyl cellulose _ ~~t'ili:~i'; .~~'=. _ '_.. ~... _ .__. '.'. _ ~ n-,-~
r~::;_ 50, 0.3'7b g disodium hydrogen phosphate dihydrate, 1.495 g sodium dihydrogen phosphate dihydrate, with water for injection (WFI) being added to bring volume of the carrier up to 100 mI.
[00128] Five animals from each group were sacrificed at weekly or biweekly intervals, and the ventral prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0.1 mg.
(00129] Ventral prostate weight was used as the endpoint because it is the sensitive organ to androgenic stimulation. Regression analysis was performed by conventional methods using the PROPI~E'C data management system previously identified.
[00130] Fig. 1 S is a graphic representation of the androgezllC assays of the actives. Each data point represents the mean (n=10) and standard error of the mean (SEM) for each prostate weight for each formulation level.
[00131] More specifically, Fig. 15 is a graph of the ventral prostate weights at weekly intervals over a 10 week period aRer the subcutaneous administration of the undecanoate (CDB-4521) in both oily and aqueous carriers, testosterone enanthate (CDB-112F) in an oily carrier, and an oily carrier ( 10% ethanol/sesame oil) alone.
The undecanoate in the aqueous vehicle exhibited the most dramatic increase and maintenance of ventral prostate weight. The area under the curve {AUC, calculated by the trapezoidal rule), was about 3 times greater for the undecanoate { 1817 mg-weeks) than for testosterone enanthate in the oily carrier (AUC 559 mg~weeks).
[00132] This experiment highlights the significance of the ability to provide the undecanoate in the form of an aqueous suspension, which provides unexpected and desirable long-term androgenic activity. This experiment also underscores the importance of the stereoconf'~guration of the C,1 substituent.

[00133] This example describes a preferred process for synthesizing 7a,11 [3-dimethyi-17~-hydraxyestt~4-en-3-one 17-undecanoate (Compound Il). Reference may be made to Fig. 16.
[00134] The synthesis of Compound 10 as described in Example b was completed. Thereafter, the undecanoate was prepared by treatment of Compound ?~i' ~ ~ '' 's~ _~~'r .~ -_,~_. _ ~. _ !''_'.. .. '~'!_ "__ with undecanoyl chloride in pyridine to provide Compound II as a white powder, in good yield.
[00135J A solution of 7x,11 Vii- dimethyl-17[i-hydroxyestri4.en-3-one (Compound 10, 252 mg, 0.83 mmol) in a mixture of benzene (20 mL) and pyridine (2.0 mL) was treated with undecanoyl chloride (Compound 12, 500 mg, 2.44 mmol).
The mixture was stirred at room temperature overnight. The mixture was then chilled in an ice bath and diluted with cold 0.1 N sodium hydroxide solution.
The resulting aqueous mixture was extracted with ether. The ether extracts were washed with water and brine, combined and dried over sodium sulfate. Evaporation of the solvent gave 525 mg of an oil. The material was chromatographed using 10%
a~cetoneJCH=C12 to yield 398 mg of an oil. The material was recrystallized from cold pentane to afford 369.2 mg of Campound II as a white powder in 94% yield; m.p.
_ 62-64°C. Analysis by reverse Phase HPLC on a NovaPak C,=Column eluted with CH3CN at a flaw rate of 1.0 mL per mm and at ~,=240 nm showed Compound Ii to have a purity of at least 99.9%. F'fTR {KBr, diffuse reflectance): v",~ 2914, 1733, 167$ and 1628 cm ~. 'I-IhIMR (CDC13) 8 0.782 {d, 3 H, J = 7.2 Hz, C7a-CH3), 0.880 (t, 3 H, J s9 Hz, ~(CH2)9CH~,), 0.922 (s, 3 H, C18-CH3), 1.058 (d, 3 H, J =
7.2 Hz, C 11 ~-CH3), 4.565 (t, 1 H, J = 8.4 Hz, C l 7a-CH) aad 5.849 (s, 1 ~I, C4-CI-I=). MS
(EI) m/z (relative intensity): 470 (M~', 100), 302 (60), 284 (78), 259 (67), 175(89), 110 (l59) and 55(96). Analysis Calculated for C3~Hso03: C, 79.10; H, 10.70.
Found: C, 79.33; H, 10.91.

[00136] This example describes a preferred process for synthesizing 7a,1 l~i-dimethyi-17~-hydroxyesu~a,-4,14-dien-3-one, 7a,11 ~i-dimethy!-17p-hydroxyestra-4,14-lien-3-one 17-undecanoate, and 7a,11 (3-dimethyl-17[3 hydroxyestra-4,14-dien-3-one 17(i-4-n-butylcyclohexanecarboxylate.
A. Pre~arintz Compound I42 From Compound 1 O1 [00137) Under a nitrogen flush, a pyridine {250 aL~acetic anhydride (25 mL) solution of Compound 1 (4.44 g, 14.7 mmol) was stirred for 24 hours. The solvent was evaporated in vacuo and residual pyridine was removed by ~o-evaporation three times with heptane to afford 5.05 g of the 17-acetate as a white powder in 100%
yield. NMR (CDC13) s a.777 (d, 3 H, J = 7.2 Hz, C7a- CH3), 0.925 (s, 3 H, C18-.rir~i=~bTv''_ilr~~l:.~:'y~ _.. _. r___ . ;:3~~'~~°;~~~ ., v..~w;1 CH3), 1.060 (d,3 H, J -- 7.5 Hz, C 1 I (3- CHs), 2.048 (s, 3 H, C 1?~i-Qac), 4.554 (t, 1 H, J = 8.1 Hz, C i?a-H) and 5.489 (s, 1 H, C4-CH=).
[0013$ An acetonitrile (180 mL) solution of the ketoacetate (5.0 g, 14.50 mmol) was treated with lithium bromide) (1.26 g, 14.50 mmol) and copper (II) bromide (6.48 g, 29.00 mmol). The mixture was stirred at room temperature for two hours and subsequently chilled in an ice bath. The reaction was diluted with cold water and extracted with ethyl acetate. 'The ethyl acetate extracts were washed with water, brine, combined and dried over sodium sulfate. Evaporation of the solvent gave 5.91 g of the crude phenol acetate. Chromatography, eluting with 2%
acetone in dichlormethane, gave 3.96 g of the pure phenol acetate as a white solid in ?9%
yield. NMR (CDCI3) 8 0.812 (d, 3 J, J ~ 7.2 Hz, C?a-CH3~, 0.843 (d, 3 H, J =
?.3 Hz, C I1[i- CH3), 0.936 (s, 3H, C 18-CH3), 2.064 (s, 3H, C1?[i-Dac), 4,648 (t, 1 H, J
= 8.03 Hz, CI?a-H), 6.521 (d, 1 H, J = 3 Hz, C4-aromatic CH-), 6.637, (dd, 1 H, J =
8.4 Hz, J' = 3 Hz, C2-aromatic CH-) and 7.032 (d, l H, J = 8.4 Hz, C 1-aromatic CH-).
[00139) This material (3.96 g, 11.48 mmol) was dissolved in methanol (400 ml) and treated with excess potassium hydroxide (2.?2 g, 4$.57 mmol in 40 m), of water). The mixture was heated at reflex for two hours and methanol was evaporated in vacuo. The materials was taken up in water and pH was adjusted to a level of 1-2 with the addition of HCI. The aqueous mixture was extracted with dichioromethane. The organic extracts were washed with water and brine, combined and dried over sodium sulfate. Evaporation of the solvent gave 3.27 g of the diol (Compound 102) as a white solid in 95% yield. FTIR (KBr, diffuse reflectance):
vm"~ 3353, 3106, 2894, 1614, 15?$, 149? arid 1243 ctri ~. NMR (CL?C13 + tr.
D4MeOH) 8 0.804 (d, 3 H, J = 7.2 Hz, C?a- CF13), 0.856 (d, 3 H, J = ?.3 Hz, C
11 [i-CH3), 0.88$ (s, 3 H, C-18- CH3), 3.? 12 (t, 1 H, J = 8.03 Hz, C 1 ?a-H), 6.521 (d, 1 H, J ° 3 Hz, C4~aromatic CH-), 6.636 (dd, i H, J = 8.4 Hz, J' -- 3 Hz, C2 -aromatic CH-) and 7.011 (d, l H, J -- 8.4 Hz, C 1-aromatic CH-).
B. Preparation o~pound 103 [00140] A THF (200 mL) solution of Compound 102 (3.27 g, 10.88 mmol) was treated with lithium hydroxide (685 mg, 16.33 mmol), followed by the addition of dimethyl sulfate (I .14 mL, 11.97 mmol) and the mixture was heated at reflex for 2 hours. The mixture was cooled to room temperature, filtered through Celite and iJfi h b_'~fi '_ ~:_~ ,~~'.. _ ~~. ... ~~ ._'_i 1. ~~J'a~'v' the filtrate was evaporated. The residue was taken up in ether and washed with water and brine. The ether solution was dried over sodium sulfate. Evaporation of the solvent gave 3.35 g of the methyl ether, Compound 103. The crude material was dissolved in acetone (150 mL) and chilled in an ice bath. The cold solution was treated dropwise with Jones reagent until the orange color of Cr(IV) persisted. The mixture was diluted with cold water and extracted with ether. The ether extracts were washed with water, brine, combined and dried over sodium sulfate.
Evaporation of the solvent gave 3.28 g of the ketone as a white solid in 96%
yield.
Recrystalli~ation of a small sample from ether/hexane provided an analytical sample with a melting point between l 21-123 'C. FTIR (KBr, diffuse ret~ectancej:
vm"~
2962, 1736, 1612m 1573m 1500 and 1048 cm_~. NMR (CDCl3) s 0.847 (d, 6 H, C7a-CH3), C 11 (~-CH3), 1.061 (s, 3 H, C 18- CI-I3), 3.077 (s, 3 H, C3-OCH3), 6.597 (d, 1 H, J = 3 Hz, C4-aromatic CH-), b.730 (dd, 1 H, J = 8.4 Hz, J' = 3 Hz, C2 -aromatic CH-) and 7.093 (d, 1 H, ~ = 8.4 Hz, C 1-aromatic CH-). MS (El) ml~
(relative intensity: 312 {M~, 213, 200, 185, 174 and 159. Analysis calculated for C2lI"12802: C, 80.70; H, 9.00 Found: C, 81.00; H, 9.20.
C. Prenarati~ of Compound 104 [00141] A THh (10 mL) solution of Compound 103 (520 mg, 1.66 mmol) was added dropwise over 10-12 minutes to a 2.0 M lithium diisopropylamide solution ( 1.66 mL, 3.33 mmol) chilled to -78 'C for 15 minutes, before methyl amine {0.b2 mL, 4.4p mmol) was added, followed by the addition o~ chlorotrimethylsilane in THF (1.0 M) (3.33 mL, 3.33 moral). The reaction mixture was allowed to come to room temperature for 25 minutes before being diluted with cold saturated bicarbonate solution. The mixture was extracted with Ethyl Acetate. The ethyl acetate extracts were washed with water, brine, combine and dried over sodium sulfate. Evaporatioa of the solvent gave 632 mg of a yellow oil in 99% yield that was homogeneous by Thin Layer Chromatography (TLC) and used without father purification in the subsequent reaction.
[00142] This enol trimethylsilyl ether was dissolved iz~ dichloromethane (12 mfr) and acetonitrile (4.0 mL) and palladium acetate (39S mg, 1.76 mmol) was added. The mixture was stirred at 35 - 40 °C for three hours. The solvent was evaporated in vacuo and the residue was chromatographed, eluting with 2%
acetone in dichloromethane, to afford 352 mg ofthe enone (Compound 104) as a light ,b c _ :~t'0~=~E'n'_'Jr~','_,'_. _. _, __.. .. ::~~~~~~;~, ~.~_ yellow solid in 68% yield along with the recovered of 108 mg of the ketone, Compound 103. Recrystallization of a small sample of Compound 104 from etherlhexanes provided an analytical sample with a melting point of 135-136 'C.
FTIR {KBr, diffuse reflectance): v""x 2989, 2958, 1707, 1609, 1573 and 1497 cm's.
NMTt (CDC13) b 0.917 (d, 3 H, J = 7.2 Hz, C7a- CH3), 0.984 (d, 3H,1= 7.3 H2, C 11 ~3-CHs), 1.236 (s, 3 I I, C-18-CH3), 3.781 (s, 3 H, C3-OCH3), 6.058 (m, 1 H, C16-CH=), 6.61 l (d, 1 I-1, J = 3 Hz, C4=-aromatic CH-), 6,735 (dd, 1 H, J --8.4 Hz, J' = 3 Hz, C2-aromatic Ch-) 7.098 (d, 1 H, J = 8.4 Hz, C1-aromatic CH-) and 7.585 (m,lH, C15-CH=). MS (EI) mlz (relative intensity) 310 (M+), 295, 282, 267, 253, 239, 202, 189, 174 and 159. Analysis calculated for CZ~H2602: C, 81.30; H, 8.40 Found: C, 81.13; H, 8.55.
D. Preoara ion of Cor,Opound 105 [00143] The enone (Compound 104) (1.41 g, 4.54 mmol) was dissolved in a 1:1 mixture of isopropenyl acetate and acetic anhydride {100 mL) andp~
toluenesulfonic acid monohydrate (86 mg, 0.45 mmol) was added. The mixture was heated at reflux for four hours. The mixture wag cooled to room temperature, poured into ice water and stirred for one hour. The mixture was extracted with ether.
The ether extracts were washed with saturated sodium bicarbonate solution two times, water and brine. The combined ether extracts were dried over sodium sulfate and evaporation of the solvent gave 1.78 g of a crude Compound 105.
Chromatography, eluting with 2% acetone in dichlommethane, afforded 1.34 g of the dienolacetate (Compound LOS) as a light yellow oil in 8a % yield along with the recovery of 0.12 g of the enone Compound 104. The actual conversion yield was 92%. NMR
(CDC13) 8 0.974 (d, 3 H, J - 7.2 Hz, C7a-CH3), 1.023 (d, 3 H, J = ?.3 Hz, C 11 ø-CH3), 1.215 (s, 3 H, C 18-CH3), 2.225 {s, 3 H, C 17-OAC), 3.781 (s, 3 H, C3-OCH3), 5.926 and 6.096 (d, 2 H, J = 2.25 Hz, C 15 and C l 6-CHs), 6.616 (d, 1 H, J =
3 Hz, C4-aromatic CH-), 6,730 {dd, 1 H, J -- 8.4 Hz, J' = 3 Hz, C2=aromatic CH-) and 7.098 (d, 1 H, J = 8.4 H2, C 1-aromatic CH-).
E. Preflaration of Cod l Ob [00144] The dienolacetate Compound 105 (1.598, 4.51 mmo) was dissolved in ethanol (70 tnL) and chilled in an ice-bath. A 23% aqueous ethanol (70 mL) of sodium borohydride (b40 mg, 16.92 tntnol) was chilled to 0°C and added to the solution of Compound 105. The mixture was allowed to warm to room temperature v J .

and stirred overnight. Acetic acid was added to the reaction mixture to a pH
level of 6 and the ethanol was evaporated in vacuo. The residue was diluted with water and the mixture was extracted with diclorormethane. The organic extracts were washed with water and brine, combined and dried over sodium sulfate. Evaporation of the solvent gave 1.42 g of Compound 106 as white foam in 89% yield. This product was homogeneous by TLC and used in the subsequent reaction without further purification. NMR (CDC13) b 0.$94 (m, 3-lines, 3 H, C7a-CH3 & C I 1 [3-CH3}, I
.078 (s, 3 H, C 18-CH3), 3.778 {s, 3 H, C3-OCH3), 4.024 (t, 1 H, J - 8.2 Hz, C 17 a-CH), 5.177 (br s, 1 H, C 1 S-CH=), 6.600 (d, I H, J = 3 Hz, C4-aromatic CH-), 6.732 {dd, 1 H, 3 = 8.4 Hz, J' = 3 Hz, C2-aromatic CH-) and T.167 (d, 1 H, J = 8.4 Hz, C1-aromatic CH-).
F. Preparation of Compound III
[00145] A THF (50 mL)/t-butanol (50 mL) solution of Compound i 06 (1.42 g, 4.54 mmol) was added to anhydrous liquid ammonia (distilled from sodium) at -78 'C. With vigorous stirring, lithium wire (630 mg, 90.82 mu~ol), cut into small pieces, was added. The resulting blue mixture was stirred at ammonia reflex for three hours. The reaction mixture was chilled to -78 °C and quenched through the addition of methanol. The ammonia was evaporation under a stream of nitrogen and then diluted with water. The aqueous mixture was extracted with ether. The ether extracts were washed with water and brine, combined and dried over sodium sulfate.
Evaporation of the solvent gave 1.45 g of the 1,4 dihydro derivative as a white powder in ~ 100% yield. This crude materials was dissolved in methanol (250 tn.L) and treated with 10% HCl (10 Ml) and the mixture was diluted with saturated with NaHC03. The aqueous mixture was extracted with dichloromethane. The organic extracts were washed with water, brine, combined, dried over NazS04.
Evaporation of the solvent gave 1.35 g of a stable foam. 'this crude product was subjected to chromatography, eluting with 9% acetone in dichloromethane, to afford 0.95 g of Compound III as a white powder in 70% yield and the recovery of 0.330 g of the 5( 10)-en-3-one. A small sample of Compound III was recrystallized from ether/hexanes to afford an analytical sample with melting point of149-I 51 'C.
FT'IR
{KBr, diffuse reflectance): vm,~ 3477, 2971, 2897, 1655 and 1612 ctt'1..~. NMR
(CDCl3) 8 0.837 (d, 3 H, C7a-CH3), 1.063 (s, 3 H, C18-CH3), 1.135 (d, 3H, J =
7.2 Hz, C I 1 ~- CHI), 3.895 (t, 1 H, J = 8.7 Hz, C 17a-CH), 5.141 (br s, 1 H, C I
S-CH=), .5~:~i;:fi~G ~ ~~ yi i,; !~ ~_ _. ~~__.. ., .?='~'3 ~: ,.
i a .~ ~~ _ 5.874 {br s, l H, C4-CH=). M5 (EI) m/z (relative intensity): 300 (M', 91), 2$5 (19), 256 (36}, 214 (25}, 190 (33), 173 (62), 163 (55), 161 (42), 147 (74), 145 (45), 136 (45), 119 {74), 107 (57), 105 (70), 93 (43), 91 (100}, 79 (66), 77 (74), b7 (43) and 55 (83). Analysis calculated for CzQH280z: C, 80.00; H, 9.40; Found: C, 79.77; H, 9.48.
G. Preparation of Compound IV
[OOX46j A benzene (8.0 mL)Ipyridine solution (1.0 mL) ofthe alcohol Compound 107 ( 162 mg, 0.54 mmol) was treated with an excess undecanoyl chloride (500 mg, 2.41 mxsiol) and the mixture was stirred at room temperature for two hours. The mixture was chilled in an ice bath and diluted with saturated sodium bicarbonate solution. The aqueous mixture was extracted with ether. The ether extracts were washed with water and brine. The combined ether extracts were dried over sodium sulfate and evaporation of the solvent gave 620 mg of an oil containing undecanoic acid and Compound IV. The crude material was subjected to chromatography, eluting with 1 % acetone in dichloromethane to give 25 I mg of the ester of Compound IV in 99% yield. This material exists as a low melting was and would not crystallize from a variety of solvents. FTTR (ICBr, diffuse reflectance):
vm~, 2925, 2853, 1737, 1673 and 1466 cm-i. NMR (CDC13) s a.86s (d, 3 H, J =
7.2Hz, C7 a- CH3), 1.079 (s, 3 H, C18- CH3), 1.158 (d, 3 H, J = 7.2 Hz, C11 ~-CH3), 4,889 (t, 1 H, J - 8.4 Hz, C 17 a-CH), 5.151 (br s, 1 H, C 15-CH-), and 5.873 (s, 1 H, C4-CH=}. MS (EI) m/z (relative intensity): 468.7 (M-~, 14.5), 283 {27), 282 ( 100), 189 ( 1 ?), 173 ( 15}, 147 (21 ), 119 917), 105 ( 17) 93, 917), 69 ( 17) and 57 (27). Analysis calculated for C~~H~aC>~~ 1l4 HzO: C, 78.70; H, 10.30; Found:
C, 78.78; H, 10.36.
H. Prevaration of Compound V
[00I4'7] A benzene (8.0 tnL)/pyridine (1.0 mL) solution of Compound 107 (129 mg, 0.43 mmol) was treated with traps-4-n-butylcyclohexanecarboxylic acid chloride (349 mg, 1.72 mmol) and stirred at zoom temperature for two hours.
The nsixture was chilled in an ice bath and diluted with saturated sodium bicarbonate solution. T'hc aqueous mixture was extracted with ether. T'he ether extracts were washed with water and brine, combined and dried over sodium sulfate.
Evaporation of the solvent gave 480 mg of as oil containing traps-4-n-butylcyclohexanecarboxylic acid and Compound V. The etude material was subjected to chromatography, eluting with 5% acetone in dichloromethane, to give ,.+. ,, !~ nr~~~i_t'~'_i'~'n ., _.'_.. ~: _. .... , ~~_ ~~. ~'r.

189 mg of the ester Compound V as a glass with 95 % yield. The material was recrystallized from cold pentane to afford 120 mg of pure Compound V as a white powder in 60% yield with a melting point of 84-85 'C. fFIR (KBr, diffuse reflectance): vm"~ 2929, 2854, 1673, 1613 and 1453 cm'1- NMR (CDCl3) 8 0.867 (d, 3H, J -- .2 Hz, C7 a- CH3)), 1.076 (s, 3 H, C 18- CH3) 1.158 (d, 3 H, J = 7.2 Hz, C 11 (3-CH3), 4.873 (t, 1 H, J = 8.4 Hz, C 17a-CH), 5.161 (br s, 1 H C 15-CH=), and 5,873 (s, 1 H, C4-CH=). MS (EI) m/z (relative intensity): 466 (M', 10), 283 (17), 282 ( 100), 190 ( 17), 172 927), 157 ( 19), 147 (38), 119 ( 17), 105 ( 17), 93 ( 17), 83 (50), f>9 (38) and 55 (4b). Analysis calculated for C311~03: C, 79.83; H, 9.87;
Found: C, 79.91; H, 9.96.

[00148] This example provides data on the androgenic potency of Compounds IV and V when administered orally.
[00149] Immature (about 21 day old) Sprague male rats were orchidectomizxd under anesthesia, and randomly assignee to groups of ten animals for each dose level of the active undergoing testing. Animals were maintained under standard conditions of housing and hsd free access to food and water. Illumination was controlled for 14 hour periods of light aad 10 hours of darkness. Each active was dissolved in 10% ethanoUsesame oil and administered by gavage (oral) each day for seven days beginning on the date of the orchidectomy. The animals were sacrificed 24 hours after the last dose, and the ventral prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0.1 mg. See, e.$., Hershberger, L. et al, Myotrophic Activity of 19-nortestosterone And Other Steroids Determined By Modified Levator And Muscle Method, Proc. Sec. Exptl. Biol. Med ~ 175-180 (1953). Regression analysis was performed by conventional methods using a PROPHET data management system. See, e.g., Bliss, C., The Statistics of Bioassay (Academic Press, New York, 1952); Hollister, C., Nucleic Acids Res. 1~ 1873-75 (1988).
Ventral prostate weight was used as the endpoint because it is the sensitive organ to androgenic stimulation.
[00150] As displayed in Fig. 20, about six to about eighteen times the oral activity of the standard methyltestosterone were exhibited in testing performed on Compound Y. Compound IV test results exhibited about two to about nine times the oral activity of methyltestosterone. These findings were unexpected due to the relative inactivity of testosterone and its esters on oral administration, yet it is believed that this may be explained, in part, due to the protections that the ester receives from degradation in the gastrointestinal tract and/or rapid metabolism by the liver. It is also conceivable that the lipophilic nature of Compound V
permits absorption into the thoracic lymph thus avoiding direct entrance into the portal system and "first-pass" metabolism in the liver.

[00151) This example provides data on the androgenic potency of Compounds IV and V when administered parenterally (by subcutaneous injection).
{00152] Immature (about 22-day-old) Sprague-Dawley male rats were orchidectomized under anesthesia, and randomly assignee to groups of ten animals for each dose level of the active undergoing testing. The animals were maintained under standard conditions of housing and had free access to food and water.
Illumination was controlled for 14 hour periods of light and 10 hours of darkness.
[00153] Each active was administered by subcutaneous injection of 0.6 mg of test material in aque4us suspending vehicle (ASV) andlor an oily vehicle (10%
ethanol/sesame oil) on the day of surgery. Testosterone enarithate in sesame oil was used as a standard. The ventral prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0:1 mg. Regression analysis was performed by conventional methods using a PROPHET data management system. Ventral prostate weight was used as the endpoint because it is the sensitive organ to androgenic stimulation.
[00154] As seen in Fig. 2I, both esters exhibited about one-half (0.46) times the activity of methyltestosternne following subcutaneous administration. This weak activity was surprising given the potent long-action action following a single subcutaneous injection. The lack of potent subcutaneous activity likely reflects the slow release of the drug fiocn the injection site over the 7-day administration period.

[001S5) This example further illustrates the relative activity of 17 esters of 7a,11[i-dimethyl-17~-hydroxyestra-4,14-dien-3-one (i.e., 7a,11{i-dimethyl-17(3-hydroxyestra 4,14-dien-3-one 17-undecanoate (Compound IV; CDB-4563) and 7a,1 lei-dimethyl-17~i hydroxyestra-4,14-lien-3-one 17[i-4-n-butylcyclohexanecarboxylate (Compound V; CDB.4562} compared to that of 9t' ~ _ .....'>: . ~!','_, _~ _. . _... , "a',~

as testosterone enanthate (CDB-112F) and other androgens (i.e., testosterone bucyclate, _ CDB-1?81a at 1 mg dosage; Dimethandrolone undecanoate, CDB..4521; and Dimethandrolone bucyclate, CDB-4386A} over relatively long periods of time.
[0015G] Immature {about 21-day-old) Sprague-Dawley rats were orchidectomized under anesthesia, and randomly assignee to groups of 4p or more.
Animals received a single subcutaneous injection of 0.6 mg of an active (with the exception of testosterone bucyclate of which 1 mg was administered) in 0.2 ml of an aqueous suspending cagier and/or oily carrier ( 10% ethano1190% sesame oil containing S tng/m1 chlorobutanol as a preservative, or ethyloleate} on the date of the orchidectomy. The enanthate ester was formulated using the 10%
ethanoUsesame oil or ethyloleate carrier as a first standard, with the l 0%
ethanoUsesame oil carrier used as a second standard.
[00157] In this example, the carrier used to provide the aqueous suspension was formulated as follows: l g betszyl alcohol, 0.5 g sodium carboxylethy!
cellulose 50, 0.3?6 g disodium hydrogen phosphate dihydrate, 1.495 g sodium dihydrogen phosphate dihydrate, with water for injection (WFI) being added to bring volume of the carrier up to 100 ml.
[0015$] Five animals from each group were sacrificed at weekly or biweekly intervals, and the ventral prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0.1 mg.
[00159] Ventral prostate weight was used as the endpoint because it is the sensitive organ to androgenie stimulation. Regression analysis was performed by conventional methods using the PROPHET data management system previously identified.
[00160) Fig. 22 is a graphic representation of the androgenic assays ofthe actives. Each data point represents the mean (n--10) and standard error of the mean (SEM) for each prostate weight for each formulation level.
[00161] More specifically, Fig. 22 is a graph of the ventral prostate weights at weekly intervals over a 12 week period after the subcutaneous administration of the actives in the carriers (as indicated in Fig. 22). CDB-4521 and CDB-4562 in the aqueous vehicle exhibited the most dramatic increases and maintenance of ventral prostate weight. 'fhe area under the curve (AUC, calculated by the trapezoidal rule), was about 3 times greater for CDB-4562 in the aqueous vehicle (AUC 1521 mg~
a,;~~

weeks), than for testosterone enanthate in the oily carrier (AUC 513 mg-weeks).
The aqueous vehicle control exhibited an AUC of 81 mg-weeks.
This experiment highlights the significance of the ability to provide 7a,11 ~i-dimethyl-17~ hydrnxyestra 4,14-lien-3-one 17~-4-n-burylcyclohexanecarboxylate (Compound V; CDB-4562) in the form of an acjueous suspension, which provides unexpected and desirable long-term androgenic activity. This experiment also underscores the importance of the stereoconfiguration o~ the Cu substituent.

[00152] This example provides data on the androgenic potency of Compound III (CDB-4545), 7a-methyl-17~i hydroxyestra 4,14-diem-3-one (CDB-868A), and 7a-methyl-17~ hydroxyestra-4,14-lien-3-one 17~~-n-burylcyclohexanecarboxylate (CDB-4327) when adnvnistered orally.
[00163] Immature {about 21 day old) Sprague male rats were orchidectomized under anesthesia, and randomly assignee to groups of ten animals for each dose level of the active undergoing testing. Animals were maintained under standard conditions of housing and had free access to food and water. Illumination was controlled for 14 hour periods of light and 10 hours of darkness. Each active was dissolved in 10% ethanol/sesame oil and administered by gavage (oral) each day for seven days beginning on the date of the orchidectomy. The animals were sacrificed 24 hours afttr the last dose, and the ventxal prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0.1 mg. See, e.g., Hershberger, L. et al, Myotrophic Activity of 19-nortestosterone And Other Steroids Determined $y Modified Levator And Muscle Method, Proc. Soc. Exptl. Biol. Med 83 175,180 (I953). Regression analysis was performed by conventional methods using a PROPHET data management system. See, e.g., Bliss, C., The Statistics of Bioassay (Academic Press, New York, 1952); Hollister, C., Nucleic Acids Res. 1b 1873-75 (1988).
Ventral prostate weight was used as the endpoint because it is the sensitive organ to androgenic stimulation.
[00I64] As displayed in Fig. 23, about two (1.9b) times the oral activity of the standard methyltestosterone was exhibited in testing performed on Compound III.
The results oftesting 7a-methyl-l7ji hydroxyestra-4,14-dien-.3-one (CDB-868A) and 7a-methyl-17~ hydroxyestra-4,14-lien-3-one 17{3-4-n-butylcyclohexanecatboxylate (CDB-4327) indicated that these actives exhibited Fs,~ in:

about five (at least about 3 times, 5.14) and about 18 (at least about 10 times, 18.77}
times the oral activity of methyltestosterone. These findings were unexpected due to the relative inactivity of testosterone and its esters on oral administration, yet it is believed that this may be explained, in part, due to the protections that the ester receives from degradation in the gastrointestinal tract and/or rapid metabolism by the liver.

(00165] This example provides data on the androgenic potency of Compound III (CDB-4545) and 7a-methyl-17ø hydroxyestra-4,14-dien-3-one (CDB-868A), when administered parenterally (by subcutaneous injection).
[OOlb6J Immature (about 22-day-o!d) Sprague-Dawley male rats were orclaidectomized under anesthesia, and randomly assignee to groups of ten animals for each dose level of the active undergoing testing. The animals were maintained under standard conditions of housing and had free access to food and water.
Illumination was controlled for 14 hour periods of light and 10 hours of darkness.
[00167] Each active was administered by subcutaneous injection of test material in an oily vehicle (10% ethanol/sesame oil) on the day of surgery.
Testosterone in sesame oil was used as a standard. The ventral prostate and seminal vesicles were excised, cleaned of fat and connective tissue, blotted on moist filter paper and weighed to the nearest 0.1 mg. Regression analysis was performed by conventional methods using a PROPHET data management system. Ventral prostate weight was used as the endpoint because it is the sewsitive organ to androgenic stimulation.
[00160) As seen in Fig. 24, both actives exhibited high activity {Compound III, at least about 10, lO.Ob; 7a-methyl-17ø hydroxyestra.4,14-dies-3-one (CDB-86$A), at least about 50, 51.13} times the activity oftestostemne following subcutaneous administration.
(00169] Any reference cited herein, including patents, patent applications, and publications, are hereby incorporated in their entireties by reference.
Further, any reference herein to a component in the singular is intended to indicate and include at least one of that particular component, i.e., one or more.
[00170] While this invention has been described with an emphasis upon preferred embodiments, it will be obvious to those of ordinary skill in the art that variations of the preferred embodiments may be used and that it is intended that the r t. J

invention may be practiced otherwise than as specifically described herein.
Accordingly, this invention includes all modifications encompassed within the spirit and scope of the invention as defined by the following claims.
~ '~ i ~. - , , , i 1S, t'~._ r~-_~l , ~ ~~.lll I~~~;J_'

Claims (148)

We claim as our invention:

1. A method for providing hormonal therapy to a patient comprising the oral administration of an androgen selected from the group consisting of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one, 17-ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one, a 17 ester of 7.alpha.-methyl-17.beta.
hydroxyestra-4,14-dien-3-one or mixtures thereof in an amount effective to provide hormonal therapy to a patient in need thereof.

2. The method of claim 1, wherein an average dosage of about 1 mg to about 50 mg per day of the androgen is orally administered to the patient.

3. The method of claim 2, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra 4,14-dien-3-one.

4. The method of claim 1, wherein the androgen is a 17 ester of 7.alpha.,11.beta.-dimethyl-17.beta.3-hydroxyestra-4,14-dien-3-one.

5. The method of claim 4, wherein the androgen is 7.alpha.,11.beta.3-dimethyl-17.beta.
hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

6. The method of claim 5, wherein an average dosage of about 5 mg to about 40 mg per day of the androgen is orally administered to the patient.

7. The method of claim 4, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.

8. The method of claim 7, wherein an average dosage of about 5 mg to about 40 mg per day of the androgen is orally administered to the patient.

9. The method of claim 2, wherein the oral administration is completed on a daily basis for at least one month.

10. The method of claim 9, wherein the hormonal therapy continues at least 3 months.

11. The method of claim 1, wherein the hormonal therapy is the treatment of hypogonadism in a male patient.

12. The method of claim 11, wherein an average dosage of about 1 mg to about 50 mg per day of the androgen is orally administered to the patient.

13. The method of claim 12, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

14. The method of claim 11, wherein the androgen is a 17 ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

15. The method of claim 14, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta. hydroxyestra-4,14-dien-3-one 17.beta.3-4-n-butylcyclohexanecarboxylate.

16. The method of claim 15, wherein an average dosage of about 5 mg to about 40 mg per day of the androgen is orally administered to the patient.

17. The method of claim 14, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.

18. The method of claim 17, wherein an average dosage of about 5 mg to about 40 mg per day of the androgen is orally administered to the patient.

19. The method of claim 12, wherein the oral administration is completed on a daily basis for at least one month.

20. The method of claim 19, wherein the hormonal therapy continues at least 3 months.

21. The method of claim 1, wherein the hormonal therapy is male contraception.

22. The method of claim 21, wherein an average dosage of about 1 mg to about 50 mg per day of the androgen is orally administered to the patient.

23. The method of claim 22, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

24. The method of claim 21, wherein the androgen is a 17 ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

25. The method of claim 24, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta. hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

26. The method of claim 25, wherein an average dosage of about 5 mg to about 40 mg per day of the androgen is orally administered to the patient.

27. The method of claim 24, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.

28. The method of claim 27, wherein an average dosage of about 5 mg to about 40 mg per day of the androgen is orally administered to the patient.

29. The method of claim 22, wherein the oral administration is completed on a daily basis for at least one month.

30. The method of claim 29, wherein the hormonal therapy continues at least 3 months.

31. The method of claim 1, wherein the hormonal therapy is the promotion and maintenance of muscle mass in a patient.

32. The method of claim 31, wherein the therapy continues for at least 3 months.

33. The method of claim 31, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

34. The method of claim 31, wherein the androgen is a 17 ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

35. The method of claim 31, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta. hydroxyestra 4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

36. The method of claim 31, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.

37. The method of claim 1, wherein the hormonal therapy is the pilliative treatment of breast cancer.

38. The method of claim 37, wherein the therapy continues for at least 3 months.

39. The method of claim 37, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

40. The method of claim 37, wherein the androgen is a 17 ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

41. The method of claim 40, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta. hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

42. The method of claim 40, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.

43. The method of claim 1, wherein the hormonal therapy is hormone replacement therapy in females.

44. The method of claim 43, further comprising the administration of estrogen or an analog thereof.

45. The method of claim 44, further comprising the administration of a progestin.

46. The method of claim 44, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

47. The method of claim 44, wherein the androgen is a 17 ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

48. The method of claim 47, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta. hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

49. The method of claim 47, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.

50. The method of claim 1, wherein the androgen is administered as a formulation comprising the androgen and a pharmaceutically-acceptable oily carrier.

51. A method for providing hormonal therapy to a patient comprising administering parenterally to the patient an androgen selected from the group consisting of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one, a 17-ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one, a 17 ester of 7.alpha.-methyl-17.beta.
hydroxyestra-4,14-dien-3-one or mixtures thereof in an amount effective to provide hormonal therapy to the patient.

52. The method of claim 51, wherein an average dosage of about 1 to about 400 mg of the androgen is parenterally administered to the patient.

53. The method of claim 52, wherein the androgen is administered to the patient about once every month.

54. The method of claim 53, wherein the androgen is a 17-ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

55. The method of claim 51, wherein the androgen is administered to the patient about once every two to four months.

56. The method of claim 55, wherein the androgen is a 17-ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

57. The method of claim 56, wherein an average dosage of about 1 to about 400 mg of the androgen is parenterally administered to the patient.

58. The method of claim 52, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

59. The method of claim 52, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.

60. The method of claim 51, wherein the average amount of the androgen administered during the period of hormonal therapy is from about 1 to about 40 mg per week.

61. The method of claim 51, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate and is administered as a formulation comprising 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra 4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate and a pharmaceutically-acceptable aqueous carrier.

62. The method of claim 61, wherein the 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate is crystalline and the formulation comprises a suspension of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate in the pharmaceutically-acceptable aqueous carrier.

63. The method of claim 62, wherein the formulation is administered about once every month.

64. The method of claim 62, wherein the formulation is administered about once every two to four months.

65. The method of claim 64, wherein from about 100 mg to about 400 mg of the androgen is administered to the patient.

66. The method of claim 51, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one and is administered as a formulation comprising 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one and a pharmaceutically-acceptable aqueous carrier.

67. The method of claim 66, wherein the 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one is crystalline and the formulation comprises a suspension of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one in the pharmaceutically-acceptable aqueous carrier.

68. The method of claim 67, wherein the formulation is administered about once every month.

69. The method of claim 67, wherein the formulation is administered about once every two to four months.

70. The method of claim 69, wherein from about 100 mg to about 400 mg of the androgen is administered to the patient.

71. The method of claim 51, wherein the hormonal treatment is the treatment of hypogonadism in male patients,

72. The method of claim 71, wherein an average dosage of about 1 to about 400 mg of the androgen is parenterally administered to the patient.

73. The method of claim 72, wherein the androgen is administered to the patient about once every month.

74. The method of claim 71, wherein the androgen is a 17-ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

75. The method of claim 71, wherein the androgen is administered to the patient about once every two to four months.

76. The method of claim 71, wherein the androgen is a 17-ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

77. The method of claim 75, wherein an average dosage of about 1 to about 400 mg of the androgen is parenterally administered to the patient.

78. The method of claim 71, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

79. The method of claim 71, wherein the androgen is 7.alpha., 11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.

80. The method of claim 71, wherein the average amount of the androgen administered during the period of hormonal therapy is from about 1 to about 40 mg per week.

81. The method of claim 71, wherein the androgen is 7a.alpha.11 .beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate and is administered as a formulation comprising 7.alpha., 11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate and a pharmaceutically-acceptable aqueous carrier.

82. The method of claim 81, wherein the .alpha.a,11.beta.-dimethyl=17.beta.-hydroxyestra 4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate is crystalline and the formulation comprises a suspension of 7.alpha., 11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate in the pharmaceutically-acceptable aqueous carrier.

83. The method of claim 82, wherein the formulation is administered about once every month.

84. The method of claim 82, wherein the formulation is administered about once every two to four months.

8S. The method of claim 82, wherein from about 100 mg to about 400 mg of the androgen is administered to the patient.

86. The method of claim 71, wherein the androgen is 7.alpha., 11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate and is administered as a formulation comprising 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate and a pharmaceutically-acceptable aqueous carrier.

87. The method of claim 86, wherein the 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate is crystalline and the formulation comprises a suspension of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate in the pharmaceutically acceptable aqueous carrier.

88. The method of claim 86, wherein the formulation is administered about once every month.

89. The method of claim 86, wherein the formulation is administered about once every two to four months.

90. The method of claim 89, wherein from about 100 mg to about 400 mg of the androgen is administered to the patient.

91. The method of claim 51, wherein the hormonal treatment is male contraception.

92. The method of claim 89, wherein an average dosage of about 1 to about 400 mg of the androgen is parenterally administered to the patient.

93. The method of claim 90, wherein the androgen is administered to the patient about once every month.

94. The method of claim 91, wherein the androgen is a 17-ester of 7.alpha.,11.beta.-dimethyl-17.beta.hydroxyestra-4,14-dien-3-one.

95. The method of claim 91 , wherein the androgen is administered to the patient about once every two to four months.

96.The method of claim 91, wherein the androgen is a 17-ester of 7.alpha.,11..beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

97. The method of claim 94, wherein an average dosage of about 1 to about 400 mg of the androgen is parenterally administered to the patient.

98. The method of claim 91, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta. hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

99. The method of claim 91, wherein the androgen is 7.alpha.e,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.

100. The method of claim 91, wherein the average amount of the androgen administered during the period of hormonal therapy is from about 1 to about 40 mg per week.

101. The method of claim 91, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate and is administered as a formulation comprising 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate and a pharmaceutically-acceptable aqueous carrier.

102. The method of claim 91, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one and is administered as a formulation comprising 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyelohexanecarboxylate and a pharmaceutically acceptable aqueous carrier.

103. The method of claim 100, wherein the androgen is a 17-ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

104. An oral dosage formulation comprising an androgen selected from the group consisting of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one, a 17-ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one, a 17 ester of 7.alpha.-methyl-17.beta. hydroxyestra-4,14-dien-3-one or mixtures thereof and a pharmaceutically-acceptable carrier.

105. The oral dosage form of claim 104, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

106. The oral dosage form of claim 104, wherein the androgen is a 17 ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

107. The oral dosage form of claim 106, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

108. The oral dosage form of claim 106, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.

109. The oral dosage form of claim 104, further comprising estrogen or an analog thereof.

110. The oral dosage form of claim 104, wherein the androgen is present in an amount sufficient to provide hormonal therapy to a patient in need of such therapy.

111. The oral dosage form of claim 104, wherein the androgen is present in an amount ranging from about 0.1 to about 100 mg.

112. The oral dosage form of claim 106, wherein the androgen is present in an amount ranging fiom about 0.1 to about 50 mg.

113. A parenteral dosage formulation comprising an androgen selected from the group consisting of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one, a 17-ester of 7.alpha.,11.beta.-dimethyl-17.beta.hydroxyestra 4,14-dien-3-one, a 17 ester of 7.alpha.-methyl-17.beta. hydroxyestra-4, 14-dien-3-one or mixtures thereof and a pharmaceutically-acceptable liquid carrier, the androgen being present in an amount sufficient to provide hormonal therapy to a human patient in need thereof.

114. The parenteral dosage form of claim 113, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

115. The parenteral dosage form of claim 113, wherein the androgen is a 17 ester of 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one.

116. The parenteral dosage form of claim 115, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

117. The parenteral dosage form of claim 115, wherein the androgen is 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one 17-undecanoate.
118. The parenteral dosage form of claim 113, further comprising estrogen or an analog thereof.

118. The parenteral dosage form of claim 113, wherein the androgen is present in an amount ranging from about 1 to about 600 mg.

119. The parenteral dosage form of claim 118, wherein the androgen is present in an amount ranging from about 50 to about 400 mg.

120. The parenteral dosage form of claim 113, further comprising a syringe filled with androgen and a pharmaceutically acceptable liquid carrier.

121. The parenteral dosage form of claim 113, wherein the androgen is in a pharmaceutically-acceptable aqueous liquid carrier.

122. The parenteral dosage form of claim 121, wherein the androgen is crystalline while in the carrier.

123. A method far preparing 7.alpha.,11.beta.-dimethyl-17.beta.-hydroxyestra-4,14-dien-3-one (III) comprising the steps of:
(a) acetylating, aromatizing and hydrolyzing Compound 101 to provide Compound 102;
(b) methylating the phenolic functionality of Compound 102 and oxidizing the hydroxyl group to provide Compound 103;
(c) dehydrogenating Compound 103 to provide Compound 104;

(d) enolacetylating Compound 104 to provide Compound 105;
(e) reducing and hydrolyzing Compound 105 to provide Compound 106; and (f) reducing Compound 106 to provide 7.alpha.,11.beta.-dimethyi-17.beta.-hydroxyestra-4,14-dien-3-one (Compound III).

124. The process of claim 123, further comprising, esterifying Compound III at the 17-position.

125. The process of claim 124, wherein the esterified compound is Compound (IV)

126. The process of claim 124, wherein the esterified compound is Compound (V)

127. The compound of formula III
and 17-esters thereof.

128. The compound of formula III

129. The compound of formula IV

130. The compound of formula V

131. The compounds of claim 127, wherein the compounds are in crystalline form.

132. A crystalline compound of formula III.

133. A crystalline compound of formula V

134. The crystalline compound of claim 132, wherein the melting point is 149-151°C.

135. The compound of claim 128, wherein the purity of the compound is at least 98%.

136. The crystalline compound of claim 133, wherein the melting point is 84-85°C,

137.The compound of claim 129, wherein the purity of the compound is at least 98%.

138. The compound of claim 130, wherein the purity of the compound is at least 98%.

139. The method according to claim 1, wherein the androgen is a 17 ester of 7.alpha.-methyl-17.beta. hydroxyestra 4,14-dien-3-one.

140. The method according to claim 139, wherein the androgen is 7.alpha.-methyl-17.beta. hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

141. The method according to claim 51, wherein the androgen is a 17 ester of 7.alpha.-methyl-17.beta. hydroxyestra-4,14-dien-3-one.

142. The method according to claim 141, wherein the androgen is 7.alpha.-methyl-17.beta. hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

143. The oral formulation according to claim 104, wherein the androgen is a 17 ester of 7.alpha.-methyl-17.beta. hydroxyestra-4,14-dien-3-one.

144. The method according to claim 143, wherein the androgen is 7.alpha.-methyl-17.beta. hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.

145. The parenteral formulation according to claim 113, wherein the androgen is a 17 ester of 7.alpha.-methyl-17.beta. hydroxyestra-4,14-dien-3-one.

146. The method according to claim 145, wherein the androgen is 7.alpha.-methyl-17.beta. hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyolohexanecarboxylate.

147. 17 esters of a compound having the formula 7.alpha.-methyl-17.beta.
hydroxyestra-4,14-dien-3-one.

148. A compound having the formula 7.alpha.-methyl-17.beta. hydroxyestra-4,14-dien-3-one 17.beta.-4-n-butylcyclohexanecarboxylate.