WO2002002112A1 - Combinaison pharmaceutique d'anti-androgene et d'anastrozole conçue pour produire un effet anti-androgene et une inhibition de l'aromatase - Google Patents

Combinaison pharmaceutique d'anti-androgene et d'anastrozole conçue pour produire un effet anti-androgene et une inhibition de l'aromatase Download PDF

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Publication number
WO2002002112A1
WO2002002112A1 PCT/SE2001/001546 SE0101546W WO0202112A1 WO 2002002112 A1 WO2002002112 A1 WO 2002002112A1 SE 0101546 W SE0101546 W SE 0101546W WO 0202112 A1 WO0202112 A1 WO 0202112A1
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WIPO (PCT)
Prior art keywords
androgen
patient
solvate
pharmaceutically acceptable
acceptable salt
Prior art date
Application number
PCT/SE2001/001546
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English (en)
Inventor
Ian Cockshott
Barrington Furr
Original Assignee
Astrazeneca Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GB0016427A external-priority patent/GB0016427D0/en
Priority claimed from GB0020769A external-priority patent/GB0020769D0/en
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Priority to AU6800101A priority Critical patent/AU6800101A/xx
Publication of WO2002002112A1 publication Critical patent/WO2002002112A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4166—1,3-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. phenytoin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4196—1,2,4-Triazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
    • A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
    • A61P5/28—Antiandrogens

Definitions

  • the present invention relates to a pharmaceutical product, daily dose or dose regimen comprising an anti-androgen and anastrozole, wherein the anti-androgen is selected from flutamide, nilutamide, chlormadinone acetate and cyproterone.
  • the invention also relates to a method of providing an anti-androgenic effect and aromatase inhibition in a patient, wherein the aromatase inhibition is provided substantially without causing an additional increase in the levels of circulating androgens.
  • the invention relates to the use of an anti-androgen and anastrozole in the manufacture of a pharmaceutical product for this purpose, wherein the anti-androgen is selected from flutamide, nilutamide, chlormadinone acetate and cyproterone.
  • Anastrozole an aromatase inhibitor
  • AstraZeneca trade name an aromatase inhibitor
  • Anastrozole is known as 2,2'-[5-(lH-l,2,4-triazol-l-ylmethyl)-l,3- phenylene]di(2-methyl-propionitrile), which is disclosed in US re-issue No. 36,617.
  • An alternative name is 2,2'-dimethyl-2,2'-[5-(lH-l,2,4-triazol-l-ylmethyl)-l,3- phenylene]bis(propiononitrile). The corresponding structure is shown in formula I:-
  • Flutamide an anti-androgen, is known by the trade name EULEXLN . Flutamide is also known by the alternative names 2-methyl-N-[4-nitro-3- (trifluoromethyl)phenyl]propanamide; , ⁇ , ⁇ -trifluoro-2-methyl-4'-nitro-m- propionotoluidide; and 4'-nitro-3'-trifiuoromethylisobutyranilide. Flutamide is disclosed in US 3,847,988. The corresponding structure is shown in formula II:-
  • Nilutamide an anti-androgen, is known by the trade name NILANDRON . Nilutamide is also known by the alternative names 5,5-dimethyl-3-[4-nitro-3-(trifluoromethyl)phenyl]- 2,4-imidazolidinedione; and l-(3 '-trifiuoromethyl-4'-nitrophenyl)-4,4- dimethylimidazoline-2,5-dione. Nilutamide is disclosed in US 4,097,578. The corresponding structure is shown in formula III:-
  • Chlormadinone in its acetate form, is an anti-androgen.
  • the acetate form is known by the alternative names 17-(acetyloxy)-6-chloropregna-4,6-diene-3,20-dione; 6-chloro-17- hydroxypregna-4,6-diene-3 ,20-dione acetate; 6-chloro-6-dehydro- 17 ⁇ - hydroxyprogesterone acetate; 6-chloro-6-dehydro-17 ⁇ -acetoxyprogesterone; and 17 ⁇ - acetoxy-6-choro-6,7-dehydroprogesterone.
  • Chormadinone is disclosed in US 3,485,852.
  • Cyproterone is known by the alternative names (l ⁇ ,2 ⁇ )-6-chloro-l,2-dihydro-17-hydroxy- 3 'H-cy clopropa[ 1 ,2]pregna- 1 ,4,6-triene-3 ,20 dione; 6-chloro- 17-hydroxy- 1 ⁇ ,2 - methylenepregna-4,6-diene-3 ,20-dione; 6-chloro-6-dehydro- 17 ⁇ -hydroxy- 1 ,2 ⁇ - methyleneprogesterone; and 6-chloro-l,2 ⁇ -methylene-4,6-pregnadien-17 ⁇ -ol-3,20-dione. Cyproterone is disclosed in US 3,234,093. Cyproterone in its free alcohol and acetate forms is an anti-androgen.
  • Anti-androgens such as flutamide and nilutamide are used in the treatment of prostate cancer. This is also the case for another anti-androgen, bicalutamide.
  • Such compounds are generally used in combination with an inhibitor of gonadotrophin secretion, for example a luteinising hormone releasing hormone (LHRH) agonist such as goserelin, buserelin, leuprorelin or triptorelin.
  • LHRH luteinising hormone releasing hormone
  • the properties and usefulness of these anti-androgens have been reviewed, for example in the following documents which are incorporated herein by way of reference :- flutamide R O Neri, J. Drug Develop.. 1987, 1 (Suppl.), 5-9 and Urology, 1989,
  • nilutamide causes an increase in the basal level of circulating testosterone (A U Decensi et al. , J. Urology, 1991, 146, 377-381). It is believed that such increases in the level of testosterone occur when sufficient of the anti-androgen gains access to the CNS and blocks androgen receptors in the hypothalamus.
  • a disadvantageous effect is produced. Namely, the increase in the levels of circulating oestrogen may cause one or more of the side effects of gynaecomastia, breast tenderness, hot flushes, impotence and reduction in libido.
  • a discussion on gynaecomastia can be found in C J Tyrrell, Prostate Cancer and Prostatic Diseases, 1999, 2(4): pp 167-171.
  • the present invention fulfils this need by providing a pharmaceutical product for administration to a patient for providing an anti-androgenic effect and aromatase inhibition in the patient, the product comprising an anti-androgen and anastrozole or a pharmaceutically acceptable salt or solvate thereof, wherein the anti-androgen is selected from flutamide, nilutamide, chlormadinone acetate" and cyproterone or a pharmaceutically acceptable salt or solvate thereof.
  • the cyproterone is in its free alcohol or acetate form.
  • the anti-androgen and anastrozole are provided in a ratio of 25 to 1000 : 0.005 to 100 respectively.
  • the aromatase inhibition is provided substantially without causing an additional increase in the levels of circulating androgens.
  • the present invention also provides a daily pharmaceutical dose for administration to a patient for providing an anti-androgenic effect and aromatase inhibition in the patient, the dose comprising an anti-androgen and from 0.005 to 100 mg of anastrozole or a pharmaceutically acceptable salt or solvate thereof, wherein the anti-androgen is selected from flutamide, nilutamide, chlormadinone acetate and cyproterone or a pharmaceutically acceptable salt or solvate thereof.
  • the present invention provides a dose regimen for such purpose comprising an anti-androgen and from 0.005 to 100 mg of anastrozole or a pharmaceutically acceptable salt or solvate thereof for simultaneous or sequential administration to the patient, wherein the anti-androgen is selected from flutamide, nilutamide, chlormadinone acetate and cyproterone or a pharmaceutically acceptable salt or solvate thereof.
  • aspects of the invention relate to the use in the manufacture of a pharmaceutical product of an anti-androgen and anastrozole or a pharmaceutically acceptable salt or solvate thereof that are simultaneously or sequentially administrable to a patient, for:-
  • anti-androgen is selected from flutamide, nilutamide, chlormadinone acetate and cyproterone or a pharmaceutically acceptable salt or solvate thereof.
  • suppressing increase in the incidence or severity of a side effect we mean providing a lower incidence or severity compared with the side effect produced when the anti- androgen is administered alone, or eliminating the side effect.
  • the present invention further provides a method of providing an anti-androgenic effect in a patient comprising simultaneously or sequentially administering an anti-androgen and anastrozole or a pharmaceutically acceptable salt or solvate thereof to the patient, wherein the method further provides aromatase inhibition in the patient substantially without causing an additional increase in the levels of circulating androgens, and wherein the anti- androgen is selected from flutamide, nilutamide, chlormadinone acetate and cyproterone or a pharmaceutically acceptable salt or solvate thereof.
  • the present invention provides both an anti-androgenic effect and aromatase inhibition in a patient, wherein the aromatase inhibition is produced substantially without causing an additional increase in the levels of circulating androgens. This is achieved by administering to the patient a product comprising an anti-androgen and anastrozole or a pharmaceutically acceptable salt or solvate thereof, wherein the anti-androgen is selected from flutamide, nilutamide, chlormadinone acetate and cyproterone or a pharmaceutically acceptable salt or solvate thereof.
  • the anti-androgen and anastrozole are provided in a ratio respectively of 25 to 1000 (preferably the lower end of the range being 50 or 100; preferably the upper end of the range being 500, 350, 300, 150 or 50; suitable values in the ranges being 750, 375, 150, 125 or 50) : 0.005 to 100 (preferably the lower end of the range being 0.05 or 0.5 ; preferably the upper end of the range being 50, 10 or 1 ; the most preferred range being 0.5 to 1 ; a suitable value in the range being 1).
  • flutamide a preferred range is 100 to 1000, and 750 or 375 is a preferred value.
  • chlormadinone acetate a preferred value is 50.
  • cyproterone a preferred range is 200 to 300.
  • nilutamide a preferred range is 50 to 500, and 300 or 150 is a preferred value.
  • product is intended to mean either a mixture of the anti-androgen and anastrozole (eg, provided as a capsule or tablet containing both compounds) or a kit comprising separate amounts of the compounds (eg, a set of anastrozole tablets and a separate set of tablets of the anti-androgen). The latter product can be used for simultaneous or sequential (ie, temporally spaced) administration of the compounds to the patient, while the pre-mixed compounds are for simultaneous administration.
  • Factors such as the rate of absorption, metabolism and the rate of excretion of each agent will affect their presence at the tumour site. Such factors are routinely considered by, and are well within the ordinary skill of, the clinician when he contemplates the treatment of a medical condition which requires the conjoint administration of two agents in order to obtain a beneficial effect.
  • the invention contemplates the use of pharmaceutically acceptable salts and solvates of the anti-androgen (for flutamide and nilutamide) and/or anastrozole.
  • Suitable salts are, for example acid addition salts, such as hydrochloride, hydrobromide, phosphate, acetate, fumarate, maleate, tartarate, citrate, oxalate, methanesulphonate or >-toluenesulphonate, or alkali metal salts such as sodium or potassium salts.
  • the anastrozole is included to provide aromatase inhibition, in that this compound inhibits conversion of testosterone to oestradiol by aromatase enzyme.
  • the anti-androgenic effect is useful for treating cancer, for example prostate cancer.
  • cancer for example prostate cancer.
  • Particular examples are advanced prostate cancer and early prostate cancer.
  • the anti- androgenic effect may be useful for prophylaxis, in order to reduce the risk of prostate cancer occurrence in patients. This could be especially useful in men genetically predisposed to prostate cancer.
  • Conventional methods are available to classify patients according to their risk of contracting prostate cancer, for example by assessment of family history and measurements over time of particular blood proteins such as prostate specific antigen (PSA).
  • PSA prostate specific antigen
  • Other uses for the anti-androgenic effect are the treatment of a non- malignant disease of the prostate gland (eg, benign prostatic hyperplasia or hypertrophy) and acne.
  • the aromatase inhibition is useful for suppressing increase in the incidence or severity of a side effect selected from gynaecomastia, breast tenderness, hot flushes, impotence, reduction in libido, nausea, vomiting, fatigue and diarrhoea.
  • a side effect selected from gynaecomastia, breast tenderness, hot flushes, impotence, reduction in libido, nausea, vomiting, fatigue and diarrhoea.
  • a side effect selected from gynaecomastia, breast tenderness, hot flushes, impotence, reduction in libido, nausea, vomiting, fatigue and diarrhoea.
  • the side effect is one or both of gynaecomastia and breast tenderness.
  • a suitable dose regimen or daily pharmaceutical dose comprises the anti-androgen and from 0.005 to 100 mg of anastrozole or a pharmaceutically acceptable salt or solvate thereof.
  • the lower end of the range is 0.05 or 0.5 mg; preferably the upper end of the range is 50, 10 or 1 mg; the most preferred range is 0.5 to 1 mg; a suitable value in the range being 1 mg.
  • the dose or the regimen preferably comprises from 25 to 1000 mg of the anti-androgen or a pharmaceutically acceptable salt or solvate thereof.
  • the lower end of the range is 50 or 100 mg; preferably the upper end of the range is 350, 300, 150 or 50 mg; suitable values in the ranges are 750, 375, 150, 125 or 50 mg.
  • a preferred range is 100 to 1000 mg, and 750 or 375 mg is a preferred value.
  • chlormadinone acetate a preferred value is 50 mg.
  • cyproterone a preferred range is 200 to 300 mg.
  • nilutamide a preferred range is 50 to 500 mg, and 300 or 150 mg is a preferred value.
  • each compound is preferably administered daily.
  • Another possible regime would be dosing of the anti-androgen on alternate days and dosing of the anastrozole also on (the same or different) alternate days.
  • the regimen may include administration instructions.
  • a dose of the anti-androgen is administered every 3, 4, 5, 6 or 7 days and the anastrozole is administered every 3, 4, 5, 6 or 7 days (eg, on the same day as the anti-androgen).
  • the regimen or daily dose comprises 3 times 250 mg of flutamide (eg, 250 mg administered every 8 hours) or 3 times 125 mg of flutamide (eg, 125 mg administered every 8 hours).
  • the patient can be a human male, eg an adult, but the treatment of other mammals (except rats) is also contemplated.
  • the products, doses and regimens of the invention may be in a form suitable for oral use (for example as tablets, capsules, aqueous or oily suspensions, emulsions or dispersible powders or granules), for topical use (for example as creams, ointments, gels, or aqueous or oily solutions or suspensions; for example for use within a transdermal patch), for parenteral administration (for example as a sterile aqueous or oily solution or suspension for intravenous, subcutaneous, intramuscular or intravascular dosing), or as a suppository for rectal dosing.
  • the compositions of the invention are in a form suitable for oral use, for example as tablets or capsules.
  • the products, doses and regimens of the invention may be obtained by conventional procedures using conventional pharmaceutically-acceptable diluents or carriers that are well known in the art.
  • Suitable pharmaceutically-acceptable diluents or carriers for a tablet formulation include, for example, inert diluents such as lactose, sodium carbonate, calcium phosphate or calcium carbonate, granulating and disintegrating agents such as corn starch or alginic acid; binding agents such as gelatin or starch; lubricating agents such as magnesium stearate, stearic acid or talc; preservative agents such as ethyl or propyl rj-hydroxybenzoate, and anti-oxidants, such as ascorbic acid.
  • Tablet formulations may be uncoated or coated either to modify their disintegration and the subsequent absorption of the active ingredient within the gastrointestinal tract, or to unprove their stability and/or appearance, in either case using conventional coating agents and procedures well known in the art.
  • Compositions for oral use may be in the form of hard gelatin capsules in which the active 5 ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules in which the active ingredient is mixed with water or an oil such as peanut oil, liquid paraffin or olive oil.
  • an inert solid diluent for example, calcium carbonate, calcium phosphate or kaolin
  • an oil such as peanut oil, liquid paraffin or olive oil.
  • CASODEXTM was administered daily at a dose of 150 mg and the ARIMIDEX TM was administered daily at a dose of 1 mg. All treatments were in tablet form and taken once daily. Daily treatment with CASODEX was for 6 weeks, and with ARIMIDEXTM for the final 2 weeks of this period. The treatment periods were selected as the minimum time to attain steady-state plasma concentrations for the drugs.
  • Day 1 samples were drawn before dosing, and therefore act as a baseline measurement.
  • CASODEX TM beyond the 4 th week, this figure would be expected to rise (corresponding to an approximate doubling of the mean total testosterone concentration).
  • Verhelst, J et al Enddocrine profiles during administration of the new non-steroidal anti-androgen Casodex in prostate cancer
  • Verhelst, J et al Clin. Endocnnol. (Oxf) 1994, Oct., 41(4), pp 525-30

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  • Health & Medical Sciences (AREA)
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  • General Health & Medical Sciences (AREA)
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Abstract

L'invention concerne un produit pharmaceutique, une dose quotidienne ou un schéma posologique, comprenant un anti-androgène et de l'anatrozole. L'anti-androgène est choisi dans flutamide, nilutamide, acétate de chlormadinone et cyprotérone, un sel ou un solvate de ceux-ci pharmaceutiquement acceptable. L'invention concerne également un procédé permettant d'obtenir un effet anti-androgène et l'inhibition de l'aromatase chez un patient, l'inhibition de l'aromatase se produisant sensiblement sans provoquer une augmentation supplémentaire des niveaux d'androgènes en circulation.
PCT/SE2001/001546 2000-07-05 2001-07-04 Combinaison pharmaceutique d'anti-androgene et d'anastrozole conçue pour produire un effet anti-androgene et une inhibition de l'aromatase WO2002002112A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU6800101A AU6800101A (en) 2000-07-05 2001-07-04 Pharmaceutical combination of an anti-androgen and anastrozole for providing an antiandrogenic effect and aromatase inhibition

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB0016427.7 2000-07-05
GB0016427A GB0016427D0 (en) 2000-07-05 2000-07-05 Pharmaceutical combination
GB0020769A GB0020769D0 (en) 2000-08-24 2000-08-24 Pharmaceutical combination
GB0020769.6 2000-08-24

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WO2002002112A1 true WO2002002112A1 (fr) 2002-01-10

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2102287A (en) * 1981-05-22 1983-02-02 Schering Ag Use of aromatase-inhibitors with antiandrogens for treatment of prostatic hyperplasia.
US4895715A (en) * 1988-04-14 1990-01-23 Schering Corporation Method of treating gynecomastia
WO1998003180A2 (fr) * 1996-07-22 1998-01-29 The Victoria University Of Manchester Utilisation de modulateurs de l'activite de steroides sexuels pour le traitement de plaies et d'etats pathologiques de type 'fibreux'
WO2001049294A1 (fr) * 1999-12-30 2001-07-12 Pharmacia Italia S.P.A. Produit pour le traitement de la gynecomastie

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2102287A (en) * 1981-05-22 1983-02-02 Schering Ag Use of aromatase-inhibitors with antiandrogens for treatment of prostatic hyperplasia.
US4895715A (en) * 1988-04-14 1990-01-23 Schering Corporation Method of treating gynecomastia
WO1998003180A2 (fr) * 1996-07-22 1998-01-29 The Victoria University Of Manchester Utilisation de modulateurs de l'activite de steroides sexuels pour le traitement de plaies et d'etats pathologiques de type 'fibreux'
WO2001049294A1 (fr) * 1999-12-30 2001-07-12 Pharmacia Italia S.P.A. Produit pour le traitement de la gynecomastie

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
JEROME P. RICHIE: "Anti-androgens and other hormonal therapies for prostate cancer", UROLOGY, vol. 54, no. 6A, 1999, pages 15 - 18, XP002948184 *
R.C. COOMBES ET AL.: "Aromatase inhibitors and their use in the sequential setting", ENDOCRINE-RELATED CANCER, vol. 6, 1999, pages 259 - 263, XP002948183 *

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