WO1997003676A1 - Nouvelle formulation pharmaceutique de dehydroepiandrosterone pour application topique percutanee - Google Patents
Nouvelle formulation pharmaceutique de dehydroepiandrosterone pour application topique percutanee Download PDFInfo
- Publication number
- WO1997003676A1 WO1997003676A1 PCT/ES1996/000153 ES9600153W WO9703676A1 WO 1997003676 A1 WO1997003676 A1 WO 1997003676A1 ES 9600153 W ES9600153 W ES 9600153W WO 9703676 A1 WO9703676 A1 WO 9703676A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- formulation
- dehydroepiandrosterone
- glycolic
- dhea
- ingredients
- Prior art date
Links
- FMGSKLZLMKYGDP-USOAJAOKSA-N dehydroepiandrosterone Chemical compound C1[C@@H](O)CC[C@]2(C)[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CC=C21 FMGSKLZLMKYGDP-USOAJAOKSA-N 0.000 title claims abstract description 10
- FMGSKLZLMKYGDP-UHFFFAOYSA-N Dehydroepiandrosterone Natural products C1C(O)CCC2(C)C3CCC(C)(C(CC4)=O)C4C3CC=C21 FMGSKLZLMKYGDP-UHFFFAOYSA-N 0.000 title claims abstract description 9
- 229960002847 prasterone Drugs 0.000 title claims abstract description 9
- 230000000699 topical effect Effects 0.000 title claims description 5
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 4
- 238000009472 formulation Methods 0.000 claims abstract description 22
- 239000000203 mixture Substances 0.000 claims abstract description 22
- 239000000499 gel Substances 0.000 claims abstract description 15
- RJKFOVLPORLFTN-LEKSSAKUSA-N Progesterone Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](C(=O)C)[C@@]1(C)CC2 RJKFOVLPORLFTN-LEKSSAKUSA-N 0.000 claims abstract description 12
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 claims abstract description 6
- 229960005309 estradiol Drugs 0.000 claims abstract description 6
- 229930182833 estradiol Natural products 0.000 claims abstract description 6
- 239000004615 ingredient Substances 0.000 claims abstract description 6
- 239000000186 progesterone Substances 0.000 claims abstract description 6
- 229960003387 progesterone Drugs 0.000 claims abstract description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229920002907 Guar gum Polymers 0.000 claims abstract description 3
- 108010003272 Hyaluronate lyase Proteins 0.000 claims abstract description 3
- 102000001974 Hyaluronidases Human genes 0.000 claims abstract description 3
- 239000001913 cellulose Substances 0.000 claims abstract description 3
- 229920002678 cellulose Polymers 0.000 claims abstract description 3
- 239000000665 guar gum Substances 0.000 claims abstract description 3
- 229960002154 guar gum Drugs 0.000 claims abstract description 3
- 235000010417 guar gum Nutrition 0.000 claims abstract description 3
- 229960002773 hyaluronidase Drugs 0.000 claims abstract description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims description 8
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 8
- 239000000284 extract Substances 0.000 claims description 7
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims description 4
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims description 4
- 241000723346 Cinnamomum camphora Species 0.000 claims description 4
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 claims description 4
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 4
- ZFMITUMMTDLWHR-UHFFFAOYSA-N Minoxidil Chemical compound NC1=[N+]([O-])C(N)=CC(N2CCCCC2)=N1 ZFMITUMMTDLWHR-UHFFFAOYSA-N 0.000 claims description 4
- 229920002125 Sokalan® Polymers 0.000 claims description 4
- 229930003268 Vitamin C Natural products 0.000 claims description 4
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- 229960000846 camphor Drugs 0.000 claims description 4
- 229930008380 camphor Natural products 0.000 claims description 4
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 claims description 4
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- 229940041616 menthol Drugs 0.000 claims description 4
- 229960003632 minoxidil Drugs 0.000 claims description 4
- 235000019154 vitamin C Nutrition 0.000 claims description 4
- 239000011718 vitamin C Substances 0.000 claims description 4
- 235000019165 vitamin E Nutrition 0.000 claims description 4
- 229940046009 vitamin E Drugs 0.000 claims description 4
- 239000011709 vitamin E Substances 0.000 claims description 4
- 235000002566 Capsicum Nutrition 0.000 claims description 3
- 240000008574 Capsicum frutescens Species 0.000 claims description 3
- 244000146462 Centella asiatica Species 0.000 claims description 3
- 235000004032 Centella asiatica Nutrition 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 3
- 230000002280 anti-androgenic effect Effects 0.000 claims description 3
- 239000000051 antiandrogen Substances 0.000 claims description 3
- 229940030495 antiandrogen sex hormone and modulator of the genital system Drugs 0.000 claims description 3
- 239000001390 capsicum minimum Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 230000002666 vasoprotective effect Effects 0.000 claims description 3
- 235000008694 Humulus lupulus Nutrition 0.000 claims description 2
- 240000006661 Serenoa repens Species 0.000 claims description 2
- 235000005318 Serenoa repens Nutrition 0.000 claims description 2
- 229960000978 cyproterone acetate Drugs 0.000 claims description 2
- UWFYSQMTEOIJJG-FDTZYFLXSA-N cyproterone acetate Chemical compound C1=C(Cl)C2=CC(=O)[C@@H]3C[C@@H]3[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(C)=O)(OC(=O)C)[C@@]1(C)CC2 UWFYSQMTEOIJJG-FDTZYFLXSA-N 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
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- 239000008280 blood Substances 0.000 description 3
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- 229940011871 estrogen Drugs 0.000 description 3
- 239000000262 estrogen Substances 0.000 description 3
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- CZWCKYRVOZZJNM-UHFFFAOYSA-N Prasterone sodium sulfate Natural products C1C(OS(O)(=O)=O)CCC2(C)C3CCC(C)(C(CC4)=O)C4C3CC=C21 CZWCKYRVOZZJNM-UHFFFAOYSA-N 0.000 description 2
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- CZWCKYRVOZZJNM-USOAJAOKSA-N dehydroepiandrosterone sulfate Chemical compound C1[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CC=C21 CZWCKYRVOZZJNM-USOAJAOKSA-N 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
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- 201000002282 venous insufficiency Diseases 0.000 description 2
- DNXHEGUUPJUMQT-UHFFFAOYSA-N (+)-estrone Natural products OC1=CC=C2C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 DNXHEGUUPJUMQT-UHFFFAOYSA-N 0.000 description 1
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- DNXHEGUUPJUMQT-CBZIJGRNSA-N Estrone Chemical compound OC1=CC=C2[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 DNXHEGUUPJUMQT-CBZIJGRNSA-N 0.000 description 1
- 241001466453 Laminaria Species 0.000 description 1
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 1
- 239000000006 Nitroglycerin Substances 0.000 description 1
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/06—Preparations for care of the skin for countering cellulitis
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- 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
- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
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- A61K31/565—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol
- A61K31/568—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol substituted in positions 10 and 13 by a chain having at least one carbon atom, e.g. androstanes, e.g. testosterone
- A61K31/5685—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids not substituted in position 17 beta by a carbon atom, e.g. estrane, estradiol substituted in positions 10 and 13 by a chain having at least one carbon atom, e.g. androstanes, e.g. testosterone having an oxo group in position 17, e.g. androsterone
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- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
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- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
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- A61K8/04—Dispersions; Emulsions
- A61K8/042—Gels
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
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Definitions
- the present invention falls within the technical field of hormonal therapy for the maintenance of certain vital functions that deteriorate with age or the treatment of various metabolic or degenerative diseases. More specifically, the present invention relates to a new form of presentation of dehydropediandrosterone (DHEA) intended for percutaneous topical application.
- DHEA dehydropediandrosterone
- DHEA Dehydroepiandrosterone
- the present invention refers to a new pharmaceutical formulation of dehydroepiandrosterone intended for percutaneous topical application.
- the applicant has been able to verify, after his investigations, that steroid hormones and, in particular, dehydroepiandrosterone are well absorbed topically, fundamentally, percutaneously. Therefore, as a result of this finding, the inventors propose a new form of pharmaceutical presentation of dehydroe ⁇ piandrosterone, as a gel, emulsion or solution intended for percutaneous application.
- This type of application allows to reach, in blood, the most convenient levels for each problem (either replenish the physiological levels of other phases of life or raise them).
- the formulation may comprise, in addition to ingredients (a) and (b) other hydrophilic gels, selected from glycolic, hydro-glycolic, hydroglycerolate, hydroalcoholic and hydropropylene glycol in similar proportions of 0.5-2% carbopol and other ingredients assets selected from 0.02-0.1% estradiol, 0.05-1% Vitamin E, 0.1-5% Vitamin C, 2-5% progesterone, 1-3% minoxidil, 0, 1-2% of tricosaccharides and tricopeptides, 0.1-5% of xanthic bases, 0.1-20% of iodinated products, 100-2000 U% of hyaluronidase, 0.1-12% of vasoprotective and capillary agents , 0.1-2% dinitrilesuccinic, 0.1-5% glycolic and hydroalcoholic extracts of capsicum and arnica, 0.1-0.75% camphor,
- the formulation of the invention can be presented in any form suitable for percutaneous application, such as gel, emulsion, lotion, ointment, paste, dermal diffusion patch, etc.
- the formulation is applied in a predetermined amount by rubbing over an area of the skin with good circulation (preferably the arms, forearms, abdomen, etc.) 1 to 3 times a day.
- the optional active ingredients depend on the type of final utility that is intended to be given to the formulation.
- DHEA In controlling the disorders of the female menstrual cycle and as a preventive of breast and gynecological malignancies, DHEA will be associated, in any of the ways described above, with estrogens (mainly estradiol, estrone and its derivatives) with a concentration of estradiol or equivalent of 0.02-0.1%. This neutralizes some of the negative effects of estrogen itself.
- estrogens mainly estradiol, estrone and its derivatives
- these preparations will be associated with Vitamin E (between 0.05 and 1%) and / or Vitamin C (between 0, one and 5%).
- DHEA can be associated with Progesterone (between 2-5%) and / or with Minoxidil (between 1 and 3%), as well as with Tricosaccharides and tricopeptides (0.1-2%) for hair maintenance.
- DHEA is associated with vasoprotective and capillary agents, both synthetic and naturally occurring (flavonoids, biflavonoids, anthocyanosides, procyanidoles and steroidal saponosides), especially glycolic and hydroalcocholic citrides (citrides) ) between 0.1-12%, the glycolic and alcoholic extracts of Ginko Biloba, between 0.1-15%, the glycolic and alcoholic extracts of Black and Red Currant, of Black Mirtilo and Red Vine between 0 , 1-15%.
- DHEA can be associated with vesicant and rubefacient substances for topical therapies derived from congestion, hyperemias, bruises and muscle aches glycolic and hydroalcoholic extracts of capsicum and arnica between 0.1-5%; Camphor between 0.1-0.75%) and that of these substances with antipruritic substances (menthol, 0.01-0.5%, and glycolic and hydro-glycolic extract of Centella Asiatica, between 0.1-5% ).
- DHEA can be associated with the natural (1-15%) or synthetic (0.1-5%) antiandrogens indicated above.
- DHEA could be associated with any combination of the substances described in the previous sections.
- This formulation can also be applied by dermal diffusion patches.
- EXAMPLE 1 This Example illustrates various formulations according to the present invention, indicating the amounts of active ingredients used and the application to which they were intended: Formulation 1 DHEA 3%
- Tricopeptides 1% This formulation is useful for the maintenance of axillary hair and hair as well as the treatment of certain forms of alopecia.
- This formulation is useful for the treatment of congestion, hyperemias, bruises and muscle aches.
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Abstract
La nouvelle formulation comprend: (a) 0,1 à 5 % en poids de déhydroepiandrostérone; (b) 0,5-3 % d'un gel acrylique, 1-3 % de gomme guar ou 1-3 % d'un gel dérivé de cellulose; et, éventuellement, d'autres ingrédients tels que des gels hydrophiles, un estradiol, des vitamines, la progestérone, le minoxydile, des bases xantiques, une hyaluronidase, des vasoprotecteurs, des extraits de plantes, etc. La formulation a diverses applications pharmacologiques, par exemple pour le traitement de troubles de la menstruation chez la femme, des néoplasies mammaires et gynécologiques, des lipodystrophies, des paniculopathies et des troubles circulatoires, des contusions, des douleurs musculaires, l'obésité, le diabète, l'ostéoporose, le vieillissement, etc.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU64196/96A AU6419696A (en) | 1995-07-21 | 1996-07-19 | Novel pharmaceutical formulation of dehydroepiandrosterone for percutaneous topical application |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES9501471A ES2098193B1 (es) | 1995-07-21 | 1995-07-21 | Nueva formulacion farmaceutica de dehidroepiandrosterona para aplicacion topica percutanea. |
ESP9501471 | 1995-07-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997003676A1 true WO1997003676A1 (fr) | 1997-02-06 |
Family
ID=8291123
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/ES1996/000153 WO1997003676A1 (fr) | 1995-07-21 | 1996-07-19 | Nouvelle formulation pharmaceutique de dehydroepiandrosterone pour application topique percutanee |
Country Status (3)
Country | Link |
---|---|
AU (1) | AU6419696A (fr) |
ES (1) | ES2098193B1 (fr) |
WO (1) | WO1997003676A1 (fr) |
Cited By (28)
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WO1999048502A1 (fr) * | 1998-03-24 | 1999-09-30 | Universidad Miguel Hernandez | UTILISATION DU 17β ESTRADIOL, DE SES ANALOGUES ET DE SES DERIVES DANS LE TRAITEMENT DU DIABETE SUCRE ET SES MANIFESTATIONS |
EP0963201A1 (fr) * | 1996-07-12 | 1999-12-15 | Carolyn V. Shaak | Application transdermique d'hormones stero diennes d'origine naturelle |
WO1999063973A2 (fr) * | 1998-06-11 | 1999-12-16 | Endorecherche, Inc. | COMPOSITIONS PHARMACEUTIQUES ET UTILISATIONS POUR L'ANDROST-5-ENE-3β,17β-DIOL |
WO2001019365A1 (fr) * | 1999-09-15 | 2001-03-22 | Roche Consumer Health Ag | Compositions pharmaceutiques et/ou cosmetiques |
EP1092423A2 (fr) * | 1999-10-13 | 2001-04-18 | L'oreal | Utilisation de la DHEA ou de ses précurseurs ou dérivés métaboliques comme dépigmentant |
WO2001070258A1 (fr) * | 2001-03-19 | 2001-09-27 | Santana, Cristiano, Alberto, Ribeiro | COMPOSITION PHARMACEUTIQUE POUR EXCIPIENT POUR PRODUITS A BASE DE VITAMINE E, DE BROMELINE ET D'HYALURONIDASE |
EP1172094A1 (fr) * | 2000-07-13 | 2002-01-16 | L'oreal | Composition, notamment cosmétique, comprenant la DHEA et/ou un précurseur ou dérivé, et au moins un composé augmentant la synthèse des glycosaminoglycanes |
FR2811562A1 (fr) * | 2000-07-13 | 2002-01-18 | Oreal | Composition, notamment cosmetique, renfermant la dhea et un isoflavonoide |
FR2811567A1 (fr) * | 2000-07-13 | 2002-01-18 | Oreal | Composition, notamment cosmetique, comprenant la dhea et/ou un precurseur ou derive de celle-ci, en association avec au moins un inhibiteur de no-synthase |
EP1189619A1 (fr) * | 1999-06-11 | 2002-03-27 | Watson Pharmaceuticals, Inc. | Administration de steroides androgenes non oraux aux femmes |
WO2002034230A1 (fr) * | 2000-10-26 | 2002-05-02 | L'oreal | Composition cosmetique renfermant la dhea et un agent anti-irritant |
WO2002047631A1 (fr) * | 2000-12-15 | 2002-06-20 | L'oreal | Composition, notamment cosmetique, renfermant la 7-hydroxy dhea et/ou la 7-ceto dhea et au moins un isoflavonoïde |
WO2002047647A1 (fr) * | 2000-12-15 | 2002-06-20 | L'oreal | Composition renfermant la 7-hydroxy dhea et/ou la 7-ceto dhea et au moins un agent depigmentant |
WO2002047655A1 (fr) * | 2000-12-15 | 2002-06-20 | L'oreal | Composition, notamment cosmetique, comprenant la 7-hydroxy dhea et/ou la 7-ceto dhea et au moins un inhibiteur de no-synthase |
FR2847475A1 (fr) * | 2002-11-25 | 2004-05-28 | Oreal | COMPOSITION COSMETIQUE OU PHARMACEUTIQUE ASSOCIANT UN AGENT MODULATEUR DE L'EXPRESSION DE L'OXYSTEROL 7alpha-HYDROXYLASE ET UN SUBSTRAT BIOLOGIQUE DE LADITE ENZYME |
WO2005102372A1 (fr) * | 2004-04-26 | 2005-11-03 | Obschestvo S Ogranichennoi Otvetstvennostyu 'rusgen' | Compositions de correction de changements du systeme endocrinien humain dus a l'age et procede de fabrication d'une forme pharmaceutique sur la base de ces compositions |
US6994864B2 (en) | 2000-12-15 | 2006-02-07 | L'oreal | Composition containing 7-hydroxy DHEA and/or 7-keto DHEA and at least a carotenoid |
US7198801B2 (en) | 2000-08-03 | 2007-04-03 | Antares Pharma Ipl Ag | Formulations for transdermal or transmucosal application |
US7354956B2 (en) | 2002-04-12 | 2008-04-08 | L'oreal | Composition containing a sapogenin and use thereof |
US7404965B2 (en) | 2000-08-03 | 2008-07-29 | Antares Pharma Ipl Ag | Composition for transdermal and/or transmucosal administration of active compounds that ensures adequate therapeutic levels |
US7425340B2 (en) | 2004-05-07 | 2008-09-16 | Antares Pharma Ipl Ag | Permeation enhancing compositions for anticholinergic agents |
US7442369B1 (en) | 2000-08-09 | 2008-10-28 | Mcneil Ab | Compositions of minoxidil |
US8268346B2 (en) | 2006-04-21 | 2012-09-18 | Antares Pharma Ipl Ag | Methods of treating hot flashes with formulations for transdermal or transmucosal application |
US8338400B2 (en) | 2005-05-27 | 2012-12-25 | Antares Pharma Ipl Ag | Methods and apparatus for transdermal or transmucosal application of testosterone |
US8652491B2 (en) | 2000-08-03 | 2014-02-18 | Antares Pharma Ipl Ag | Transdermal compositions for anticholinergic agents |
US8980309B2 (en) | 2003-10-10 | 2015-03-17 | Antares Pharma Ipl Ag | Transdermal testosterone formulation for minimizing skin residues |
US9320744B2 (en) | 2011-10-19 | 2016-04-26 | Dhea Llc | DHEA bioadhesive controlled release gel |
US11324690B2 (en) | 2019-02-12 | 2022-05-10 | Dawn Marie Cutillo | Composition for restorative vaginal lubrication and a method of use thereof |
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MX350336B (es) | 2011-12-29 | 2017-09-04 | Univ Chile | Anillo vaginal que comprende dhea o dhea sulfato y opcionalmente un agente modulador de la liberacion del principio activo, util para aumentar la reserva ovarica en mujeres y para aliviar sintomas asociados a la menopausia. |
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JPS60161912A (ja) * | 1984-02-01 | 1985-08-23 | Kanebo Ltd | 皮膚化粧料 |
US4542129A (en) * | 1982-08-16 | 1985-09-17 | Norman Orentreich | DHEA Formulations and methods for treating dry skin |
US4628052A (en) * | 1985-05-28 | 1986-12-09 | Peat Raymond F | Pharmaceutical compositions containing dehydroepiandrosterone and other anesthetic steroids in the treatment of arthritis and other joint disabilities |
WO1994016709A2 (fr) * | 1993-01-19 | 1994-08-04 | Endorecherche Inc. | Procedes therapeutiques et systemes d'apport de deshydroepiandrosterone |
-
1995
- 1995-07-21 ES ES9501471A patent/ES2098193B1/es not_active Expired - Fee Related
-
1996
- 1996-07-19 WO PCT/ES1996/000153 patent/WO1997003676A1/fr active Application Filing
- 1996-07-19 AU AU64196/96A patent/AU6419696A/en not_active Abandoned
Patent Citations (4)
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US4542129A (en) * | 1982-08-16 | 1985-09-17 | Norman Orentreich | DHEA Formulations and methods for treating dry skin |
JPS60161912A (ja) * | 1984-02-01 | 1985-08-23 | Kanebo Ltd | 皮膚化粧料 |
US4628052A (en) * | 1985-05-28 | 1986-12-09 | Peat Raymond F | Pharmaceutical compositions containing dehydroepiandrosterone and other anesthetic steroids in the treatment of arthritis and other joint disabilities |
WO1994016709A2 (fr) * | 1993-01-19 | 1994-08-04 | Endorecherche Inc. | Procedes therapeutiques et systemes d'apport de deshydroepiandrosterone |
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Title |
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CHEMICAL ABSTRACTS, vol. 104, no. 2, 13 January 1986, Columbus, Ohio, US; abstract no. 10399s, KANEBO LTD.: "Cosmetics containing dehydroepiandrosterone" XP002018211 * |
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Also Published As
Publication number | Publication date |
---|---|
AU6419696A (en) | 1997-02-18 |
ES2098193B1 (es) | 1997-12-01 |
ES2098193A1 (es) | 1997-04-16 |
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