AU2002231622A1 - Oral compositions for the treatment of scalp disorders - Google Patents
Oral compositions for the treatment of scalp disordersInfo
- Publication number
- AU2002231622A1 AU2002231622A1 AU2002231622A AU2002231622A AU2002231622A1 AU 2002231622 A1 AU2002231622 A1 AU 2002231622A1 AU 2002231622 A AU2002231622 A AU 2002231622A AU 2002231622 A AU2002231622 A AU 2002231622A AU 2002231622 A1 AU2002231622 A1 AU 2002231622A1
- Authority
- AU
- Australia
- Prior art keywords
- extract
- pharmaceutical
- treatment
- cosmetic compositions
- zinc
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
Description
ORAL COMPOSITIONS FOR THE TREATMENT OF SCALP DISORDES
The present invention relates to pharmaceutical and/or cosmetic oral compositions for the treatment and the prevention of disorders of the scalp, containing ingredients of vegetable origin.
More particularly, the present invention relates to pharmaceutical and/or cosmetic oral compositions for the treatment and the prevention of disorders of the scalp, containing as active components extracts of Serenoa repens and of Vitis vinifera.
Dandruff, seborrhea and hair loss or alopecia are among the most common disorders of the scalp. A number of studies have proved that androgenetic alopecia is a physiological process in genetically predisposed individuals, although its very high frequency, in particular in Caucasians, makes any attempt to establish the heritability mode difficult. Although such heritability is strongly autosomic, the number of the involved genes has not yet been established. There is evidence of the relationship between androgens and development of androgenetic alopecia: for example, pattern baldness is related with reduced time in hair anagen growth phase, and androgens are known to induce shorter anagen growth phases in scalp hair follicles, which become finer and thinner. Tissue androgens, testosterone and more potent dihydrotestosterone (DHT), can reach the skin through blood circulation or can be locally produced in hair follicles and sebaceous glands by specific enzymes in the steroid cascade. The kinetic constants of a number of enzymes which mediate the formation of DHT, 5-alpha-reductase included, in hair follicles and sebaceous glands of human hair from scalps of man and women
affected with androgenetic alopecia have been evaluated; furthermore, androgen receptors specifically binding DHT have been identified in sebocytes and human hair.
Recently, binding studies showed that the dermal papilla of hair follicles of balding subjects contains more androgen receptors than that of normal subjects. As a consequence of this hormone pathway, abnormal sebum secretion may occur, which in turn induces further worsening of baldness as well as overproduction of sebum and dandruff.
Two isoforms of 5-alpha-reductase are known: type 1 and type 2. Prostate contains the type 2 isoenzyme, whereas skin and cutaneous appendages (hair and sebaceous glands) contain both type 1 and type 2. Finasteride, a type 2 5-alpha-reductase inhibitor originally used for the therapy of prostate hyperplasy, revealed active also in the treatment of androgenetic alopecia; furthermore, a relationship between baldness seriousness and benign prostate hyperplasy seriousness has been observed.
In addition to 5-alpha-reductase, also oxidative stress (pollution, atmospheric agents and the like) and poor intake of oligoelements and sulfated amino acids (such as methionine, cysteine and cystine) through diet adversely affect the hair. The numerous pharmaceutical or cosmetic formulations for the treatment of dandruff and alopecia at present commercially available have not yet satisfactorily solved these problems.
It has now been found, and this is the object of the present invention, that pharmaceutical and/or cosmetic oral formulations containing a combination of active principles of vegetable origin induce excellent results in the treatment of scalp disorders, in particular alopecia and dandruff, as a result of the combination of the different activities of the various components, which exert, inter alia, antiandrogenic, antiradicalic, antiaging activities.
The compositions of the invention act on the factors which contribute to the development of said scalp disorders, in particular on androgens, oxidative stress, oligoelements and sulfated amino acids present in the diet.
More particularly, the present invention relates to oral pharmaceutical and/or cosmetic compositions containing: a) extract of Serenoa repens, b) standardized extract of Vitis vinifera, in the free form and/or as phospholipid complexes.
The components of the compositions of the present invention are all known and used in the pharmaceutical and/or in cosmetic fields. However, it should be noted that the single components, when used separately, exert by far lower activity than that obtained with the compositions of the present invention, in which the various components have been found to exert a synergistic effect of in the prevention and treatment of scalp disorders. a) The extract of Serenoa repens is a vegetable remedy effective in benign prostate hyperplasy due to its antiandrogenic action. This product contains a specific mixture of fatty acids extracted from the plant by means of C02 in supercritical conditions, as disclosed in EP 250,953, and when tested "in vitro" on prostate isolated cells, it revealed strong affinity to androgen receptors, as demonstrated by displacement with radiolabelled 3H- methyltrienolone . b) The extract of Vitis vinifera, disclosed in GB 1,541,469, includes gallic acid, as well as catechin and epicatechin monomers, dimers, trimers, tetramers, pentamers, hexamers and heptamers in the free form or esterified as gallates. Extensive searches proved its many properties: a) strong, complete antioxidant profile which allow to remove the more reactive radicals, thereby counteracting all the phenomena related to free radicals activity; b) ability to inhibit xanthine-oxidase and to chelate Cu++ and Fe++, thus preventing the
enzymatic release of free radicals into tissues; c) ability to inhibit collagenase, hyaluronidase, elastase and beta-glucuronidase, thus protecting blood vessels and connective tissue against the damages caused by proteolytic enzymes released following UV radiations, oxidative stress and during the development of the inflammatory response.
As mentioned above, the extract of Vitis vinifera may also be present in the form of phospholipid complexes as disclosed in US 4,963,527.
The compositions of the present invention may optionally contain, in addition to the above stated components, further ingredients having useful or anyway complementary actions, for example oligoelements, such as zinc, copper, iron, selenium, magnesium; amino acids, such as L-lysine, L-proline,
L-hydroxyproline, L-leucine, L-isoleucine, L-methionine, L-cysteine,
L-cystine; vitamins, such as the vitamins B complex, vitamin E and vitamin C.
The compositions of the invention will be formulated in oral dosage forms, according to conventional techniques, as described, for example, in
"Remington: The Science and Practice of Pharmacy", Lippincott, Williams and Wilkins Eds, Dec. 2000). Said compositions may be in the form of tablets, capsules, oral preparations, powders, granules, lozenges, powders for reconstitution, injectable solutions or suspensions, and liquids for infusions or suppositories.
Tablets and capsules for the oral administration will usually be presented in the form of unitary dosage, and will contain conventional excipients such as binders, diluents, tabletting agents, lubricants, disinte grants, dyes, flavors and wetting agents. Tablets may be coated according to methods well known in the art.
According to an embodiment of the invention, the compositions will be presented in the form of two capsules for the simultaneous administration, one containing the extracts of the invention and the other containing the
oligoelements mentioned above.
The oral liquid preparations may, for example, be in the form of aqueous or oily solutions or suspensions, emulsions, syrup or elixir, or dry products for reconstitution with water or other suitable carrier before use. Said liquid preparations may contain conventional excipients such as suspending agents, emulsifiers, non aqueous carriers, preservatives, flavors or dyes.
The compositions of the present invention will be used in such dosage forms as to provide a components daily intake within the following ranges: a) standardized extract of Serenoa repens (40-320 mg/day); b) standardized extract of Vitis vinifera in the free form and/or as phospholipid complexes (50 - 300 mg/day and 150 - 900 mg day, respectively).
The oligoelements can be present in such amounts as to provide a daily intake of 0.1 to 100 mg. The compositions of the invention revealed effective in the treatment of scalp disorders, with beneficial effects on trichogram, dandruff, seborrhea and baldness, and in the prevention of said disorders, ensuring healthy hair.
The results of the pharmacological tests are reported in the following. Effect on Dandruff, Sebum Production And Hair Loss 60 subjects with dandruff (scaling of the scalp skin) were randomized in four groups. The first received with one capsule prepared according to Example 1 daily for 8 weeks. Evaluations were carried out immediately before starting the treatment, at the end of the treatment (after 8 weeks) and 4 weeks after interrupting the treatment (follow-up). The second group received placebo under the same experimental conditions. The third and the fourth groups received 25 and 80 mg of extracts of Vitis vinifera and Serenoa repens, respectively.
The results reported in Table 1 evidence that after 8 weeks of treatment
the number of desquamated cells (evaluated according to Mac Ginley et al. J. Invest. Dermatol. 53,107,1969) was reduced from 85 to 18 cells/cm2. The number of desquamated cells was still significantly reduced after 4 weeks of follow-up (21 cells/cm^).
Table 1- MAC GINLEY COUNT (cells/cm2)
The results reported in Table 2 prove that the treatment with the capsules of the invention significantly reduces the mean value of scalp sebum from 105 to 92 U.S. (U.S. = arbitrary Sebometric Units). It is particularly remarkable that the value of sebometric units is still significantly reduced (95 U.S.) even 4 weeks after the end of the treatment.
Table 2 - SEBOMETRY (U.S.)
The effect on hair loss was studied by trichogram evaluation, which consists in taking a sufficient number of hair (about 50) from the higher and antero-nucal frontal areas of each subject (Bosse K., Hautzart, 18, 35, 1967; Bosse K., Hautzart, 18, 218, 1967). The percentage of hair in anagen (growth), catagen (mature), or telogen (rest) phase was evaluated by microscope observation of each single hair shaft under the microscope. Any dystrophic
anagen condition, namely the phase in which hair have miniaturized shaft, has also been evaluated in this study. A percentage of hair in telogen phase higher than 10-15% (considered normal) is an index of a clinical pathologic condition of hair loss. The results reported in Table 3 evidence that after 8 week treatment with the capsules of the invention, increase in hair bulbs in anagen phase, decrease in the value of dystrophic anagen hair and, as a consequence, reduction of bulbs in telogen phase were observed. These results were still visible after 4 weeks of follow-up. It should be noted that in the placebo group the clinical situation both at the end of the treatment and after the 4 weeks of follow-up was diametrically opposed.
Table 3 - EFFECT ON HAIR LOSS
Effect on Seborrheic Dermatitis
40 subjects affected with seborrheic dermatitis of the scalp were randomized in two groups. The first group received a capsule prepared according to Example 1 daily for 8 weeks. Instrumental sebometric evaluation was carried out immediately before starting treatment, at the end of treatment (after 8 weeks), and 4 weeks after suspension of treatment (follow-up). The second group received placebo under the same experimental conditions. The
third and fourth groups received 25 and 80 mg of extracts of Vitis vinifera and Serenoa repens, respectively.
The results reported in Table 4 clearly show that treatment with the capsules of the invention significantly reduced scalp sebum mean value in subjects with seborrheic dermatitis, whose sebum values are above 200 U.S. (U.S. = arbitrary Sebometric Units). This value is still significantly low after 4 weeks of follow-up.
Table 4 - SEBOMETRY (U.S.)
Examples of the compositions according to the invention are reported in the following.
EXAMPLE 1 - HARD-GELATIN CAPSULES
Each 326 mg capsule contains:
Extract of Serenoa repens 50.0 mg Extract of Vitis vinifera extract 25.0 mg
L-cysteine 30.0 mg
L-histidine 30.0 mg
L-methionine 30.0 mg
D-calcium pantotenate 15.0 mg Zinc citrate (equivalent to 3 mg of zinc) 10.0 mg
Copper citrate (equivalent to 0.8 mg of copper) 2.3 mg
Beta-carotene 10% W.S. 4.3 mg (equivalent to 700 U.I. of vitamin A)
Colloidal silica 30.0 mg
(Aerosil 200 - DEGUSSA)
Microcrystalline cellulose 30.0 mg
(Avicel PH 101 - FMC)
Maltodextrin 30.0 mg
(Lycatab DSH - ROQUETTE)
Pregelatinized starch 21.9 mg
(Amido STA 1500 - COLORCON)
Cross-linked sodium carboxymethylcellulose 15.0 mg
(Ac-Of-Sol - FMC)
Magnesium stearate 2.5 mg
EXAMPLE 2 - HARD-GELATIN CAPSULES
Each 326 mg capsule contains:
Extract of Serenoa repens 80.0 mg
Extract of Vitis vinifera 25.0 mg
Soy polysaccharides 83.0 mg
(Emcosoy - MENDELL)
D-calcium pantotenate 15.0 mg
Zinc gluconate (equivalent to 3 mg of zinc) 23.84 mg
Copper gluconate (equivalent to 0.8 mg of copper) 5.7 mg
Colloidal silica 6.2 mg
(aerosil 200 - DEGUSSA)
Microcrystalline cellulose 30.0 mg
(Avicel PHI 01 - FMC)
Pregelatinized starch 72.0 mg
(STA1500 starch - COLORCORN)
Magnesium stearate 2.5 mg
Claims (11)
1. Pharmaceutical and/or cosmetic oral compositions containing the following ingredients of vegetable origin: a) extract of Serenoa repens, b) extract of Vitis vinifera, in the free form and/or as phospholipid complexes, in combination with conventional excipients and carriers.
2. Pharmaceutical and/or cosmetic oral compositions as claimed in claim 1, further containing additional active ingredients selected from the group consisting of oligoelements, such as zinc, copper, iron, selenium, magnesium; amino acids, such as L-lysine, L-proline, L-hydroxyproline, L-leucine, L- isoleucine, L-methionine, L-cysteine, L-cystine; vitamins, such as the vitamins B complex, vitamin E and vitamin C.
3. Pharmaceutical and/or cosmetic compositions as claimed in claim 2, wherein the additional active ingredients are present in such amounts as to provide a daily intake from 0.1 to 100 mg.
4. Pharmaceutical and/or cosmetic compositions as claimed in the above claims, in the form of hard- gelatin capsules, containing: extract of Serenoa repens 50.0 mg extract of Vitis vinifera 25.0 mg
L-cysteine 30.0 mg
L-histidine 30.0 mg
L-methionine 30.0 mg D-calcium pantotenate 15.0 mg
Zinc citrate (equivalent to 3 mg of zinc) 10.0 mg
Copper citrate (equivalent to 0.8 mg of copper) 2.3 mg
Beta-carotene 10% W.S. 4.3 mg (equivalent to 700 U.I. of vitamin A)
Colloidal silica 30.0 mg
(Aerosil 200 - DEGUSSA)
Microcrystalline cellulose 30.0 mg (Avicel PH 101 - FMC)
Maltodextrin 30.0 mg
(Lycatab DSH - ROQUETTE)
Pregelatinized starch 21.9 mg
(Amido STA 1500 - COLORCON) Cross-linked sodium carboxymethylcellulose 15.0 mg
(Ac-Of-Sol - FMC)
Magnesium stearate 2.5 mg
5. Pharmaceutical and/or cosmetic compositions as claimed in the above claims, in the form of hard-gelatin capsules, containing: extract of Serenoa repens 80.0 mg extract of Vitis vinifera 25.0 mg
Soy polysaccharides 83.0 mg
(Emcosoy - MENDELL)
D-calcium pantotenate 15.0 mg Zinc gluconate (equivalent to 3 mg of zinc) 23.84 mg
Copper gluconate (equivalent to 0.8 mg of copper) 5.7 mg
Colloidal silica 6.2 mg
(aerosil 200 - DEGUSSA)
Microcrystalline cellulose 30.0 mg (Avicel PHlOl - FMC)
Pregelatinized starch 72.0 mg
(STA1500 starch - COLORCORN)
Magnesium stearate 2.5 mg
6. Pharmaceutical and/or cosmetic compositions as claimed in the above claims, in the form of two separate capsules for the simultaneous administration, one capsule containing: a) extract of Serenoa repens; and b) extract of Vitis vinifera in the free form and/or as phospholipid complexes; the other capsule containing the oligoelements, amino acids and vitamins as claimed in claim 2.
7. The use of: a) extract of Serenoa repens; b) extract of Vitis vinifera in the free form and/or as phospholipid complexes; for the preparation of pharmaceutical and/or cosmetic compositions for the treatment and the prevention of scalp disorders.
8. The use of: a) extract f Serenoa repens; b) extract of Vitis vinifera in the free form and/or as complexes with phospholipids; in combination with additional active ingredients selected from the group consisting of oligoelements, such as zinc, copper, iron, selenium, magnesium; amino acids, such as L-lysine, L-proline, L-hydroxyproline, L- leucine, L-isoleucine, L-methionine, L-cysteine, L-cystine; vitamins, such as the vitamins B complex, vitamin E and vitamin C, for the preparation of pharmaceutical and/or cosmetic compositions for the treatment and the prevention of scalp disorders.
9. The use of the cosmetic compositions as claimed in any one of the above claims, for the treatment and the prevention of scalp disorders.
10. The use of the cosmetic compositions as claimed in claim 9 for the treatment of alopecia and/or dandruff and/or seborrhea.
11. The use of the pharmaceutical and/or cosmetic compositions as claimed in claim 9 for the treatment of seborrheic dermatitis.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITMI2001A001732 | 2001-08-07 | ||
IT2001MI001732A ITMI20011732A1 (en) | 2001-08-07 | 2001-08-07 | ORAL PHARMACEUTICAL AND / OR COSMETIC COMPOSITIONS FOR THE TREATMENT AND PREVENTION OF HAIR LESS DISORDERS |
PCT/EP2001/013188 WO2003013561A1 (en) | 2001-08-07 | 2001-11-14 | Oral compositions for the treatment of scalp disorders |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2002231622A1 true AU2002231622A1 (en) | 2003-06-19 |
AU2002231622B2 AU2002231622B2 (en) | 2007-01-18 |
Family
ID=11448250
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2002231622A Ceased AU2002231622B2 (en) | 2001-08-07 | 2001-11-14 | Oral compositions for the treatment of scalp disorders |
Country Status (25)
Country | Link |
---|---|
US (1) | US7201931B2 (en) |
EP (1) | EP1414473B1 (en) |
JP (1) | JP4988146B2 (en) |
KR (1) | KR100846888B1 (en) |
CN (1) | CN1294956C (en) |
AT (1) | ATE318610T1 (en) |
AU (1) | AU2002231622B2 (en) |
BR (1) | BR0117098A (en) |
CA (1) | CA2456519C (en) |
CZ (1) | CZ300110B6 (en) |
DE (1) | DE60117606T2 (en) |
DK (1) | DK1414473T3 (en) |
ES (1) | ES2258563T3 (en) |
HK (1) | HK1067559A1 (en) |
HU (1) | HU228648B1 (en) |
IL (2) | IL160232A0 (en) |
IT (1) | ITMI20011732A1 (en) |
MX (1) | MXPA04001107A (en) |
NO (1) | NO331412B1 (en) |
PL (1) | PL203133B1 (en) |
PT (1) | PT1414473E (en) |
RU (1) | RU2274470C2 (en) |
SI (1) | SI1414473T1 (en) |
SK (1) | SK287743B6 (en) |
WO (1) | WO2003013561A1 (en) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10260955A1 (en) * | 2002-12-20 | 2004-07-08 | Henkel Kgaa | Use of steroid sulfatase inhibitors to reduce hair loss |
DE502004011865D1 (en) | 2003-05-09 | 2010-12-23 | Scheller Cosmetics Ag Dr | A preparation for the prevention and treatment of acne containing zinc gluconate and copper gluconate |
FR2871061B1 (en) * | 2004-06-04 | 2007-08-10 | Coletica Sa | ACTIVE PRINCIPLE CAPABLE OF INDUCING TRANSFORMATION FROM INACTIVE TGBF-LATENT TO ACTIVE TGFB |
US7897800B2 (en) * | 2006-02-03 | 2011-03-01 | Jr Chem, Llc | Chemical compositions and methods of making them |
JP5181486B2 (en) * | 2006-02-16 | 2013-04-10 | 大正製薬株式会社 | Oral composition containing zinc compound |
JP2007246509A (en) * | 2006-02-16 | 2007-09-27 | Taisho Pharmaceut Co Ltd | Oral composition compounded with copper compound |
KR101277530B1 (en) * | 2007-01-26 | 2013-06-21 | 주식회사 엘지생활건강 | Composition for scalp-care before haircoloring |
DE102008012988A1 (en) | 2008-03-07 | 2009-09-10 | S.W. Patentverwertungs Ltd. | Composition and uses for influencing hair growth |
EP2158906A1 (en) * | 2008-08-28 | 2010-03-03 | ProxiPHARM GmbH | Composition for the treatment of alopecia |
KR101106723B1 (en) * | 2009-08-12 | 2012-01-18 | 박용현 | One body type screen and projector frame moving apparatus |
FR2954124B1 (en) * | 2009-12-18 | 2012-04-06 | Fabre Pierre Dermo Cosmetique | USE OF 2,3-DIHYDROXYPROPYL DODECANOATE FOR THE TREATMENT OF SEBORRHEA |
US20130059913A1 (en) | 2010-04-07 | 2013-03-07 | Otsuka Pharmaceutical Factory, Inc. | Composition for amelioration of hypoalbuminemia |
ES2354103B1 (en) * | 2010-12-27 | 2011-12-05 | Cosmetica Cosbar S.L. | COMPOSITION CAPILLARY ACTIVATOR OF THE SIRTUINS AND USE OF THE SAME. |
ES2765174T3 (en) * | 2011-07-07 | 2020-06-08 | Elc Man Llc | Methods and compositions useful for the treatment of Fitzpatrick type IV, V or VI skin |
DE102012014042A1 (en) | 2012-07-14 | 2014-01-16 | Friedrich Haas | Dietary supplement for oral intake, useful as agent against hair loss, agent for increasing hair volume, agent for reducing relubrication of hair, comprises selenium, vitamin D, carrier and/or optionally further additives |
WO2014105249A2 (en) | 2012-10-05 | 2014-07-03 | University Of Florida Research Foundation Inc. | Use of anoctamin as biomarker for radiation biodosimetry |
CN107596049A (en) * | 2017-11-01 | 2018-01-19 | 安徽大学 | A kind of pharmaceutical composition of hair growth disease and preparation method thereof |
WO2021184125A1 (en) * | 2020-03-19 | 2021-09-23 | Idunn Technologies | Discovery of fifteen new anti-aging plant extracts and identification of cellular processes they affect as new caloric restriction mimetics |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1201151B (en) * | 1987-01-14 | 1989-01-27 | Indena Spa | PHOSPHOLIPID COMPLEXES WITH EXTRACTS FROM VITIS VINIFERA, PROCEDURE FOR THEIR PREPARATION AND COMPOSITIONS THAT CONTAIN THEM |
JPH02145509A (en) * | 1988-11-28 | 1990-06-05 | Shiseido Co Ltd | Dandruff-preventing cosmetic |
FR2704394B1 (en) * | 1993-04-27 | 1995-06-02 | Boiron | Absorbable nutritional supplement for the treatment of hair and nails. |
WO1997002041A1 (en) * | 1995-07-03 | 1997-01-23 | Crandall Wilson T | Transdermal and oral treatment of androgenic alopecia |
FR2736828B1 (en) * | 1995-07-20 | 1997-10-10 | Fabre Pierre Dermo Cosmetique | ZINC SALICYLATE COMBINATION AND SERENOA REPENS EXTRACT FOR THE TREATMENT OF SEBORRHEA AND DERMO-COSMETIC COMPOSITIONS COMPRISING SAME |
AU2741197A (en) * | 1996-04-22 | 1997-11-12 | Henkel Corporation | Natural antioxidant composition |
GB2314019B (en) * | 1996-06-10 | 2000-03-15 | Bio Scient Ltd | The use of L-Lysine in the treatment of hair loss |
US5895652A (en) | 1996-07-29 | 1999-04-20 | Longevity Institute International | Method of metabolic adjuvanation and cellular repair |
GB9706318D0 (en) | 1997-03-26 | 1997-05-14 | Bryant Andrew E | Therapeutic formulations |
US6207694B1 (en) * | 1998-07-27 | 2001-03-27 | Howard Murad | Pharmaceutical compositions and methods for managing scalp conditions |
IL132625A (en) * | 1999-10-28 | 2007-06-17 | Avi Dascalu | Composition for inducing hair growth |
FR2816843B1 (en) * | 2000-11-23 | 2006-10-27 | Actichem | INHIBITORS OF ENZYME 5 ALPHA-REDUCTASE |
-
2001
- 2001-08-07 IT IT2001MI001732A patent/ITMI20011732A1/en unknown
- 2001-11-14 US US10/485,981 patent/US7201931B2/en not_active Expired - Fee Related
- 2001-11-14 WO PCT/EP2001/013188 patent/WO2003013561A1/en active IP Right Grant
- 2001-11-14 CZ CZ20040195A patent/CZ300110B6/en not_active IP Right Cessation
- 2001-11-14 ES ES01991723T patent/ES2258563T3/en not_active Expired - Lifetime
- 2001-11-14 JP JP2003518568A patent/JP4988146B2/en not_active Expired - Fee Related
- 2001-11-14 SI SI200130506T patent/SI1414473T1/en unknown
- 2001-11-14 AT AT01991723T patent/ATE318610T1/en active
- 2001-11-14 BR BR0117098-8A patent/BR0117098A/en not_active Application Discontinuation
- 2001-11-14 DE DE60117606T patent/DE60117606T2/en not_active Expired - Lifetime
- 2001-11-14 CN CNB018235220A patent/CN1294956C/en not_active Expired - Fee Related
- 2001-11-14 RU RU2004103422/15A patent/RU2274470C2/en not_active IP Right Cessation
- 2001-11-14 EP EP01991723A patent/EP1414473B1/en not_active Expired - Lifetime
- 2001-11-14 HU HU0401427A patent/HU228648B1/en not_active IP Right Cessation
- 2001-11-14 KR KR1020047001735A patent/KR100846888B1/en not_active IP Right Cessation
- 2001-11-14 PL PL367900A patent/PL203133B1/en unknown
- 2001-11-14 AU AU2002231622A patent/AU2002231622B2/en not_active Ceased
- 2001-11-14 MX MXPA04001107A patent/MXPA04001107A/en active IP Right Grant
- 2001-11-14 CA CA2456519A patent/CA2456519C/en not_active Expired - Fee Related
- 2001-11-14 PT PT01991723T patent/PT1414473E/en unknown
- 2001-11-14 DK DK01991723T patent/DK1414473T3/en active
- 2001-11-14 IL IL16023201A patent/IL160232A0/en unknown
- 2001-11-14 SK SK83-2004A patent/SK287743B6/en not_active IP Right Cessation
-
2004
- 2004-02-05 IL IL160232A patent/IL160232A/en not_active IP Right Cessation
- 2004-02-05 NO NO20040536A patent/NO331412B1/en not_active IP Right Cessation
-
2005
- 2005-01-07 HK HK05100114A patent/HK1067559A1/en not_active IP Right Cessation
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