CA2513773A1 - Clindamycin phosphate foam - Google Patents
Clindamycin phosphate foam Download PDFInfo
- Publication number
- CA2513773A1 CA2513773A1 CA002513773A CA2513773A CA2513773A1 CA 2513773 A1 CA2513773 A1 CA 2513773A1 CA 002513773 A CA002513773 A CA 002513773A CA 2513773 A CA2513773 A CA 2513773A CA 2513773 A1 CA2513773 A1 CA 2513773A1
- Authority
- CA
- Canada
- Prior art keywords
- composition
- alcohol
- quick
- breaking
- mixture
- 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
- 239000006260 foam Substances 0.000 title claims abstract 8
- UFUVLHLTWXBHGZ-MGZQPHGTSA-N [(2r,3r,4s,5r,6r)-6-[(1s,2s)-2-chloro-1-[[(2s,4r)-1-methyl-4-propylpyrrolidine-2-carbonyl]amino]propyl]-4,5-dihydroxy-2-methylsulfanyloxan-3-yl] dihydrogen phosphate Chemical compound CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](OP(O)(O)=O)[C@@H](SC)O1 UFUVLHLTWXBHGZ-MGZQPHGTSA-N 0.000 title claims 2
- 229960002291 clindamycin phosphate Drugs 0.000 title claims 2
- 239000000203 mixture Substances 0.000 claims abstract 60
- 150000001875 compounds Chemical class 0.000 claims abstract 8
- 239000004088 foaming agent Substances 0.000 claims abstract 7
- 238000000034 method Methods 0.000 claims abstract 6
- 230000001476 alcoholic effect Effects 0.000 claims abstract 2
- 230000000699 topical effect Effects 0.000 claims abstract 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims 8
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 claims 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 7
- 239000013543 active substance Substances 0.000 claims 4
- 229960000541 cetyl alcohol Drugs 0.000 claims 4
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 claims 4
- 229940002612 prodrug Drugs 0.000 claims 4
- 239000000651 prodrug Substances 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 239000004094 surface-active agent Substances 0.000 claims 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 3
- 239000003242 anti bacterial agent Substances 0.000 claims 3
- 229940088710 antibiotic agent Drugs 0.000 claims 3
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 2
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 claims 2
- 229960002227 clindamycin Drugs 0.000 claims 2
- KDLRVYVGXIQJDK-AWPVFWJPSA-N clindamycin Chemical compound CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@@H](SC)O1 KDLRVYVGXIQJDK-AWPVFWJPSA-N 0.000 claims 2
- 239000003974 emollient agent Substances 0.000 claims 2
- 229930195733 hydrocarbon Natural products 0.000 claims 2
- 150000002430 hydrocarbons Chemical class 0.000 claims 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims 2
- 229920005862 polyol Polymers 0.000 claims 2
- 150000003077 polyols Chemical group 0.000 claims 2
- 239000003380 propellant Substances 0.000 claims 2
- 150000004492 retinoid derivatives Chemical class 0.000 claims 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 claims 2
- 208000002874 Acne Vulgaris Diseases 0.000 claims 1
- 239000004342 Benzoyl peroxide Substances 0.000 claims 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims 1
- RRZFQNYMUQPMHE-HYEGCIPRSA-N [(2r,3r,4s,5r,6r)-6-[(1s,2s)-2-chloro-1-[[(2s,4r)-1-methyl-4-propylpyrrolidine-2-carbonyl]amino]propyl]-4,5-dihydroxy-2-methylsulfanyloxan-3-yl] dihydrogen phosphate;(2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenoic acid Chemical compound OC(=O)\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C.CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](OP(O)(O)=O)[C@@H](SC)O1 RRZFQNYMUQPMHE-HYEGCIPRSA-N 0.000 claims 1
- 206010000496 acne Diseases 0.000 claims 1
- 229940121375 antifungal agent Drugs 0.000 claims 1
- 239000003429 antifungal agent Substances 0.000 claims 1
- APQDBWGZCQHKHQ-SHSUDHJHSA-N benzoyl benzenecarboperoxoate;[(2r,3r,4s,5r,6r)-6-[(1s,2s)-2-chloro-1-[[(2s,4r)-1-methyl-4-propylpyrrolidine-2-carbonyl]amino]propyl]-4,5-dihydroxy-2-methylsulfanyloxan-3-yl] dihydrogen phosphate Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1.CN1C[C@H](CCC)C[C@H]1C(=O)N[C@H]([C@H](C)Cl)[C@@H]1[C@H](O)[C@H](O)[C@@H](OP(O)(O)=O)[C@@H](SC)O1 APQDBWGZCQHKHQ-SHSUDHJHSA-N 0.000 claims 1
- 235000019400 benzoyl peroxide Nutrition 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000002563 ionic surfactant Substances 0.000 claims 1
- 239000002736 nonionic surfactant Substances 0.000 claims 1
- 239000003002 pH adjusting agent Substances 0.000 claims 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims 1
- 229950008882 polysorbate Drugs 0.000 claims 1
- 229920000136 polysorbate Polymers 0.000 claims 1
- 229960004889 salicylic acid Drugs 0.000 claims 1
- IHCDKJZZFOUARO-UHFFFAOYSA-M sulfacetamide sodium Chemical compound O.[Na+].CC(=O)[N-]S(=O)(=O)C1=CC=C(N)C=C1 IHCDKJZZFOUARO-UHFFFAOYSA-M 0.000 claims 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000015181 infectious disease Diseases 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/046—Aerosols; Foams
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/38—Percompounds, e.g. peracids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/67—Vitamins
- A61K8/671—Vitamin A; Derivatives thereof, e.g. ester of vitamin A acid, ester of retinol, retinol, retinal
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/12—Aerosols; Foams
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/12—Aerosols; Foams
- A61K9/122—Foams; Dry foams
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
Abstract
The present invention provides various pharmaceutically active topical delivery compositions. In particular, compositions of the present invention are present in a pressurized container comprising a quick-breaking alcoholic foaming agent, such that when the composition is released, i.e., dispensed, from the pressurized container, a quick-breaking temperature sensitive foam is formed. In addition, the present invention provides various aspects related to such compositions, including methods for modulating a foam characteristic, methods for improving the shelf-life of a pharmaceutically active compound, methods for the percutaneous treatment of various diseases, infections, and illnesses, and methods for evaluating foam characteristics.
Claims (39)
1. A topical delivery composition in a pressurized container, said composition comprising:
up to 15% w/w of at least one pharmaceutically active compound, or its pharmaceutically acceptable salt or a prodrug thereof;
from about 83% to about 97.9% w/w of a quick-breaking foaming agent; and from about 2% to about 7% w/w of an aerosol propellant selected from the group consisting of a hydrocarbon, a chlorofluorocarbon, dimethyl ether, hydroflurocarbons and a mixture thereof, wherein said composition is a quick-breaking temperature sensitive foam after release from said container.
up to 15% w/w of at least one pharmaceutically active compound, or its pharmaceutically acceptable salt or a prodrug thereof;
from about 83% to about 97.9% w/w of a quick-breaking foaming agent; and from about 2% to about 7% w/w of an aerosol propellant selected from the group consisting of a hydrocarbon, a chlorofluorocarbon, dimethyl ether, hydroflurocarbons and a mixture thereof, wherein said composition is a quick-breaking temperature sensitive foam after release from said container.
2. The composition of claim 1, wherein said at least one pharmaceutically active compound is an antibiotic agent.
3. The composition of claim 2, wherein said at least one antibiotic agent is clindamycin, or a pharmaceutically acceptable salt or a prodrug thereof.
4. The composition of claim 3, wherein said at least one pharmaceutically active compound is clindamycin phosphate.
5. The composition of claim 1, wherein said at least one pharmaceutically active compound comprises a combination of active agents.
6. The composition of claim 5, wherein said combination of active agents comprises at least two agents selected from the group consisting of an antibiotic agent, an antifungal agent, a retinoid, a retinoid derivative, salicylic acid, azelaic acid, sodium sulfacetamide, and benzoyl peroxide.
7. The composition of claim 5, wherein said combination of active agents comprises clindamycin phosphate and tretinoin.
8. The composition of claim 5, wherein said combination of active agents comprises clindamycin phosphate and benzoyl peroxide.
9. The composition of claim 1, wherein said quick-breaking foaming agent comprises a C1-C6 alcohol and water.
10. The composition of claim 9, wherein the ratio of said C1-C6 alcohol to water is from about 1:7 to about 1:16.
11. The composition of claim 10, wherein the ratio of said C1-C6 alcohol to water is about 1:7.
12. The composition of claim 10, wherein the ratio of said C1-C6 alcohol to water is about 1:16.
13. The composition of claim 1, wherein said quick-breaking foaming agent comprises a C1-C6 alcohol, a C14-C22 alcohol, water, and a surfactant.
14. The composition of claim 13, wherein the foam breaking temperature of said quick-breaking temperature sensitive foam is from about 30°C to about 36°C.
15. The composition of claim 13, wherein the ratio of said C1-C6 alcohol to water is about 1.7:1.
16. The composition of claim 13, wherein said surfactant is present in an amount of from about 0.1 % to about 10 % w/w.
17. The composition of claim 16, wherein said surfactant is selected from the group consisting of an ethoxylated non-ionic surfactant, an ethoxylated ionic surfactant, and a mixture thereof.
18. The composition of claim 16, wherein said surfactant is a polysorbate.
19. The composition of claim 13, further comprising an emollient.
20. The composition of claim 19, wherein said emollient is a polyol.
21. The composition of claim 20, wherein said polyol is selected from the group consisting of propylene glycol, glycerol, and a mixture thereof.
22. The composition of claim 13, wherein the amount of said C1-C6 alcohol in said quick-breaking foaming agent is from about 55% to about 65% w/w.
23. The composition of claim 22, wherein said C1-C6 alcohol is selected from the group consisting of methanol, ethanol, isopropanol, butanol, and a mixture thereof.
24. The composition of claim 23, wherein said C1-C6 alcohol is ethanol.
25. The composition of claim 23, wherein said C1-C6 alcohol is a mixture of ethanol and at feast one other C1-C6 alcohol.
26. The composition of claim 13, wherein the amount of said C14-C22 alcohol in said quick-breaking foaming agent is from about 1 % to about 5.0% w/w.
27. The composition of claim 26, wherein said C14-C22 alcohol is a C14-C20 alcohol.
28. The composition of claim 27, wherein said C14-C20 alcohol is selected from the group consisting of cetyl alcohol, stearyl alcohol, and a mixture thereof.
29. The composition of claim 28, wherein said C14-C20 alcohol is a mixture of cetyl alcohol and stearyl alcohol.
30. The composition of claim 29, wherein the ratio of cetyl alcohol to stearyl alcohol is from about 60:40 to about 80:20.
31. The composition of claim 30, wherein the ratio of cetyl alcohol to stearyl alcohol is about 70:30.
32. The composition of claim 1, wherein said composition comprises water in an amount up to 90% w/w.
33. The composition of claim 13, wherein said composition comprises water in an amount from about 30% to about 40% w/w.
34. The composition of claim 13, further comprising a pH adjusting agent.
35. The composition of claim 34, wherein the pH of said composition is from about pH 4.0 to about pH 9Ø
36. The composition of claim 35, wherein the pH of said composition is from about pH 4.0 to about pH 6.5.
37. The composition of claim 1, wherein said composition comprises:
from about 0.1% to about 10% w/w of at least one pharmaceutically active compound, or its pharmaceutically acceptable salt or a prodrug thereof;
from about 83% to about 97.9% w/w of a quick-breaking alcoholic foaming agent; and from about 2% to about 7% w/w of an aerosol propellant selected from the group consisting of a hydrocarbon, a chlorofluorocarbon, and a mixture thereof.
from about 0.1% to about 10% w/w of at least one pharmaceutically active compound, or its pharmaceutically acceptable salt or a prodrug thereof;
from about 83% to about 97.9% w/w of a quick-breaking alcoholic foaming agent; and from about 2% to about 7% w/w of an aerosol propellant selected from the group consisting of a hydrocarbon, a chlorofluorocarbon, and a mixture thereof.
38. The composition of claim 1, wherein said composition does not contain a C1-C6 alcohol.
39. A method for the percutaneous treatment of acne, said method comprising:
applying a quick-breaking temperature sensitive foam composition to the skin of a subject in need thereof, said composition comprising an effective amount of at least one pharmaceutically active compound, wherein said at least one pharmaceutically active compound is at least clindamycin, or a pharmaceutically acceptable salt or a prodrug thereof.
applying a quick-breaking temperature sensitive foam composition to the skin of a subject in need thereof, said composition comprising an effective amount of at least one pharmaceutically active compound, wherein said at least one pharmaceutically active compound is at least clindamycin, or a pharmaceutically acceptable salt or a prodrug thereof.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US44228003P | 2003-01-24 | 2003-01-24 | |
US60/442,280 | 2003-01-24 | ||
US45483203P | 2003-03-13 | 2003-03-13 | |
US60/454,832 | 2003-03-13 | ||
PCT/AU2004/000088 WO2004064833A1 (en) | 2003-01-24 | 2004-01-23 | Clindamycin phosphate foam |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2513773A1 true CA2513773A1 (en) | 2004-08-05 |
CA2513773C CA2513773C (en) | 2013-03-26 |
Family
ID=32776128
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2513773A Expired - Lifetime CA2513773C (en) | 2003-01-24 | 2004-01-23 | Clindamycin phosphate foam |
Country Status (16)
Country | Link |
---|---|
US (6) | US7141237B2 (en) |
EP (2) | EP2289512B8 (en) |
JP (2) | JP4828404B2 (en) |
AR (2) | AR042906A1 (en) |
AU (2) | AU2004206769B2 (en) |
BR (1) | BRPI0406905B8 (en) |
CA (1) | CA2513773C (en) |
EA (2) | EA009031B1 (en) |
ES (2) | ES2450133T3 (en) |
IL (2) | IL169761A (en) |
MX (1) | MXPA05007722A (en) |
NO (1) | NO339620B1 (en) |
NZ (1) | NZ541526A (en) |
RS (1) | RS20050557A (en) |
TW (2) | TWI355267B (en) |
WO (1) | WO2004064833A1 (en) |
Families Citing this family (87)
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US8263580B2 (en) * | 1998-09-11 | 2012-09-11 | Stiefel Research Australia Pty Ltd | Vitamin formulation |
US8512718B2 (en) | 2000-07-03 | 2013-08-20 | Foamix Ltd. | Pharmaceutical composition for topical application |
US20050239675A1 (en) * | 2002-04-01 | 2005-10-27 | Munzer Makansi | Carrier foam to enhance liquid functional performance |
US20050008576A1 (en) * | 2002-04-01 | 2005-01-13 | Munzer Makansi | Carrier foam to enhance liquid functional performance |
US20040167223A1 (en) * | 2002-09-03 | 2004-08-26 | Popp Karl F. | Topical antibacterial formulations |
US20040171561A1 (en) * | 2002-09-03 | 2004-09-02 | Popp Karl F. | Topical formulations for treatment of rosacea |
US20040043946A1 (en) * | 2002-09-03 | 2004-03-04 | Popp Karl F. | Topical formulations for treatment of skin disorders |
IL152486A0 (en) | 2002-10-25 | 2003-05-29 | Meir Eini | Alcohol-free cosmetic and pharmaceutical foam carrier |
US7820145B2 (en) | 2003-08-04 | 2010-10-26 | Foamix Ltd. | Oleaginous pharmaceutical and cosmetic foam |
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MXPA05007722A (en) | 2003-01-24 | 2006-01-31 | Connetics Australia Pty Ltd | Clindamycin phosphate foam. |
US7575739B2 (en) | 2003-04-28 | 2009-08-18 | Foamix Ltd. | Foamable iodine composition |
US7186416B2 (en) * | 2003-05-28 | 2007-03-06 | Stiefel Laboratories, Inc. | Foamable pharmaceutical compositions and methods for treating a disorder |
US8486374B2 (en) | 2003-08-04 | 2013-07-16 | Foamix Ltd. | Hydrophilic, non-aqueous pharmaceutical carriers and compositions and uses |
US8795693B2 (en) | 2003-08-04 | 2014-08-05 | Foamix Ltd. | Compositions with modulating agents |
KR20060113907A (en) | 2003-09-29 | 2006-11-03 | 에테나 헬스케어 인코포레이티드 | - high alcohol content gel-like and foaming compositions |
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-
2006
- 2006-02-07 US US11/349,820 patent/US7749488B2/en not_active Expired - Lifetime
- 2006-08-09 US US11/463,573 patent/US7374747B2/en not_active Expired - Lifetime
-
2009
- 2009-11-10 AU AU2009235974A patent/AU2009235974B2/en not_active Expired
-
2010
- 2010-05-20 US US12/783,824 patent/US20100266511A1/en not_active Abandoned
-
2011
- 2011-06-10 JP JP2011130433A patent/JP5480201B2/en not_active Expired - Lifetime
- 2011-07-14 IL IL214118A patent/IL214118A/en active IP Right Grant
- 2011-08-01 AR ARP110102768A patent/AR082432A2/en not_active Application Discontinuation
- 2011-11-30 US US13/307,533 patent/US8586008B2/en not_active Expired - Lifetime
-
2013
- 2013-10-14 US US14/053,085 patent/US9486394B2/en not_active Expired - Lifetime
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