NO327712B1 - Azelainsyreholdig preparat og anvendelse derav - Google Patents

Azelainsyreholdig preparat og anvendelse derav Download PDF

Info

Publication number: NO327712B1
Authority: NO; Norway
Prior art keywords: preparation; weight; concentration; preparation according; present
Prior art date: 1997-11-19

Application number

NO20002487A

Other languages

English (en)

Norwegian (no)

Other versions

NO20002487D0 (no

NO20002487L (no

Inventor

Clemens Guenther

Patrick Franke

Jutta Riedl

Original Assignee

Intendis Gmbh

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.)

1997-11-19

Filing date

2000-05-12

Publication date

2009-09-14

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27217979&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO327712(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2000-05-12 Application filed by Intendis Gmbh filed Critical Intendis Gmbh

2000-05-12 Publication of NO20002487D0 publication Critical patent/NO20002487D0/no

2000-07-18 Publication of NO20002487L publication Critical patent/NO20002487L/no

2009-09-14 Publication of NO327712B1 publication Critical patent/NO327712B1/no

Links

BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 title claims abstract description 63
238000002360 preparation method Methods 0.000 title claims description 60
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims abstract description 42
229920000136 polysorbate Polymers 0.000 claims abstract description 13
150000003626 triacylglycerols Chemical class 0.000 claims abstract description 13
229920002125 Sokalan® Polymers 0.000 claims abstract description 12
239000004584 polyacrylic acid Substances 0.000 claims abstract description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
239000000017 hydrogel Substances 0.000 claims abstract description 8
150000003839 salts Chemical class 0.000 claims abstract description 8
238000011282 treatment Methods 0.000 claims abstract description 8
239000008347 soybean phospholipid Substances 0.000 claims abstract description 6
201000004700 rosacea Diseases 0.000 claims abstract description 4
206010008570 Chloasma Diseases 0.000 claims abstract description 3
208000003351 Melanosis Diseases 0.000 claims abstract description 3
241001303601 Rosacea Species 0.000 claims abstract description 3
206010040880 Skin irritation Diseases 0.000 claims abstract description 3
230000036556 skin irritation Effects 0.000 claims abstract description 3
231100000475 skin irritation Toxicity 0.000 claims abstract description 3
239000000787 lecithin Substances 0.000 claims description 11
235000010445 lecithin Nutrition 0.000 claims description 11
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims description 7
229940067606 lecithin Drugs 0.000 claims description 7
239000008346 aqueous phase Substances 0.000 claims description 6
239000003814 drug Substances 0.000 claims description 6
229940068965 polysorbates Drugs 0.000 claims description 6
PZNPLUBHRSSFHT-RRHRGVEJSA-N 1-hexadecanoyl-2-octadecanoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCCCC(=O)O[C@@H](COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCCCCCCCCCC PZNPLUBHRSSFHT-RRHRGVEJSA-N 0.000 claims description 5
230000000144 pharmacologic effect Effects 0.000 claims description 5
239000000126 substance Substances 0.000 claims description 5
208000002874 Acne Vulgaris Diseases 0.000 claims description 4
206010000496 acne Diseases 0.000 claims description 4
239000000654 additive Substances 0.000 claims description 3
239000004480 active ingredient Substances 0.000 claims description 2
102000004856 Lectins Human genes 0.000 claims 1
108090001090 Lectins Proteins 0.000 claims 1
239000002523 lectin Substances 0.000 claims 1
229950008882 polysorbate Drugs 0.000 abstract description 5
239000000203 mixture Substances 0.000 abstract description 4
239000000470 constituent Substances 0.000 abstract 1
239000008194 pharmaceutical composition Substances 0.000 abstract 1
210000003491 skin Anatomy 0.000 description 23
239000000825 pharmaceutical preparation Substances 0.000 description 11
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
239000006071 cream Substances 0.000 description 8
239000013543 active substance Substances 0.000 description 7
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 6
239000000499 gel Substances 0.000 description 6
239000007908 nanoemulsion Substances 0.000 description 6
210000000056 organ Anatomy 0.000 description 4
239000005711 Benzoic acid Substances 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
235000010233 benzoic acid Nutrition 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
238000000034 method Methods 0.000 description 3
239000002245 particle Substances 0.000 description 3
239000003755 preservative agent Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
229940124599 anti-inflammatory drug Drugs 0.000 description 2
230000008901 benefit Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000000969 carrier Substances 0.000 description 2
238000009792 diffusion process Methods 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000003925 fat Substances 0.000 description 2
235000019197 fats Nutrition 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
230000004060 metabolic process Effects 0.000 description 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 2
230000035515 penetration Effects 0.000 description 2
239000002304 perfume Substances 0.000 description 2
239000000546 pharmaceutical excipient Substances 0.000 description 2
230000001225 therapeutic effect Effects 0.000 description 2
238000011200 topical administration Methods 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
WSWCOQWTEOXDQX-MQQKCMAXSA-M (E,E)-sorbate Chemical compound C\C=C\C=C\C([O-])=O WSWCOQWTEOXDQX-MQQKCMAXSA-M 0.000 description 1
ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
239000012981 Hank's balanced salt solution Substances 0.000 description 1
OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
239000000232 Lipid Bilayer Substances 0.000 description 1
102000018697 Membrane Proteins Human genes 0.000 description 1
108010052285 Membrane Proteins Proteins 0.000 description 1
241000699670 Mus sp. Species 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
235000021319 Palmitoleic acid Nutrition 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
235000020661 alpha-linolenic acid Nutrition 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
239000012620 biological material Substances 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
210000004027 cell Anatomy 0.000 description 1
210000000170 cell membrane Anatomy 0.000 description 1
SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
239000002537 cosmetic Substances 0.000 description 1
238000013461 design Methods 0.000 description 1
238000001514 detection method Methods 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
230000002500 effect on skin Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000000284 extract Substances 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000003889 eye drop Substances 0.000 description 1
229940012356 eye drops Drugs 0.000 description 1
230000001815 facial effect Effects 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000010685 fatty oil Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000012634 fragment Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
208000002672 hepatitis B Diseases 0.000 description 1
238000004128 high performance liquid chromatography Methods 0.000 description 1
238000010874 in vitro model Methods 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
230000002458 infectious effect Effects 0.000 description 1
230000002757 inflammatory effect Effects 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
238000011835 investigation Methods 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
235000020778 linoleic acid Nutrition 0.000 description 1
OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
229960004488 linolenic acid Drugs 0.000 description 1
KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
239000002502 liposome Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000008291 lyophilic colloid Substances 0.000 description 1
229960003511 macrogol Drugs 0.000 description 1
229940057917 medium chain triglycerides Drugs 0.000 description 1
239000012528 membrane Substances 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
239000003921 oil Substances 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
235000021313 oleic acid Nutrition 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
-1 polyethylene Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
229940068968 polysorbate 80 Drugs 0.000 description 1
229920000053 polysorbate 80 Polymers 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
230000000069 prophylactic effect Effects 0.000 description 1
239000002994 raw material Substances 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
208000017520 skin disease Diseases 0.000 description 1
229940075554 sorbate Drugs 0.000 description 1
239000001593 sorbitan monooleate Substances 0.000 description 1
229940035049 sorbitan monooleate Drugs 0.000 description 1
235000011069 sorbitan monooleate Nutrition 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
210000000434 stratum corneum Anatomy 0.000 description 1
238000012360 testing method Methods 0.000 description 1
230000000699 topical effect Effects 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
229960005486 vaccine Drugs 0.000 description 1

Classifications

- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
- 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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
- 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
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/23—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms
- 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
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/24—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing atoms other than carbon, hydrogen, oxygen, halogen, nitrogen or sulfur, e.g. cyclomethicone or phospholipids
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/32—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers, poly(meth)acrylates, or polyvinyl pyrrolidone

Landscapes

Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Chemical & Material Sciences (AREA)
General Health & Medical Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Medicinal Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Epidemiology (AREA)
Bioinformatics & Cheminformatics (AREA)
Dermatology (AREA)
Engineering & Computer Science (AREA)
Organic Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Emergency Medicine (AREA)
Urology & Nephrology (AREA)
Vascular Medicine (AREA)
Cardiology (AREA)
Heart & Thoracic Surgery (AREA)
Medicinal Preparation (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

NO20002487A 1997-11-19 2000-05-12 Azelainsyreholdig preparat og anvendelse derav NO327712B1 (no)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
DE19753044		1997-11-19
US7485098P	1998-02-12	1998-02-12
DE19808086		1998-02-20
PCT/EP1998/007370 WO1999025332A1 (de)	1997-11-19	1998-11-18	Zusammensetzung mit azelainsäure

Publications (3)

Publication Number	Publication Date
NO20002487D0 NO20002487D0 (no)	2000-05-12
NO20002487L NO20002487L (no)	2000-07-18
NO327712B1 true NO327712B1 (no)	2009-09-14

Family

ID=27217979

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO20002487A NO327712B1 (no)	1997-11-19	2000-05-12	Azelainsyreholdig preparat og anvendelse derav

Country Status (21)

Country	Link
US (1)	US6534070B1 (is)
EP (1)	EP1032379B1 (is)
JP (1)	JP3867123B2 (is)
KR (1)	KR100534511B1 (is)
AT (1)	ATE210438T1 (is)
AU (1)	AU743437B2 (is)
BR (1)	BR9814214B1 (is)
CA (1)	CA2311128C (is)
CZ (1)	CZ299116B6 (is)
DE (2)	DE59802473D1 (is)
DK (1)	DK1032379T3 (is)
ES (1)	ES2169566T3 (is)
HU (1)	HU226592B1 (is)
IL (1)	IL136101A (is)
IS (1)	IS2257B (is)
NO (1)	NO327712B1 (is)
PL (1)	PL202454B1 (is)
PT (1)	PT1032379E (is)
SK (1)	SK284338B6 (is)
TR (1)	TR200001393T2 (is)
WO (1)	WO1999025332A1 (is)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ATE369866T1 (de) *	2003-06-10	2007-09-15	Intendis Gmbh	Zusammensetzung aus alkandicarbonsäuren und einem pharmazeutischen wirkstoff
US20050026982A1 (en) *	2003-06-10	2005-02-03	Soenke Johannsen	Composition that consists of alkanedicarboxylic acids and a pharmaceutical active ingredient
ATE347367T1 (de) *	2003-10-13	2006-12-15	Zoser B Salama	Pharmazeutische zusammensetzung umfassend oxoplatin und dessen salze
DE10356288B4 (de)	2003-11-28	2014-04-03	Siemens Aktiengesellschaft	Röntgendetektorlade
CA2600054A1 (en) *	2005-03-09	2006-09-21	Combe Incorporated	Stable mixed emulsions
CA2600288A1 (en) *	2005-09-19	2007-04-12	Combe Incorporated	Stable emulsion systems with high salt tolerance
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1998
- 1998-11-18 US US09/554,738 patent/US6534070B1/en not_active Expired - Lifetime
- 1998-11-18 AT AT98962351T patent/ATE210438T1/de active
- 1998-11-18 CZ CZ20001844A patent/CZ299116B6/cs not_active IP Right Cessation
- 1998-11-18 HU HU0004375A patent/HU226592B1/hu unknown
- 1998-11-18 EP EP98962351A patent/EP1032379B1/de not_active Expired - Lifetime
- 1998-11-18 JP JP2000520766A patent/JP3867123B2/ja not_active Expired - Lifetime
- 1998-11-18 BR BRPI9814214-3A patent/BR9814214B1/pt not_active IP Right Cessation
- 1998-11-18 TR TR2000/01393T patent/TR200001393T2/xx unknown
- 1998-11-18 KR KR10-2000-7005430A patent/KR100534511B1/ko not_active Expired - Lifetime
- 1998-11-18 DK DK98962351T patent/DK1032379T3/da active
- 1998-11-18 ES ES98962351T patent/ES2169566T3/es not_active Expired - Lifetime
- 1998-11-18 PL PL340631A patent/PL202454B1/pl unknown
- 1998-11-18 SK SK708-2000A patent/SK284338B6/sk not_active IP Right Cessation
- 1998-11-18 CA CA002311128A patent/CA2311128C/en not_active Expired - Lifetime
- 1998-11-18 PT PT98962351T patent/PT1032379E/pt unknown
- 1998-11-18 DE DE59802473T patent/DE59802473D1/de not_active Expired - Lifetime
- 1998-11-18 WO PCT/EP1998/007370 patent/WO1999025332A1/de not_active Ceased
- 1998-11-18 DE DE19881737T patent/DE19881737D2/de not_active Ceased
- 1998-11-18 IL IL13610198A patent/IL136101A/xx not_active IP Right Cessation
- 1998-11-18 AU AU17551/99A patent/AU743437B2/en not_active Expired
2000
- 2000-05-09 IS IS5484A patent/IS2257B/is unknown
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Publication number	Publication date
KR20010032229A (ko)	2001-04-16
BR9814214B1 (pt)	2010-07-13
PT1032379E (pt)	2002-06-28
ES2169566T3 (es)	2002-07-01
CZ299116B6 (cs)	2008-04-30
JP2001522879A (ja)	2001-11-20
HU226592B1 (en)	2009-04-28
DK1032379T3 (da)	2002-04-02
CZ20001844A3 (cs)	2000-10-11
KR100534511B1 (ko)	2005-12-08
TR200001393T2 (tr)	2000-10-23
AU1755199A (en)	1999-06-07
CA2311128C (en)	2008-01-29
EP1032379A1 (de)	2000-09-06
US6534070B1 (en)	2003-03-18
DE59802473D1 (de)	2002-01-24
IL136101A (en)	2005-08-31
JP3867123B2 (ja)	2007-01-10
BR9814214A (pt)	2000-10-03
HUP0004375A2 (hu)	2001-08-28
IS5484A (is)	2000-05-09
CA2311128A1 (en)	1999-05-27
PL202454B1 (pl)	2009-06-30
WO1999025332A1 (de)	1999-05-27
EP1032379B1 (de)	2001-12-12
NO20002487D0 (no)	2000-05-12
SK284338B6 (sk)	2005-02-04
AU743437B2 (en)	2002-01-24
NO20002487L (no)	2000-07-18
PL340631A1 (en)	2001-02-12
SK7082000A3 (en)	2001-06-11
DE19881737D2 (de)	2001-03-22
IS2257B (is)	2007-06-15
IL136101A0 (en)	2001-05-20
ATE210438T1 (de)	2001-12-15
HUP0004375A3 (en)	2006-06-28

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2018-12-10	MK1K	Patent expired

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