UA74778C2 - Pharmaceutical formulation for controlled release of clarithromycin - Google Patents

Pharmaceutical formulation for controlled release of clarithromycin Download PDF

Info

Publication number: UA74778C2
Authority: UA; Ukraine
Prior art keywords: pharmaceutical composition; composition according; fact; clarithromycin; controlled release
Prior art date: 1999-02-19

Application number

UA2001096230A

Other languages

English (en)

Ukrainian (uk)

Original Assignee

Lec Tovarna Pharmacevtskih In

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.)

1999-02-19

Filing date

2000-02-17

Publication date

2006-02-15

2000-02-17 Application filed by Lec Tovarna Pharmacevtskih In filed Critical Lec Tovarna Pharmacevtskih In

2006-02-15 Publication of UA74778C2 publication Critical patent/UA74778C2/uk

Links

AGOYDEPGAOXOCK-KCBOHYOISA-N clarithromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@](C)([C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)OC)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 AGOYDEPGAOXOCK-KCBOHYOISA-N 0.000 title claims abstract description 26
229960002626 clarithromycin Drugs 0.000 title claims abstract description 26
239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 19
238000013270 controlled release Methods 0.000 title claims abstract description 10
239000004094 surface-active agent Substances 0.000 claims abstract description 6
239000000203 mixture Substances 0.000 claims description 25
OKMWKBLSFKFYGZ-UHFFFAOYSA-N 1-behenoylglycerol Chemical group CCCCCCCCCCCCCCCCCCCCCC(=O)OCC(O)CO OKMWKBLSFKFYGZ-UHFFFAOYSA-N 0.000 claims description 10
238000000034 method Methods 0.000 claims description 10
229940049654 glyceryl behenate Drugs 0.000 claims description 9
239000011248 coating agent Substances 0.000 claims description 7
238000000576 coating method Methods 0.000 claims description 7
238000002360 preparation method Methods 0.000 claims description 7
239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 6
235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 6
229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 6
UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical group OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 6
239000002253 acid Substances 0.000 claims description 4
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 2
239000008363 phosphate buffer Substances 0.000 claims description 2
238000007873 sieving Methods 0.000 claims description 2
239000002904 solvent Substances 0.000 claims description 2
208000035143 Bacterial infection Diseases 0.000 claims 1
239000000654 additive Substances 0.000 claims 1
208000022362 bacterial infectious disease Diseases 0.000 claims 1
238000003825 pressing Methods 0.000 claims 1
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239000011159 matrix material Substances 0.000 abstract description 17
239000013543 active substance Substances 0.000 abstract description 15
ULGZDMOVFRHVEP-RWJQBGPGSA-N Erythromycin Chemical compound O([C@@H]1[C@@H](C)C(=O)O[C@@H]([C@@]([C@H](O)[C@@H](C)C(=O)[C@H](C)C[C@@](C)(O)[C@H](O[C@H]2[C@@H]([C@H](C[C@@H](C)O2)N(C)C)O)[C@H]1C)(C)O)CC)[C@H]1C[C@@](C)(OC)[C@@H](O)[C@H](C)O1 ULGZDMOVFRHVEP-RWJQBGPGSA-N 0.000 description 7
UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 7
238000004090 dissolution Methods 0.000 description 6
239000003814 drug Substances 0.000 description 6
239000002245 particle Substances 0.000 description 6
229940079593 drug Drugs 0.000 description 5
239000000126 substance Substances 0.000 description 5
239000000725 suspension Substances 0.000 description 5
238000005516 engineering process Methods 0.000 description 4
210000001035 gastrointestinal tract Anatomy 0.000 description 4
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 3
235000021355 Stearic acid Nutrition 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
238000009792 diffusion process Methods 0.000 description 3
229960003276 erythromycin Drugs 0.000 description 3
239000008101 lactose Substances 0.000 description 3
150000002632 lipids Chemical class 0.000 description 3
239000000314 lubricant Substances 0.000 description 3
239000003120 macrolide antibiotic agent Substances 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
238000004859 neutralization-reionization mass spectrometry Methods 0.000 description 3
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
239000008203 oral pharmaceutical composition Substances 0.000 description 3
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239000008117 stearic acid Substances 0.000 description 3
210000002784 stomach Anatomy 0.000 description 3
239000000454 talc Substances 0.000 description 3
229910052623 talc Inorganic materials 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
229920002153 Hydroxypropyl cellulose Polymers 0.000 description 2
229920000168 Microcrystalline cellulose Polymers 0.000 description 2
RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 2
229920002125 Sokalan® Polymers 0.000 description 2
-1 acetal diethylaminoacetate Chemical class 0.000 description 2
235000010443 alginic acid Nutrition 0.000 description 2
229920000615 alginic acid Polymers 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
230000003115 biocidal effect Effects 0.000 description 2
229960001631 carbomer Drugs 0.000 description 2
229920003086 cellulose ether Polymers 0.000 description 2
230000006378 damage Effects 0.000 description 2
238000007922 dissolution test Methods 0.000 description 2
238000001035 drying Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000013265 extended release Methods 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
239000001863 hydroxypropyl cellulose Substances 0.000 description 2
235000010977 hydroxypropyl cellulose Nutrition 0.000 description 2
239000007788 liquid Substances 0.000 description 2
230000000873 masking effect Effects 0.000 description 2
239000002609 medium Substances 0.000 description 2
229940016286 microcrystalline cellulose Drugs 0.000 description 2
235000019813 microcrystalline cellulose Nutrition 0.000 description 2
239000008108 microcrystalline cellulose Substances 0.000 description 2
239000003921 oil Substances 0.000 description 2
235000019198 oils Nutrition 0.000 description 2
239000001267 polyvinylpyrrolidone Substances 0.000 description 2
229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
239000000243 solution Substances 0.000 description 2
230000008961 swelling Effects 0.000 description 2
239000006188 syrup Substances 0.000 description 2
235000020357 syrup Nutrition 0.000 description 2
238000005550 wet granulation Methods 0.000 description 2
LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
244000215068 Acacia senegal Species 0.000 description 1
235000021357 Behenic acid Nutrition 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
241000192125 Firmicutes Species 0.000 description 1
229920002907 Guar gum Polymers 0.000 description 1
229920000084 Gum arabic Polymers 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
235000010489 acacia gum Nutrition 0.000 description 1
239000000205 acacia gum Substances 0.000 description 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
230000002730 additional effect Effects 0.000 description 1
239000003463 adsorbent Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229940072056 alginate Drugs 0.000 description 1
239000000783 alginic acid Substances 0.000 description 1
229960001126 alginic acid Drugs 0.000 description 1
150000004781 alginic acids Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
230000000845 anti-microbial effect Effects 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
229940116226 behenic acid Drugs 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
229960000074 biopharmaceutical Drugs 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
239000002775 capsule Substances 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
230000007423 decrease Effects 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
229960000878 docusate sodium Drugs 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000011049 filling Methods 0.000 description 1
238000009472 formulation Methods 0.000 description 1
229920001002 functional polymer Polymers 0.000 description 1
210000004051 gastric juice Anatomy 0.000 description 1
239000000499 gel Substances 0.000 description 1
239000007903 gelatin capsule Substances 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
150000002314 glycerols Chemical class 0.000 description 1
229940075507 glyceryl monostearate Drugs 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
238000000227 grinding Methods 0.000 description 1
239000000665 guar gum Substances 0.000 description 1
235000010417 guar gum Nutrition 0.000 description 1
229960002154 guar gum Drugs 0.000 description 1
230000036571 hydration Effects 0.000 description 1
238000006703 hydration reaction Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000002596 lactones Chemical group 0.000 description 1
230000001050 lubricating effect Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
229940126601 medicinal product Drugs 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
230000011987 methylation Effects 0.000 description 1
238000007069 methylation reaction Methods 0.000 description 1
239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
229940126701 oral medication Drugs 0.000 description 1
230000003204 osmotic effect Effects 0.000 description 1
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
150000004804 polysaccharides Chemical class 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
238000012216 screening Methods 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000005063 solubilization Methods 0.000 description 1
230000007928 solubilization Effects 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000005846 sugar alcohols Chemical class 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229940124597 therapeutic agent Drugs 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
230000007704 transition Effects 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
239000001069 triethyl citrate Substances 0.000 description 1
VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
235000013769 triethyl citrate Nutrition 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
229920003169 water-soluble polymer Polymers 0.000 description 1
230000003313 weakening effect Effects 0.000 description 1
238000009736 wetting Methods 0.000 description 1
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239000000230 xanthan gum Substances 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
239000001052 yellow pigment Substances 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7048—Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin, digitoxin or digoxin
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/2833—Organic macromolecular compounds
- A61K9/286—Polysaccharides, e.g. gums; Cyclodextrin
- A61K9/2866—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
- 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

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Epidemiology (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Molecular Biology (AREA)
Communicable Diseases (AREA)
Oncology (AREA)
Chemical Kinetics & Catalysis (AREA)
Bioinformatics & Cheminformatics (AREA)
Biophysics (AREA)
Engineering & Computer Science (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicinal Preparation (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

UA2001096230A 1999-02-19 2000-02-17 Pharmaceutical formulation for controlled release of clarithromycin UA74778C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
SI9900039A SI20150A (sl)	1999-02-19	1999-02-19	Direktno stisljivi matriks za nadzorovano sproščanje celodnevne doze klaritromicina
PCT/SI2000/000002 WO2000048607A1 (en)	1999-02-19	2000-02-17	Directly compressible matrix for controlled release of single daily doses of clarithromycin

Publications (1)

Publication Number	Publication Date
UA74778C2 true UA74778C2 (en)	2006-02-15

Family

ID=20432410

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
UA2001096230A UA74778C2 (en)	1999-02-19	2000-02-17	Pharmaceutical formulation for controlled release of clarithromycin

Country Status (21)

Country	Link
EP (1)	EP1150686B1 (sr)
AT (1)	ATE286736T1 (sr)
AU (1)	AU776912B2 (sr)
BG (1)	BG65324B1 (sr)
CY (1)	CY1107454T1 (sr)
CZ (1)	CZ302781B6 (sr)
DE (1)	DE60017361T2 (sr)
DK (1)	DK1150686T3 (sr)
EE (1)	EE05422B1 (sr)
ES (1)	ES2235834T3 (sr)
HR (1)	HRP20010684B1 (sr)
HU (1)	HUP0105481A3 (sr)
PL (1)	PL196665B1 (sr)
PT (1)	PT1150686E (sr)
RS (1)	RS50298B (sr)
RU (1)	RU2237480C2 (sr)
SI (2)	SI20150A (sr)
SK (1)	SK287525B6 (sr)
TR (1)	TR200102396T2 (sr)
UA (1)	UA74778C2 (sr)
WO (1)	WO2000048607A1 (sr)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
TR200000054A2 (tr) *	2000-01-05	2001-08-21	Sanovel İlaç San. Ve Ti̇c. Anoni̇m Şi̇rketi̇	Klaritromisin içeren sürekli salım sağlayan tablet formülasyonları.
US6544555B2 (en)	2000-02-24	2003-04-08	Advancis Pharmaceutical Corp.	Antibiotic product, use and formulation thereof
IN192748B (sr) *	2000-08-29	2004-05-15	Ranbaxy Lab Ltd
US20020068078A1 (en)	2000-10-13	2002-06-06	Rudnic Edward M.	Antifungal product, use and formulation thereof
WO2003017981A1 (en)	2001-08-29	2003-03-06	Ranbaxy Laboratories Limited	Controlled release formulation of clarithromycin or tinidazol
CA2405918A1 (en) *	2001-10-01	2003-04-01	Ind-Swift Limited	Controlled release macrolide pharmaceutical formulations
SE0103369D0 (sv) *	2001-10-09	2001-10-09	Astrazeneca Ab	Pharmaceutical formulation
CA2465405A1 (en)	2001-11-02	2003-05-08	Wockhardt Limited	Controlled release compositions for macrolide antimicrobial agents
US20050163857A1 (en) *	2002-04-03	2005-07-28	Ashok Rampal	Clarithromycin formulations having improved bioavailability
US20060083759A1 (en) *	2002-07-17	2006-04-20	Aleksander Resman	Stabilization of the profile of release of active substances from a formulation
EP1534238A1 (en) *	2002-07-29	2005-06-01	ALZA Corporation	Formulations and dosage forms for controlled delivery of topiramate
US20050232995A1 (en)	2002-07-29	2005-10-20	Yam Nyomi V	Methods and dosage forms for controlled delivery of paliperidone and risperidone
US8062672B2 (en)	2003-08-12	2011-11-22	Shionogi Inc.	Antibiotic product, use and formulation thereof
WO2005023221A1 (en) *	2003-09-05	2005-03-17	Ranbaxy Laboratories Limited	Clarithromycin formulations having improved biovailability
US7943585B2 (en) *	2003-12-22	2011-05-17	Sandoz, Inc.	Extended release antibiotic composition
AU2005235237A1 (en) *	2004-03-24	2005-11-03	Lupin Limited	Clarithromycin extended release formulation
EP2283824B1 (en)	2009-07-30	2017-04-19	Special Products Line S.p.A.	Compositions and formulations based on swellable matrices for sustained release of poorly soluble drugs such as clarithromycin

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4331803A (en) *	1980-06-04	1982-05-25	Taisho Pharmaceutical Co., Ltd.	Novel erythromycin compounds
JPS60163823A (ja) *	1984-02-03	1985-08-26	Taisho Pharmaceut Co Ltd	経口投与製剤
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1999
- 1999-02-19 SI SI9900039A patent/SI20150A/sl not_active IP Right Cessation
2000
- 2000-02-17 CZ CZ20012964A patent/CZ302781B6/cs not_active IP Right Cessation
- 2000-02-17 SI SI200030647T patent/SI1150686T1/xx unknown
- 2000-02-17 DK DK00905514T patent/DK1150686T3/da active
- 2000-02-17 ES ES00905514T patent/ES2235834T3/es not_active Expired - Lifetime
- 2000-02-17 DE DE60017361T patent/DE60017361T2/de not_active Expired - Lifetime
- 2000-02-17 UA UA2001096230A patent/UA74778C2/uk unknown
- 2000-02-17 TR TR2001/02396T patent/TR200102396T2/xx unknown
- 2000-02-17 PL PL350419A patent/PL196665B1/pl unknown
- 2000-02-17 AT AT00905514T patent/ATE286736T1/de active
- 2000-02-17 WO PCT/SI2000/000002 patent/WO2000048607A1/en active IP Right Grant
- 2000-02-17 EE EEP200100433A patent/EE05422B1/xx not_active IP Right Cessation
- 2000-02-17 RS YUP-592/01A patent/RS50298B/sr unknown
- 2000-02-17 HU HU0105481A patent/HUP0105481A3/hu unknown
- 2000-02-17 SK SK1197-2001A patent/SK287525B6/sk not_active IP Right Cessation
- 2000-02-17 RU RU2001125667A patent/RU2237480C2/ru not_active IP Right Cessation
- 2000-02-17 PT PT00905514T patent/PT1150686E/pt unknown
- 2000-02-17 EP EP00905514A patent/EP1150686B1/en not_active Expired - Lifetime
- 2000-02-17 AU AU27049/00A patent/AU776912B2/en not_active Ceased
2001
- 2001-09-18 HR HR20010684A patent/HRP20010684B1/xx not_active IP Right Cessation
- 2001-09-19 BG BG105914A patent/BG65324B1/bg unknown
2005
- 2005-03-10 CY CY20051100330T patent/CY1107454T1/el unknown

Also Published As

Publication number	Publication date
ES2235834T3 (es)	2005-07-16
HRP20010684A2 (en)	2002-10-31
DK1150686T3 (da)	2005-04-04
EP1150686A1 (en)	2001-11-07
HUP0105481A2 (hu)	2002-05-29
SK11972001A3 (sk)	2002-02-05
EP1150686B1 (en)	2005-01-12
ATE286736T1 (de)	2005-01-15
HRP20010684B1 (en)	2011-01-31
RU2237480C2 (ru)	2004-10-10
AU776912B2 (en)	2004-09-23
YU59201A (sh)	2004-07-15
TR200102396T2 (tr)	2002-01-21
PL350419A1 (en)	2002-12-16
SI1150686T1 (en)	2005-06-30
BG105914A (bg)	2002-05-31
SK287525B6 (sk)	2011-01-04
EE200100433A (et)	2002-12-16
DE60017361D1 (de)	2005-02-17
SI20150A (sl)	2000-08-31
CY1107454T1 (el)	2012-12-19
PL196665B1 (pl)	2008-01-31
CZ20012964A3 (cs)	2002-01-16
DE60017361T2 (de)	2005-12-22
RS50298B (sr)	2009-09-08
BG65324B1 (bg)	2008-02-29
HUP0105481A3 (en)	2003-04-28
EE05422B1 (et)	2011-06-15
AU2704900A (en)	2000-09-04
CZ302781B6 (cs)	2011-11-02
PT1150686E (pt)	2005-05-31
WO2000048607A1 (en)	2000-08-24

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