SK284036B6 - Lipozomálna parenterálna kompozícia - Google Patents

Lipozomálna parenterálna kompozícia Download PDF

Info

Publication number: SK284036B6
Authority: SK; Slovakia
Prior art keywords: cholesterol; liposomal composition; erythropoietin; liposomal; composition
Prior art date: 1998-02-23

Application number

SK1222-2000A

Other languages

English (en)

Slovak (sk)

Other versions

SK12222000A3 (sk

Inventor

Rainer N�ff

Sandro Delmenico

Andr Wetter

Frank-Ulrich Fl�ther

Original Assignee

Cilag Ag International

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.)

1998-02-23

Filing date

1999-02-12

Publication date

2004-08-03

1999-02-12 Application filed by Cilag Ag International filed Critical Cilag Ag International

2001-11-06 Publication of SK12222000A3 publication Critical patent/SK12222000A3/sk

2004-08-03 Publication of SK284036B6 publication Critical patent/SK284036B6/sk

Links

102000003951 Erythropoietin Human genes 0.000 title claims abstract description 51
108090000394 Erythropoietin Proteins 0.000 title claims abstract description 51
229940105423 erythropoietin Drugs 0.000 title claims abstract description 49
OXCMYAYHXIHQOA-UHFFFAOYSA-N potassium;[2-butyl-5-chloro-3-[[4-[2-(1,2,4-triaza-3-azanidacyclopenta-1,4-dien-5-yl)phenyl]phenyl]methyl]imidazol-4-yl]methanol Chemical compound [K+].CCCCC1=NC(Cl)=C(CO)N1CC1=CC=C(C=2C(=CC=CC=2)C2=N[N-]N=N2)C=C1 OXCMYAYHXIHQOA-UHFFFAOYSA-N 0.000 title claims abstract description 48
239000006185 dispersion Substances 0.000 title description 17
239000000203 mixture Substances 0.000 claims abstract description 65
239000002502 liposome Substances 0.000 claims abstract description 36
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 32
HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims abstract description 31
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 abstract description 20
235000012000 cholesterol Nutrition 0.000 claims abstract description 17
239000000787 lecithin Substances 0.000 claims abstract description 10
229940067606 lecithin Drugs 0.000 claims abstract description 10
235000010445 lecithin Nutrition 0.000 claims abstract description 10
150000001841 cholesterols Chemical class 0.000 claims abstract description 9
-1 lipid compound Chemical class 0.000 claims abstract description 7
239000002202 Polyethylene glycol Chemical class 0.000 claims abstract description 5
150000001840 cholesterol esters Chemical class 0.000 claims abstract description 5
229920001223 polyethylene glycol Chemical class 0.000 claims abstract description 5
239000008363 phosphate buffer Substances 0.000 claims abstract description 3
150000002632 lipids Chemical class 0.000 claims description 12
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 10
239000004480 active ingredient Substances 0.000 claims description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
OOSZCNKVJAVHJI-UHFFFAOYSA-N 1-[(4-fluorophenyl)methyl]piperazine Chemical group C1=CC(F)=CC=C1CN1CCNCC1 OOSZCNKVJAVHJI-UHFFFAOYSA-N 0.000 claims description 8
208000007502 anemia Diseases 0.000 claims description 8
210000003743 erythrocyte Anatomy 0.000 claims description 8
238000004519 manufacturing process Methods 0.000 claims description 8
229940074545 sodium dihydrogen phosphate dihydrate Drugs 0.000 claims description 8
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Natural products NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 7
239000000872 buffer Substances 0.000 claims description 7
KDQPSPMLNJTZAL-UHFFFAOYSA-L disodium hydrogenphosphate dihydrate Chemical compound O.O.[Na+].[Na+].OP([O-])([O-])=O KDQPSPMLNJTZAL-UHFFFAOYSA-L 0.000 claims description 7
239000003381 stabilizer Substances 0.000 claims description 7
230000004071 biological effect Effects 0.000 claims description 5
239000011780 sodium chloride Substances 0.000 claims description 5
239000004471 Glycine Substances 0.000 claims description 4
210000002798 bone marrow cell Anatomy 0.000 claims description 4
239000003755 preservative agent Substances 0.000 claims description 4
210000001995 reticulocyte Anatomy 0.000 claims description 4
239000000654 additive Substances 0.000 claims description 3
150000001875 compounds Chemical class 0.000 claims description 3
QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 claims description 2
BVKFQEAERCHBTG-UHFFFAOYSA-N 17,18,19-trihydroxypentatriacontane-16,20-dione Chemical compound CCCCCCCCCCCCCCCC(=O)C(O)C(O)C(O)C(=O)CCCCCCCCCCCCCCC BVKFQEAERCHBTG-UHFFFAOYSA-N 0.000 claims description 2
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 claims description 2
239000003963 antioxidant agent Substances 0.000 claims description 2
PORPENFLTBBHSG-MGBGTMOVSA-N 1,2-dihexadecanoyl-sn-glycerol-3-phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCC PORPENFLTBBHSG-MGBGTMOVSA-N 0.000 claims 2
PZNPLUBHRSSFHT-RRHRGVEJSA-N 1-hexadecanoyl-2-octadecanoyl-sn-glycero-3-phosphocholine Chemical class CCCCCCCCCCCCCCCCCC(=O)O[C@@H](COP([O-])(=O)OCC[N+](C)(C)C)COC(=O)CCCCCCCCCCCCCCC PZNPLUBHRSSFHT-RRHRGVEJSA-N 0.000 claims 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
230000003078 antioxidant effect Effects 0.000 claims 1
125000004432 carbon atom Chemical group C* 0.000 claims 1
239000008139 complexing agent Substances 0.000 claims 1
QJMBVMLTKGQFKW-UHFFFAOYSA-L disodium dihydrogen phosphate dihydrate Chemical compound O.O.[Na+].[Na+].OP(O)([O-])=O.OP(O)([O-])=O QJMBVMLTKGQFKW-UHFFFAOYSA-L 0.000 claims 1
125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 claims 1
239000008194 pharmaceutical composition Substances 0.000 claims 1
230000002335 preservative effect Effects 0.000 claims 1
229910052708 sodium Inorganic materials 0.000 claims 1
239000011734 sodium Substances 0.000 claims 1
238000000034 method Methods 0.000 abstract description 16
102000008100 Human Serum Albumin Human genes 0.000 abstract description 9
108091006905 Human Serum Albumin Proteins 0.000 abstract description 9
238000002347 injection Methods 0.000 abstract description 6
239000007924 injection Substances 0.000 abstract description 6
150000007524 organic acids Chemical class 0.000 abstract description 4
239000006201 parenteral dosage form Substances 0.000 abstract description 2
238000009472 formulation Methods 0.000 abstract 1
150000002334 glycols Chemical class 0.000 abstract 1
239000000243 solution Substances 0.000 description 11
238000004166 bioassay Methods 0.000 description 10
210000004027 cell Anatomy 0.000 description 9
238000001727 in vivo Methods 0.000 description 6
230000001476 alcoholic effect Effects 0.000 description 5
239000012062 aqueous buffer Substances 0.000 description 5
238000000338 in vitro Methods 0.000 description 5
239000012071 phase Substances 0.000 description 5
102000003886 Glycoproteins Human genes 0.000 description 4
108090000288 Glycoproteins Proteins 0.000 description 4
239000013543 active substance Substances 0.000 description 4
238000004220 aggregation Methods 0.000 description 4
230000002776 aggregation Effects 0.000 description 4
230000000694 effects Effects 0.000 description 4
239000008213 purified water Substances 0.000 description 4
108010074604 Epoetin Alfa Proteins 0.000 description 3
235000010469 Glycine max Nutrition 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
241000699666 Mus <mouse, genus> Species 0.000 description 3
241000699670 Mus sp. Species 0.000 description 3
239000002253 acid Substances 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
210000004369 blood Anatomy 0.000 description 3
239000008280 blood Substances 0.000 description 3
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
230000002209 hydrophobic effect Effects 0.000 description 3
238000001990 intravenous administration Methods 0.000 description 3
235000005985 organic acids Nutrition 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
238000007920 subcutaneous administration Methods 0.000 description 3
239000002691 unilamellar liposome Substances 0.000 description 3
YFWHNAWEOZTIPI-DIPNUNPCSA-N 1,2-dioctadecanoyl-sn-glycerol-3-phosphate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(O)=O)OC(=O)CCCCCCCCCCCCCCCCC YFWHNAWEOZTIPI-DIPNUNPCSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical class OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
238000002965 ELISA Methods 0.000 description 2
244000068988 Glycine max Species 0.000 description 2
229910021578 Iron(III) chloride Inorganic materials 0.000 description 2
239000000232 Lipid Bilayer Substances 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
206010028980 Neoplasm Diseases 0.000 description 2
241000382509 Vania Species 0.000 description 2
150000001413 amino acids Chemical class 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
201000011510 cancer Diseases 0.000 description 2
238000002512 chemotherapy Methods 0.000 description 2
208000020832 chronic kidney disease Diseases 0.000 description 2
208000022831 chronic renal failure syndrome Diseases 0.000 description 2
238000000326 densiometry Methods 0.000 description 2
208000035475 disorder Diseases 0.000 description 2
229940048820 edetates Drugs 0.000 description 2
229960003388 epoetin alfa Drugs 0.000 description 2
238000010348 incorporation Methods 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
239000013554 lipid monolayer Substances 0.000 description 2
239000012528 membrane Substances 0.000 description 2
LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 2
150000003904 phospholipids Chemical class 0.000 description 2
239000011148 porous material Substances 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
206010002068 Anaemia neonatal Diseases 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
239000004255 Butylated hydroxyanisole Substances 0.000 description 1
239000004322 Butylated hydroxytoluene Substances 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
206010061452 Complication of pregnancy Diseases 0.000 description 1
201000003883 Cystic fibrosis Diseases 0.000 description 1
ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 1
208000019255 Menstrual disease Diseases 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
KPBYZDRYGZZKIG-UHFFFAOYSA-N [hexadecanoyloxy(hydroxy)phosphoryl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OP(O)(=O)OC(=O)CCCCCCCCCCCCCCC KPBYZDRYGZZKIG-UHFFFAOYSA-N 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
230000001154 acute effect Effects 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
230000001464 adherent effect Effects 0.000 description 1
230000032683 aging Effects 0.000 description 1
201000000975 anemia of prematurity Diseases 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
125000003289 ascorbyl group Chemical group [H]O[C@@]([H])(C([H])([H])O*)[C@@]1([H])OC(=O)C(O*)=C1O* 0.000 description 1
238000003556 assay Methods 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
230000033228 biological regulation Effects 0.000 description 1
229940088623 biologically active substance Drugs 0.000 description 1
230000037396 body weight Effects 0.000 description 1
210000001185 bone marrow Anatomy 0.000 description 1
235000019282 butylated hydroxyanisole Nutrition 0.000 description 1
CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
229940043253 butylated hydroxyanisole Drugs 0.000 description 1
235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
229940095259 butylated hydroxytoluene Drugs 0.000 description 1
230000015556 catabolic process Effects 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
238000004113 cell culture Methods 0.000 description 1
230000010261 cell growth Effects 0.000 description 1
238000001516 cell proliferation assay Methods 0.000 description 1
230000001413 cellular effect Effects 0.000 description 1
238000002144 chemical decomposition reaction Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
WLNARFZDISHUGS-MIXBDBMTSA-N cholesteryl hemisuccinate Chemical compound C1C=C2C[C@@H](OC(=O)CCC(O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 WLNARFZDISHUGS-MIXBDBMTSA-N 0.000 description 1
150000001860 citric acid derivatives Chemical class 0.000 description 1
GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
230000002950 deficient Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
201000010099 disease Diseases 0.000 description 1
239000003814 drug Substances 0.000 description 1
239000008151 electrolyte solution Substances 0.000 description 1
238000005538 encapsulation Methods 0.000 description 1
229940089118 epogen Drugs 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000011521 glass Substances 0.000 description 1
230000012010 growth Effects 0.000 description 1
230000003394 haemopoietic effect Effects 0.000 description 1
229910001385 heavy metal Inorganic materials 0.000 description 1
230000002489 hematologic effect Effects 0.000 description 1
230000002440 hepatic effect Effects 0.000 description 1
208000006454 hepatitis Diseases 0.000 description 1
231100000283 hepatitis Toxicity 0.000 description 1
150000002433 hydrophilic molecules Chemical class 0.000 description 1
239000012678 infectious agent Substances 0.000 description 1
239000007972 injectable composition Substances 0.000 description 1
239000008384 inner phase Substances 0.000 description 1
210000003734 kidney Anatomy 0.000 description 1
239000007788 liquid Substances 0.000 description 1
210000004185 liver Anatomy 0.000 description 1
239000002609 medium Substances 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
239000004292 methyl p-hydroxybenzoate Substances 0.000 description 1
229960002216 methylparaben Drugs 0.000 description 1
230000003278 mimic effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
235000021313 oleic acid Nutrition 0.000 description 1
150000002889 oleic acids Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000008103 phosphatidic acids Chemical class 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229920000223 polyglycerol Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
239000002243 precursor Substances 0.000 description 1
230000035935 pregnancy Effects 0.000 description 1
208000012113 pregnancy disease Diseases 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
239000002994 raw material Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000012216 screening Methods 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
208000007056 sickle cell anemia Diseases 0.000 description 1
239000008347 soybean phospholipid Substances 0.000 description 1
208000020431 spinal cord injury Diseases 0.000 description 1
238000010186 staining Methods 0.000 description 1
238000011146 sterile filtration Methods 0.000 description 1
230000004936 stimulating effect Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
229940124597 therapeutic agent Drugs 0.000 description 1
238000011287 therapeutic dose Methods 0.000 description 1
210000001519 tissue Anatomy 0.000 description 1
239000003104 tissue culture media Substances 0.000 description 1
235000010384 tocopherol Nutrition 0.000 description 1
239000011732 tocopherol Substances 0.000 description 1
229960001295 tocopherol Drugs 0.000 description 1
229930003799 tocopherol Natural products 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000402 unacceptable toxicity Toxicity 0.000 description 1
239000008215 water for injection Substances 0.000 description 1
GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1

Classifications

- 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
- A61K9/127—Synthetic bilayered vehicles, e.g. liposomes or liposomes with cholesterol as the only non-phosphatidyl surfactant
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/18—Growth factors; Growth regulators
- A61K38/1816—Erythropoietin [EPO]
- 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
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
- 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
- A61K47/16—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing nitrogen, e.g. nitro-, nitroso-, azo-compounds, nitriles, cyanates
- A61K47/18—Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids
- A61K47/183—Amino acids, e.g. glycine, EDTA or aspartame

Landscapes

Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
Medicinal Chemistry (AREA)
General Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Pharmacology & Pharmacy (AREA)
Epidemiology (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
General Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Zoology (AREA)
Diabetes (AREA)
Hematology (AREA)
Gastroenterology & Hepatology (AREA)
Immunology (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Dermatology (AREA)
Medicinal Preparation (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

SK1222-2000A 1998-02-23 1999-02-12 Lipozomálna parenterálna kompozícia SK284036B6 (sk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP98103111A EP0937456B1 (en)	1998-02-23	1998-02-23	Erythropoietin liposomal dispersion
PCT/IB1999/000249 WO1999042085A1 (en)	1998-02-23	1999-02-12	Erythropoietin liposomal dispersion

Publications (2)

Publication Number	Publication Date
SK12222000A3 SK12222000A3 (sk)	2001-11-06
SK284036B6 true SK284036B6 (sk)	2004-08-03

Family

ID=8231466

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1222-2000A SK284036B6 (sk)	1998-02-23	1999-02-12	Lipozomálna parenterálna kompozícia

Country Status (23)

Country	Link
US (2)	US6645522B2 (pt)
EP (1)	EP0937456B1 (pt)
JP (1)	JP4613294B2 (pt)
KR (1)	KR100591871B1 (pt)
CN (1)	CN1184958C (pt)
AT (1)	ATE271376T1 (pt)
AU (1)	AU750481B2 (pt)
BR (1)	BR9908202A (pt)
CA (1)	CA2320072C (pt)
CZ (1)	CZ296415B6 (pt)
DE (1)	DE69825137T2 (pt)
DK (1)	DK0937456T3 (pt)
ES (1)	ES2224299T3 (pt)
HU (1)	HUP0101026A2 (pt)
IL (2)	IL137808A0 (pt)
NO (1)	NO20004186L (pt)
NZ (1)	NZ506429A (pt)
PL (1)	PL194502B1 (pt)
PT (1)	PT937456E (pt)
RU (1)	RU2218914C2 (pt)
SI (1)	SI0937456T1 (pt)
SK (1)	SK284036B6 (pt)
WO (1)	WO1999042085A1 (pt)

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1998
- 1998-02-23 ES ES98103111T patent/ES2224299T3/es not_active Expired - Lifetime
- 1998-02-23 AT AT98103111T patent/ATE271376T1/de active
- 1998-02-23 DE DE69825137T patent/DE69825137T2/de not_active Expired - Lifetime
- 1998-02-23 SI SI9830684T patent/SI0937456T1/xx unknown
- 1998-02-23 PT PT98103111T patent/PT937456E/pt unknown
- 1998-02-23 EP EP98103111A patent/EP0937456B1/en not_active Expired - Lifetime
- 1998-02-23 DK DK98103111T patent/DK0937456T3/da active
1999
- 1999-02-12 IL IL13780899A patent/IL137808A0/xx active IP Right Grant
- 1999-02-12 RU RU2000124317/14A patent/RU2218914C2/ru not_active IP Right Cessation
- 1999-02-12 BR BR9908202-0A patent/BR9908202A/pt not_active Application Discontinuation
- 1999-02-12 WO PCT/IB1999/000249 patent/WO1999042085A1/en active IP Right Grant
- 1999-02-12 JP JP2000532102A patent/JP4613294B2/ja not_active Expired - Fee Related
- 1999-02-12 HU HU0101026A patent/HUP0101026A2/hu unknown
- 1999-02-12 AU AU21808/99A patent/AU750481B2/en not_active Ceased
- 1999-02-12 SK SK1222-2000A patent/SK284036B6/sk not_active IP Right Cessation
- 1999-02-12 KR KR1020007009202A patent/KR100591871B1/ko not_active IP Right Cessation
- 1999-02-12 CA CA002320072A patent/CA2320072C/en not_active Expired - Fee Related
- 1999-02-12 CN CNB998052590A patent/CN1184958C/zh not_active Expired - Fee Related
- 1999-02-12 CZ CZ20002959A patent/CZ296415B6/cs not_active IP Right Cessation
- 1999-02-12 PL PL99342514A patent/PL194502B1/pl unknown
- 1999-02-12 NZ NZ506429A patent/NZ506429A/xx not_active IP Right Cessation
- 1999-02-18 US US09/252,563 patent/US6645522B2/en not_active Expired - Lifetime
2000
- 2000-08-10 IL IL137808A patent/IL137808A/en not_active IP Right Cessation
- 2000-08-22 NO NO20004186A patent/NO20004186L/no not_active Application Discontinuation
2003
- 2003-09-10 US US10/659,097 patent/US20040052838A1/en not_active Abandoned

Also Published As

Publication number	Publication date
DK0937456T3 (da)	2004-11-08
DE69825137D1 (de)	2004-08-26
WO1999042085A1 (en)	1999-08-26
BR9908202A (pt)	2000-10-24
CA2320072C (en)	2009-04-07
AU750481B2 (en)	2002-07-18
RU2218914C2 (ru)	2003-12-20
DE69825137T2 (de)	2005-07-21
JP4613294B2 (ja)	2011-01-12
IL137808A0 (en)	2001-10-31
US6645522B2 (en)	2003-11-11
KR100591871B1 (ko)	2006-06-23
KR20010041152A (ko)	2001-05-15
IL137808A (en)	2007-07-24
HUP0101026A2 (hu)	2001-08-28
SK12222000A3 (sk)	2001-11-06
PT937456E (pt)	2004-10-29
AU2180899A (en)	1999-09-06
ATE271376T1 (de)	2004-08-15
NO20004186D0 (no)	2000-08-22
CZ296415B6 (cs)	2006-03-15
EP0937456A1 (en)	1999-08-25
CN1184958C (zh)	2005-01-19
SI0937456T1 (en)	2004-12-31
US20040052838A1 (en)	2004-03-18
CA2320072A1 (en)	1999-08-26
CN1298296A (zh)	2001-06-06
PL194502B1 (pl)	2007-06-29
CZ20002959A3 (cs)	2001-10-17
JP2002503685A (ja)	2002-02-05
PL342514A1 (en)	2001-06-18
NZ506429A (en)	2003-03-28
US20020028236A1 (en)	2002-03-07
NO20004186L (no)	2000-08-22
ES2224299T3 (es)	2005-03-01
EP0937456B1 (en)	2004-07-21

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2017-11-03	MM4A	Patent lapsed due to non-payment of maintenance fees	Effective date: 20170212