HRP20180999T1 - Formulacija krutog farmaceutskog oblika doziranja koja sadrži lopinavir - Google Patents
Formulacija krutog farmaceutskog oblika doziranja koja sadrži lopinavir Download PDFInfo
- Publication number
- HRP20180999T1 HRP20180999T1 HRP20180999TT HRP20180999T HRP20180999T1 HR P20180999 T1 HRP20180999 T1 HR P20180999T1 HR P20180999T T HRP20180999T T HR P20180999TT HR P20180999 T HRP20180999 T HR P20180999T HR P20180999 T1 HRP20180999 T1 HR P20180999T1
- Authority
- HR
- Croatia
- Prior art keywords
- dosage form
- pharmaceutically acceptable
- use according
- copolymer
- polyoxyethylene
- Prior art date
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- 239000007787 solid Substances 0.000 title claims 11
- KJHKTHWMRKYKJE-SUGCFTRWSA-N Kaletra Chemical compound N1([C@@H](C(C)C)C(=O)N[C@H](C[C@H](O)[C@H](CC=2C=CC=CC=2)NC(=O)COC=2C(=CC=CC=2C)C)CC=2C=CC=CC=2)CCCNC1=O KJHKTHWMRKYKJE-SUGCFTRWSA-N 0.000 title claims 5
- 229960004525 lopinavir Drugs 0.000 title claims 5
- 238000009472 formulation Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 239000002552 dosage form Substances 0.000 claims 27
- -1 polyoxyethylene Polymers 0.000 claims 17
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims 12
- 229920001577 copolymer Polymers 0.000 claims 11
- 239000008180 pharmaceutical surfactant Substances 0.000 claims 9
- 229920003169 water-soluble polymer Polymers 0.000 claims 6
- 239000000243 solution Substances 0.000 claims 5
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 4
- 235000014113 dietary fatty acids Nutrition 0.000 claims 4
- 239000000194 fatty acid Substances 0.000 claims 4
- 229930195729 fatty acid Natural products 0.000 claims 4
- 229920002556 Polyethylene Glycol 300 Polymers 0.000 claims 3
- NCDNCNXCDXHOMX-UHFFFAOYSA-N Ritonavir Natural products C=1C=CC=CC=1CC(NC(=O)OCC=1SC=NC=1)C(O)CC(CC=1C=CC=CC=1)NC(=O)C(C(C)C)NC(=O)N(C)CC1=CSC(C(C)C)=N1 NCDNCNXCDXHOMX-UHFFFAOYSA-N 0.000 claims 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims 3
- 229920002678 cellulose Polymers 0.000 claims 3
- 239000006185 dispersion Substances 0.000 claims 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 3
- 229920001519 homopolymer Polymers 0.000 claims 3
- GSGDTSDELPUTKU-UHFFFAOYSA-N nonoxybenzene Chemical compound CCCCCCCCCOC1=CC=CC=C1 GSGDTSDELPUTKU-UHFFFAOYSA-N 0.000 claims 3
- 229920000642 polymer Polymers 0.000 claims 3
- NCDNCNXCDXHOMX-XGKFQTDJSA-N ritonavir Chemical compound N([C@@H](C(C)C)C(=O)N[C@H](C[C@H](O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1SC=NC=1)CC=1C=CC=CC=1)C(=O)N(C)CC1=CSC(C(C)C)=N1 NCDNCNXCDXHOMX-XGKFQTDJSA-N 0.000 claims 3
- 229960000311 ritonavir Drugs 0.000 claims 3
- 239000007962 solid dispersion Substances 0.000 claims 3
- 239000006104 solid solution Substances 0.000 claims 3
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 claims 2
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 claims 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 2
- 229930006000 Sucrose Natural products 0.000 claims 2
- 239000001913 cellulose Substances 0.000 claims 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 2
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims 2
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims 2
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims 2
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound 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 2
- 229940035044 sorbitan monolaurate Drugs 0.000 claims 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims 2
- 239000005720 sucrose Substances 0.000 claims 2
- 229920002554 vinyl polymer Polymers 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- OMDQUFIYNPYJFM-XKDAHURESA-N (2r,3r,4s,5r,6s)-2-(hydroxymethyl)-6-[[(2r,3s,4r,5s,6r)-4,5,6-trihydroxy-3-[(2s,3s,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)[C@H](O)[C@H](O)[C@H](O)O1 OMDQUFIYNPYJFM-XKDAHURESA-N 0.000 claims 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 claims 1
- QIZPVNNYFKFJAD-UHFFFAOYSA-N 1-chloro-2-prop-1-ynylbenzene Chemical compound CC#CC1=CC=CC=C1Cl QIZPVNNYFKFJAD-UHFFFAOYSA-N 0.000 claims 1
- CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 claims 1
- FDCJDKXCCYFOCV-UHFFFAOYSA-N 1-hexadecoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC FDCJDKXCCYFOCV-UHFFFAOYSA-N 0.000 claims 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims 1
- CTXGTHVAWRBISV-UHFFFAOYSA-N 2-hydroxyethyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCO CTXGTHVAWRBISV-UHFFFAOYSA-N 0.000 claims 1
- BHIZVZJETFVJMJ-UHFFFAOYSA-N 2-hydroxypropyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(C)O BHIZVZJETFVJMJ-UHFFFAOYSA-N 0.000 claims 1
- 208000030507 AIDS Diseases 0.000 claims 1
- 229920000623 Cellulose acetate phthalate Polymers 0.000 claims 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims 1
- 239000001856 Ethyl cellulose Substances 0.000 claims 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- 229920000926 Galactomannan Polymers 0.000 claims 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims 1
- OFFWOVJBSQMVPI-RMLGOCCBSA-N Kaletra Chemical compound N1([C@@H](C(C)C)C(=O)N[C@H](C[C@H](O)[C@H](CC=2C=CC=CC=2)NC(=O)COC=2C(=CC=CC=2C)C)CC=2C=CC=CC=2)CCCNC1=O.N([C@@H](C(C)C)C(=O)N[C@H](C[C@H](O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1SC=NC=1)CC=1C=CC=CC=1)C(=O)N(C)CC1=CSC(C(C)C)=N1 OFFWOVJBSQMVPI-RMLGOCCBSA-N 0.000 claims 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims 1
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 claims 1
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 239000004372 Polyvinyl alcohol Substances 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 1
- IYFATESGLOUGBX-YVNJGZBMSA-N Sorbitan monopalmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O IYFATESGLOUGBX-YVNJGZBMSA-N 0.000 claims 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 claims 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims 1
- KGUHOFWIXKIURA-VQXBOQCVSA-N [(2r,3s,4s,5r,6r)-6-[(2s,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl dodecanoate Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](COC(=O)CCCCCCCCCCC)O[C@@H]1O[C@@]1(CO)[C@@H](O)[C@H](O)[C@@H](CO)O1 KGUHOFWIXKIURA-VQXBOQCVSA-N 0.000 claims 1
- FOLJTMYCYXSPFQ-CJKAUBRRSA-N [(2r,3s,4s,5r,6r)-6-[(2s,3s,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)-2-(octadecanoyloxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl octadecanoate Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](COC(=O)CCCCCCCCCCCCCCCCC)O[C@@H]1O[C@@]1(COC(=O)CCCCCCCCCCCCCCCCC)[C@@H](O)[C@H](O)[C@@H](CO)O1 FOLJTMYCYXSPFQ-CJKAUBRRSA-N 0.000 claims 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 claims 1
- 150000005215 alkyl ethers Chemical class 0.000 claims 1
- 239000002775 capsule Substances 0.000 claims 1
- 239000000679 carrageenan Substances 0.000 claims 1
- 235000010418 carrageenan Nutrition 0.000 claims 1
- 229920001525 carrageenan Polymers 0.000 claims 1
- 229940113118 carrageenan Drugs 0.000 claims 1
- 229940081734 cellulose acetate phthalate Drugs 0.000 claims 1
- 229920003086 cellulose ether Polymers 0.000 claims 1
- 229940075614 colloidal silicon dioxide Drugs 0.000 claims 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims 1
- 239000008298 dragée Substances 0.000 claims 1
- FYUWIEKAVLOHSE-UHFFFAOYSA-N ethenyl acetate;1-ethenylpyrrolidin-2-one Chemical compound CC(=O)OC=C.C=CN1CCCC1=O FYUWIEKAVLOHSE-UHFFFAOYSA-N 0.000 claims 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 claims 1
- 229920001249 ethyl cellulose Polymers 0.000 claims 1
- 235000019325 ethyl cellulose Nutrition 0.000 claims 1
- 235000013305 food Nutrition 0.000 claims 1
- 150000004676 glycans Chemical class 0.000 claims 1
- 239000008187 granular material Substances 0.000 claims 1
- 229920013821 hydroxy alkyl cellulose Polymers 0.000 claims 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims 1
- 229920003132 hydroxypropyl methylcellulose phthalate Polymers 0.000 claims 1
- 229940031704 hydroxypropyl methylcellulose phthalate Drugs 0.000 claims 1
- 229920000639 hydroxypropylmethylcellulose acetate succinate Polymers 0.000 claims 1
- 229940120922 lopinavir and ritonavir Drugs 0.000 claims 1
- 229920000609 methyl cellulose Polymers 0.000 claims 1
- 239000001923 methylcellulose Substances 0.000 claims 1
- 235000010981 methylcellulose Nutrition 0.000 claims 1
- 239000002736 nonionic surfactant Substances 0.000 claims 1
- ZPIRTVJRHUMMOI-UHFFFAOYSA-N octoxybenzene Chemical compound CCCCCCCCOC1=CC=CC=C1 ZPIRTVJRHUMMOI-UHFFFAOYSA-N 0.000 claims 1
- 229920001542 oligosaccharide Polymers 0.000 claims 1
- 150000002482 oligosaccharides Chemical class 0.000 claims 1
- 229940094335 peg-200 dilaurate Drugs 0.000 claims 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims 1
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- 229920000233 poly(alkylene oxides) Polymers 0.000 claims 1
- 229920002401 polyacrylamide Polymers 0.000 claims 1
- 229920000058 polyacrylate Polymers 0.000 claims 1
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- 229920000193 polymethacrylate Polymers 0.000 claims 1
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- 229920001282 polysaccharide Polymers 0.000 claims 1
- 239000005017 polysaccharide Substances 0.000 claims 1
- 229920002689 polyvinyl acetate Polymers 0.000 claims 1
- 239000011118 polyvinyl acetate Substances 0.000 claims 1
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 229940026235 propylene glycol monolaurate Drugs 0.000 claims 1
- 239000001593 sorbitan monooleate Substances 0.000 claims 1
- 235000011069 sorbitan monooleate Nutrition 0.000 claims 1
- 229940035049 sorbitan monooleate Drugs 0.000 claims 1
- 239000001570 sorbitan monopalmitate Substances 0.000 claims 1
- 235000011071 sorbitan monopalmitate Nutrition 0.000 claims 1
- 229940031953 sorbitan monopalmitate Drugs 0.000 claims 1
- 229950011392 sorbitan stearate Drugs 0.000 claims 1
- 229940086735 succinate Drugs 0.000 claims 1
- 229940032085 sucrose monolaurate Drugs 0.000 claims 1
- 229940035023 sucrose monostearate Drugs 0.000 claims 1
- 239000003826 tablet Substances 0.000 claims 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims 1
- 239000000230 xanthan gum Substances 0.000 claims 1
- 229920001285 xanthan gum Polymers 0.000 claims 1
- 235000010493 xanthan gum Nutrition 0.000 claims 1
- 229940082509 xanthan gum Drugs 0.000 claims 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 claims 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1682—Processes
- A61K9/1694—Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
- A61K9/2077—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
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- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1635—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
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Claims (14)
1. Kruti farmaceutski oblik doziranja za upotrebu u liječenju pacijenta s HIV-om, te liječenje obuhvaća davanje navedenom pacijentu navedenog krutog farmaceutskog oblika doziranja bez hrane, naznačen time da navedeni oblik doziranja sadrži otopinu ili disperziju krutog lopinavira u barem jednom farmaceutski prihvatljivom polimeru koji je topljiv u vodi koji ima Tg od barem 50 °C i barem jednom farmaceutski prihvatljivom neionskom surfaktantu.
2. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da navedeni oblik doziranja sadrži od 50 do 85 masenih % oblika doziranja farmaceutski prihvatljivog polimera koji je topljiv u vodi.
3. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da oblik doziranja nadalje sadrži ritonavir.
4. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da navedeni farmaceutski prihvatljiv surfaktant ima HLB vrijednost od 4 do 10.
5. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da navedena otopina krutih tvari ili navedena disperzija krutih tvari sadrži barem jedan farmaceutski prihvatljiv polimer koji je topljiv u vodi odabran iz skupine koja sadrži homopolimer N-vinil laktama, kopolimer N-vinil laktama, celuloza ester, celuloza eter, visoko molekularni polialkilen oksid, poliakrilat, polimetakrilat, poliakrilamid, polivinil alkohol, vinil acetat polimer, oligosaharid, te polisaharid, te pri čemu navedena kruta otopina ili kruta disperzija sadrži barem jedan farmaceutski prihvatljiv surfaktant koji ima HLB vrijednost od 4 do 10 odabran iz skupine koja sadrži polioksietilen alkil eter, polioksietilen alkilaril eter, polietilen glikol ester masne kiseline, alkilen glikol mono ester masne kiseline, saharoza ester masne kiseline, te sorbitan mono ester masne kiseline.
6. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da navedena otopina krutih tvari ili navedena disperzija krutih tvari sadrži barem jedan farmaceutski prihvatljiv polimer koji je topljiv u vodi odabran iz skupine koja sadrži homopolimer N-vinil pirolidona, kopolimer N-vinil pirolidona, kopolimer N-vinil pirolidona i vinil acetata, kopolimer N-vinil pirolidona i vinil propionata, polivinilpirolidon, metilcelulozu, etilcelulozu, hidroksialkilceluloze, hidroksipropilcelulozu, hidroksialkilalkil celulozu, hidroksipropilmetilcelulozu, celuloza ftalat, celuloza sukcinat, celuloza acetat ftalat, hidroksipropilmetil celuloza ftalat, hidroksipropilmetil celuloza sukcinat, hidroksipropilmetil celuloza acetat sukcinat, polietilen oksid, polipropilen oksid, kopolimer etilen oksida i propilen oksida, kopolimer metakrilna kiselina/etil akrilat, kopolimer metakrilna kiselina/metil metakrilat, kopolimer butil metakrilat/2-dimetilaminoetil metakrilat, poli(hidroksialkil akrilat), poli(hidroksialkil metakrilate), kopolimer vinil acetata i krotonske kiseline, djelomično hidrolizirani polivinil acetat, karagenan, galaktomanan, i ksantan guma, te pri čemu navedena kruta otopina ili kruta disperzija sadrži barem jedan farmaceutski prihvatljiv surfaktant koji ima HLB vrijednost od 4 do 10 odabran iz skupine koja sadrži polioksietilen (3) lauril eter, polioksietilen (5) cetil eter, polioksietilen (2) stearil eter, polioksietilen (5) stearil eter, polioksietilen (2) nonilfenil eter, polioksietilen (3) nonilfenil eter, polioksietilen (4) nonilfenil eter, polioksietilen (3) oktilfenil eter, PEG-200 monolaurat, PEG-200 dilaurat, PEG-300 dilaurat, PEG-400 dilaurat, PEG-300 distearat, PEG-300 dioleat, propilen glikol monolaurat, saharoza monostearat, saharoza distearat, saharoza monolaurat, saharoza dilaurat, sorbitan mono laurat, sorbitan monooleat, sorbitan monopalmitat, i sorbitan stearat.
7. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da navedeni oblik doziranja sadrži otopinu krutog ili disperziju krutog ritonavira i lopinavira u navedenom barem jednom farmaceutski prihvatljivom polimeru koji je topljiv u vodi i navedenom barem jednom farmaceutski prihvatljivom surfaktantu, i navedeni farmaceutski prihvatljiv polimer koji je topljiv u vodi je homopolimer ili kopolimer N-vinil pirolidona.
8. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da navedeni oblik doziranja sadrži od 2 do 20 masenih % ukupnog oblika doziranja farmaceutski prihvatljivog surfaktanta.
9. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da navedeni oblik doziranja sadrži otopinu krutog lopinavira u navedenom barem jednom farmaceutski prihvatljivom polimeru koji je topljiv u vodi i navedenom barem jednom farmaceutski prihvatljivom surfaktantu, te navedeni farmaceutski prihvatljiv surfaktant ima HLB vrijednost od 4 do 10.
10. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da navedeni oblik doziranja sadrži otopinu krutog ritonavira i lopinavira u navedenom barem jednom farmaceutski prihvatljivom polimeru koji je topljiv u vodi i navedenom barem jednom farmaceutski prihvatljivom surfaktantu, te navedeni farmaceutski prihvatljiv surfaktant ima HLB vrijednost od 4 do 10.
11. Oblik doziranja za uporabu prema zahtjevu 3, naznačen time da sadrži ukupno 18-22.5 masenih % lopinavira i ritonavira, 65-75 masenih % kopolimera N-vinil pirolidon/vinil acetat 60:40, 4-10 masenih % sorbitan monolaurata, 0-10 masenih % polioksietilenglikol oksistearata, te 0-3 masenih % koloidnog silicijevog dioksida.
12. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da se navedeni oblik doziranja treba davati oralno.
13. Oblik doziranja za uporabu prema zahtjevu 12, naznačen time da je navedeni oblik doziranja kapsula, dražeja, granula, pilula, prah ili tableta.
14. Oblik doziranja za uporabu prema zahtjevu 1, naznačen time da je navedeni oblik doziranja za upotrebu u liječenju ljudskog pacijenta koji boluje od HIV/AIDS.
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EP10159672.4A EP2206500B1 (en) | 2005-02-23 | 2006-02-21 | A solid pharmaceutical dosage formulation comprising lopinavir |
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Families Citing this family (40)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE60028754T2 (de) * | 1999-11-12 | 2007-05-31 | Abbott Laboratories, Abbott Park | Feste dispersion mit ritonavir, fenofibrat oder griseofulvin |
US20050048112A1 (en) | 2003-08-28 | 2005-03-03 | Jorg Breitenbach | Solid pharmaceutical dosage form |
US8025899B2 (en) | 2003-08-28 | 2011-09-27 | Abbott Laboratories | Solid pharmaceutical dosage form |
US8377952B2 (en) * | 2003-08-28 | 2013-02-19 | Abbott Laboratories | Solid pharmaceutical dosage formulation |
CA2568378C (en) * | 2004-05-28 | 2013-03-19 | Abbott Gmbh & Co. Kg | Formulation obtained from a powder mixture comprising an inorganic pigment |
AR045841A1 (es) * | 2004-09-28 | 2005-11-16 | Richmond Sa Com Ind Y Financie | Una composicion farmaceutica solida que comprende al tiazolil metil ester del acido [5s-(5r*, 8r*, 10r*,11r*)] -10- hidroxi-2- metil-5-(1-metiletil)-1-[2-(1-metiletil)-4-tiazolil]-3,6-dioxo-8,11-bis(fenilmetil)-2,4,7,12- tetraazatridecan-13-oico y un procedimiento para prepararla. |
JP2009502969A (ja) * | 2005-07-28 | 2009-01-29 | アイエスピー インヴェストメンツ インコーポレイテッド | 非晶質エファビレンツ及びその製造 |
UY30535A1 (es) * | 2006-08-10 | 2008-03-31 | Cipla Ltd | Composicion comprendiendo farmacos antirretrovirales y al menos un polimero insoluble en agua, proceso de preparacion y aplicaciones. |
WO2008029417A2 (en) * | 2006-09-04 | 2008-03-13 | Matrix Laboratories Limited | Pharmaceutical formulation for use in hiv therapy |
US20080085310A1 (en) * | 2006-10-06 | 2008-04-10 | Maria Oksana Bachynsky | Capecitabine rapidly disintegrating tablets |
EP2112925A4 (en) * | 2006-11-15 | 2013-01-09 | Abbott Lab | SOLID PHARMACEUTICAL DOSAGE FORMULATIONS |
US20080152717A1 (en) * | 2006-12-14 | 2008-06-26 | Isp Investments, Inc. | Amorphous valsartan and the production thereof |
US8613946B2 (en) * | 2006-12-21 | 2013-12-24 | Isp Investment Inc. | Carotenoids of enhanced bioavailability |
CN101622302B (zh) * | 2007-01-26 | 2013-01-23 | Isp投资公司 | 生产喷雾干燥产品的制剂工艺方法 |
WO2008092046A2 (en) * | 2007-01-26 | 2008-07-31 | Isp Investments Inc. | Amorphous oxcarbazepine and the production thereof |
EP2152244B1 (en) * | 2007-04-26 | 2015-12-02 | Technion Research & Development Foundation Ltd. | Oral administration of proteins and peptides |
US20110224435A1 (en) * | 2007-08-07 | 2011-09-15 | Ranbaxy Laboratories Limited | Process for preparation of amorphous lopinavir |
WO2009056818A1 (en) * | 2007-10-29 | 2009-05-07 | Cipla Limited | Novel antiretroviral combination |
WO2009084036A2 (en) * | 2007-12-20 | 2009-07-09 | Matrix Laboratories Limited | Composition for treatment of viral infections |
PA8809601A1 (es) * | 2007-12-24 | 2009-07-23 | Cipla Ltd | Combinación anti-retroviral |
CN101959506A (zh) * | 2008-02-28 | 2011-01-26 | 雅培制药有限公司 | 片剂和其制备方法 |
US20100222315A1 (en) * | 2008-09-24 | 2010-09-02 | Harbor BioSciencs, Inc. | Patient populations and treatment methods |
TWI540132B (zh) | 2009-06-08 | 2016-07-01 | 亞培公司 | Bcl-2族群抑制劑之口服醫藥劑型 |
WO2011013110A1 (en) * | 2009-07-31 | 2011-02-03 | Ranbaxy Laboratories Limited | Unit dosage forms of hiv protease inhibitors |
US20110034489A1 (en) | 2009-07-31 | 2011-02-10 | Ranbaxy Laboratories Limited | Solid dosage forms of hiv protease inhibitors |
EP2568810B1 (en) * | 2010-05-10 | 2018-09-19 | Hetero Research Foundation | Darunavir compositions |
UA113500C2 (xx) | 2010-10-29 | 2017-02-10 | Одержані екструзією розплаву тверді дисперсії, що містять індукуючий апоптоз засіб | |
EP2564832A1 (en) * | 2011-08-29 | 2013-03-06 | Hexal AG | Solid dosage form of HIV protease inhibitors |
KR101794032B1 (ko) * | 2011-09-21 | 2017-11-07 | (주)바이오시네틱스 | 나노입자 제조방법 |
JP6314131B2 (ja) * | 2012-05-03 | 2018-04-18 | シプラ・リミテッド | 抗レトロウイルス組成物 |
CN103655571B (zh) * | 2012-09-11 | 2016-04-20 | 上海星泰医药科技有限公司 | 一种洛匹那韦和利托那韦复方高均匀度纳米共分散体及其制备方法 |
WO2014130553A2 (en) * | 2013-02-20 | 2014-08-28 | Abbvie Inc. | Tablet dosage forms |
US10034865B2 (en) | 2015-09-10 | 2018-07-31 | Kashiv Pharma, Llc | Surfactant-free HIV protease inhibitor composition and method of manufacturing thereof |
RU2619840C1 (ru) * | 2016-09-21 | 2017-05-18 | Общество с ограниченной ответственностью "Изварино Фарма" | Фармацевтическая композиция для лечения ВИЧ-инфекции |
CN108186578A (zh) * | 2018-03-27 | 2018-06-22 | 聊城大学 | 一种利托那韦固体分散体的制备方法 |
EP3569225A1 (en) | 2018-05-18 | 2019-11-20 | Pharmaceutical Oriented Services Ltd | Solid dispersion containing ritonavir |
GB201808564D0 (en) | 2018-05-24 | 2018-07-11 | Douglas Pharmaceuticals Ltd | Treatments |
EA202191371A1 (ru) * | 2018-12-14 | 2021-12-27 | Фуджифилм Корпорэйшн | Фармацевтическая композиция и способ ее получения |
GB201907305D0 (en) * | 2019-05-23 | 2019-07-10 | Douglas Pharmaceuticals Ltd | Treatment of conditions |
CN112263554B (zh) * | 2020-10-22 | 2022-09-30 | 安徽贝克生物制药有限公司 | 一种洛匹那韦利托那韦复方片剂及其制备方法 |
Family Cites Families (405)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE973095C (de) | 1955-01-19 | 1959-12-03 | Kalle & Co Ag | Verfahren zur UEberfuehrung von OElen in streufaehige Pulver durch Spruehtrocknung von OEl-in-Wasser-Emulsionen |
HU176101B (en) | 1977-12-29 | 1980-12-28 | Gyogyszerkutato Intezet | Process for producing bis-bracket-nitrozo-ureido-bracket closed-polyol derivatives |
DE3013839A1 (de) | 1979-04-13 | 1980-10-30 | Freunt Ind Co Ltd | Verfahren zur herstellung einer aktivierten pharmazeutischen zusammensetzung |
CA1146866A (en) | 1979-07-05 | 1983-05-24 | Yamanouchi Pharmaceutical Co. Ltd. | Process for the production of sustained release pharmaceutical composition of solid medical material |
FR2525108B1 (fr) | 1982-04-19 | 1989-05-12 | Elan Corp Ltd | Medicaments a haut degre de solubilite et procede pour leur obtention |
US4629621A (en) | 1984-07-23 | 1986-12-16 | Zetachron, Inc. | Erodible matrix for sustained release bioactive composition |
JPS61205208A (ja) | 1985-03-08 | 1986-09-11 | Yamanouchi Pharmaceut Co Ltd | 難溶性医薬品の速溶性製剤 |
US4590065A (en) | 1985-04-18 | 1986-05-20 | Colgate-Palmolive Company | Stable flavor-containing dentifrice |
US4758427A (en) | 1985-08-08 | 1988-07-19 | Ciba-Geigy Corporation | Enhanced absorption of psychoactive 2-aryl-pyrazolo quinolines as a solid molecular dispersion in polyvinylpyrrolidone |
PH22025A (en) | 1985-08-19 | 1988-05-13 | Johnson & Son Inc S C | Aqueous pyrethroid insecticidal formulations and method of increasing the stability thereof |
DE3612212A1 (de) | 1986-04-11 | 1987-10-15 | Basf Ag | Verfahren zur herstellung von festen pharmazeutischen formen |
DE3612211A1 (de) | 1986-04-11 | 1987-10-15 | Basf Ag | Kontinuierliches verfahren zum tablettieren |
ES2040697T3 (es) | 1986-12-18 | 1993-11-01 | Kurt H. Prof. Dr. Bauer | Concentrado de nifedipina estabilizado frente a la influencia de la luz, y procedimiento para su preparacion. |
US4804699A (en) * | 1987-05-15 | 1989-02-14 | Ici Americas Inc. | Monomeric and oligomeric glutarate-based light stabilizers for plastics |
IL87710A (en) | 1987-09-18 | 1992-06-21 | Ciba Geigy Ag | Covered floating retard form for controlled release in gastric juice |
AU2902289A (en) | 1987-12-08 | 1989-07-05 | Mark Chasin | Method of forming bioerodible implants for improved controlled drug release |
DE3812567A1 (de) | 1988-04-15 | 1989-10-26 | Basf Ag | Verfahren zur herstellung pharmazeutischer mischungen |
DE3830353A1 (de) | 1988-09-07 | 1990-03-15 | Basf Ag | Verfahren zur kontinuierlichen herstellung von festen pharmazeutischen formen |
US5368864A (en) | 1988-11-25 | 1994-11-29 | Henning Berlin Gmbh Chemie- Und Pharmawerk | Formulation of oxypurinol and/or its alkali and alkaline earth salts |
GB8903328D0 (en) | 1989-02-14 | 1989-04-05 | Ethical Pharma Ltd | Nifedipine-containing pharmaceutical compositions and process for the preparation thereof |
US5696270A (en) | 1989-05-23 | 1997-12-09 | Abbott Laboratories | Intermediate for making retroviral protease inhibiting compounds |
US5354866A (en) | 1989-05-23 | 1994-10-11 | Abbott Laboratories | Retroviral protease inhibiting compounds |
HU204529B (en) | 1989-08-10 | 1992-01-28 | Richter Gedeon Vegyeszet | Process for producing new 1-oxa-2-oxo-8-aza-spiro(4,5)decane derivatives and pharmaceutical compositions containing them |
US5075291A (en) | 1989-11-22 | 1991-12-24 | Ici Americas Inc. | Crystalline sugar alcohol containing uniformly dispersed particulate pharmaceutical compound |
AU648573B2 (en) | 1990-06-01 | 1994-04-28 | Research Corporation Technologies, Inc. | Self-emulsifying glasses |
SE9003296L (sv) | 1990-10-16 | 1992-04-17 | Kabi Pharmacia Ab | Foerfarande foer att formulera laekemedel |
KR0166096B1 (ko) | 1990-11-28 | 1999-01-15 | 우에하라 아키라 | 6-0-메틸에리쓰로마이신 a 유도체 |
ATE159426T1 (de) | 1991-04-16 | 1997-11-15 | Nippon Shinyaku Co Ltd | Verfahren zur herstellung einer festen dispersion |
WO1993007859A1 (en) | 1991-10-23 | 1993-04-29 | Warner-Lambert Company | Novel pharmaceutical pellets and process for their production |
DE4138513A1 (de) | 1991-11-23 | 1993-05-27 | Basf Ag | Feste pharmazeutische retardform |
AU671811B2 (en) | 1991-12-18 | 1996-09-12 | Warner-Lambert Company | A process for the preparation of a solid dispersion |
DE4200821A1 (de) | 1992-01-15 | 1993-07-22 | Bayer Ag | Geschmacksmaskierte pharmazeutische mittel |
DE4201179A1 (de) | 1992-01-17 | 1993-07-22 | Alfatec Pharma Gmbh | Wirkstoff(e) enthaltendes granulat oder pellet mit einem geruest aus hydrophilen makromolekuelen und verfahren zu seiner herstellung |
DE69331930T2 (de) | 1992-02-18 | 2003-01-09 | Pharmos Corp | Trockene zusammensetzungen zur herstellung von emulsionen im submikron-bereich |
US5654003A (en) | 1992-03-05 | 1997-08-05 | Fuisz Technologies Ltd. | Process and apparatus for making tablets and tablets made therefrom |
WO1993020138A2 (en) | 1992-03-30 | 1993-10-14 | Alza Corporation | Polymer system containing a partially soluble compound |
CA2095776C (en) | 1992-05-12 | 2007-07-10 | Richard C. Fuisz | Rapidly dispersable compositions containing polydextrose |
IT1256026B (it) | 1992-06-12 | 1995-11-20 | Sali del glutatione etilestere | |
DE4220782A1 (de) | 1992-06-25 | 1994-01-05 | Basf Ag | Verfahren zur Herstellung von festen pharmazeutischen Retardformen |
DE4226753A1 (de) | 1992-08-13 | 1994-02-17 | Basf Ag | Wirkstoffe enthaltende Zubereitungen in Form fester Teilchen |
US5968942A (en) | 1992-08-25 | 1999-10-19 | G. D. Searle & Co. | α- and β-amino acid hydroxyethylamino sulfonamides useful as retroviral protease inhibitors |
IS2334B (is) | 1992-09-08 | 2008-02-15 | Vertex Pharmaceuticals Inc., (A Massachusetts Corporation) | Aspartyl próteasi hemjari af nýjum flokki súlfonamíða |
US5484926A (en) | 1993-10-07 | 1996-01-16 | Agouron Pharmaceuticals, Inc. | HIV protease inhibitors |
GB9306887D0 (en) | 1993-04-01 | 1993-05-26 | Graham Neil B | Random block copolymers |
US6312726B1 (en) | 1993-08-20 | 2001-11-06 | Nippon Shinyaku Co., Ltd. | Gastric remaining preparation, swollen molding, and production process |
US5773025A (en) | 1993-09-09 | 1998-06-30 | Edward Mendell Co., Inc. | Sustained release heterodisperse hydrogel systems--amorphous drugs |
IL110752A (en) | 1993-09-13 | 2000-07-26 | Abbott Lab | Liquid semi-solid or solid pharmaceutical composition for an HIV protease inhibitor |
US5559158A (en) | 1993-10-01 | 1996-09-24 | Abbott Laboratories | Pharmaceutical composition |
ATE317397T1 (de) | 1993-11-17 | 2006-02-15 | Athena Neurosciences Inc | Transparente flüssigkeit zur verabreichung von verkapselten medikamenten |
KR100354702B1 (ko) | 1993-11-23 | 2002-12-28 | 유로-셀티크 소시에떼 아노뉨 | 약학조성물의제조방법및서방형조성물 |
IL111991A (en) | 1994-01-28 | 2000-07-26 | Abbott Lab | Liquid pharmaceutical composition of HIV protease inhibitors in organic solvent |
US6787156B1 (en) | 1994-02-23 | 2004-09-07 | Bm Research A/S | Controlled release composition |
DE4413350A1 (de) | 1994-04-18 | 1995-10-19 | Basf Ag | Retard-Matrixpellets und Verfahren zu ihrer Herstellung |
IL129871A (en) | 1994-05-06 | 2003-11-23 | Pharmacia & Upjohn Inc | Process for preparing 4-phenyl-substituted octanoyl-oxazolidin-2-one intermediates that are useful for preparing pyran-2-ones useful for treating retroviral infections |
DE19509807A1 (de) | 1995-03-21 | 1996-09-26 | Basf Ag | Verfahren zur Herstellung von Wirkstoffzubereitungen in Form einer festen Lösung des Wirkstoffs in einer Polymermatrix sowie mit diesem Verfahren hergestellte Wirkstoffzubereitungen |
US5443178A (en) | 1994-06-23 | 1995-08-22 | Allergan, Inc. | Tablet dispensing system |
FR2722984B1 (fr) | 1994-07-26 | 1996-10-18 | Effik Lab | Procede de preparation de formes pharmaceutiques seches et les compositions pharmaceutiques ainsi realisees |
ATE198152T1 (de) | 1994-09-30 | 2001-01-15 | Takeda Chemical Industries Ltd | Oral anzuwendende arzneizubereitung mit verzögerter wirkstoffabgabe |
US5965161A (en) | 1994-11-04 | 1999-10-12 | Euro-Celtique, S.A. | Extruded multi-particulates |
DE4446470A1 (de) | 1994-12-23 | 1996-06-27 | Basf Ag | Verfahren zur Herstellung von teilbaren Tabletten |
DE4446467A1 (de) | 1994-12-23 | 1996-06-27 | Basf Ag | Verfahren zur Herstellung von linsenförmigen Tabletten durch Schmelzkalandrierung |
DE4446468A1 (de) | 1994-12-23 | 1996-06-27 | Basf Ag | Verfahren zur Herstellung von umhüllten Tabletten |
US5545628A (en) | 1995-01-10 | 1996-08-13 | Galephar P.R. Inc. | Pharmaceutical composition containing fenofibrate |
DE19500977C2 (de) | 1995-01-14 | 1999-01-07 | Lohmann Therapie Syst Lts | Feste Arzneimittelform mit in polymerem Material verteiltem Wirkstoff |
NZ270439A (en) | 1995-02-02 | 1996-04-26 | Bernard Charles Sherman | Solid slow release pharmaceutical composition: carrier is polyethylene glycol and hydrophilic gel-forming polymer |
DE19504832A1 (de) | 1995-02-14 | 1996-08-22 | Basf Ag | Feste Wirkstoff-Zubereitungen |
DE19509806A1 (de) | 1995-03-21 | 1996-09-26 | Basf Ag | Lagerstabile Arzneiformen |
DE19509805A1 (de) | 1995-03-21 | 1996-09-26 | Basf Ag | Transparente, schnell freisetzende Zubereitungen von nichtsteroidalen Analgetica |
AU706195B2 (en) | 1995-04-14 | 1999-06-10 | Inhale Therapeutic Systems | Powdered pharmaceutical formulations having improved dispersibility |
SI9500173B (sl) | 1995-05-19 | 2002-02-28 | Lek, | Trofazna farmacevtska oblika s konstantnim in kontroliranim sproščanjem amorfne učinkovine za enkrat dnevno aplikacijo |
US5567823A (en) | 1995-06-06 | 1996-10-22 | Abbott Laboratories | Process for the preparation of an HIV protease inhibiting compound |
SE9502244D0 (sv) | 1995-06-20 | 1995-06-20 | Bioglan Ab | A composition and a process for the preparation thereof |
US6037157A (en) | 1995-06-29 | 2000-03-14 | Abbott Laboratories | Method for improving pharmacokinetics |
BE1009856A5 (fr) | 1995-07-14 | 1997-10-07 | Sandoz Sa | Composition pharmaceutique sous la forme d'une dispersion solide comprenant un macrolide et un vehicule. |
TW487582B (en) | 1995-08-11 | 2002-05-21 | Nissan Chemical Ind Ltd | Method for converting sparingly water-soluble medical substance to amorphous state |
DE69617245T2 (de) | 1995-08-17 | 2002-07-25 | Csir Pretoria | Produkte mit gesteuerter freisetzung |
DE19531277A1 (de) | 1995-08-25 | 1997-02-27 | Basf Ag | Verwendung von Lipiden als Hilfsmittel bei der Herstellung von festen Arzneiformen nach dem Schmelzextrusionsverfahren |
US6391338B1 (en) | 1995-09-07 | 2002-05-21 | Biovail Technologies Ltd. | System for rendering substantially non-dissoluble bio-affecting agents bio-available |
GB9519363D0 (en) | 1995-09-22 | 1995-11-22 | Euro Celtique Sa | Pharmaceutical formulation |
DE19536394A1 (de) | 1995-09-29 | 1997-04-03 | Basf Ag | Feste Arzneiformen, erhältlich durch Extrusion einer Isomalt enthaltenden Polymer-Wirkstoff-Schmelze |
DE19536387A1 (de) | 1995-09-29 | 1997-04-03 | Basf Ag | Verfahren zur Herstellung von vitaminhaltigen festen Zubereitungen |
EP0862420A4 (en) | 1995-10-13 | 1999-11-03 | Penn State Res Found | SYNTHESIS OF DRUG SPRAY DRUG NANOPARTICLES |
DE19539361A1 (de) | 1995-10-23 | 1997-04-24 | Basf Ag | Verfahren zur Herstellung von mehrschichtigen, festen Arzneiformen zur oralen oder rektalen Verabreichung |
DE19539574A1 (de) | 1995-10-25 | 1997-04-30 | Boehringer Mannheim Gmbh | Zubereitungen und Verfahren zur Stabilisierung biologischer Materialien mittels Trocknungsverfahren ohne Einfrieren |
US5914332A (en) | 1995-12-13 | 1999-06-22 | Abbott Laboratories | Retroviral protease inhibiting compounds |
US5858401A (en) | 1996-01-22 | 1999-01-12 | Sidmak Laboratories, Inc. | Pharmaceutical composition for cyclosporines |
DE19602206A1 (de) | 1996-01-23 | 1997-07-24 | Basf Ag | Zubereitungen nichtsteroidaler Analgetika |
US5958455A (en) | 1996-02-09 | 1999-09-28 | Quadrant Holdings Cambridge Ltd | Oral solid dosage forms, methods of making same and compositions thereof |
US5762961A (en) | 1996-02-09 | 1998-06-09 | Quadrant Holdings Cambridge Ltd. | Rapidly soluble oral solid dosage forms, methods of making same, and compositions thereof |
GB2311027B (en) | 1996-03-15 | 1999-10-27 | Johnson & Johnson Medical | Coated bioabsorbable beads for wound treatment |
US20030064108A1 (en) | 1996-04-23 | 2003-04-03 | Stefan Lukas | Taste masked pharmaceutical compositions |
DE19617716A1 (de) | 1996-05-03 | 1997-11-06 | Basf Ag | In wäßriger Lösung redispergierbare Polymerpulver |
US5834472A (en) | 1996-05-24 | 1998-11-10 | Schering Corporation | Antifungal composition with enhanced bioavailability |
US6764690B2 (en) | 1996-05-29 | 2004-07-20 | Delsitech Oy | Dissolvable oxides for biological applications |
AU3146997A (en) | 1996-06-03 | 1998-01-05 | Merck & Co., Inc. | Pediatric formulation for hiv protease inhibitors |
US5935936A (en) | 1996-06-03 | 1999-08-10 | Genzyme Corporation | Compositions comprising cationic amphiphiles and co-lipids for intracellular delivery of therapeutic molecules |
DE19624607A1 (de) | 1996-06-20 | 1998-01-02 | Basf Ag | Verfahren zur Herstellung von Salzen von Säuregruppen tragenden pharmazeutischen Wirkstoffen |
DE69739343D1 (de) | 1996-06-26 | 2009-05-14 | Univ Texas | Heiss-geschmolzene extrudierbare pharmazeutische formulierung |
DE19629753A1 (de) | 1996-07-23 | 1998-01-29 | Basf Ag | Verfahren zur Herstellung von festen Arzneiformen |
DE19635676A1 (de) | 1996-09-03 | 1998-03-05 | Basf Ag | Feste geschäumte Wirkstoffzubereitungen |
DE19637479A1 (de) | 1996-09-13 | 1998-03-19 | Basf Ag | Verfahren zur Herstellung fester pharmazeutischer Formen |
HRP970485A2 (en) | 1996-09-13 | 1998-08-31 | Joerg Rosenberg | Process for producing solid pharmaceutical forms |
US6649186B1 (en) | 1996-09-20 | 2003-11-18 | Ethypharm | Effervescent granules and methods for their preparation |
US6071539A (en) | 1996-09-20 | 2000-06-06 | Ethypharm, Sa | Effervescent granules and methods for their preparation |
US6488961B1 (en) | 1996-09-20 | 2002-12-03 | Ethypharm, Inc. | Effervescent granules and methods for their preparation |
US5727878A (en) | 1996-10-17 | 1998-03-17 | Cdf Corporation | Liner for a mixing container and an assembly and method for mixing fluid components |
US8828432B2 (en) | 1996-10-28 | 2014-09-09 | General Mills, Inc. | Embedding and encapsulation of sensitive components into a matrix to obtain discrete controlled release particles |
US20010006677A1 (en) | 1996-10-29 | 2001-07-05 | Mcginity James W. | Effervescence polymeric film drug delivery system |
ATE275942T1 (de) | 1996-11-15 | 2004-10-15 | Merck Patent Gmbh | Verfahren zur herstellung von geformten oder ungeformten polyolmassen und hergestelle zusammensetzungen |
US6232333B1 (en) | 1996-11-21 | 2001-05-15 | Abbott Laboratories | Pharmaceutical composition |
ZA9710071B (en) | 1996-11-21 | 1998-05-25 | Abbott Lab | Pharmaceutical composition. |
TW486370B (en) | 1996-12-25 | 2002-05-11 | Yamanouchi Pharma Co Ltd | Rapidly disintegrable pharmaceutical composition |
US6045829A (en) | 1997-02-13 | 2000-04-04 | Elan Pharma International Limited | Nanocrystalline formulations of human immunodeficiency virus (HIV) protease inhibitors using cellulosic surface stabilizers |
US6197787B1 (en) | 1997-03-03 | 2001-03-06 | Sanofi-Synthelabo | Pharmaceutical formulations containing poorly soluble drug substances |
DE19709663A1 (de) | 1997-03-10 | 1998-09-17 | Basf Ag | Verwendung von redispergierbaren Polymerpulvern oder Polymergranulaten als Bindemittel zur Herstellung von festen pharmazeutischen Darreichungsformen |
DE19710009A1 (de) | 1997-03-12 | 1998-09-24 | Knoll Ag | Mehrphasige wirkstoffhaltige Zubereitungsformen |
DE19710213A1 (de) | 1997-03-12 | 1998-09-17 | Basf Ag | Verfahren zur Herstellung von festen Kombinationsarzneiformen |
US5948426A (en) | 1997-05-03 | 1999-09-07 | Jefferies; Steven R. | Method and article to induce hematopoietic expansion |
US6610764B1 (en) | 1997-05-12 | 2003-08-26 | Metabolix, Inc. | Polyhydroxyalkanoate compositions having controlled degradation rates |
DE19721467A1 (de) | 1997-05-22 | 1998-11-26 | Basf Ag | Verfahren zur Herstellung kleinteiliger Zubereitungen biologisch aktiver Stoffe |
GB9710699D0 (en) | 1997-05-24 | 1997-07-16 | Danbiosyst Uk | Gastro-retentive controlled release system |
JPH1125076A (ja) | 1997-06-30 | 1999-01-29 | Fujitsu Ltd | 文書管理装置および文書管理プログラム記憶媒体 |
US5955475A (en) | 1997-06-30 | 1999-09-21 | Endo Pharmaceuticals Inc. | Process for manufacturing paroxetine solid dispersions |
US5889051A (en) | 1997-07-15 | 1999-03-30 | Development Center For Biotechnology | Stabilization of prostaglandin drug |
DE19733505A1 (de) | 1997-08-01 | 1999-02-04 | Knoll Ag | Schnell wirksames Analgeticum |
DK0901786T3 (da) | 1997-08-11 | 2007-10-08 | Pfizer Prod Inc | Faste farmaceutiske dispersioner med foröget biotilgængelighed |
HN1998000115A (es) | 1997-08-21 | 1999-06-02 | Warner Lambert Co | Formas de dosificación farmacéuticas sólidas |
DE69828635T2 (de) | 1997-09-19 | 2005-06-16 | Shire Laboratories, Inc. | Feste lösungskügelchen |
JP3460538B2 (ja) | 1997-10-08 | 2003-10-27 | 救急薬品工業株式会社 | 速溶性フィルム製剤 |
US20020164374A1 (en) | 1997-10-29 | 2002-11-07 | John Jackson | Polymeric systems for drug delivery and uses thereof |
US6027747A (en) | 1997-11-11 | 2000-02-22 | Terracol; Didier | Process for the production of dry pharmaceutical forms and the thus obtained pharmaceutical compositions |
ATE214595T1 (de) | 1997-11-28 | 2002-04-15 | Knoll Ag | Verfahren zur herstellung von lösungsmittelfreien nicht-kristallinen biologisch aktiven substanzen |
DE19753298A1 (de) | 1997-12-01 | 1999-06-02 | Basf Ag | Verfahren zur Herstellung von festen Dosierungsformen |
US6632455B2 (en) | 1997-12-22 | 2003-10-14 | Schering Corporation | Molecular dispersion composition with enhanced bioavailability |
JPH11271927A (ja) * | 1998-01-20 | 1999-10-08 | Mitsubishi Paper Mills Ltd | 画像材料用支持体 |
GB9802088D0 (en) | 1998-01-30 | 1998-03-25 | Scherer Ltd R P | Pharmaceutical products |
US6787157B1 (en) | 1998-03-10 | 2004-09-07 | Abbott Laboratories | Multiphase active ingredient-containing formulations |
RU2204996C2 (ru) | 1998-03-16 | 2003-05-27 | Яманоути Фармасьютикал Ко., Лтд. | Таблетка, быстро распадающаяся в щечном кармане, и способ ее изготовления |
DE19812688A1 (de) | 1998-03-23 | 1999-09-30 | Basf Ag | Verfahren zur Herstellung von festen Dosierungsformen |
US5945123A (en) | 1998-04-02 | 1999-08-31 | K-V Pharmaceutical Company | Maximizing effectiveness of substances used to improve health and well being |
DE19814730A1 (de) | 1998-04-02 | 1999-10-07 | Basf Ag | Verwendung von N-Vinyllacram oder N-Vinylamin haltigen Copolymeren als Matrix zur Herstellung von festen pharmazeutischen und kosmetischen Darreichungsformen |
US20040062802A1 (en) | 1998-04-02 | 2004-04-01 | Hermelin Victor M. | Maximizing effectiveness of substances used to improve health and well being |
DE19814739A1 (de) | 1998-04-02 | 1999-10-07 | Basf Ag | Verwendung von Polyalkylenoxid-haltigen Pfropfpolymerisaten als Solubilisatoren |
CA2327655C (en) | 1998-04-08 | 2010-03-09 | Kyowa Hakko Kogyo Co., Ltd. | Tablet production method and tablet |
WO1999055774A1 (en) | 1998-04-24 | 1999-11-04 | Eastman Chemical Company | Coprecipitation of cellulose esters with functional additives and compositions thus obtainable |
JP4027535B2 (ja) | 1998-05-26 | 2007-12-26 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 脂溶性薬物を含有した粉末 |
CA2334449A1 (en) | 1998-06-05 | 1999-12-16 | Radka K. Milanova | Compositions comprising phytosterol, phytostanol or mixtures of both having enhanced solubility and dispersability and incorporation thereof into foods, beverages, pharmaceuticals, nutraceuticals and the like |
JP2002517431A (ja) | 1998-06-11 | 2002-06-18 | イーエム インダストリーズ インコーポレイテッド | マイクロ浸透圧制御薬物送達システム |
KR100336090B1 (ko) | 1998-06-27 | 2002-05-27 | 윤승원 | 오일, 지방산 또는 이들의 혼합물을 함유한 난용성 약물의 고형분산제제 |
CO5090830A1 (es) * | 1998-07-20 | 2001-10-30 | Abbott Lab | Poliformo de un agente farmaceutico |
US6894171B1 (en) | 1998-07-20 | 2005-05-17 | Abbott Laboratories | Polymorph of a pharmaceutical |
US6323180B1 (en) | 1998-08-10 | 2001-11-27 | Boehringer Ingelheim (Canada) Ltd | Hepatitis C inhibitor tri-peptides |
US20010021372A1 (en) | 1998-08-18 | 2001-09-13 | Tore Omtveit | Apparatus having partially gold-plated surface |
DE19839276A1 (de) | 1998-08-28 | 2000-03-02 | Basf Ag | Verfahren zur Herstellung von festen Dosierungsformen |
DE19840256A1 (de) | 1998-09-03 | 2000-03-09 | Basf Ag | Verfahren zur Herstellung von beschichteten festen Dosierungsformen |
DE19841244A1 (de) | 1998-09-09 | 2000-03-16 | Knoll Ag | Verfahren und Vorrichtung zum Herstellen von Tabletten |
DE19842753A1 (de) | 1998-09-18 | 2000-03-23 | Bayer Ag | Agitationsunabhängige pharmazeutische Retardzubereitungen und Verfahren zu ihrer Herstellung |
DE19842914A1 (de) | 1998-09-18 | 2000-03-23 | Basf Ag | Testsystem zur Charakterisierung der Verträglichkeit von biologisch aktiven Substanzen und Polyvinylpyrrolidon |
DE19843904A1 (de) | 1998-09-24 | 2000-03-30 | Basf Ag | Feste Dosierungsform mit polymerem Bindemittel |
US20040013613A1 (en) | 2001-05-18 | 2004-01-22 | Jain Rajeev A | Rapidly disintegrating solid oral dosage form |
US6383594B2 (en) * | 1998-10-07 | 2002-05-07 | Johns Manville International, Inc. | Pre-cut fibrous insulation for custom fitting building cavities of different widths |
DE19847618A1 (de) | 1998-10-15 | 2000-04-20 | Basf Ag | Verfahren zur Herstellung von festen Dosierungsformen |
US6502135B1 (en) | 1998-10-30 | 2002-12-31 | Science Applications International Corporation | Agile network protocol for secure communications with assured system availability |
DE19853985A1 (de) | 1998-11-23 | 2000-05-25 | Basf Ag | Verfahren zur Herstellung von festen Dosierungsformen |
DE19855440A1 (de) | 1998-12-01 | 2000-06-08 | Basf Ag | Verfahren zum Herstellen fester Darreichungsformen mittels Schmelzextrusion |
DE19856147A1 (de) | 1998-12-04 | 2000-06-08 | Knoll Ag | Teilbare feste Dosierungsformen und Verfahren zu ihrer Herstellung |
DE19856432A1 (de) | 1998-12-08 | 2000-06-15 | Basf Ag | Nanopartikuläre Kern-Schale Systeme sowie deren Verwendung in pharmazeutischen und kosmetischen Zubereitungen |
AT407111B (de) | 1998-12-22 | 2000-12-27 | Gergely Dr & Co | Zucker- und/oder zuckeralkoholhältiges matrixmaterial und verfahren zu seiner herstellung |
EP1058539A1 (en) | 1999-01-06 | 2000-12-13 | Korea Research Institute Of Chemical Technology | Method of preparing pharmaceutical active ingredient comprising water-insoluble drug and pharmaceutical composition for oral administration comprising the same |
DE19901383A1 (de) | 1999-01-15 | 2000-07-20 | Knoll Ag | Verfahren zur Herstellung unterschiedlicher fester Dosierungsformen |
DE60039379D1 (de) | 1999-02-10 | 2008-08-21 | Pfizer Prod Inc | Pharmazeutische feste Dispersionen |
US6706283B1 (en) | 1999-02-10 | 2004-03-16 | Pfizer Inc | Controlled release by extrusion of solid amorphous dispersions of drugs |
DE60039802D1 (de) | 1999-02-10 | 2008-09-25 | Pfizer Prod Inc | Vorrichtung mit matrixgesteuerter Wirkstofffreisetzung |
US6440946B1 (en) * | 1999-02-25 | 2002-08-27 | Takeda Chemical Industries, Ltd. | Multiple-agents-binding compound, production and use thereof |
US6248363B1 (en) | 1999-11-23 | 2001-06-19 | Lipocine, Inc. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
US6294192B1 (en) | 1999-02-26 | 2001-09-25 | Lipocine, Inc. | Triglyceride-free compositions and methods for improved delivery of hydrophobic therapeutic agents |
DE19911097A1 (de) | 1999-03-12 | 2000-09-14 | Basf Ag | Verfahren zur Herstellung von festen cyclodextrinhaltigen Dosierungsformen |
CA2362728C (en) | 1999-03-24 | 2009-06-23 | Fmc Corporation | Improved aqueous solubility pharmaceutical formulations |
DE19913692A1 (de) * | 1999-03-25 | 2000-09-28 | Basf Ag | Mechanisch stabile pharmazeutische Darreichungsformen, enthaltend flüssige oder halbfeste oberflächenaktive Substanzen |
DE19913606A1 (de) | 1999-03-25 | 2000-09-28 | Basf Ag | Pulverförmige Solubilisationshilfsstoffe für feste pharmazeutische Darreichungsformen |
US6383471B1 (en) | 1999-04-06 | 2002-05-07 | Lipocine, Inc. | Compositions and methods for improved delivery of ionizable hydrophobic therapeutic agents |
FR2793689B1 (fr) | 1999-05-19 | 2001-08-24 | Pf Medicament | Dispositif transdermique pour l'administration de testosterone ou d'un de ses derives |
US7919119B2 (en) | 1999-05-27 | 2011-04-05 | Acusphere, Inc. | Porous drug matrices and methods of manufacture thereof |
US6465011B2 (en) | 1999-05-29 | 2002-10-15 | Abbott Laboratories | Formulations comprising lipid-regulating agents |
NL1012300C2 (nl) | 1999-06-11 | 2000-12-12 | Rijksuniversiteit | Stabilisator voor farmaca. |
FR2795326B1 (fr) | 1999-06-28 | 2001-08-31 | Adir | Composition pharmaceutique solide thermoformable a liberation controlee |
DE19930454A1 (de) | 1999-07-02 | 2001-01-04 | Knoll Ag | Feste Paroxetin enthaltende Zubereitungen |
DE19934610A1 (de) | 1999-07-23 | 2001-01-25 | Bayer Ag | Schnellfreisetzende Extrudate und Verfahren zu ihrer Herstellung sowie daraus erhältliche Zubereitungen |
US6284270B1 (en) | 1999-08-04 | 2001-09-04 | Drugtech Corporation | Means for creating a mass having structural integrity |
SE9903236D0 (sv) | 1999-09-10 | 1999-09-10 | Astra Ab | Method to obtain microparticles |
DE19943501A1 (de) | 1999-09-10 | 2001-03-15 | Basf Ag | Unterwassergranulation wirkstoffhaltiger Schmelzen |
CA2386312A1 (en) | 1999-09-29 | 2001-04-05 | R.P. Scherer Technologies, Inc. | Hydrolyzed cellulose granulations of salts of drugs |
DE19949897A1 (de) | 1999-10-15 | 2001-04-19 | Rainer Rogasch | Formkörper und Verfahren zu dessen Herstellung |
US6264981B1 (en) | 1999-10-27 | 2001-07-24 | Anesta Corporation | Oral transmucosal drug dosage using solid solution |
US6372259B1 (en) | 1999-11-10 | 2002-04-16 | University Of Iowa Research Foundation | Palatable, sustained release drug granules |
DE60028754T2 (de) | 1999-11-12 | 2007-05-31 | Abbott Laboratories, Abbott Park | Feste dispersion mit ritonavir, fenofibrat oder griseofulvin |
WO2001034118A2 (en) | 1999-11-12 | 2001-05-17 | Abbott Laboratories | Solid dispersion pharmaceutical formulations |
US7364752B1 (en) | 1999-11-12 | 2008-04-29 | Abbott Laboratories | Solid dispersion pharamaceutical formulations |
DE19958007A1 (de) | 1999-12-02 | 2001-06-07 | Roehm Gmbh | Spritzgußverfahren für (Meth)acrylat-Copolymere mit teritiären Ammoniumgruppen |
DE19960494A1 (de) | 1999-12-15 | 2001-06-21 | Knoll Ag | Vorrichtung und Verfahren zum Herstellen von festen wirkstoffhaltigen Formen |
DE19961334A1 (de) | 1999-12-17 | 2001-06-21 | Roehm Gmbh | Spritzgußverfahren für neutrale und säuregruppenhaltige (Meth)acrylat-Copolymere |
JP5159012B2 (ja) | 1999-12-23 | 2013-03-06 | メイン・ファ−マ・インタ−ナショナル・プロプライエタリ−・リミテッド | 不良溶解性の薬物に対する改良された医薬組成物 |
AU784340B2 (en) | 1999-12-23 | 2006-03-16 | Pfizer Products Inc. | Pharmaceutical compositions providing enhanced drug concentrations |
KR100523127B1 (ko) | 1999-12-23 | 2005-10-20 | 화이자 프로덕츠 인코포레이티드 | 하이드로겔계 약물 투여 형태 |
DE10000792A1 (de) | 2000-01-11 | 2001-07-19 | Bernhard C Lippold | Formulierungen von Wirkstoffen in Form einer festen Dispersion |
US7029700B2 (en) | 2000-01-14 | 2006-04-18 | Brown University Research Foundation | Micronized freeze-dried particles |
JP2001217428A (ja) | 2000-01-25 | 2001-08-10 | Samsung Electronics Co Ltd | 低温多結晶シリコン形薄膜トランジスタ−及びその製造方法 |
GB0003782D0 (en) | 2000-02-17 | 2000-04-05 | Dumex Ltd As | Process |
GB0005016D0 (en) | 2000-03-01 | 2000-04-26 | Jumik Technologies Limited | PVA-Containing compositions |
PT1263413E (pt) | 2000-03-09 | 2006-08-31 | Univ Ohio State Res Found | Metodo de preparacao de dispersoes solidas |
AR028253A1 (es) | 2000-03-16 | 2003-04-30 | Pfizer Prod Inc | Inhibidores de la glucogeno fosforilasa |
DE10013289A1 (de) | 2000-03-17 | 2001-09-20 | Knoll Ag | Torasemid enthaltende pharmazeutische Zubereitungen |
DE10015479A1 (de) | 2000-03-29 | 2001-10-11 | Basf Ag | Feste orale Darreichungsformen mit retardierter Wirkstofffreisetzung und hoher mechanischer Stabilität |
US6608198B2 (en) | 2000-03-30 | 2003-08-19 | Abbott Laboratories | Crystalline pharmaceutical |
GB0008785D0 (en) | 2000-04-10 | 2000-05-31 | Novartis Ag | Organic compounds |
DE10021539C1 (de) | 2000-05-03 | 2002-02-28 | Henkel Kgaa | Vorrichtung zur Sprühtrocknung von lösungsmittelhaltigen Zusammensetzungen |
US20020001617A1 (en) | 2000-05-26 | 2002-01-03 | Chang-Hyun Lee | Rapidly disintegrating tablet and process for the manufacture thereof |
DE10026698A1 (de) | 2000-05-30 | 2001-12-06 | Basf Ag | Selbstemulgierende Wirkstoffformulierung und Verwendung dieser Formulierung |
DE10026699A1 (de) | 2000-05-30 | 2001-12-06 | Basf Ag | Formulierung auf Heparin-, Glycosaminoglycan- oder Heparinoidbasis und Verwendung der Formulierung sowie der Formulierungsgrundlage |
DE10029201A1 (de) | 2000-06-19 | 2001-12-20 | Basf Ag | Verfahren zur Herstellung fester oraler Darreichungsformen mit retardierender Wirkstoffreisetzung |
US20100010101A1 (en) | 2000-07-05 | 2010-01-14 | Capricorn Pharma, Inc. | Rapid-Melt Compositions and Methods of Making Same |
AU2001279284A1 (en) | 2000-07-05 | 2002-01-14 | Capricorn Pharma, Inc | Rapid-melt semi-solid compositions, methods of making same and methods of using same |
IT1318618B1 (it) | 2000-07-10 | 2003-08-27 | A C R Applied Coating Res S A | Microsfere bioadesive a rilascio rapido per la somministrazionesublinguale di principi attivi. |
AU2001289653A1 (en) | 2000-07-14 | 2002-01-30 | Universiteit Gent | Composite solid shaped articles for the controlled delivery of biologically active ingredients |
DE10038571A1 (de) | 2000-08-03 | 2002-02-14 | Knoll Ag | Zusammensetzungen und Dosierungsformen zur Anwendung in der Mundhöhle bei der Bhandlung von Mykosen |
CA2418490A1 (en) | 2000-08-11 | 2002-02-21 | Eisai Co., Ltd. | Drug-containing solid dispersion having improved solubility |
US6372905B1 (en) * | 2000-08-31 | 2002-04-16 | Abbott Laboratories | Processes and intermediates for preparing retroviral protease inhibitors |
DE10046541A1 (de) | 2000-09-19 | 2002-03-28 | Knoll Ag | Mechanisch stabile darreichungsformen, enthaltend Ubichinone |
FR2814366A1 (fr) | 2000-09-22 | 2002-03-29 | Rhodia Chimie Sa | Procede de granulation de matieres actives par extrusion basse pression pour l'obtention de granules directement compressibles |
WO2002024168A1 (fr) | 2000-09-25 | 2002-03-28 | Nippon Shinyaku Co., Ltd. | Procede de production d'une dispersion solide medicinale |
JP2004509739A (ja) | 2000-09-27 | 2004-04-02 | ベリオン インコーポレイテッド | 即時水溶解性カプセルおよびその製法 |
US6579521B2 (en) * | 2000-10-20 | 2003-06-17 | Chiron Corporation | Methods of therapy for HIV infection |
WO2002035991A2 (en) | 2000-10-30 | 2002-05-10 | The Board Of Regents, The University Of Texas System | Spherical particles produced by a hot-melt extrusion/spheronization process |
GB0026593D0 (en) | 2000-10-31 | 2000-12-13 | Quadrant Holdings Cambridge | Derivatised carbohydrates and their use in solid delivery systems |
AU2002212102A1 (en) | 2000-11-08 | 2002-05-21 | Aeromatic-Fielder Ag | A process for production of particles for pharmaceutical compositions having increased bioavailability |
CN100408099C (zh) | 2000-11-09 | 2008-08-06 | 阿斯特拉曾尼卡有限公司 | 含有嵌段共聚物的口服药物组合物 |
GB0027357D0 (en) | 2000-11-09 | 2000-12-27 | Bradford Particle Design Plc | Particle formation methods and their products |
US6733781B2 (en) | 2000-12-06 | 2004-05-11 | Wyeth | Fast dissolving tablet |
GB0029843D0 (en) | 2000-12-07 | 2001-01-24 | Univ Belfast | Drug delivery system |
US20050175687A1 (en) | 2001-01-30 | 2005-08-11 | Mcallister Stephen M. | Pharmaceutical formulations |
US7883721B2 (en) | 2001-01-30 | 2011-02-08 | Smithkline Beecham Limited | Pharmaceutical formulation |
US7842308B2 (en) | 2001-01-30 | 2010-11-30 | Smithkline Beecham Limited | Pharmaceutical formulation |
MXPA03007092A (es) | 2001-02-13 | 2003-11-18 | Astrazeneca Ab | Nueva formulacion de liberacion modificada. |
GB0104752D0 (en) | 2001-02-27 | 2001-04-18 | Astrazeneca Ab | Pharmaceutical compositions |
US6713081B2 (en) | 2001-03-15 | 2004-03-30 | The United States Of America As Represented By The Department Of Health And Human Services | Ocular therapeutic agent delivery devices and methods for making and using such devices |
EP1387684A1 (en) * | 2001-05-01 | 2004-02-11 | Abbott Laboratories | Compositions comprising lopinavir and methods for enhancing the bioavailability of pharmaceutical agents |
DE60201988T2 (de) | 2001-05-03 | 2005-12-15 | F. Hoffmann-La Roche Ag | Pharmazeutische dosierungsform von amorphem nilfenavir mesylat |
AR033711A1 (es) | 2001-05-09 | 2004-01-07 | Novartis Ag | Composiciones farmaceuticas |
US20030096791A1 (en) | 2001-05-31 | 2003-05-22 | Cima Labs Inc. | Taste masking of highly water-soluble drugs |
DE10127134A1 (de) | 2001-06-05 | 2002-12-12 | Roehm Gmbh | verfahren zur Herstellung von Formkörpern aus (Meth)acrylat-Copolymeren mittels Spritzguß |
US6730319B2 (en) | 2001-06-06 | 2004-05-04 | Hoffmann-La Roche Inc. | Pharmaceutical compositions having depressed melting points |
US20030212102A1 (en) | 2001-06-12 | 2003-11-13 | Koretke Todd W | Novel solid dispersion compositions |
MXPA03011933A (es) | 2001-06-22 | 2004-03-26 | Pfizer Prod Inc | Composiciones farmaceuticas de farmacos y polimeros acidos neutralizados. |
AU2002302903B2 (en) | 2001-06-22 | 2007-05-17 | Pfizer Products Inc. | Pharmaceutical compositions of adsorbates of amorphous drug |
EP1269994A3 (en) | 2001-06-22 | 2003-02-12 | Pfizer Products Inc. | Pharmaceutical compositions comprising drug and concentration-enhancing polymers |
BR0211028A (pt) | 2001-06-22 | 2004-06-15 | Pfizer Prod Inc | Solução aquosa, método para formação de associações de fármaco e polìmero, composições farmacêuticas, método para formação de uma composição farmacêutica e produto |
JP2004534812A (ja) | 2001-06-22 | 2004-11-18 | ファイザー・プロダクツ・インク | 薬物および中性ポリマーの分散物の医薬組成物 |
JP2005500313A (ja) | 2001-06-22 | 2005-01-06 | ファイザー・プロダクツ・インク | 基材中の低可溶性薬物の固体分散体および溶解度向上性ポリマーを含有する医薬品組成物 |
ITMI20011337A1 (it) | 2001-06-26 | 2002-12-26 | Farmatron Ltd | Composizioni farmaceutiche orali a rilascio modificato del principio attivo |
ITMI20011338A1 (it) | 2001-06-26 | 2002-12-26 | Farmatron Ltd | Composizioni farmaceutiche orali a rilascio immediato del principio attivo |
CN101961317A (zh) | 2001-07-06 | 2011-02-02 | 生命周期药物公司 | 受控制的凝聚 |
US20030044474A1 (en) | 2001-08-03 | 2003-03-06 | Shaklee Corporation | High molecular weight, lipophilic, orally ingestible bioactive agents in formulations having improved bioavailability |
FR2828380B1 (fr) | 2001-08-10 | 2005-07-29 | Fontarome | Composition a structure composite contenant des substances aromatiques et/ou des substances non aromatiques volatiles et/ou sensibles aux agents exterieurs, et son procede de fabrication |
JP4644397B2 (ja) | 2001-09-05 | 2011-03-02 | 信越化学工業株式会社 | 難溶性薬物を含む医薬用固形製剤の製造方法 |
US20050019399A1 (en) | 2001-09-21 | 2005-01-27 | Gina Fischer | Controlled release solid dispersions |
MXPA04002979A (es) | 2001-09-28 | 2005-06-20 | Johnson & Johnson | Formas de dosificacion de liberacion modificada. |
US6982094B2 (en) | 2001-09-28 | 2006-01-03 | Mcneil-Ppc, Inc. | Systems, methods and apparatuses for manufacturing dosage forms |
US7122143B2 (en) | 2001-09-28 | 2006-10-17 | Mcneil-Ppc, Inc. | Methods for manufacturing dosage forms |
DE10151290A1 (de) | 2001-10-22 | 2003-04-30 | Roehm Gmbh | Verfahren zur Herstellung von wirkstoffhaltigen Pellets |
US20030091630A1 (en) | 2001-10-25 | 2003-05-15 | Jenny Louie-Helm | Formulation of an erodible, gastric retentive oral dosage form using in vitro disintegration test data |
US20030099708A1 (en) | 2001-10-29 | 2003-05-29 | Therics, Inc | Printing or dispensing a suspension such as three-dimensional printing of dosage forms |
US7491407B2 (en) | 2001-10-31 | 2009-02-17 | North Carolina State University | Fiber-based nano drug delivery systems (NDDS) |
JP2003146869A (ja) | 2001-11-14 | 2003-05-21 | Scg:Kk | 口腔内崩壊型固形製剤及びその製造方法 |
US6524606B1 (en) | 2001-11-16 | 2003-02-25 | Ap Pharma, Inc. | Bioerodible polyorthoesters containing amine groups |
US20030129250A1 (en) | 2001-11-20 | 2003-07-10 | Advanced Inhalation Research Inc. | Particulate compositions for improving solubility of poorly soluble agents |
US7179488B2 (en) | 2001-11-29 | 2007-02-20 | Bob Sherwood | Process for co-spray drying liquid herbal extracts with dry silicified MCC |
WO2003047551A1 (en) | 2001-11-29 | 2003-06-12 | Penwest Pharmaceutical Company | Agglomerated particles including an active agent coprocessed with silicified microcrystalline cellulose |
US20030206978A1 (en) | 2001-11-29 | 2003-11-06 | Bob Sherwood | Agglomerated particles including an active agent coprocessed with silicified microcrystalline cellulose |
EP1460897A4 (en) | 2001-12-10 | 2006-09-13 | Spherics Inc | PROCESSES AND PRODUCTS SUITED TO THE FORMATION AND ISOLATION OF MICROPARTICLES |
CA2471948A1 (en) | 2002-01-03 | 2003-07-17 | Smithkline Beecham Corporation | Novel pharmaceutical dosage forms and method for producing same |
EP1469830A2 (en) | 2002-02-01 | 2004-10-27 | Pfizer Products Inc. | Method for making homogeneous spray-dried solid amorphous drug dispersions using pressure nozzles |
EP1469832B2 (en) | 2002-02-01 | 2016-10-26 | Bend Research, Inc. | Pharmaceutical compositions of amorphous dispersions of drugs and lipophilic microphase-forming materials |
BR0307333A (pt) | 2002-02-01 | 2004-12-07 | Pfizer Prod Inc | Métodos para a preparação de dispersões homogéneas de fármacos sólidos amorfos atomizados utilizando um sistema de secagem por pulverização |
BR0307516A (pt) | 2002-02-01 | 2004-12-07 | Pfizer Prod Inc | Formas de dosagem de liberação imediata contendo dispersões de uma droga sólida |
AR038681A1 (es) | 2002-02-14 | 2005-01-26 | Solvay Pharm Bv | Formulacion oral de solucion solida de una sustancia activa pobremente soluble en agua |
DE10208344A1 (de) | 2002-02-27 | 2003-09-04 | Roehm Gmbh | Schmelzextrusion von Wirkstoffsalzen |
GB0205253D0 (en) | 2002-03-06 | 2002-04-17 | Univ Gent | Immediate release pharmaceutical granule compositions and a continuous process for making them |
CA2478519C (en) | 2002-03-07 | 2011-08-02 | Eurand Pharmaceuticals Limited | Process for loading and thermodynamically activating drugs on polymers by means of supercritical fluids |
DE60222734T2 (de) | 2002-03-15 | 2008-07-17 | Alrise Biosystems Gmbh | Mikropartikel und Verfahren zur deren Herstellung |
DE10213242A1 (de) | 2002-03-25 | 2003-10-16 | Abbott Gmbh & Co Kg | Testsystem zur Evaluierung der Kompatibilität biologisch aktiver Substanzen mit Copolymeren |
DE10213977A1 (de) | 2002-03-28 | 2003-10-16 | Krauss Maffei Kunststofftech | Verfahren zum Herstellen von Wirkstoffe enthaltenden Formkörpern |
CN102813654A (zh) | 2002-04-05 | 2012-12-12 | 欧洲凯尔蒂克公司 | 含有羟氢可待酮和烯丙羟吗啡酮的药物制剂 |
CA2484100C (en) | 2002-04-19 | 2012-01-03 | Novartis Ag | Novel biomaterials, their preparation and use |
US20030203027A1 (en) | 2002-04-26 | 2003-10-30 | Ethicon, Inc. | Coating technique for deposition of drug substance on a substrate |
US7205413B2 (en) | 2002-05-03 | 2007-04-17 | Transform Pharmaceuticals, Inc. | Solvates and polymorphs of ritonavir and methods of making and using the same |
BR0309844A (pt) | 2002-05-07 | 2005-02-15 | Control Delivery Sys Inc | Processos para formação de um dispositivo para a distribuição de droga |
GB0214013D0 (en) | 2002-06-18 | 2002-07-31 | Euro Celtique Sa | Pharmaceutical product |
AU2003243699B2 (en) | 2002-06-21 | 2009-01-15 | Transform Pharmaceuticals, Inc. | Pharmaceutical compositions with improved dissolution |
AR039744A1 (es) | 2002-06-26 | 2005-03-09 | Alza Corp | Metodos y formas de dosificacion para aumentar la solubilidad de las composiciones de farmacos para la administracion controlada |
CN100515388C (zh) | 2002-06-26 | 2009-07-22 | 金拓 | 难溶药物快速溶出固体剂型 |
US7155459B2 (en) * | 2002-06-28 | 2006-12-26 | Miccrosoft Corporation | Time-bound database tuning |
AU2003246351B2 (en) | 2002-07-04 | 2009-02-19 | Janssen Pharmaceutica N.V. | Solid dispersions comprising two different polymer matrixes |
US7985422B2 (en) | 2002-08-05 | 2011-07-26 | Torrent Pharmaceuticals Limited | Dosage form |
TW200410714A (en) | 2002-08-07 | 2004-07-01 | Smithkline Beecham Corp | Electrospun amorphous pharmaceutical compositions |
MXPA05000977A (es) | 2002-08-12 | 2005-05-16 | Pfizer Prod Inc | Composiciones farmaceuticas de farmacos semiordenados y polimeros. |
CA2494188A1 (en) | 2002-08-13 | 2004-02-19 | Medtronic, Inc. | Active agent delivery system including a hydrophobic cellulose derivative |
AU2003258209A1 (en) | 2002-08-13 | 2004-02-25 | Medtronic, Inc. | Active agent delivery systems, medical devices, and methods |
ES2355723T3 (es) | 2002-09-11 | 2011-03-30 | Elan Pharma International Limited | Composiciones de agente activo en nanopartículas estabilizadas en gel. |
US20040062778A1 (en) | 2002-09-26 | 2004-04-01 | Adi Shefer | Surface dissolution and/or bulk erosion controlled release compositions and devices |
DE10247037A1 (de) | 2002-10-09 | 2004-04-22 | Abbott Gmbh & Co. Kg | Herstellung von festen Dosierungsformen unter Verwendung eines vernetzten nichtthermoplastischen Trägers |
AU2003304108B2 (en) | 2002-10-30 | 2007-03-22 | Spherics, Inc. | Nanoparticulate bioactive agents |
FR2846557B1 (fr) | 2002-10-30 | 2007-06-08 | Statice Sante | Structure implantable pour la liberation prolongee et controlee d'un principe actif |
DE10250711A1 (de) | 2002-10-31 | 2004-05-19 | Degussa Ag | Pharmazeutische und kosmetische Zubereitungen |
WO2004050068A1 (en) | 2002-11-29 | 2004-06-17 | Janssen Pharmaceutica N.V. | Pharmaceutical compositions comprising a basic respectively acidic drug compound, a surfactant and a physiologically tolerable water-soluble acid respectively base |
US7670627B2 (en) | 2002-12-09 | 2010-03-02 | Salvona Ip Llc | pH triggered targeted controlled release systems for the delivery of pharmaceutical active ingredients |
DE60313359T2 (de) | 2002-12-17 | 2008-01-03 | Abbott Gmbh & Co. Kg | Fenofibratsäure enthaltende pharmazeutische zusammensetzung und deren physiologisch verträgliche salze und derivate |
US6872799B2 (en) | 2002-12-18 | 2005-03-29 | Ethicon, Inc. | Functionalized polymers for medical applications |
US20040121003A1 (en) | 2002-12-19 | 2004-06-24 | Acusphere, Inc. | Methods for making pharmaceutical formulations comprising deagglomerated microparticles |
BR0317392A (pt) | 2002-12-19 | 2005-12-20 | Pharmacia Corp | Formulação não-higroscópica incluindo uma droga higroscópica |
ITMI20022748A1 (it) | 2002-12-23 | 2004-06-24 | Eurand Int | Dispersioni solide stabilizzate di farmaco in un carrier organico e procedimento per la loro preparazione. |
AU2003205543A1 (en) | 2003-01-14 | 2004-08-10 | Lifecycle Pharma A/S | Dry dispersions |
DE10304403A1 (de) | 2003-01-28 | 2004-08-05 | Röhm GmbH & Co. KG | Verfahren zur Herstellung einer oralen Arzneiform mit unmittelbarem Zerfall und Wirkstofffreisetzung |
US20040258752A1 (en) | 2003-01-31 | 2004-12-23 | Paruthi Manoj Kumar | Taste masking pharmaceutical composition and process for its preparation |
EP1594468A2 (en) | 2003-02-03 | 2005-11-16 | Novartis AG | Process for preparing a solid dispersion pharmaceutical product |
US20040156894A1 (en) | 2003-02-07 | 2004-08-12 | Grother Leon Paul | Use of edible acids in fast-dispersing pharmaceutical solid dosage forms |
US6931888B2 (en) | 2003-02-07 | 2005-08-23 | Ferro Corporation | Lyophilization method and apparatus for producing particles |
US20060286169A1 (en) | 2003-02-13 | 2006-12-21 | Phares Pharmaceutical Research N.V. | Lipophilic compositions |
GB0304726D0 (en) | 2003-03-01 | 2003-04-02 | Ardana Bioscience Ltd | New Process |
GB0305941D0 (en) | 2003-03-14 | 2003-04-23 | Camurus Ab | Composition |
US20040185170A1 (en) | 2003-03-21 | 2004-09-23 | Shubha Chungi | Method for coating drug-containing particles and formulations and dosage units formed therefrom |
EP2186510B1 (en) | 2003-03-26 | 2013-07-10 | Egalet Ltd. | Matrix compositions for controlled delivery of drug substances |
US20040208928A1 (en) | 2003-04-15 | 2004-10-21 | Animal Technology Institute Taiwan | Method for preparing an orally administrable formulation for controlled release |
CA2523218A1 (en) | 2003-04-22 | 2004-11-04 | Dr. Reddy's Laboratories Limited | Oral pharmaceutical formulations of acid-labile active ingredients and process for making same |
GB0310300D0 (en) | 2003-05-06 | 2003-06-11 | Univ Belfast | Nanocomposite drug delivery composition |
WO2004100883A2 (en) | 2003-05-06 | 2004-11-25 | Bpsi Holdings, Inc. | Method for preparing thermoformed compositions containing acrylic polymer binders, pharmaceutual dosage forms and methods of preparing the same |
JP2004339162A (ja) | 2003-05-16 | 2004-12-02 | Shin Etsu Chem Co Ltd | 難溶性薬物を含む医薬用固形製剤とその製造方法 |
EP1479381A1 (en) | 2003-05-19 | 2004-11-24 | Euro-Celtique S.A. | Pharmaceutical dosage form comprising a solid solution |
KR20120080243A (ko) | 2003-05-28 | 2012-07-16 | 노바르티스 아게 | 아미노산 및/또는 인지질로 부분 또는 완전 코팅된 수불용성 활성제 미립자의 제조를 위한 알코올성 수용액의 분무 건조법 |
US20040247624A1 (en) | 2003-06-05 | 2004-12-09 | Unger Evan Charles | Methods of making pharmaceutical formulations for the delivery of drugs having low aqueous solubility |
DE10325989A1 (de) | 2003-06-07 | 2005-01-05 | Glatt Gmbh | Verfahren zur Herstellung von und daraus resultierende Mikropellets sowie deren Verwendung |
WO2004112755A1 (en) | 2003-06-18 | 2004-12-29 | John Michael Newton | Controlled release devices with lumens |
US20040265378A1 (en) | 2003-06-25 | 2004-12-30 | Yingxu Peng | Method and compositions for producing granules containing high concentrations of biologically active substances |
CA2531486C (en) | 2003-07-11 | 2012-10-02 | Antonio A. Albano | Saquinavir mesylate oral dosage form |
DE10332160A1 (de) | 2003-07-15 | 2005-02-03 | Röhm GmbH & Co. KG | Multipartikuläre Arzneiform, enthaltend mucoadhaesiv formulierte Peptid- oder Protein-Wirkstoffe, sowie ein Verfahren zur Herstellung der Arzneiform |
TW200526274A (en) | 2003-07-21 | 2005-08-16 | Smithkline Beecham Plc | Pharmaceutical formulations |
BR0302523A (pt) | 2003-07-23 | 2005-04-05 | Cristalia Prod Quimicos Farm | Composição farmacêutica estável para administração de inibidores da hiv protease e processo de obtenção de composição farmacêutica concentrada para a administração de inibidores da hiv protease |
US7645474B1 (en) | 2003-07-31 | 2010-01-12 | Advanced Cardiovascular Systems, Inc. | Method and system of purifying polymers for use with implantable medical devices |
US7785512B1 (en) | 2003-07-31 | 2010-08-31 | Advanced Cardiovascular Systems, Inc. | Method and system of controlled temperature mixing and molding of polymers with active agents for implantable medical devices |
WO2005014162A1 (en) | 2003-08-04 | 2005-02-17 | Camurus Ab | Method for improving the properties of amphiphile particles |
ATE540671T1 (de) | 2003-08-04 | 2012-01-15 | Bend Res Inc | Pharmazeutische zusammensetzungen von adsorbaten von amorphen arzneimitteln und lipophilen mikrophasen-bildenden materialien |
CL2004001884A1 (es) | 2003-08-04 | 2005-06-03 | Pfizer Prod Inc | Procedimiento de secado por pulverizacion para la formacion de dispersiones solidas amorfas de un farmaco y polimeros. |
WO2005011740A1 (en) | 2003-08-05 | 2005-02-10 | Fuji Photo Film B.V. | Use of recombinant or synthetic gelatin-like proteins as stabiliser in lyophilized pharmaceutical compositions |
DE10339197A1 (de) | 2003-08-22 | 2005-03-24 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Sprühgetrocknete amorphe Pulver mit geringer Restfeuchte und guter Lagerstabilität |
US8025899B2 (en) | 2003-08-28 | 2011-09-27 | Abbott Laboratories | Solid pharmaceutical dosage form |
US20050048112A1 (en) | 2003-08-28 | 2005-03-03 | Jorg Breitenbach | Solid pharmaceutical dosage form |
US8377952B2 (en) | 2003-08-28 | 2013-02-19 | Abbott Laboratories | Solid pharmaceutical dosage formulation |
EP1675576A1 (en) | 2003-10-03 | 2006-07-05 | LifeCycle Pharma A/S | A method for preparing modified release pharmaceutical compositions |
AU2004279855A1 (en) | 2003-10-08 | 2005-04-21 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-binding cassette transporters containing cycloalkyl or pyranyl groups |
EP1674083B1 (en) | 2003-10-15 | 2018-08-01 | Fuji Chemical Industry Co., Ltd. | Tablet quickly disintegrating in oral cavity |
US8349361B2 (en) | 2003-10-15 | 2013-01-08 | Fuji Chemical Industry Co., Ltd. | Composition for rapid disintegrating tablet in oral cavity |
PT1677827E (pt) | 2003-10-27 | 2009-03-13 | Vertex Pharma | Associações para o tratamento do vhc |
US7413690B1 (en) | 2003-10-29 | 2008-08-19 | The University Of Mississippi | Process and apparatus for producing spherical pellets using molten solid matrices |
EP1694303A1 (en) | 2003-12-15 | 2006-08-30 | Council Of Scientific And Industrial Research | Taste masked pharmaceutical composition comprising ph sensitive polymer |
CA2568378C (en) | 2004-05-28 | 2013-03-19 | Abbott Gmbh & Co. Kg | Formulation obtained from a powder mixture comprising an inorganic pigment |
US20050281876A1 (en) | 2004-06-18 | 2005-12-22 | Shun-Por Li | Solid dosage form for acid-labile active ingredient |
DE102004040104A1 (de) | 2004-08-18 | 2006-02-23 | Basf Ag | Verwendung von amphiphilen Copolymerisaten als Solubilisatoren |
GB0501835D0 (en) | 2005-01-28 | 2005-03-09 | Unilever Plc | Improvements relating to spray dried compositions |
US20090104269A1 (en) | 2005-02-11 | 2009-04-23 | Brian Graham | Nanoformulations |
RU2007129642A (ru) | 2005-02-25 | 2009-03-27 | Ф.Хоффманн-Ля Рош Аг (Ch) | Таблетки с улучшенным распределением лекарственного вещества |
EP1885455A1 (en) | 2005-06-03 | 2008-02-13 | Horizon Science Pty. Ltd. | Delivery systems |
WO2007002041A2 (en) | 2005-06-21 | 2007-01-04 | Foster Corporation | Drug-filled polymer films |
US20080199516A1 (en) | 2005-07-26 | 2008-08-21 | Glaxo Group Limited | Encapsulation Of Lipid-Based Formulations In Enteric Polymers |
JP2009504590A (ja) | 2005-08-08 | 2009-02-05 | アボット ゲーエムベーハー ウント コンパニー カーゲー | 改善された生物学的利用能をもつ剤型 |
CN101283008A (zh) | 2005-08-11 | 2008-10-08 | 巴斯夫欧洲公司 | 基于n-乙烯基已内酰胺的共聚物及其作为增溶剂的用途 |
RU2385712C2 (ru) | 2005-08-24 | 2010-04-10 | Рубикон Рисёч Пвт Лтд. | Рецептура с контролируемым высвобождением |
US20070077305A1 (en) | 2005-10-03 | 2007-04-05 | Le Tien C | Biocompatible polymeric matrix and preparation thereof |
WO2007050631A2 (en) | 2005-10-25 | 2007-05-03 | Cima Labs Inc. | Dosage form with coated active |
ITMI20052461A1 (it) | 2005-12-22 | 2007-06-23 | Univ Degli Studi Milano | Sistemi microparticellari per la somministrazione orale di sostanze biologicamente attive |
WO2007091856A1 (en) | 2006-02-10 | 2007-08-16 | Lg Household & Health Care Ltd. | In-situ melting and gelling tablet composition for oral care |
JP2009530382A (ja) | 2006-03-23 | 2009-08-27 | シェーリング コーポレイション | Hcvプロテアーゼインヒビターとcyp3a4インヒビターとの組み合わせ、および関連する処置方法 |
US7771632B2 (en) | 2006-05-15 | 2010-08-10 | American Leistritz Extruder Corp. | Continuous melt spheronization apparatus and process for the production of pharmaceutical pellets |
WO2007141182A2 (de) | 2006-06-07 | 2007-12-13 | Basf Se | Verwendung von vinylacetat-sulfonat-copolymeren als solubilisatoren für in wasser schwerlösliche verbindungen |
US8343548B2 (en) | 2006-08-08 | 2013-01-01 | Shin-Etsu Chemical Co., Ltd. | Solid dosage form comprising solid dispersion |
US7923026B2 (en) | 2006-10-20 | 2011-04-12 | Solvay Pharmaceuticals B.V. | Embedded micellar nanoparticles |
EP2112925A4 (en) | 2006-11-15 | 2013-01-09 | Abbott Lab | SOLID PHARMACEUTICAL DOSAGE FORMULATIONS |
WO2008065502A1 (en) | 2006-11-29 | 2008-06-05 | Pfizer Products Inc. | Pharmaceutical compositions based on a) nanoparticles comprising enteric polymers and b) casein |
DE102007009242A1 (de) | 2007-02-22 | 2008-09-18 | Evonik Röhm Gmbh | Pellets mit magensaftresistenter Wirkstoff-Matix |
CN101765616A (zh) | 2007-07-26 | 2010-06-30 | 巴斯夫欧洲公司 | 制备通过接枝聚合在溶液中获得的并基于固体聚醚的共聚物的方法 |
EP2022805A3 (en) | 2007-08-03 | 2009-02-25 | Basf Se | Copolymers based on N-vinyllactams and olefins as their use as solubilizers for slightly water-soluble compounds |
MX2010003928A (es) | 2007-10-11 | 2010-09-10 | Philip Morris Prod | Producto de tabaco sin humo. |
US8722094B2 (en) | 2008-03-11 | 2014-05-13 | Aska Pharmaceutical Co., Ltd. | Solid dispersion and pharmaceutical composition of the same, and production processes thereof |
AR071375A1 (es) | 2008-04-22 | 2010-06-16 | Solvay Pharm Gmbh | Formulaciones para ingredientes farmaceuticos activos de permeabilidad deficiente, proceso de preparacion y producto |
WO2010017053A1 (en) | 2008-08-06 | 2010-02-11 | Isp Investments, Inc. | Solid excipient compositions |
GB0815852D0 (en) | 2008-09-01 | 2008-10-08 | Unilever Plc | Improvements relating to pharmaceutical compositions |
WO2010028489A1 (en) | 2008-09-15 | 2010-03-18 | Labopharm Inc. | Starch-based microparticles for the release of agents disposed therein |
US8778401B2 (en) | 2008-10-28 | 2014-07-15 | Agency For Science, Technology And Research | Mesoporous material excipients for poorly aqueous soluble ingredients |
US8715715B2 (en) | 2008-11-03 | 2014-05-06 | Nal Pharmaceuticals Ltd. | Dosage form for insertion into the mouth |
WO2010078429A1 (en) | 2008-12-30 | 2010-07-08 | Impax Laboratories, Inc. | Pharmaceutical dosage forms and methods of manufacturing same |
CN101444494B (zh) | 2008-12-31 | 2011-03-30 | 江苏大学 | 难溶性药物高效长效缓释制剂及其制法 |
EP2393484A1 (en) | 2009-02-06 | 2011-12-14 | Egalet Ltd. | Immediate release composition resistant to abuse by intake of alcohol |
EP2311435A1 (en) | 2009-10-07 | 2011-04-20 | LEK Pharmaceuticals d.d. | Pharmaceutical composition comprising poorly soluble active ingredient and hyperbranched polymer |
WO2011090724A2 (en) | 2009-12-29 | 2011-07-28 | Impax Laboratories, Inc. | Gastroretentive solid oral dosage forms with lipid-based low-density excipient |
CN102821754B (zh) | 2010-03-26 | 2014-06-18 | 陶氏环球技术有限责任公司 | 多层熔融挤出膜 |
US20110288181A1 (en) | 2010-05-21 | 2011-11-24 | Basf Se | Preparations of biologically active substances with enlarged surface based on amphiphilic copolymers |
EP2579896B1 (en) | 2010-06-14 | 2016-07-20 | Dow Global Technologies LLC | Hydroxypropyl methyl cellulose acetate succinate with enhanced acetate and succinate substitution |
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