JP2014530875A5 - - Google Patents
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- JP2014530875A5 JP2014530875A5 JP2014537311A JP2014537311A JP2014530875A5 JP 2014530875 A5 JP2014530875 A5 JP 2014530875A5 JP 2014537311 A JP2014537311 A JP 2014537311A JP 2014537311 A JP2014537311 A JP 2014537311A JP 2014530875 A5 JP2014530875 A5 JP 2014530875A5
- Authority
- JP
- Japan
- Prior art keywords
- pharmaceutical composition
- fatty acid
- composition according
- drug
- acid diester
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 235000014113 dietary fatty acids Nutrition 0.000 claims description 109
- 239000000194 fatty acid Substances 0.000 claims description 109
- 239000008194 pharmaceutical composition Substances 0.000 claims description 95
- 229920001223 polyethylene glycol Polymers 0.000 claims description 94
- 150000004665 fatty acids Chemical class 0.000 claims description 81
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Chemical group CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 claims description 54
- 239000003814 drug Substances 0.000 claims description 43
- 229940079593 drugs Drugs 0.000 claims description 43
- 150000003839 salts Chemical class 0.000 claims description 37
- 239000011780 sodium chloride Substances 0.000 claims description 37
- 239000000203 mixture Substances 0.000 claims description 31
- 239000002202 Polyethylene glycol Substances 0.000 claims description 19
- 239000000654 additive Substances 0.000 claims description 19
- HVFLCNVBZFFHBT-ZKDACBOMSA-N Cefepime Chemical compound S([C@@H]1[C@@H](C(N1C=1C([O-])=O)=O)NC(=O)\C(=N/OC)C=2N=C(N)SC=2)CC=1C[N+]1(C)CCCC1 HVFLCNVBZFFHBT-ZKDACBOMSA-N 0.000 claims description 17
- 230000000996 additive Effects 0.000 claims description 17
- 229960002100 cefepime Drugs 0.000 claims description 17
- 150000001780 cephalosporins Chemical class 0.000 claims description 16
- 201000009910 diseases by infectious agent Diseases 0.000 claims description 16
- YZBQHRLRFGPBSL-RXMQYKEDSA-N carbapenem Chemical compound C1C=CN2C(=O)C[C@H]21 YZBQHRLRFGPBSL-RXMQYKEDSA-N 0.000 claims description 12
- 150000001720 carbohydrates Chemical class 0.000 claims description 12
- BJHIKXHVCXFQLS-UYFOZJQFSA-N Fructose Natural products OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO BJHIKXHVCXFQLS-UYFOZJQFSA-N 0.000 claims description 10
- 230000035536 Oral bioavailability Effects 0.000 claims description 6
- 239000003782 beta lactam antibiotic agent Substances 0.000 claims description 6
- 230000036220 oral bioavailability Effects 0.000 claims description 6
- 239000002132 β-lactam antibiotic Substances 0.000 claims description 6
- 239000005715 Fructose Substances 0.000 claims description 5
- CZMRCDWAGMRECN-GDQSFJPYSA-N Sucrose Natural products O([C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1)[C@@]1(CO)[C@H](O)[C@@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-GDQSFJPYSA-N 0.000 claims description 5
- 239000005720 sucrose Substances 0.000 claims description 5
- 125000000185 sucrose group Chemical group 0.000 claims description 5
- 229960003644 Aztreonam Drugs 0.000 claims description 4
- WZPBZJONDBGPKJ-VEHQQRBSSA-N Aztreonam Chemical compound O=C1N(S([O-])(=O)=O)[C@@H](C)[C@@H]1NC(=O)C(=N/OC(C)(C)C(O)=O)\C1=CSC([NH3+])=N1 WZPBZJONDBGPKJ-VEHQQRBSSA-N 0.000 claims description 4
- 206010060945 Bacterial infection Diseases 0.000 claims description 4
- ZCCUWMICIWSJIX-NQJJCJBVSA-N Ceftaroline fosamil Chemical compound S([C@@H]1[C@@H](C(N1C=1C([O-])=O)=O)NC(=O)\C(=N/OCC)C=2N=C(NP(O)(O)=O)SN=2)CC=1SC(SC=1)=NC=1C1=CC=[N+](C)C=C1 ZCCUWMICIWSJIX-NQJJCJBVSA-N 0.000 claims description 4
- JWCSIUVGFCSJCK-CAVRMKNVSA-N Disodium Moxalactam Chemical compound N([C@]1(OC)C(N2C(=C(CSC=3N(N=NN=3)C)CO[C@@H]21)C(O)=O)=O)C(=O)C(C(O)=O)C1=CC=C(O)C=C1 JWCSIUVGFCSJCK-CAVRMKNVSA-N 0.000 claims description 4
- JUZNIMUFDBIJCM-ANEDZVCMSA-N Invanz Chemical compound O=C([C@H]1NC[C@H](C1)SC=1[C@H](C)[C@@H]2[C@H](C(N2C=1C(O)=O)=O)[C@H](O)C)NC1=CC=CC(C(O)=O)=C1 JUZNIMUFDBIJCM-ANEDZVCMSA-N 0.000 claims description 4
- DMJNNHOOLUXYBV-PQTSNVLCSA-N Meropenem Chemical compound C=1([C@H](C)[C@@H]2[C@H](C(N2C=1C(O)=O)=O)[C@H](O)C)S[C@@H]1CN[C@H](C(=O)N(C)C)C1 DMJNNHOOLUXYBV-PQTSNVLCSA-N 0.000 claims description 4
- 229940049954 Penicillin Drugs 0.000 claims description 4
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 claims description 4
- 229960000626 benzylpenicillin Drugs 0.000 claims description 4
- 239000002775 capsule Substances 0.000 claims description 4
- JSVCEVCSANKFDY-SFYZADRCSA-N carbacephem Chemical compound C1CC(C)=C(C(O)=O)N2C(=O)[C@@H](NC(=O)C)[C@H]21 JSVCEVCSANKFDY-SFYZADRCSA-N 0.000 claims description 4
- RGFBRLNVZCCMSV-BIRGHMBHSA-N ceftaroline Chemical compound S([C@@H]1[C@@H](C(N1C=1C([O-])=O)=O)NC(=O)\C(=N/OCC)C=2N=C(N)SN=2)CC=1SC(SC=1)=NC=1C1=CC=[N+](C)C=C1 RGFBRLNVZCCMSV-BIRGHMBHSA-N 0.000 claims description 4
- 229940036735 ceftaroline Drugs 0.000 claims description 4
- 229960004828 ceftaroline fosamil Drugs 0.000 claims description 4
- 239000002552 dosage form Substances 0.000 claims description 4
- 229960002770 ertapenem Drugs 0.000 claims description 4
- 229960002260 meropenem Drugs 0.000 claims description 4
- 239000006186 oral dosage form Substances 0.000 claims description 4
- HHXMXAQDOUCLDN-RXMQYKEDSA-N penem Chemical compound S1C=CN2C(=O)C[C@H]21 HHXMXAQDOUCLDN-RXMQYKEDSA-N 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 208000002633 Febrile Neutropenia Diseases 0.000 claims description 3
- 206010046577 Urinary tract infection Diseases 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 239000007938 effervescent tablet Substances 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 235000014666 liquid concentrate Nutrition 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 claims description 2
- AVAACINZEOAHHE-VFZPANTDSA-N Doripenem Chemical compound C=1([C@H](C)[C@@H]2[C@H](C(N2C=1C(O)=O)=O)[C@H](O)C)S[C@@H]1CN[C@H](CNS(N)(=O)=O)C1 AVAACINZEOAHHE-VFZPANTDSA-N 0.000 claims 2
- 229960000895 doripenem Drugs 0.000 claims 2
- 229920001451 Polypropylene glycol Polymers 0.000 description 73
- -1 fatty acid esters Chemical class 0.000 description 37
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- 210000003491 Skin Anatomy 0.000 description 6
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- 150000001875 compounds Chemical class 0.000 description 4
- 150000003626 triacylglycerols Chemical class 0.000 description 4
- 238000007912 intraperitoneal administration Methods 0.000 description 3
- 210000001519 tissues Anatomy 0.000 description 3
- XAKKNLNAJBNLPC-MAYKBZFQSA-N (6R,7R)-3-[(E)-3-[(2-amino-2-oxoethyl)-ethyl-methylazaniumyl]prop-1-enyl]-7-[[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(fluoromethoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Chemical compound N([C@H]1[C@@H]2N(C1=O)C(=C(CS2)/C=C/C[N+](C)(CC)CC(N)=O)C([O-])=O)C(=O)C(=N/OCF)\C1=NSC(N)=N1 XAKKNLNAJBNLPC-MAYKBZFQSA-N 0.000 description 2
- DKOQGJHPHLTOJR-PUIFZAHNSA-N (6R,7R)-7-[[(2E)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(6,7-dihydro-5H-cyclopenta[b]pyridin-1-ium-1-ylmethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Chemical compound N([C@@H]1C(N2C(=C(C[N+]=3C=4CCCC=4C=CC=3)CS[C@@H]21)C([O-])=O)=O)C(=O)/C(=N/OC)C1=CSC(N)=N1 DKOQGJHPHLTOJR-PUIFZAHNSA-N 0.000 description 2
- HCCFUFNFJIUPHS-MZYBJUSBSA-O (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(2-carboxypropan-2-yloxyimino)acetyl]amino]-3-[(1-methylpyridin-1-ium-4-yl)sulfanylmethyl]-5,8-dioxo-5$l^{4}-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Chemical compound C1=C[N+](C)=CC=C1SCC1=C(C(O)=O)N2C(=O)[C@@H](NC(=O)C(=N/OC(C)(C)C(O)=O)\C=3N=C(N)SC=3)[C@H]2S(=O)C1 HCCFUFNFJIUPHS-MZYBJUSBSA-O 0.000 description 2
- ORFOPKXBNMVMKC-DWVKKRMSSA-O (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-(2-carboxypropan-2-yloxyimino)acetyl]amino]-8-oxo-3-(pyridin-1-ium-1-ylmethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid Chemical compound S([C@@H]1[C@@H](C(N1C=1C(O)=O)=O)NC(=O)\C(=N/OC(C)(C)C(O)=O)C=2N=C(N)SC=2)CC=1C[N+]1=CC=CC=C1 ORFOPKXBNMVMKC-DWVKKRMSSA-O 0.000 description 2
- YWKJNRNSJKEFMK-PQFQYKRASA-N (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-8-oxo-3-(5,6,7,8-tetrahydroquinolin-1-ium-1-ylmethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate Chemical compound N([C@@H]1C(N2C(=C(C[N+]=3C=4CCCCC=4C=CC=3)CS[C@@H]21)C([O-])=O)=O)C(=O)\C(=N/OC)C1=CSC(N)=N1 YWKJNRNSJKEFMK-PQFQYKRASA-N 0.000 description 2
- 241001225321 Aspergillus fumigatus Species 0.000 description 2
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- 229950001334 Cefluprenam Drugs 0.000 description 2
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- LNZMRLHZGOBKAN-KAWPREARSA-N Cefpimizole Chemical compound N1=CNC(C(=O)N[C@@H](C(=O)N[C@@H]2C(N3C(=C(C[N+]=4C=CC(CCS(O)(=O)=O)=CC=4)CS[C@@H]32)C([O-])=O)=O)C=2C=CC=CC=2)=C1C(=O)O LNZMRLHZGOBKAN-KAWPREARSA-N 0.000 description 2
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- 229940106196 Cephaloridine Drugs 0.000 description 2
- CZTQZXZIADLWOZ-CRAIPNDOSA-N Cephaloridine Chemical compound O=C([C@@H](NC(=O)CC=1SC=CC=1)[C@H]1SC2)N1C(C(=O)[O-])=C2C[N+]1=CC=CC=C1 CZTQZXZIADLWOZ-CRAIPNDOSA-N 0.000 description 2
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- JYIKNQVWKBUSNH-WVDDFWQHSA-N Caspofungin Chemical compound C1([C@H](O)[C@@H](O)[C@H]2C(=O)N[C@H](C(=O)N3CC[C@H](O)[C@H]3C(=O)N[C@H](NCCN)[C@H](O)C[C@@H](C(N[C@H](C(=O)N3C[C@H](O)C[C@H]3C(=O)N2)[C@@H](C)O)=O)NC(=O)CCCCCCCC[C@@H](C)C[C@@H](C)CC)[C@H](O)CCN)=CC=C(O)C=C1 JYIKNQVWKBUSNH-WVDDFWQHSA-N 0.000 description 1
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- 241000235645 Pichia kudriavzevii Species 0.000 description 1
- 241000233870 Pneumocystis Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229940055033 Proteus mirabilis Drugs 0.000 description 1
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- 206010037596 Pyelonephritis Diseases 0.000 description 1
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- 229940076185 Staphylococcus aureus Drugs 0.000 description 1
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- 229940031000 Streptococcus pneumoniae Drugs 0.000 description 1
- 241000193998 Streptococcus pneumoniae Species 0.000 description 1
- 229940076156 Streptococcus pyogenes Drugs 0.000 description 1
- 241000193996 Streptococcus pyogenes Species 0.000 description 1
- 206010042938 Systemic candida Diseases 0.000 description 1
- 208000002474 Tinea Diseases 0.000 description 1
- 241000130764 Tinea Species 0.000 description 1
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- 206010048038 Wound infection Diseases 0.000 description 1
- 206010061418 Zygomycosis Diseases 0.000 description 1
- NWGKJDSIEKMTRX-HSACVWGTSA-N [(2R)-2-[(2R,3R,4S)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] (E)-octadec-9-enoate Chemical compound CCCCCCCC\C=C\CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-HSACVWGTSA-N 0.000 description 1
- FBCLKBXYZRAXNA-PDIPHZEPSA-N aculeacin A Chemical compound C1([C@H](O)[C@@H](O)[C@H]2C(=O)N[C@H](C(=O)N3C[C@H](C)[C@H](O)[C@H]3C(=O)N[C@H](O)[C@H](O)C[C@@H](C(N[C@H](C(=O)N3C[C@H](O)C[C@H]3C(=O)N2)[C@@H](C)O)=O)NC(=O)CCCCCCCCCCCCCCC)[C@H](O)CC(N)=O)=CC=C(O)C=C1 FBCLKBXYZRAXNA-PDIPHZEPSA-N 0.000 description 1
- 108010081349 aculeacin A Proteins 0.000 description 1
- 230000001154 acute Effects 0.000 description 1
- JHVAMHSQVVQIOT-MFAJLEFUSA-N anidulafungin Chemical compound C1=CC(OCCCCC)=CC=C1C1=CC=C(C=2C=CC(=CC=2)C(=O)N[C@@H]2C(N[C@H](C(=O)N3C[C@H](O)C[C@H]3C(=O)N[C@H](C(=O)N[C@H](C(=O)N3C[C@H](C)[C@H](O)[C@H]3C(=O)N[C@H](O)[C@H](O)C2)[C@@H](C)O)[C@H](O)[C@@H](O)C=2C=CC(O)=CC=2)[C@@H](C)O)=O)C=C1 JHVAMHSQVVQIOT-MFAJLEFUSA-N 0.000 description 1
- 201000002909 aspergillosis Diseases 0.000 description 1
- 230000001580 bacterial Effects 0.000 description 1
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- 201000003486 coccidioidomycosis Diseases 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
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- FAUOJMHVEYMQQG-HVYQDZECSA-N echinocandin B Chemical compound C1([C@H](O)[C@@H](O)[C@H]2C(=O)N[C@H](C(=O)N3C[C@H](C)[C@H](O)[C@H]3C(=O)N[C@H](O)[C@H](O)C[C@@H](C(N[C@H](C(=O)N3C[C@H](O)C[C@H]3C(=O)N2)[C@@H](C)O)=O)NC(=O)CCCCCCC\C=C/C\C=C/CCCCC)[C@@H](C)O)=CC=C(O)C=C1 FAUOJMHVEYMQQG-HVYQDZECSA-N 0.000 description 1
- 108010062092 echinocandin B Proteins 0.000 description 1
- 230000002538 fungal Effects 0.000 description 1
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- 201000002563 histoplasmosis Diseases 0.000 description 1
- 230000004301 light adaptation Effects 0.000 description 1
- 201000009906 meningitis Diseases 0.000 description 1
- PIEUQSKUWLMALL-YABMTYFHSA-N micafungin Chemical compound C1=CC(OCCCCC)=CC=C1C1=CC(C=2C=CC(=CC=2)C(=O)N[C@@H]2C(N[C@H](C(=O)N3C[C@H](O)C[C@H]3C(=O)N[C@H](C(=O)N[C@H](C(=O)N3C[C@H](C)[C@H](O)[C@H]3C(=O)N[C@H](O)[C@H](O)C2)[C@H](O)CC(N)=O)[C@H](O)[C@@H](O)C=2C=C(OS(O)(=O)=O)C(O)=CC=2)[C@@H](C)O)=O)=NO1 PIEUQSKUWLMALL-YABMTYFHSA-N 0.000 description 1
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- 201000009890 sinusitis Diseases 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 201000004647 tinea pedis Diseases 0.000 description 1
- 201000007096 vulvovaginal candidiasis Diseases 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161549882P | 2011-10-21 | 2011-10-21 | |
| US61/549,882 | 2011-10-21 | ||
| PCT/US2012/061125 WO2013059664A1 (en) | 2011-10-21 | 2012-10-19 | Pharmaceutical compositions and uses thereof |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018029249A Division JP2018109037A (ja) | 2011-10-21 | 2018-02-22 | 医薬組成物及びそれらの使用 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014530875A JP2014530875A (ja) | 2014-11-20 |
| JP2014530875A5 true JP2014530875A5 (US20030027995A1-20030206-C00005.png) | 2015-12-03 |
| JP6329486B2 JP6329486B2 (ja) | 2018-05-23 |
Family
ID=48141411
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014537311A Expired - Fee Related JP6329486B2 (ja) | 2011-10-21 | 2012-10-19 | 医薬組成物及びそれらの使用 |
| JP2018029249A Withdrawn JP2018109037A (ja) | 2011-10-21 | 2018-02-22 | 医薬組成物及びそれらの使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018029249A Withdrawn JP2018109037A (ja) | 2011-10-21 | 2018-02-22 | 医薬組成物及びそれらの使用 |
Country Status (5)
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6329486B2 (ja) * | 2011-10-21 | 2018-05-23 | シーチェイド ファーマシューティカルズ，インコーポレーテッド | 医薬組成物及びそれらの使用 |
| US20160074322A1 (en) * | 2013-04-25 | 2016-03-17 | Seachaid Pharmaceuticals, Inc. | Oral cefepime compositions and uses thereof |
| WO2021006267A1 (ja) * | 2019-07-08 | 2021-01-14 | グリーン・テック株式会社 | ピラゾール誘導体の塩及びピラゾール誘導体の製剤 |
| CN111053755B (zh) * | 2019-12-31 | 2022-03-29 | 金日制药（中国）有限公司 | 一种高渗透性的头孢克肟胶囊制剂制备方法 |
| CN111450057A (zh) * | 2020-06-03 | 2020-07-28 | 江苏中牧倍康药业有限公司 | 一种硫酸头孢喹肟自微乳及其制备方法 |
| AU2021104067A4 (en) * | 2021-07-12 | 2021-09-09 | Pharmachem Australia Pty Ltd | Oral antibiotic formulation |
| WO2023178324A1 (en) | 2022-03-17 | 2023-09-21 | Bristol-Myers Squibb Company | Pharmaceutical compositions comprising salts of salcaprozate and nicotinamide for improving oral bioavailability |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57146722A (en) * | 1981-03-06 | 1982-09-10 | Toyo Jozo Co Ltd | Pharmaceutical preparation having improved absorption |
| US4537772A (en) | 1984-05-02 | 1985-08-27 | Merck & Co., Inc. | Enhancing absorption of drugs from gastrointestinal tract using acylcarnitines |
| JPS61267528A (ja) | 1984-11-26 | 1986-11-27 | Yamanouchi Pharmaceut Co Ltd | 吸収促進剤を含有するカルシトニン経鼻剤 |
| JP3440315B2 (ja) * | 1994-12-02 | 2003-08-25 | 小林製薬株式会社 | トイレ用洗浄剤組成物 |
| US6248363B1 (en) * | 1999-11-23 | 2001-06-19 | Lipocine, Inc. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
| US7235583B1 (en) * | 1999-03-09 | 2007-06-26 | Luitpold Pharmaceuticals, Inc., | Fatty acid-anticancer conjugates and uses thereof |
| US6309663B1 (en) * | 1999-08-17 | 2001-10-30 | Lipocine Inc. | Triglyceride-free compositions and methods for enhanced absorption of hydrophilic therapeutic agents |
| US20030180352A1 (en) * | 1999-11-23 | 2003-09-25 | Patel Mahesh V. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
| US6858580B2 (en) | 2001-06-04 | 2005-02-22 | Nobex Corporation | Mixtures of drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same |
| US7713932B2 (en) | 2001-06-04 | 2010-05-11 | Biocon Limited | Calcitonin drug-oligomer conjugates, and uses thereof |
| US6828305B2 (en) | 2001-06-04 | 2004-12-07 | Nobex Corporation | Mixtures of growth hormone drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same |
| US6828297B2 (en) | 2001-06-04 | 2004-12-07 | Nobex Corporation | Mixtures of insulin drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same |
| US6713452B2 (en) | 2001-06-04 | 2004-03-30 | Nobex Corporation | Mixtures of calcitonin drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same |
| US7196059B2 (en) | 2001-09-07 | 2007-03-27 | Biocon Limited | Pharmaceutical compositions of insulin drug-oligomer conjugates and methods of treating diseases therewith |
| WO2004002458A1 (en) * | 2002-06-28 | 2004-01-08 | Shire Laboratories Inc. | Formulations of fenofibrate and/or fenofibrate derivatives with improved oral bioavailability |
| JP4829783B2 (ja) | 2003-06-24 | 2011-12-07 | バイオコン・リミテッド | カルシトニン薬−オリゴマーコンジュゲートの混合物および疼痛治療における使用方法 |
| US20050123602A1 (en) * | 2003-09-25 | 2005-06-09 | Michaelis Arthur F. | Rifalazil formulations |
| US8329958B2 (en) | 2004-07-02 | 2012-12-11 | Biocon Limited | Combinatorial synthesis of PEG oligomer libraries |
| AU2006242535B2 (en) * | 2005-04-29 | 2012-08-09 | Merck Sharp & Dohme Corp. | Therapeutic compositions |
| JP4343153B2 (ja) | 2005-05-12 | 2009-10-14 | 基博 中島 | 抗腫瘍組成物の製造方法 |
| US20080145411A1 (en) | 2006-10-06 | 2008-06-19 | Kaneka Corporation | Composition of high absorbability for oral administration comprising oxidized coenzyme q10 |
| MX2009006912A (es) * | 2006-12-28 | 2009-08-12 | Repros Therapeutics Inc | Metodos y formulaciones para biodisponibilidad mejorada de antiprogestinas. |
| US8362083B2 (en) * | 2008-01-15 | 2013-01-29 | C.B. Fleet Company Inc. | Taste-masked docusate compositions |
| WO2009131995A1 (en) | 2008-04-21 | 2009-10-29 | Nanobio Corporation | Nanoemulsion influenza vaccine |
| US9241519B2 (en) | 2008-09-19 | 2016-01-26 | Ironclad Performance Wear Corporation | Glove for use in the oil and natural gas extraction industries |
| EP2338480A1 (en) * | 2009-12-22 | 2011-06-29 | LEK Pharmaceuticals d.d. | Coating of particles comprising a pharmaceutically active ingredient with a carbonate salt or phosphate salt |
| JP6329486B2 (ja) * | 2011-10-21 | 2018-05-23 | シーチェイド ファーマシューティカルズ，インコーポレーテッド | 医薬組成物及びそれらの使用 |
| US20160074322A1 (en) | 2013-04-25 | 2016-03-17 | Seachaid Pharmaceuticals, Inc. | Oral cefepime compositions and uses thereof |
-
2012
- 2012-10-19 JP JP2014537311A patent/JP6329486B2/ja not_active Expired - Fee Related
- 2012-10-19 US US14/352,966 patent/US9308263B2/en not_active Expired - Fee Related
- 2012-10-19 WO PCT/US2012/061125 patent/WO2013059664A1/en active Application Filing
- 2012-10-19 IN IN3214CHN2014 patent/IN2014CN03214A/en unknown
- 2012-10-19 EP EP12841549.4A patent/EP2775831A4/en not_active Withdrawn
-
2018
- 2018-02-22 JP JP2018029249A patent/JP2018109037A/ja not_active Withdrawn
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