JP2011522834A5 - - Google Patents
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- JP2011522834A5 JP2011522834A5 JP2011512703A JP2011512703A JP2011522834A5 JP 2011522834 A5 JP2011522834 A5 JP 2011522834A5 JP 2011512703 A JP2011512703 A JP 2011512703A JP 2011512703 A JP2011512703 A JP 2011512703A JP 2011522834 A5 JP2011522834 A5 JP 2011522834A5
- Authority
- JP
- Japan
- Prior art keywords
- pegylated
- interferon
- patients
- hepatitis
- pharmaceutical composition
- 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.)
- Pending
Links
- 108010047761 Interferon-alpha Proteins 0.000 claims description 32
- 102000006992 Interferon-alpha Human genes 0.000 claims description 32
- 229920001184 polypeptide Polymers 0.000 claims description 28
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 28
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 28
- 239000003814 drug Substances 0.000 claims description 26
- 208000005176 Hepatitis C Diseases 0.000 claims description 25
- 239000008194 pharmaceutical composition Substances 0.000 claims description 24
- 108010018844 interferon type III Proteins 0.000 claims description 21
- 238000011282 treatment Methods 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 102000002227 Interferon Type I Human genes 0.000 claims description 19
- 108010014726 Interferon Type I Proteins 0.000 claims description 19
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 claims description 18
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical compound N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 claims description 17
- 229960000329 ribavirin Drugs 0.000 claims description 13
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 claims description 13
- 241000711549 Hepacivirus C Species 0.000 claims description 12
- NHKZSTHOYNWEEZ-AFCXAGJDSA-N taribavirin Chemical group N1=C(C(=N)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 NHKZSTHOYNWEEZ-AFCXAGJDSA-N 0.000 claims description 11
- 208000015181 infectious disease Diseases 0.000 claims description 10
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims description 9
- 229920001427 mPEG Polymers 0.000 claims description 9
- 229950006081 taribavirin Drugs 0.000 claims description 9
- 206010016654 Fibrosis Diseases 0.000 claims description 7
- 125000000539 amino acid group Chemical group 0.000 claims description 7
- 241000725303 Human immunodeficiency virus Species 0.000 claims description 6
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 claims description 5
- 229940079593 drug Drugs 0.000 claims description 5
- 239000000137 peptide hydrolase inhibitor Substances 0.000 claims description 5
- 229960000517 boceprevir Drugs 0.000 claims description 4
- LHHCSNFAOIFYRV-DOVBMPENSA-N boceprevir Chemical compound O=C([C@@H]1[C@@H]2[C@@H](C2(C)C)CN1C(=O)[C@@H](NC(=O)NC(C)(C)C)C(C)(C)C)NC(C(=O)C(N)=O)CC1CCC1 LHHCSNFAOIFYRV-DOVBMPENSA-N 0.000 claims description 4
- 230000007882 cirrhosis Effects 0.000 claims description 3
- 208000019425 cirrhosis of liver Diseases 0.000 claims description 3
- 210000004185 liver Anatomy 0.000 claims description 3
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- 238000002054 transplantation Methods 0.000 claims description 3
- 208000006454 hepatitis Diseases 0.000 claims description 2
- 231100000283 hepatitis Toxicity 0.000 claims description 2
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- 229940123066 Polymerase inhibitor Drugs 0.000 claims 1
- 238000000034 method Methods 0.000 description 92
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- 229940079322 interferon Drugs 0.000 description 6
- SCVHJVCATBPIHN-SJCJKPOMSA-N (3s)-3-[[(2s)-2-[[2-(2-tert-butylanilino)-2-oxoacetyl]amino]propanoyl]amino]-4-oxo-5-(2,3,5,6-tetrafluorophenoxy)pentanoic acid Chemical group N([C@@H](C)C(=O)N[C@@H](CC(O)=O)C(=O)COC=1C(=C(F)C=C(F)C=1F)F)C(=O)C(=O)NC1=CC=CC=C1C(C)(C)C SCVHJVCATBPIHN-SJCJKPOMSA-N 0.000 description 4
- OIIMUKXVVLRCAF-UHFFFAOYSA-N 10-(4,5-dimethoxy-2-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)decyl-triphenylphosphanium Chemical group O=C1C(OC)=C(OC)C(=O)C(CCCCCCCCCC[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1C OIIMUKXVVLRCAF-UHFFFAOYSA-N 0.000 description 4
- 229940122806 Cyclophilin inhibitor Drugs 0.000 description 4
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- 102100020992 Interferon lambda-3 Human genes 0.000 description 4
- 101710099621 Interferon lambda-3 Proteins 0.000 description 4
- 102100025315 Mannosyl-oligosaccharide glucosidase Human genes 0.000 description 4
- TVRCRTJYMVTEFS-ICGCPXGVSA-N [(2r,3r,4r,5r)-5-(4-amino-2-oxopyrimidin-1-yl)-4-hydroxy-2-(hydroxymethyl)-4-methyloxolan-3-yl] (2s)-2-amino-3-methylbutanoate Chemical compound C[C@@]1(O)[C@H](OC(=O)[C@@H](N)C(C)C)[C@@H](CO)O[C@H]1N1C(=O)N=C(N)C=C1 TVRCRTJYMVTEFS-ICGCPXGVSA-N 0.000 description 4
- YQNQNVDNTFHQSW-UHFFFAOYSA-N acetic acid [2-[[(5-nitro-2-thiazolyl)amino]-oxomethyl]phenyl] ester Chemical group CC(=O)OC1=CC=CC=C1C(=O)NC1=NC=C([N+]([O-])=O)S1 YQNQNVDNTFHQSW-UHFFFAOYSA-N 0.000 description 4
- 239000000556 agonist Substances 0.000 description 4
- 229940124599 anti-inflammatory drug Drugs 0.000 description 4
- 239000003443 antiviral agent Substances 0.000 description 4
- IIBYAHWJQTYFKB-UHFFFAOYSA-N bezafibrate Chemical compound C1=CC(OC(C)(C)C(O)=O)=CC=C1CCNC(=O)C1=CC=C(Cl)C=C1 IIBYAHWJQTYFKB-UHFFFAOYSA-N 0.000 description 4
- 229960000516 bezafibrate Drugs 0.000 description 4
- 239000000134 cyclophilin inhibitor Substances 0.000 description 4
- ZVTDLPBHTSMEJZ-JSZLBQEHSA-N danoprevir Chemical compound O=C([C@@]12C[C@H]1\C=C/CCCCC[C@@H](C(N1C[C@@H](C[C@H]1C(=O)N2)OC(=O)N1CC2=C(F)C=CC=C2C1)=O)NC(=O)OC(C)(C)C)NS(=O)(=O)C1CC1 ZVTDLPBHTSMEJZ-JSZLBQEHSA-N 0.000 description 4
- 229950000234 emricasan Drugs 0.000 description 4
- 230000004761 fibrosis Effects 0.000 description 4
- 108010050669 glucosidase I Proteins 0.000 description 4
- 102000018358 immunoglobulin Human genes 0.000 description 4
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- 229940121354 immunomodulator Drugs 0.000 description 4
- 230000004054 inflammatory process Effects 0.000 description 4
- VKHAHZOOUSRJNA-GCNJZUOMSA-N mifepristone Chemical group C1([C@@H]2C3=C4CCC(=O)C=C4CC[C@H]3[C@@H]3CC[C@@]([C@]3(C2)C)(O)C#CC)=CC=C(N(C)C)C=C1 VKHAHZOOUSRJNA-GCNJZUOMSA-N 0.000 description 4
- 229940127255 pan-caspase inhibitor Drugs 0.000 description 4
- 108010092853 peginterferon alfa-2a Proteins 0.000 description 4
- 108010092851 peginterferon alfa-2b Proteins 0.000 description 4
- 239000003970 toll like receptor agonist Substances 0.000 description 4
- 108010078233 Thymalfasin Proteins 0.000 description 3
- HTJGLYIJVSDQAE-VWNXEWBOSA-N [(1s,6s,7s,8r,8ar)-1,7,8-trihydroxy-1,2,3,5,6,7,8,8a-octahydroindolizin-6-yl] butanoate Chemical group O[C@H]1[C@H](O)[C@@H](OC(=O)CCC)CN2CC[C@H](O)[C@@H]21 HTJGLYIJVSDQAE-VWNXEWBOSA-N 0.000 description 3
- 239000000825 pharmaceutical preparation Substances 0.000 description 3
- 230000000306 recurrent effect Effects 0.000 description 3
- 230000001225 therapeutic effect Effects 0.000 description 3
- NZVYCXVTEHPMHE-ZSUJOUNUSA-N thymalfasin Chemical compound CC(=O)N[C@@H](CO)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(N)=O)C(O)=O NZVYCXVTEHPMHE-ZSUJOUNUSA-N 0.000 description 3
- 229960004231 thymalfasin Drugs 0.000 description 3
- 230000003442 weekly effect Effects 0.000 description 3
- RNEACARJKXYVND-KQGZCTBQSA-N (2r)-2-[[(5z)-5-[(5-ethylfuran-2-yl)methylidene]-4-oxo-1,3-thiazol-2-yl]amino]-2-(4-fluorophenyl)acetic acid Chemical compound O1C(CC)=CC=C1\C=C/1C(=O)N=C(N[C@@H](C(O)=O)C=2C=CC(F)=CC=2)S\1 RNEACARJKXYVND-KQGZCTBQSA-N 0.000 description 2
- HLQXYDHLDZTWDW-KAWPREARSA-N (2r,4s,5r)-1-(4-tert-butyl-3-methoxybenzoyl)-4-(methoxymethyl)-2-(pyrazol-1-ylmethyl)-5-(1,3-thiazol-2-yl)pyrrolidine-2-carboxylic acid Chemical compound C([C@]1(C[C@@H]([C@@H](N1C(=O)C=1C=C(OC)C(=CC=1)C(C)(C)C)C=1SC=CN=1)COC)C(O)=O)N1C=CC=N1 HLQXYDHLDZTWDW-KAWPREARSA-N 0.000 description 2
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 description 2
- ROSNVSQTEGHUKU-UHFFFAOYSA-N 4-[4-(4-chloro-phenoxy)-benzenesulfonylmethyl]-tetrahydro-pyran-4-carboxylic acid hydroxyamide Chemical compound C=1C=C(OC=2C=CC(Cl)=CC=2)C=CC=1S(=O)(=O)CC1(C(=O)NO)CCOCC1 ROSNVSQTEGHUKU-UHFFFAOYSA-N 0.000 description 2
- TZYVRXZQAWPIAB-FCLHUMLKSA-N 5-amino-3-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4h-[1,3]thiazolo[4,5-d]pyrimidine-2,7-dione Chemical compound O=C1SC=2C(=O)NC(N)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O TZYVRXZQAWPIAB-FCLHUMLKSA-N 0.000 description 2
- OLROWHGDTNFZBH-XEMWPYQTSA-N Alisporivir Chemical group CC[C@@H]1NC(=O)[C@H]([C@H](O)[C@H](C)C\C=C\C)N(C)C(=O)[C@H](C(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](CC(C)C)N(C)C(=O)[C@@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)N(C)C(=O)[C@H](C(C)C)NC(=O)[C@H](C(C)C)N(CC)C(=O)[C@@H](C)N(C)C1=O OLROWHGDTNFZBH-XEMWPYQTSA-N 0.000 description 2
- 241000272190 Falco peregrinus Species 0.000 description 2
- 229940126656 GS-4224 Drugs 0.000 description 2
- LLEUXCDZPQOJMY-AAEUAGOBSA-N Glu-Trp Chemical compound C1=CC=C2C(C[C@H](NC(=O)[C@H](CCC(O)=O)N)C(O)=O)=CNC2=C1 LLEUXCDZPQOJMY-AAEUAGOBSA-N 0.000 description 2
- CATMPQFFVNKDEY-YPMHNXCESA-N Golotimod Chemical group C1=CC=C2C(C[C@H](NC(=O)CC[C@@H](N)C(O)=O)C(O)=O)=CNC2=C1 CATMPQFFVNKDEY-YPMHNXCESA-N 0.000 description 2
- 102100040018 Interferon alpha-2 Human genes 0.000 description 2
- 108010079944 Interferon-alpha2b Proteins 0.000 description 2
- 102000008070 Interferon-gamma Human genes 0.000 description 2
- 108010074328 Interferon-gamma Proteins 0.000 description 2
- 241001481166 Nautilus Species 0.000 description 2
- 241000276498 Pollachius virens Species 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- -1 Schering-Plough) Chemical compound 0.000 description 2
- 102400000800 Thymosin alpha-1 Human genes 0.000 description 2
- 229940123384 Toll-like receptor (TLR) agonist Drugs 0.000 description 2
- 108010080374 albuferon Proteins 0.000 description 2
- 229940054685 alinia Drugs 0.000 description 2
- 108010058359 alisporivir Proteins 0.000 description 2
- 239000002260 anti-inflammatory agent Substances 0.000 description 2
- 229960005475 antiinfective agent Drugs 0.000 description 2
- 239000004599 antimicrobial Substances 0.000 description 2
- 208000020403 chronic hepatitis C virus infection Diseases 0.000 description 2
- 229940055354 copegus Drugs 0.000 description 2
- 108010049353 golotimod Proteins 0.000 description 2
- 102000011749 human hepatitis C immune globulin Human genes 0.000 description 2
- 108010062138 human hepatitis C immune globulin Proteins 0.000 description 2
- 230000002584 immunomodulator Effects 0.000 description 2
- 229940090438 infergen Drugs 0.000 description 2
- 238000001802 infusion Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 108010010648 interferon alfacon-1 Proteins 0.000 description 2
- 229950003954 isatoribine Drugs 0.000 description 2
- 108010046177 locteron Proteins 0.000 description 2
- 229960000907 methylthioninium chloride Drugs 0.000 description 2
- 229960003248 mifepristone Drugs 0.000 description 2
- 229960002480 nitazoxanide Drugs 0.000 description 2
- 229940002988 pegasys Drugs 0.000 description 2
- 229940106366 pegintron Drugs 0.000 description 2
- 230000006320 pegylation Effects 0.000 description 2
- FWZLYKYJQSQEPN-SKLAJPBESA-N peregrine Chemical compound OC1[C@H]2[C@@H]3C4([C@@H]5C6OC(C)=O)C(OC)CC[C@@]5(C)CN(CC)[C@H]4C6[C@@]2(OC)C[C@H](OC)[C@H]1C3 FWZLYKYJQSQEPN-SKLAJPBESA-N 0.000 description 2
- FWZLYKYJQSQEPN-UHFFFAOYSA-N peregrine Natural products OC1C2C3C4(C5C6OC(C)=O)C(OC)CCC5(C)CN(CC)C4C6C2(OC)CC(OC)C1C3 FWZLYKYJQSQEPN-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- RYXIBQLRUHDYEE-UHFFFAOYSA-M potassium;5-(cyclohexen-1-yl)-3-[(4-methoxycyclohexyl)-(4-methylcyclohexanecarbonyl)amino]thiophene-2-carboxylate Chemical compound [K+].C1CC(OC)CCC1N(C1=C(SC(=C1)C=1CCCCC=1)C([O-])=O)C(=O)C1CCC(C)CC1 RYXIBQLRUHDYEE-UHFFFAOYSA-M 0.000 description 2
- 229940053146 rebetol Drugs 0.000 description 2
- 229960002091 simeprevir Drugs 0.000 description 2
- JTZZSQYMACOLNN-VDWJNHBNSA-N simeprevir Chemical compound O=C([C@@]12C[C@H]1\C=C/CCCCN(C)C(=O)[C@H]1[C@H](C(N2)=O)C[C@H](C1)OC=1C2=CC=C(C(=C2N=C(C=1)C=1SC=C(N=1)C(C)C)C)OC)NS(=O)(=O)C1CC1 JTZZSQYMACOLNN-VDWJNHBNSA-N 0.000 description 2
- SSERCMQZZYTNBY-UHFFFAOYSA-M sodium;3-[(4-hydroxycyclohexyl)-(4-methylcyclohexanecarbonyl)amino]-5-phenylthiophene-2-carboxylate Chemical compound [Na+].C1CC(C)CCC1C(=O)N(C1=C(SC(=C1)C=1C=CC=CC=1)C([O-])=O)C1CCC(O)CC1 SSERCMQZZYTNBY-UHFFFAOYSA-M 0.000 description 2
- 229960002935 telaprevir Drugs 0.000 description 2
- BBAWEDCPNXPBQM-GDEBMMAJSA-N telaprevir Chemical compound N([C@H](C(=O)N[C@H](C(=O)N1C[C@@H]2CCC[C@@H]2[C@H]1C(=O)N[C@@H](CCC)C(=O)C(=O)NC1CC1)C(C)(C)C)C1CCCCC1)C(=O)C1=CN=CC=N1 BBAWEDCPNXPBQM-GDEBMMAJSA-N 0.000 description 2
- 108010017101 telaprevir Proteins 0.000 description 2
- 229950002810 valopicitabine Drugs 0.000 description 2
- 241000700721 Hepatitis B virus Species 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229950007843 bavituximab Drugs 0.000 description 1
- 229950003414 celgosivir Drugs 0.000 description 1
- 238000011461 current therapy Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229960001438 immunostimulant agent Drugs 0.000 description 1
- 239000003022 immunostimulating agent Substances 0.000 description 1
- 230000003308 immunostimulating effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
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Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5923708P | 2008-06-05 | 2008-06-05 | |
| US61/059,237 | 2008-06-05 | ||
| US10945508P | 2008-10-29 | 2008-10-29 | |
| US61/109,455 | 2008-10-29 | ||
| US16776309P | 2009-04-08 | 2009-04-08 | |
| US61/167,763 | 2009-04-08 | ||
| PCT/US2009/046451 WO2009149377A1 (en) | 2008-06-05 | 2009-06-05 | Use of pegylated type iii interferons for the treatment of hepatitis c |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011522834A JP2011522834A (ja) | 2011-08-04 |
| JP2011522834A5 true JP2011522834A5 (enExample) | 2012-05-17 |
Family
ID=41020837
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011512703A Pending JP2011522834A (ja) | 2008-06-05 | 2009-06-05 | Ｃ型肝炎の治療のためのペグ化ｉｉｉ型インターフェロンの使用 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20110165121A1 (enExample) |
| EP (1) | EP2296691A1 (enExample) |
| JP (1) | JP2011522834A (enExample) |
| CN (2) | CN103536906A (enExample) |
| AU (1) | AU2009255994B2 (enExample) |
| CA (1) | CA2727026A1 (enExample) |
| RU (1) | RU2496514C2 (enExample) |
| WO (1) | WO2009149377A1 (enExample) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE360696T1 (de) | 2000-06-30 | 2007-05-15 | Zymogenetics Inc | Interferon-ähnliches protein zcyto21 |
| US7910313B2 (en) | 2001-04-20 | 2011-03-22 | Zymogenetics, Inc. | Cytokine protein family |
| PT2251353E (pt) | 2003-08-07 | 2013-05-07 | Zymogenetics Inc | Preparações homogéneas de il-28 e il-29 |
| JP4896005B2 (ja) | 2004-04-02 | 2012-03-14 | ザイモジェネティクス リミテッド ライアビリティ カンパニー | Ｉｌ−２８およびｉｌ−２９システイン変異体を用いるウイルス感染を治療するための方法 |
| UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
| US20120308517A1 (en) | 2010-02-09 | 2012-12-06 | Digna Biotech, S.L. | Compositions for the treatment of infectious and tumoural diseases |
| EP2614144B1 (en) * | 2010-09-08 | 2015-07-22 | Twincore Zentrum für Experimentelle und Klinische Infektionsforschung GmbH | Use of inhibitors of phospholipase a2 for the treatment or prevention of flavivirus infection |
| EP2619215B1 (en) | 2010-09-22 | 2018-09-05 | Alios Biopharma, Inc. | Azido nucleosides and nucleotide analogs |
| CN103534256B (zh) | 2010-12-30 | 2016-08-10 | 益安药业 | 大环丙型肝炎丝氨酸蛋白酶抑制剂 |
| WO2012092411A2 (en) | 2010-12-30 | 2012-07-05 | Enanta Pharmaceuticals, Inc. | Phenanthridine macrocyclic hepatitis c serine protease inhibitors |
| CN102584979B (zh) * | 2011-01-18 | 2015-10-14 | 北京凯因科技股份有限公司 | PEG化干扰素λ |
| US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
| WO2013029062A1 (en) * | 2011-08-25 | 2013-02-28 | Nanogen Pharmaceutical Biotechnology Co., Ltd | Peginterferon lambda 1 conjugates, processes for their preparation, pharmaceutical compositions containing these conjugates and processes for making the same |
| EP2748328A4 (en) * | 2011-08-25 | 2015-03-04 | Nanogen Pharmaceutical Biotechnology | PEG-INTERFERON LAMBDA 1 CONJUGATES |
| CN104023726A (zh) | 2011-10-21 | 2014-09-03 | 艾伯维公司 | 用于治疗hcv的一种或多种daa的联合治疗(例如，与abt-072或abt-333) |
| US8492386B2 (en) | 2011-10-21 | 2013-07-23 | Abbvie Inc. | Methods for treating HCV |
| CA2811203C (en) | 2011-10-21 | 2015-05-05 | Abbvie Inc. | Methods for treating hcv |
| US8466159B2 (en) | 2011-10-21 | 2013-06-18 | Abbvie Inc. | Methods for treating HCV |
| CN102533840A (zh) * | 2011-12-13 | 2012-07-04 | 江南大学 | 毕赤酵母制备人白细胞介素29成熟肽的方法 |
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| CN104045704B (zh) * | 2013-03-11 | 2016-08-10 | 中国医学科学院基础医学研究所 | PEG化重组人IFN-λ1、其制备方法和用途 |
| WO2015103490A1 (en) | 2014-01-03 | 2015-07-09 | Abbvie, Inc. | Solid antiviral dosage forms |
| CN109293782A (zh) * | 2014-01-08 | 2019-02-01 | 德益阳光生物技术（北京）有限责任公司 | 融合多肽及使用方法 |
| WO2015136455A1 (en) * | 2014-03-13 | 2015-09-17 | Novartis Ag | New treatments of hepatitis c virus infection |
| EP3142649B1 (en) * | 2014-05-12 | 2019-07-24 | Conatus Pharmaceuticals, Inc. | Treatment of the complications of chronic liver disease with caspase inhibitor emricasan |
| US11759500B2 (en) * | 2014-07-24 | 2023-09-19 | Abion Inc. | PEGylated interferon-beta variant |
| JP7129703B2 (ja) | 2016-04-28 | 2022-09-02 | エモリー ユニバーシティー | アルキン含有ヌクレオチド及びヌクレオシド治療組成物並びにそれらに関連した使用 |
| GB201621728D0 (en) * | 2016-12-20 | 2017-02-01 | Ucb Biopharma Sprl | Methods |
| RU2678332C1 (ru) | 2017-09-08 | 2019-01-28 | Общество с ограниченной ответственностью "Саентифик Фьючер Менеджмент" (ООО "СФМ") | Пегилированный интерферон лямбда, обладающий высокой биодоступностью при пероральном применении, и способ его получения |
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| ATE360696T1 (de) * | 2000-06-30 | 2007-05-15 | Zymogenetics Inc | Interferon-ähnliches protein zcyto21 |
| US7038032B2 (en) * | 2001-04-20 | 2006-05-02 | Zymogenetics, Inc. | Cytokine protein family |
| DK3025726T3 (da) * | 2002-01-18 | 2019-12-09 | Biogen Ma Inc | Polyalkylenpolymerforbindelser og anvendelser deraf |
| JP2006509041A (ja) * | 2002-10-23 | 2006-03-16 | ザイモジェネティクス，インコーポレイティド | Ｉｌ−２８およびｉｌ−２９を用いるウイルス感染を治療するための方法 |
| PT2251353E (pt) * | 2003-08-07 | 2013-05-07 | Zymogenetics Inc | Preparações homogéneas de il-28 e il-29 |
| JP4896005B2 (ja) * | 2004-04-02 | 2012-03-14 | ザイモジェネティクス リミテッド ライアビリティ カンパニー | Ｉｌ−２８およびｉｌ−２９システイン変異体を用いるウイルス感染を治療するための方法 |
| WO2006012644A2 (en) * | 2004-07-29 | 2006-02-02 | Zymogenetics, Inc. | Use of il-28 and il-29 to treat cancer |
| US20070004635A1 (en) * | 2005-06-02 | 2007-01-04 | Schering Corporation | Method of treating interferon non-responders using HCV protease inhibitor |
| AU2006269908A1 (en) * | 2005-07-20 | 2007-01-25 | Bristol-Myers Squibb Company | IL28 and IL29 truncated cysteine mutants and antiviral methods of using same |
| AU2006272937A1 (en) * | 2005-07-20 | 2007-02-01 | Bristol-Myers Squibb Company | Use of truncated cysteine IL28 and IL29 mutants to treat cancers and autoimmune disorders |
| DK1931704T3 (da) * | 2005-10-04 | 2011-03-14 | Zymogenetics L L C | Frembringelse og rensning af IL-29 |
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2009
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- 2009-06-05 CN CN201310408018.0A patent/CN103536906A/zh active Pending
- 2009-06-05 JP JP2011512703A patent/JP2011522834A/ja active Pending
- 2009-06-05 EP EP09759535A patent/EP2296691A1/en not_active Withdrawn
- 2009-06-05 WO PCT/US2009/046451 patent/WO2009149377A1/en not_active Ceased
- 2009-06-05 CN CN2009801261152A patent/CN102099051A/zh active Pending
- 2009-06-05 CA CA2727026A patent/CA2727026A1/en not_active Abandoned
- 2009-06-05 US US12/996,358 patent/US20110165121A1/en not_active Abandoned
- 2009-06-05 RU RU2010154092/15A patent/RU2496514C2/ru active
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