PE20001386A1 - COMBINATION THERAPY FOR HCV BY INDUCTION OF RIBAVIRIN-INTERFERON ALPHA - Google Patents
COMBINATION THERAPY FOR HCV BY INDUCTION OF RIBAVIRIN-INTERFERON ALPHAInfo
- Publication number
- PE20001386A1 PE20001386A1 PE1999001294A PE00129499A PE20001386A1 PE 20001386 A1 PE20001386 A1 PE 20001386A1 PE 1999001294 A PE1999001294 A PE 1999001294A PE 00129499 A PE00129499 A PE 00129499A PE 20001386 A1 PE20001386 A1 PE 20001386A1
- Authority
- PE
- Peru
- Prior art keywords
- interferon alpha
- miu
- weeks
- ribavirin
- combination therapy
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/21—Interferons [IFN]
- A61K38/212—IFN-alpha
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
Abstract
SE REFIERE A EL USO DE RIVABIRINA EN ASOCIACION CON INTERFERON ALFA EN DOS PERIODOS DE TRATAMIENTO: a) 800-1200mg/DIA DE RIVABIRINA MAS INTERFERON ALFA ADMINISTRANDO 10 MIU DURANTE 2 SEMANAS SEGUIDO DE 5 MIU POR 6 SEMANAS, SEGUIDO DE 3 MIU POR 16 SEMANAS PARA DISMINUIR EL NIVEL DE ARN DE VHC DETECTABLE; b)800-1200mg/DIA DE RIBAVIRINA MAS 3 MIU DE INTERFERON ALFA POR UN PERIODO DE 20 A 30 SEMANAS PARA ERRADICAR EL ARN DEL VHC DETECTABLE. EL INTERFERON ALFA ES SELECCIONADO DE INTERFERON ALFA-2a, INTERFERON ALFA-2b, INTERFERON DE CONSENSO, PRODUCTO DE INTERFERON ALFA PURIFICADO. LA TERAPIA DE COMBINACION ES UTIL EN PACIENTES CON HEPATITIS C CRONICA INFECTADOS CON GENOTIPOS DE VHC MULTIPLE TIPO 1, 2 Y 3REFERS TO THE USE OF RIVABIRIN IN ASSOCIATION WITH INTERFERON ALPHA IN TWO PERIODS OF TREATMENT: a) 800-1200mg / DAY OF RIVABIRIN PLUS INTERFERON ALPHA ADMINISTERING 10 MIU FOR 2 WEEKS FOLLOWED BY 5 MIU FOR 6 WEEKS, FOLLOWED BY 3 MIU FOR 16 WEEKS TO REDUCE DETECTABLE HCV RNA LEVEL; b) 800-1200mg / DAY OF RIBAVIRIN PLUS 3 MIU OF ALPHA INTERFERED FOR A PERIOD OF 20 TO 30 WEEKS TO ERADICATE DETECTABLE HCV RNA. THE INTERFERON ALPHA IS SELECTED FROM INTERFERON ALPHA-2a, INTERFERON ALPHA-2b, INTERFERON OF CONSENSUS, INTERFERON ALPHA PURIFIED PRODUCT. COMBINATION THERAPY IS USEFUL IN PATIENTS WITH CHRONIC HEPATITIS C INFECTED WITH MULTIPLE HCV TYPE 1, 2 AND 3 GENOTYPES
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21587598A | 1998-12-18 | 1998-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20001386A1 true PE20001386A1 (en) | 2000-12-14 |
Family
ID=22804763
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE1999001294A PE20001386A1 (en) | 1998-12-18 | 1999-12-17 | COMBINATION THERAPY FOR HCV BY INDUCTION OF RIBAVIRIN-INTERFERON ALPHA |
Country Status (4)
Country | Link |
---|---|
AR (1) | AR022116A1 (en) |
AU (1) | AU2156900A (en) |
PE (1) | PE20001386A1 (en) |
WO (1) | WO2000037097A1 (en) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7179791B2 (en) * | 2001-01-11 | 2007-02-20 | Duke University | Inhibiting GS-FDH to modulate NO bioactivity |
WO2006016657A1 (en) | 2004-08-11 | 2006-02-16 | Chugai Seiyaku Kabushiki Kaisha | Drug for treating or preventing hcv infection |
US7723310B2 (en) | 2004-10-18 | 2010-05-25 | Three Rivers Pharmaceuticals, Llc | Large dose ribavirin formulations |
CA2652333A1 (en) * | 2006-05-16 | 2007-11-22 | Tokyo Metropolitan Organization For Medical Research | Pharmaceutical composition for treating or preventing hcv infection |
EP1977759A1 (en) * | 2007-03-27 | 2008-10-08 | 4Sc Ag | Pharmaceutical composition comprising a cytokine |
WO2008116919A1 (en) * | 2007-03-27 | 2008-10-02 | 4Sc Ag | Pharmaceutical composition comprising a cytokine |
US20110270212A1 (en) * | 2007-10-05 | 2011-11-03 | Medtronic, Inc. | Pharmacokinetic control for optimized interferon delivery |
EP2610343A3 (en) | 2008-11-26 | 2013-09-25 | Chugai Seiyaku Kabushiki Kaisha | Method for designing siRNA and oligoribonucleotides inhibiting HCV |
DE202012013117U1 (en) | 2011-10-21 | 2015-01-16 | Abbvie Inc. | Combination treatment (e.g., with ABT-072 or ABT-333 from DAAs for use in the treatment of HCV) |
US8466159B2 (en) | 2011-10-21 | 2013-06-18 | Abbvie Inc. | Methods for treating HCV |
US8492386B2 (en) | 2011-10-21 | 2013-07-23 | Abbvie Inc. | Methods for treating HCV |
DE112012003510T5 (en) | 2011-10-21 | 2015-03-19 | Abbvie Inc. | Method for the treatment of HCV comprising at least two direct-acting antiviral agents, ribavirin but not interferon |
CN109689063A (en) | 2016-04-28 | 2019-04-26 | 埃默里大学 | Nucleotide containing alkynes and nucleosides therapeutic combination and its associated uses |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6387365B1 (en) * | 1995-05-19 | 2002-05-14 | Schering Corporation | Combination therapy for chronic hepatitis C infection |
EP0903148B1 (en) * | 1997-09-21 | 2001-10-10 | Schering Corporation | Combination therapy for eradicating detectable HCV-RNA in patients having chronic hepatitis C infection |
-
1999
- 1999-12-16 AU AU21569/00A patent/AU2156900A/en not_active Abandoned
- 1999-12-16 WO PCT/US1999/027934 patent/WO2000037097A1/en active Application Filing
- 1999-12-16 AR ARP990106463A patent/AR022116A1/en unknown
- 1999-12-17 PE PE1999001294A patent/PE20001386A1/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
AR022116A1 (en) | 2002-09-04 |
WO2000037097A1 (en) | 2000-06-29 |
AU2156900A (en) | 2000-07-12 |
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