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A Study of Combination Therapy With PEGASYS (Pegylated Interferon Alfa-2a (40KD)) and Copegus (Ribavirin) in Patients With Chronic Hepatitis C Genotype 2 or 3 Who Do Not Achieve a Rapid Viral Response

15 juli 2013 uppdaterad av: Hoffmann-La Roche

A Randomized, Open-label Study of the Effects of 24 vs 48 Weeks of Combination Therapy With PEGASYS (Peginterferon Alfa-2a 40KD) Plus COPEGUS (Ribavirin) on Sustained Virological Response in Patients With Chronic Hepatitis C, Genotype 2 or 3 Who do Not Achieve a Rapid Viral Response

This study will evaluate the efficacy and safety of peginterferon alfa-2a 40KD + ribavirin combination therapy given for 24 weeks versus 48 weeks in patients with chronic hepatitis C, genotype 2/3.

Studieöversikt

Status

Avslutad

Betingelser

Intervention / Behandling

Detaljerad beskrivning

During a pre-study run-in phase patients with chronic hepatitis C genotype 2/3, who had started therapy with PEG-IFN alfa-2a plus ribavirin according to local standard of care and did not achieve a rapid viral response (RVR) (defined as Hepatitis C virus (HCV) RNA <15 IU/mL at Week 4 of treatment measured with the Roche COBAS AmpliPrep / COBAS TaqMan® HCV Test) were eligible for the study and entered the screening phase between treatment Week 4 and 8 as soon as the result of the Week 4 HCV RNA test was available.

Eligible patients entered the study and continued with the dose regimens of PEG-IFN alfa-2a and ribavirin they were taking prior to enrolment into the trial up to Week 24 of treatment. Patients who achieved at least a 2-log10 drop of HCV RNA at Week 12 (as compared to HCV RNA levels prior to treatment initiation) or had HCV RNA <15 IU/mL, and who were still taking study medication at treatment Week 24, were randomized at treatment Week 24 to one of the two study groups. Upon randomization, participants either stopped treatment (equaling 24 weeks of treatment) or continued treatment for another 24 weeks (equaling 48 weeks of treatment). A treatment free follow-up period of 24 weeks (for participants in the 48-week treatment group) or 48 weeks (participants in the 24-week treatment group) completed the study.

Studietyp

Interventionell

Inskrivning (Faktisk)

235

Fas

  • Fas 3

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

  • Australien
      • Darlinghurst, Australien, 2010
      • Fremantle, Australien, 6160
      • Melbourne, Australien, 3186
      • Nedlands, Australien, 6009
      • Sydney, Australien, 2139
  • Belgien
      • Antwerpen, Belgien, 2650
      • Bruxelles, Belgien, 1020
      • Bruxelles, Belgien, 1070
      • Bruxelles, Belgien, 1000
      • Gent, Belgien, 9000
      • Kortrijk, Belgien, 8500
      • Liege, Belgien, 4000
  • Brasilien
      • Brasilia, Brasilien, 70335-000
      • Campinas, Brasilien, 13081-970
      • Campinas, Brasilien, 13012-970
      • Porto Alegre, Brasilien, 90020-090
      • Porto Alegre, Brasilien, 90035-003
      • Ribeirao Preto, Brasilien, 14049-900
      • Rio de Janeiro, Brasilien, 20020-022
      • Santo Andre, Brasilien, 09060-650
      • Sao Luis, Brasilien, 78048-790
      • Sao Paulo, Brasilien, 04040-003
      • Sorocaba, Brasilien, 18047-600
      • Vitoria, Brasilien, 29043-260
  • Förenta staterna
    • Alabama
      • Birmingham, Alabama, Förenta staterna, 35294
    • California
      • La Jolla, California, Förenta staterna, 92037-1030
      • Lancaster, California, Förenta staterna, 93534
      • Long Beach, California, Förenta staterna, 90822
      • Los Angeles, California, Förenta staterna, 90048
      • Los Angeles, California, Förenta staterna, 90057
      • Sacramento, California, Förenta staterna, 95817
      • Sacramento, California, Förenta staterna, 95816
      • San Diego, California, Förenta staterna, 92103-8465
      • Torrance, California, Förenta staterna, 90505
    • Colorado
      • Aurora, Colorado, Förenta staterna, 80045
    • Florida
      • Jacksonville, Florida, Förenta staterna, 32256
      • Orlando, Florida, Förenta staterna, 32803
    • Georgia
      • Atlanta, Georgia, Förenta staterna, 30308
      • Marietta, Georgia, Förenta staterna, 30060
    • Hawaii
      • Honolulu, Hawaii, Förenta staterna, 96813
    • Louisiana
      • Baton Rouge, Louisiana, Förenta staterna, 70890
      • Opelousas, Louisiana, Förenta staterna, 70520
    • Massachusetts
      • Boston, Massachusetts, Förenta staterna, 02114
    • Mississippi
      • Tupelo, Mississippi, Förenta staterna, 38801
    • Missouri
      • St Louis, Missouri, Förenta staterna, 63110
      • St Louis, Missouri, Förenta staterna, 63104
    • New Jersey
      • Egg Harbour Township, New Jersey, Förenta staterna, 08234
      • Hackensack, New Jersey, Förenta staterna, 07601
    • New Mexico
      • Albuquerque, New Mexico, Förenta staterna, 87131
    • New York
      • New York, New York, Förenta staterna, 10016
      • Syracuse, New York, Förenta staterna, 13210
    • North Carolina
      • Asheville, North Carolina, Förenta staterna, 28801
      • Chapel Hill, North Carolina, Förenta staterna, 27599-7080
      • Winston-salem, North Carolina, Förenta staterna, 27103
    • Oklahoma
      • Oklahoma City, Oklahoma, Förenta staterna, 73112-4481
    • Oregon
      • Portland, Oregon, Förenta staterna, 97239
    • Tennessee
      • Kingsport, Tennessee, Förenta staterna, 37660
    • Texas
      • Fort Sam Houston, Texas, Förenta staterna, 78234-3879
    • Utah
      • Salt Lake City, Utah, Förenta staterna, 84132
    • Virginia
      • Charlottesville, Virginia, Förenta staterna, 22908
      • Fairfax, Virginia, Förenta staterna, 22031
      • Richmond, Virginia, Förenta staterna, 23249
  • Kanada
    • Alberta
      • Edmonton, Alberta, Kanada, T6G 2B7
    • British Columbia
      • Vancouver, British Columbia, Kanada, V6Z 2K5
    • Ontario
      • Hamilton, Ontario, Kanada, L8N 4A6
      • Mississauga, Ontario, Kanada, L5M 4N4
  • Mexiko
      • Guadalajara, Mexiko, 44160
      • Guadalajara, Mexiko, 44670
      • Mexicali, Mexiko, 21000
      • Mexico City, Mexiko, 14050
      • Mexico Df, Mexiko, 11649
      • Puebla, Mexiko, 72560
  • Puerto Rico
      • Santurce, Puerto Rico, 00909
  • Schweiz
      • Lausanne, Schweiz, 1005
      • Lugano, Schweiz, 6903
      • St. Gallen, Schweiz, 9007
      • Zürich, Schweiz, 8091
  • Tyskland
      • Berlin, Tyskland, 13353
      • Berlin, Tyskland, 10969
      • Bonn, Tyskland, 53127
      • Düsseldorf, Tyskland, 40225
      • Düsseldorf, Tyskland, 40237
      • Frankfurt Am Main, Tyskland, 60590
      • Freiburg, Tyskland, 79106
      • Giessen, Tyskland, 35392
      • Hamburg, Tyskland, 20099
      • Heidelberg, Tyskland, 69120
      • Jena, Tyskland, 07747
      • Kiel, Tyskland, 24105
      • Köln, Tyskland, 50937
      • Mainz, Tyskland, 55101
      • München, Tyskland, 81675
      • Offenburg, Tyskland, 77654
      • Tübingen, Tyskland, 72076
      • ULM, Tyskland, 89081
  • Österrike
      • Graz, Österrike, 8036
      • Innsbruck, Österrike, 6020
      • Linz, Österrike, 4010
      • Oberndorf, Österrike, 5110
      • Wien, Österrike, 1160
      • Wien, Österrike, 1090

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • adult patients, >=18 years of age;
  • serological evidence of chronic hepatitis C (CHC);
  • CHC genotype 2 or 3;
  • receiving PEGASYS + Copegus according to local standard of care and no rapid viral response (RVR);
  • compensated liver disease.

Exclusion Criteria:

  • pegylated interferon, standard interferon or ribavirin therapy at any time prior to initiation of current therapy with PEGASYS + Copegus;
  • coinfection with hepatitis A or B, or human immunodeficiency virus (HIV);
  • history or other evidence of decompensated liver disease.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: PEG-IFN alfa-2a + Ribavirin for 24 weeks
After 24 weeks of treatment with pegylated interferon alfa-2a (PEG-IFN alfa-2a) 180 μg/week plus ribavirin 800-1200 mg/day participants who achieved at least a 2-log10 drop of hepatitis C virus (HCV) ribonucleic acid (RNA) at Week 12 (as compared to HCV RNA levels prior to treatment initiation) or had HCV RNA <15 IU/mL, and who were still taking study medication at treatment Week 24 were randomized into the study, at which time treatment was stopped. Participants were followed for an additional 48 weeks during the treatment-free follow-up period.
Läkemedel: Ribavirin
Andra namn:
  • Copegus®
Läkemedel: peginterferon alfa-2a
Andra namn:
  • Pegasys®
  • PEG-IFN alfa-2a
Aktiv komparator: PEG-IFN alfa-2a + Ribavirin for 48 weeks
After 24 weeks of treatment with PEG-IFN alfa-2a 180 μg/week plus ribavirin 800-1200 mg/day participants who achieved at least a 2-log10 drop of HCV RNA at Week 12 (as compared to HCV RNA levels prior to treatment initiation) or had HCV RNA <15 IU/mL, and who were still taking study medication at treatment Week 24 were randomized into the study, and continued treatment for another 24 weeks (for a total of 48 weeks of treatment). Participants were followed for an additional 24 weeks during the treatment-free follow-up period.
Läkemedel: Ribavirin
Andra namn:
  • Copegus®
Läkemedel: peginterferon alfa-2a
Andra namn:
  • Pegasys®
  • PEG-IFN alfa-2a

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Percentage of Participants With a Sustained Virologic Response 24 Weeks After Scheduled Completion of Treatment
Tidsram: 24 weeks after scheduled treatment completion (approximately Week 48 for participants in the 24-week treatment group and Week 72 for participants in the 48-week treatment group.

Sustained virological response (SVR) is defined as a single last HCV RNA measurement <15 IU/ml (measured using the Roche COBAS AmpliPrep / COBAS TaqMan HCV Test) 24 weeks after scheduled treatment completion, defined as Week 44 or later for participants randomized to the 24-week treatment period or Week 68 or later for participants randomized to the 48-week treatment period.

Participants without measurements at the end of the 24-week untreated follow-up period were considered non-responders in the analysis.
24 weeks after scheduled treatment completion (approximately Week 48 for participants in the 24-week treatment group and Week 72 for participants in the 48-week treatment group.
Percentage of Participants With a Sustained Virologic Response 24 Weeks After Actual End of Treatment
Tidsram: 24 weeks after actual end of treatment (range from Week 48 to Week 72).
Sustained virological response (SVR) is defined as a single last HCV RNA measurement <15 IU/ml (measured using the Roche COBAS AmpliPrep / COBAS TaqMan HCV Test) at 24 weeks after actual end of study treatment. For participants in the 48-week treatment group who stopped study treatment prior to Week 48 for any reason, the HCV RNA measurements 24 weeks after actual end of treatment were used in the analysis. Participants without a 24-week post treatment measurement are considered non-responders.
24 weeks after actual end of treatment (range from Week 48 to Week 72).

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Percentage of Participants With Virological Response 72 Weeks After Treatment Initiation
Tidsram: Week 72

Virological response 72 weeks after treatment initiation is defined as the percentage of participants with HCV RNA <15 IU/mL as measured by the Roche COBAS AmpliPrep / COBAS TaqMan® HCV Test at 48 weeks post completion of the 24 week treatment period and 24 weeks post completion of the 48 week treatment period.

Participants without Week 72 measurements were considered non-responders in the analysis.
Week 72
Percentage of Participants With Virological Response at End of Treatment
Tidsram: End of Treatment (Week 24 and Week 48 for each treatment group respectively).
Virological response at the end of treatment was defined as the percentage of participants with HCV RNA <15 IU/mL as measured by the Roche COBAS AmpliPrep / COBAS TaqMan® HCV Test after the last dose of study medication.
End of Treatment (Week 24 and Week 48 for each treatment group respectively).
Percentage of Participants With Virological Relapse
Tidsram: End of treatment (Weeks 24 or 48) and 24 weeks after the end of treatment (weeks 48 and 72 in each treatment group respectively).

Virological relapse defined as the percentage of participants with a virological response at end of treatment but who did not have a sustained virological response 24 weeks after the end of treatment.

Virological response at end of treatment is defined as a single last HCV RNA measurement <15 IU/ml measured using the Roche COBAS AmpliPrep / COBAS TaqMan HCV Test at the day of last dose of study medication.

Sustained virological response 24 weeks after the actual treatment end (SVR24) is defined as a single last HCV RNA measurement <15 IU/ml at least 20 weeks after treatment end.
End of treatment (Weeks 24 or 48) and 24 weeks after the end of treatment (weeks 48 and 72 in each treatment group respectively).
Percentage of Participants With a Sustained Virologic Response 12 Weeks After Actual End of Treatment
Tidsram: 12 weeks after actual end of treatment (range from Week 36 to Week 60)
Sustained virological response (SVR) is defined as a single last HCV RNA measurement <15 IU/ml (measured using the Roche COBAS AmpliPrep / COBAS TaqMan HCV Test) at 12 weeks after actual end of study treatment. For participants in the 48-week treatment group who stopped study treatment prior to Week 48 for any reason, the HCV RNA measurements 12 weeks after actual end of treatment were used in the analysis. Participants without a 12-week post treatment measurement are considered non-responders.
12 weeks after actual end of treatment (range from Week 36 to Week 60)
Number of Participants With Adverse Events (AEs)
Tidsram: From Week 1 through Week 72.
An AE was defined as a sign or symptom, including intercurrent illness, that occurred during the course of the clinical study after treatment had started. A related AE is an event assessed by the Investigator to be remotely, possibly, or probably related to study treatment according to criteria provided in the protocol. A severe AE was an event graded by the Investigator as "incapacitating with inability to work or perform normal daily activity". A serious AE (SAE) was defined as any experience that suggests a significant hazard, contraindication, side effect or precaution. This includes any experience which was fatal; was life-threatening; required inpatient hospitalization or prolongation of an existing hospitalization; resulted in persistent or significant disability/incapacity; was a congenital anomaly/ birth defect; was medically significant or required intervention to prevent one or other of the outcomes listed above.
From Week 1 through Week 72.

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Hoffmann-La Roche

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 juni 2008

Primärt slutförande (Faktisk)

1 maj 2012

Avslutad studie (Faktisk)

1 maj 2012

Studieregistreringsdatum

Först inskickad

18 februari 2008

Först inskickad som uppfyllde QC-kriterierna

18 februari 2008

Första postat (Uppskatta)

26 februari 2008

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

22 juli 2013

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

15 juli 2013

Senast verifierad

1 juli 2013

Mer information

Termer relaterade till denna studie

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • MV21371
  • 2007-004993-15

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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