Unique ID issued by UMIN | UMIN000007071 |
---|---|
Receipt number | R000008328 |
Scientific Title | The effect and safety in Telaprevir with combined peginterferon alpha-2b plus ribavirin for chronic hepatitis C patients |
Date of disclosure of the study information | 2015/12/31 |
Last modified on | 2016/01/06 11:20:15 |
The effect and safety in Telaprevir with combined peginterferon alpha-2b plus ribavirin for chronic hepatitis C patients
Drug adjustment on adverse effect of telaprevir combined therapy (TPR-dose trial)
The effect and safety in Telaprevir with combined peginterferon alpha-2b plus ribavirin for chronic hepatitis C patients
Drug adjustment on adverse effect of telaprevir combined therapy (TPR-dose trial)
Japan |
Chronic hepatitis C
Hepato-biliary-pancreatic medicine |
Others
NO
Examination of efficacy and safety of adjustment of drug dose in combination therapy with Telaprevir/ Peginterferon alpha 2a/Ribavirin for chronic hepatitis C patients.
Safety,Efficacy
Sustained Virological Response ( SVR ) at week 24
ALT normalization
Safety
Interventional
Parallel
Randomized
Cluster
Open -no one is blinded
Dose comparison
2
Treatment
Medicine |
Telaprevir reduction
Peginterferon alpha 2b
Ribavirin
Telaprevir
Peginterferon alpha 2b
Ribavirin reduction
20 | years-old | <= |
70 | years-old | >= |
Male and Female
The following chronic hepatitis C patients with Genotype 1 and high viral lord were eligible to enter the trial
HCV-RNA >= 5.0 LogIU/mL
WBC counts>=3,000/microL
Neutrophil counts>=1,500/microL
Hemoglobin concentration>=12g/dL
Platelet counts>=90,000/microL
Presence of liver biopsy is not asked
Presence of the IFN treatment history is not asked
Patients who provided written informed consent to participate the study prior to enrollment
The following patients were excluded
women of childbearing potential and pregnancy, lactating women
allergic to ribavirin or other nucleoside analogues
an uncontrollable heart trouble( myocardial infarction, heart failure, or arrhythmia)
hemoglobibopathy ( thalassemia, sickle cell disease)
severe renal disease or Ccr<50mL/min
severe depression or psychosomatic disorders
severe liver disease
autoimmune hepatitis or HBV
drug allergy against interferon
100
1st name | |
Middle name | |
Last name | Akihiro Tamori |
Osaka City University, Graduate School of Medicine
Department of Hepatology
1-4-3, Asahimachi, Abeno-ku, Osaka
06-6645-3811
atamori@med.osaka-cu.ac.jp
1st name | |
Middle name | |
Last name | Akihiro Tamori |
Osaka City University, Graduate School of Medicine
Department of Hepatology
1-4-3, Asahimachi, Abeno-ku, Osaka 545-8585, JAPAN
06-6645-3435
webmaster@med.osaka-cu.ac.jp
Department of Hepatology, Osaka City University , Graduate School of Medicine
Osaka City University , Graduate School of Medicine
Self funding
NO
2015 | Year | 12 | Month | 31 | Day |
Published
Telaprevir dose adjustment could prevent anemia progression without weakening the anti-viral effect during triple therapy in patients with HCV.
Completed
2011 | Year | 11 | Month | 30 | Day |
2012 | Year | 01 | Month | 01 | Day |
2014 | Year | 02 | Month | 28 | Day |
2014 | Year | 03 | Month | 10 | Day |
2014 | Year | 03 | Month | 20 | Day |
2014 | Year | 03 | Month | 31 | Day |
Tamori A, Kioka K, Sakaguchi H, Enomoto M, Hai H, Kawamura E, Hagihara A, Fujii H, Uchida-Kobayashi S, Iwai S, Morikawa H, Murakami Y, Kawasaki Y, Tsuruta D, Kawada N. Effects on anemia of drug adjustment in patients with chronic hepatitis C during telaprevir-combined therapy. Ann Hepatol. 2015 Jan-Feb;14(1):28-35.
2012 | Year | 01 | Month | 16 | Day |
2016 | Year | 01 | Month | 06 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008328