Unique ID issued by UMIN | UMIN000015229 |
---|---|
Receipt number | R000000920 |
Scientific Title | Open-label, randomized, controlled study peginterferon alpa-2b plus dose-escalation of ribavirin in patients with chronic hepatitis C |
Date of disclosure of the study information | 2014/10/01 |
Last modified on | 2015/06/26 22:26:05 |
Open-label, randomized, controlled study peginterferon alpa-2b plus dose-escalation of ribavirin in patients with chronic hepatitis C
Randomized study evaluating dose-escalation of combination therapy in chronic hepatitis C patients
Open-label, randomized, controlled study peginterferon alpa-2b plus dose-escalation of ribavirin in patients with chronic hepatitis C
Randomized study evaluating dose-escalation of combination therapy in chronic hepatitis C patients
Japan |
Chronic hepatitis C
Hepato-biliary-pancreatic medicine |
Others
NO
To compare efficacy and safety of peginterferon alpha-2b plus ribavirin administered with standard versus dose-escalation manner in patients with chronic hepatitis C
Safety,Efficacy
Rate of negative results of qualitative HCV RNA test (end-of-treatment and 24 weeks after terminating therapy
1. Sustained virological response rate accordong to the time point of viral disappearance
2. Rate of anemia (defined as hemoglobin concentration < 10 g/dL) at every week up to week 8 and every 4 weeks therafter
3. Incidence of dose modification and discontinuation of therapy
Interventional
Parallel
Randomized
Individual
Open -no one is blinded
Active
YES
NO
Institution is not considered as adjustment factor.
NO
Central registration
2
Treatment
Medicine |
Standard therapy of 48 weeks according to package insert of peginterferon alpha 2b plus ribavirin
Starting with lower dose of ribavirin than standard dose according to package insert by 200 mg in combination with peginterferon alpha-2b, followed by dose-escalation of ribavirin by 100 mg, when hemoglobin concentration maintained at or above 12 g/dL at week 4 an 8
18 | years-old | <= |
Not applicable |
Male and Female
1. HCV genotype 1 an HCV RNA level 100,000 IU/mL or more
2. Cirrhosis has been excluded by histological data, image diagnosis, and laboratory tests
3. Without omplication with hepatocellular carcinoma
1. Hemoglobin values at entry visit less than 12 g/dL
2. Allergic to interferon or vaccine preparations
3. Allergic to ribavirin or other nucleos(t)ide preparations
4. Pregnant or under breast feeding
5. Uncontrolled cardiovascular diseases
6. Abnormal hemoglobinemia
7. Chronic renal failure or creatinine clearance value less than 50 mL/min
8. Neurologic or psychiatric disease
9. Sever or decompensated liver disease
10. Hypertension or diabetes
11. History of apoplexy
12. Autoimmune hepatitis
13. Chronic hepatitis B or excessive daily intake of alcohol
14. Concomitant immunosuppressive or herbal medication such as Sho-saiko-to
15. Other conditions considered inappropriate by attending physician
380
1st name | |
Middle name | |
Last name | Yoshiaki Iwasaki |
Okayama University Hospital
Department of Gastroenterology and Hepatology
2-5-1, Shikata-cho, Okayama-city, Okayama, Japan
086-235-7219
yiwasaki@cc.okayama-u.ac.jp
1st name | |
Middle name | |
Last name | Yoshiaki Iwasaki |
Okayama University Hospital
Department of Gastroenterology and Hepatology
2-5-1, Shikata-cho, Okayama-city, Okayama, Japan
086-235-7219
yiwasaki@cc.okayama-u.ac.jp
Okayama University Hospital
Not applicable
Self funding
NO
2014 | Year | 10 | Month | 01 | Day |
Published
http://onlinelibrary.wiley.com/doi/10.1002/jmv.24097/abstract
Completed
2005 | Year | 11 | Month | 05 | Day |
2006 | Year | 01 | Month | 01 | Day |
2012 | Year | 06 | Month | 01 | Day |
2014 | Year | 09 | Month | 23 | Day |
2015 | Year | 06 | Month | 26 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000000920