Unique ID issued by UMIN | UMIN000020124 |
---|---|
Receipt number | R000023247 |
Scientific Title | Efficacy of preceding administration of Entecavir with PEG-IFN-alfa2a for patients with chronic hepatitis B, positive with HBe antigen in young aged populations |
Date of disclosure of the study information | 2015/12/08 |
Last modified on | 2015/12/08 22:25:04 |
Efficacy of preceding administration of Entecavir with PEG-IFN-alfa2a for patients with chronic hepatitis B, positive with HBe antigen in young aged populations
Efficacy of preceding administration of Entecavir with PEG-IFN-alfa2a for patients with chronic hepatitis B, positive with HBe antigen in young aged populations
Efficacy of preceding administration of Entecavir with PEG-IFN-alfa2a for patients with chronic hepatitis B, positive with HBe antigen in young aged populations
Efficacy of preceding administration of Entecavir with PEG-IFN-alfa2a for patients with chronic hepatitis B, positive with HBe antigen in young aged populations
Japan |
Chronic hepatitis B
Hepato-biliary-pancreatic medicine |
Others
NO
Evaluation of the safety, and efficacy of the preceding administration of Entecavir with PEG-IFN-alfa2a for young patients with chronic hepatitis B
Safety,Efficacy
The ratio of HBV-DNA titer, below 4 log copies/mL after 48 weeks of preceding administration of Entecavir with PEG-IFN-alfa2a
Interventional
Single arm
Non-randomized
Open -no one is blinded
Uncontrolled
1
Treatment
Medicine |
Administration of Entecavir for at least 24 weeks since the beginning of treatment
At 20 weeks, HBV-DNA titer below 4log, then switch to PEG-IFN-alfa2a
At 20 weeks, HBV-DNA titer more than 4log, Entecavir would be continued
At the onset of HBV-DNA below 4log, switch to PEG-IFN-alfa2a, continued for 48 weeks
The maxim duration of Entecavir would be 48 weeks
20 | years-old | <= |
40 | years-old | > |
Male and Female
1. Age below 40 years old
2. Patient with chronic hepatitis B, untreated with IFN or nuclear analogue
Non-cirrhosis
3. Genotype C, HBe Antigen positive, HBV-DNA over 7log copies, ALT over 100IU/L
Just before the trial, Neutrophil more than 1,500/ul, Platelet more than 90,000/ul, hemoglobin more than 10g/dl
4. ECOG performance status 0 or 1
5. Obtained an informed consent from all study participants
1. HCV antibody positive
2. Liver cirrhosis
3. Pregnancy or lactation period
4. Entecavir or interferon therapy before the study
5. Treated with shou-saikotou (Kampo medicine)
6. Past history of interstitial pneumoniae
7. Past history of autoimmune hepatitis
8. Allergy with vaccination
9. Severe mentally disordered, severe psychotic disease
10. Others
26
1st name | |
Middle name | |
Last name | Michihiro Suzuki |
St. Marianna University School of Medicine
Division of Gastroenterology and Hepatology, Department of Internal Medicine
2-16-1 Sugao, Miyamae-ku, Kawasaki City, Kanagawa 216-8511, Japan
044-977-8111
michstmu@marianna-u.ac.jp
1st name | |
Middle name | |
Last name | Hiroki Ikeda |
St. Marianna University School of Medicine
Division of Gastroenterology and Hepatology, Department of Internal Medicine
2-16-1 Sugao, Miyamae-ku, Kawasaki City, Kanagawa 216-8511, Japan
044-977-8111
ikedahi@marianna-u.ac.jp
Division of Gastroenterology and Hepatology, Department of Internal Medicine, St. Marianna University School of Medicine,
Division of Gastroenterology and Hepatology, Department of Internal Medicine, St. Marianna University School of Medicine,
Self funding
NO
2015 | Year | 12 | Month | 08 | Day |
Unpublished
Enrolling by invitation
2014 | Year | 03 | Month | 01 | Day |
2014 | Year | 03 | Month | 01 | Day |
2015 | Year | 12 | Month | 08 | Day |
2015 | Year | 12 | Month | 08 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000023247