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A multicenter open-label randomized controlled trial comparing interferon-entecavir sequential therapy with interferon monotherapy for chronic hepatitis B

A multicenter open-label randomized controlled trial comparing interferon-entecavir sequential therapy with interferon monotherapy for chronic hepatitis B - Interferon-entecavir sequential therapy for chronic hepatitis B: a randomized controlled trial

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000000595
Enrollment
170
Registered
2007-08-01
Start date
2006-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic hepatitis B

Interventions

Interferon-entecavir sequential therapy arm:A single dose of 6 mega units of recombinant interferon-alpha2b (brand name: intron A) or natural IFN-alpha (brand name: Sumiferon) is administered subcutan

Sponsors

Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)The chronic hepatitis B patients with positive HBsAg, positive HBeAg, HBV DNA above 5.0 log copies/ml, abnormal ALT, and platelet counts over 140,000/microliter are eligible. (2)Liver cirrhosis is denied by physical examination, imaging and laboratory test. (3)Hepatocellular carcinoma is not detected by imaging.

Exclusion criteria

Exclusion criteria: (1)The patients who have an allergy against interferons (2)The patients who have an allergy against nucleos(t)ide analogues (3)The patients who have received interferon or nucleoside analogue within 6 months before registration (4)Pregnant women, or women who are nursing (5)The patients with an uncontrollable heart trouble (myocardial infarction, heart failure, or arrhythmia) (6)The patients with chronic renal failure, or chronic respiratory failure (7)The patients with a severe mental disease such as depression, a suicide consideration, or a suicide project, or the past history of such conditions (8)The patients with liver cirrhosis or severe hepatic diseases (9)The patients having a past history of cerebral hemorrhage or cerebral infarction (10)The patients with other liver diseases such as autoimmune hepatitis, primary biliary cirrhosis, alcoholic liver injury, or chronic hepatitis C (11)The patients having non-liver autoimmune diseases, such as rheumatoid arthritis (12)The patients who are prescribed with Shoh-saiko-toh (13)The patients who were judged inappropriate for the study by the doctor.

Design outcomes

Primary

MeasureTime frame
(1)Change of HBV DNA level from baseline (2)Fall of HBV DNA to less than 2.6 log copies/ml (3)HBeAg clearance (4)HBeAg seroconversion (5)Emergence of entecavir-resistance

Secondary

MeasureTime frame
(1)ALT (2)Albumin (3)Prothrombin time(%) (4)Total Bilirubin (5)Platelet count (6)Ascites (7)Hepatic encephalopathy (8)Child-Pugh score (9)Development of hepatocellular carcinoma (10)HBV precore mutation (11)HBV core promoter mutation

Countries

Japan

Contacts

Public ContactHaruhiko Kobashi

Okayama university hospital Department of gastroenterology and hepatology

hkobashi@md.okayama-u.ac.jp086-235-7219

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026