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Novaferon for chronic hepatitis B: a phase ?randomized open-label control trial

Novaferon for chronic hepatitis B: a phase ?randomized open-label control trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10000982
Enrollment
Unknown
Registered
2010-08-16
Start date
2010-07-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Chronic Hepatitis B

Interventions

1:Novaferon, 10ug intramuscular injection, once daily in the first day
Day 2 to day 7 not given the medication
followed injection 10ug a day, during week 2 to week 7
2:Novaferon, 10ug intramuscular injection, thrice weekly for week 1-6
3:Novaferon, 10ug intramuscular injection, once daily for the first week
followed by 20ug, thrice weekly for week 2-6

Sponsors

Beijing YouAn Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients with Chronic hepatitis B participate in this clinical trial voluntarily and may benefit from this trial; 2. Diagnosis of Chronic hepatitis B based on the guidelines of Chronic hepatitis B(2005). Patients are HBeAg -positive; 3. Patients who have a serum HBV DNA level above 105 cps/ml; 4. 18~60 years of age, regardless of gender; 5. Female: Women of childbearing potential must have a negative serum or urine pregnancy test at screening, and use an approved contraception. Male: Must be surgically sterile or compliant with an adequate contraception during, and for 3 months after the treatment; 6. The signed informed consent must be obtained prior to performing any study specific procedures.

Exclusion criteria

Exclusion criteria: 1. Patients who have a history of interferon or antiviral use within 6 months before signing informed consent form; 2. Patients with known allergy to interferon-adrugs; 3. Patients who had taken other investigational products within 3 months preceding the informed consent was signed; 4. Patients who are receiving other antiviral therapies at the same time; 5. Pregnant or breast-feeding women.

Design outcomes

Primary

MeasureTime frame
Advers event;HBV DNA level;

Secondary

MeasureTime frame
HBeAg;ALT;HBsAg;

Countries

China

Contacts

Public ContactNing Li
Liningbiyah@vip.sina.com+86 010 83997001

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026