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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01210287
Other study ID # 201010HBV
Secondary ID
Status Active, not recruiting
Phase Phase 2/Phase 3
First received September 27, 2010
Last updated January 7, 2014
Start date October 2010
Est. completion date August 2014

Study information

Verified date January 2014
Source Fudan University
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Interventional

Clinical Trial Summary

The aim of this study is to identify the incidence of hepatitis B virus reactivation rate in Diffuse Large B Cell or high grade Follicular lymphoma patients with prior resolved hepatitis B undergoing RCHOP immuno-chemotherapy.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 110
Est. completion date August 2014
Est. primary completion date August 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Naive DLBCL or high grade FL patients

- Age range 18-75 years old

- ECOG performance status 0-3

- Life expectancy of more than 3 months

- Adequate organ function

- HBsAg negative/HBcAb positive at baseline

Exclusion Criteria:

- Infection of HAV,HCV,HIV

- Pregnant or lactating women

- Serious uncontrolled diseases

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Drug:
nucleoside analog reverse transcriptase inhibitor
tablets 100mg qd

Locations

Country Name City State
China Fudan University Cancer Hospital Shanghai Shanghai
China Fudan University Shanghai Cancer Center Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Fudan University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary incidence of HBV reactivation HBV reactivation is defined as- the level of HBV-DNA exceeds the upper limit of normal(ULN). from the first cycle of RCHOP (day 1) to six months after the last cycle of RCHOP Yes
Secondary the outcome of antiviral therapy in HBV-DNA abnormal patients Once the level of HBV-DNA exceeds the upper limit of normal, antiviral therapy will be given immediately.Liver function and serum HBsAg and HBcAg of these patients will be monitored until six months after the last dosing of RCHOP. from the initiation of antiviral thearpy to six months after the last cycle of RCHOP Yes
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