Viewing Study NCT03253250


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Study NCT ID: NCT03253250
Status: UNKNOWN
Last Update Posted: 2017-09-08
First Post: 2017-08-15
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: The Investigation of Peginterferon Alfa-2a on the RFS of the Subjects With HCC Who Have Been Treated by Resection
Sponsor: Huashan Hospital
Organization:

Study Overview

Official Title: A Prospective, Randomized, Multicenter, Open-label, Exploratory Study of Utilizing of Peginterferon Alfa-2a on the Relapse Rate of the Subjects With Hepatocellular Carcinoma Who Have Been Treated by Resection
Status: UNKNOWN
Status Verified Date: 2017-09
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The current study is a prospective, randomized, open, multi-center investigation. The aim of current study is to investigate whether the Recurrence-free Survival Rate (RFS)of the hepatitis B related -hepatocellular carcinoma subjects who have been treated by resection can be improved by peginterferon alfa-2a
Detailed Description: The subjects who have been treated by resection due to hepatocellular carcinoma (HCC) will be randomized into 2 groups: the subjects in group A will be treated by Nucleotide analogues (NAs)( ETV, 0.5mg,qd;tenofovir disoproxil fumarate(TDF),300mg,qd;ADV,10mg,qd)for 96 weeks; the subjects in group B will be treated by peginterferon alfa-2a (135μg/week)combination with NAs (ETV\\TDF\\ADV)for 96 weeks.

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: