Effectiveness and Safety of Direct-Acting Antiviral Agents for the Treatment of Chronic Hepatitis C

UnknownOBSERVATIONAL
Enrollment

300

Participants

Timeline

Start Date

March 6, 2019

Primary Completion Date

July 31, 2021

Study Completion Date

August 31, 2021

Conditions
Hepatitis C, Chronic
Interventions
DRUG

Direct-acting antiviral agents

The initial DAA treatment and its dose for all patients is determined by the infectionist or hepatologist based on the clinical diagnosis and treatment routine. The administration dose in the instructions for use for current DAAs marketed in China Mainland unnecessary to combine with any IFN is shown but not limited as follows: Sofosbuvir, Ombitasvir/Paritaprevir/Ritonavir, Dasabuvir, Daclatasvir, Asunaprevir, Elbasvir/Grazoprevir, Sofosbuvir/Velpatasvir and Ledipasvir/Sofosbuvir.

Trial Locations (11)

200025

RECRUITING

Rui Jin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai

200040

RECRUITING

Huashan Hospital, Shanghai

201058

RECRUITING

Shanghai Public Health Clinical Center, Shanghai

210003

RECRUITING

The Second Hospital of Nanjing, Nanjing

210008

RECRUITING

Nanjing Drum Tower Hospital, Nanjing

210029

RECRUITING

Jiangsu Province Hospital, Nanjing

213001

RECRUITING

Changzhou Third People's Hospital, Changzhou

214016

RECRUITING

Wuxi No. 5 People's Hospital, Wuxi

215007

RECRUITING

The Fifth People's Hospital of Suzhou, Suzhou

314000

RECRUITING

The First Hospital of Jiaxing, Jiaxing

315010

RECRUITING

Hwa Mei Hospital, Ningbo

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Gilead Sciences

INDUSTRY

collaborator

Tigermed Consulting Co., Ltd

INDUSTRY

lead

Qing XIe

OTHER

NCT04952207 - Effectiveness and Safety of Direct-Acting Antiviral Agents for the Treatment of Chronic Hepatitis C | Biotech Hunter | Biotech Hunter