Postmarketing Surveillance of the Safety & Effectiveness of Daclatasvir &

Clinical Trial Summary

The primary objective of this study is to describe the safety of the combination of Daklinza (daclatasvir) and Sunvepra (asunaprevir) when used for the treatment of chronic hepatitis C (CHC) genotype 1b patients in real-life conditions when used according to its registered indications.

See also
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NCT number	NCT02727933
Study type	Observational [Patient Registry]
Source	Bristol-Myers Squibb
Contact
Status	Completed
Phase
Start date	November 3, 2015
Completion date	July 5, 2020

Postmarketing Surveillance of the Safety and Effectiveness of Daclatasvir and Asunaprevir for the Treatment of Chronic HCV Genotype 1B Infection in the Routine Clinical Practice in Korea

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms