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Clinical Trial Summary

The primary objective of this post-marketing surveillance study is to collect and assess data related to the safety and effectiveness of Harvoni® (ledipasvir/sofosbuvir (LDV/SOF)) treatment regimen, per the approved Korea prescribing information for Harvoni, in routine clinical practice in Korea and to report the results to the Ministry of Food and Drug Safety (MFDS). Participants will be treated as part of routine practice at Korean healthcare centers by accredited physicians.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02951364
Study type Observational
Source Gilead Sciences
Contact
Status Completed
Phase
Start date December 5, 2016
Completion date June 11, 2021

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