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Clinical Trial Summary

This study is intended to evaluate if 12 or 24 weeks of treatment with GSK3228836 followed by up to 24 weeks of pegylated interferon (PegIFN) can increase the rate of hepatitis B virus surface antigen (HBsAg) loss in participants on stable nucleos(t)ide analogue (NA) therapy, and whether virologic response can be sustained once PegIFN treatment is discontinued. Participants will be randomized to receive GSK3228836 for 12 or 24 weeks followed by up to 24 weeks of PegIFN.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04676724
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 2
Start date January 28, 2021
Completion date February 17, 2023

See also
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