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Clinical Trial Summary

DCR-HBVS will be evaluated for safety and efficacy in healthy volunteers and chronic hepatitis B patients.


Clinical Trial Description

DCR HBVS is being developed for the treatment of chronic hepatitis B (CHB) in adults. The study will be conducted in 3 parts, a single ascending-dose (SAD) phase in normal healthy volunteers (Group A), a single-dose (SD) phase in patients with CHB (Group B), and a multiple ascending-dose (MAD) phase in patients with CHB (Group 1c-3c). Cohort 4c is a single ascending dose with a possible duration of up to 48 weeks. Cohort 5c is a multiple dose cohort with a possible duration of up to 72 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03772249
Study type Interventional
Source Dicerna Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 1
Start date December 28, 2018
Completion date July 12, 2022

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