Safety and Efficacy Study of Retreated Clevudine in Chronic HBV Patients Who Received Clevudine in L-FMAU-201
NCT00362700 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 33
Last updated 2017-02-01
Summary
The purpose of this study is to determine the safety and antiviral activity of Clevudine, when retreated to patients previously treated with Clevudine
Conditions
Interventions
- DRUG
-
Clevudine
Sponsors & Collaborators
-
Bukwang Pharmaceutical
lead INDUSTRY
Principal Investigators
-
Hyo Suk Lee, M.D., Ph.D. · Seoul National University Hospital
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2003-07-31
- Completion
- 2005-10-31
Countries
- South Korea
Study Locations
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