Clinical trial
Safety and Antiviral Activity Study of Clevudine 30 mg QD in Patients With…
NCT00313274 · Bukwang Pharmaceutical, Industry · Terminated
Key facts
| NCT number | NCT00313274 |
|---|---|
| Title | Safety and Antiviral Activity Study of Clevudine 30 mg QD in Patients With HBeAg(-) Chronic HBV |
| Official title | A Double-Blind, Randomized, Parallel, Placebo-Controlled Phase III Study to Evaluate the Safety and Antiviral Activity of Clevudine (L-FMAU) 30 mg QD in Patients With HBeAg Negative Chronic Hepatitis B |
| Lead sponsor | Bukwang Pharmaceutical, Industry |
| Status | Terminated |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Hepatitis B |
| Intervention type | Drug |
| Interventions | Clevudine |
| Enrollment | 80 |
| Start date | Jul 1, 2003 |
| Completion | Dec 1, 2004 |
| First posted | Apr 12, 2006 |
| Last update posted | Feb 1, 2017 |
| Countries | South Korea |
At a glance
- 10–99 Study sites
- No Results posted
- 1–9 Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: