drugset / Trial / NCT00230503

Dose-Ranging Study of Pradefovir in Patients With Compensated Hepatitis B

NCT00230503

Phase 2 Completed 220 enrolled Bausch Health Americas, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

* Compare the safety of four oral doses of pradefovir after 48 weeks of treatment * Select the dose of pradefovir for Phase 3 studies

Timeline

Start
2004-06
Primary completion
2006-12
Completion
2006-12

Drugs

EvaluationDrugModalityDoseRoute
Subject adefovir dipivoxyl Unknown
Subject pradefovir Small molecule 30 mg Oral
Subject pradefovir Small molecule 45 mg Oral
Subject pradefovir Small molecule 60 mg Oral
Subject pradefovir Small molecule 75 mg Oral