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