Clinical trial

Study Comparing Tenofovir Disoproxil Fumarate (TDF), Emtricitabine (FTC)/TDF…

NCT00298363 · Gilead Sciences, Industry · Completed

Key facts

NCT number NCT00298363
Title Study Comparing Tenofovir Disoproxil Fumarate (TDF), Emtricitabine (FTC)/TDF, and Entecavir (ETV) in the Treatment of Chronic HBV in Subjects With Decompensated Liver Disease.
Official title A Phase 2, Double-Blind, Multi-center, Randomized Study Comparing Tenofovir Disoproxil Fumarate, Emtricitabine Plus Tenofovir Disoproxil Fumarate, and Entecavir in the Treatment of Chronic Hepatitis B Subjects With Decompensated Liver Disease and in the Prevention of Hepatitis B Recurrence…
Lead sponsor Gilead Sciences, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Chronic Hepatitis B
Intervention type Drug
Interventions Tenofovir disoproxil fumarate (tenofovir DF, TDF), Emtricitabine/tenofovir disoproxil fumarate (FTC/TDF), Entecavir (ETV), TDF placebo, FTC/TDF placebo, ETV placebo
Enrollment 112
Start date Apr 1, 2006
Primary completion Apr 1, 2011
Completion Apr 1, 2011
First posted Mar 2, 2006
Last update posted Apr 25, 2013
Countries Canada, France, Germany, Greece, Italy, Poland, Singapore, Spain, Taiwan, Turkey (Türkiye), United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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