drugset / Trial / NCT00936715

Rollover Protocol Continued Access to Emtricitabine/Tenofovir Disoproxil Fumarate for Adults in United States

NCT00936715

Phase 2 Completed 24 enrolled Gilead Sciences
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to provide open label emtricitabine/tenofovir disoproxil fumarate (FTC/TDF) for an additional 5 years (240 weeks) to adults completing study GS-US-203-0107.

Timeline

Start
2009-08
Primary completion
2015-11
Completion
2015-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Tenofovir disoproxil fumarate Small molecule 300 mg Oral
Subject emtricitabine Other / unclassified 200 mg Oral