drugset / Trial / NCT00270556

Phase II Comparator Study of Substitution of Tenofovir or Abacavir Receiving Thymidine Analogue as Part of HAART.

NCT00270556

Phase 2 Completed 100 enrolled Gilead Sciences

Summary

This 48 week study is designed to compare the substitution of the thymidine analogues zidovudine (ZDV) or stavudine (D4T) with either tenofovir DF or abacavir, in patients treated with highly active antiretroviral therapy (HAART), and show improved outcomes on total limb fat mass, improved body shape by dual energy x-ray absorptiometry (DEXA) and computed tomography (CT) scans and improved cholesterol and tryglicerides.

Timeline

Start
2003-01
Primary completion
Completion
2004-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Abacavir Other / unclassified
Subject Tenofovir disoproxil fumarate Small molecule