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Clinical trial

A Phase IV Multicenter Study of the Efficacy and Safety of 48-Week Induction Treatment With TRIZIVIR (Abacavir 300 Mg/Lamivudine 150 Mg/Zidovudine 300 Mg Combination Tablet BID) With Efavirenz (600 Mg QD) Followed by 48-Week Randomized, Open-Label, Maintenance Treatment With TRIZIVIR With or Without Efavirenz in HIV-1 Infected Antiretroviral Therapy Naive Subjects

NCT00011895 is registered in ClinicalTrials.gov with GlaxoSmithKline as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase IV Multicenter Study of the Efficacy and Safety of 48-Week Induction Treatment With TRIZIVIR (Abacavir 300 Mg/Lamivudine 150 Mg/Zidovudine 300 Mg Combination Tablet BID) With Efavirenz (600 Mg QD) Followed by 48-Week Randomized, Open-Label, Maintenance Treatment With TRIZIVIR With or Without Efavirenz in HIV-1 Infected Antiretroviral Therapy Naive Subjects
Lead sponsor
GlaxoSmithKline
Phase
Phase 4
Overall status
Unknown status
Start date
February 28, 2001
Completion date
Not reported
Enrollment
400
Sites
42

Conditions

As the registry lists them; a condition with its own page is linked.