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Last Updated: October 17, 2019

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CLINICAL TRIALS PROFILE FOR EPZICOM

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Clinical Trials for Epzicom

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00244712 Abacavir/Lamivudine Versus Emtricitabine/Tenofovir Both In Combination With Lopinavir/Ritonavir For The Treatment Of HIV Completed GlaxoSmithKline Phase 4 2005-07-01 This study was designed to test the safety and effectiveness of EPZICOM(abacavir/lamivudine) and TRUVADA (emtricitabine/tenofovir) for the treatment of HIV infection when both are used in combination with KALETRA (lopinavir/ritonavir) over 96 weeks
NCT00280969 Comparing the Effectiveness Between Ritonavir Boosted Atazanavir and Efavirenz for the First HIV Treatment Completed Ministry of Health, Labour and Welfare, Japan Phase 3 2005-09-01 A selection study in treatment naive HIV patients to compare the virologic success rate of once daily antiretroviral treatment regimens at the 48th week with Epzicom(lamivudine and abacavir) plus efavirenz and Epzicom plus ritonavir boosted atazanavir. The superior regimen will be hired to the comparative study to the current first line regimen (tenofovir plus lamivudine plus efavirenz)
NCT00280969 Comparing the Effectiveness Between Ritonavir Boosted Atazanavir and Efavirenz for the First HIV Treatment Completed International Medical Center of Japan Phase 3 2005-09-01 A selection study in treatment naive HIV patients to compare the virologic success rate of once daily antiretroviral treatment regimens at the 48th week with Epzicom(lamivudine and abacavir) plus efavirenz and Epzicom plus ritonavir boosted atazanavir. The superior regimen will be hired to the comparative study to the current first line regimen (tenofovir plus lamivudine plus efavirenz)
NCT00335270 A Randomized, Prospective Study of the Efficacy, Safety and Tolerability of Two Doses of GW433908Ritonavir Given With Abacavir/Lamivudine Fixed Dose Combination Completed GlaxoSmithKline Phase 4 2006-03-01 The purpose of this study is to evaluate the antiretroviral efficacy, safety, and tolerability of fos-amprenavir boosted with either of two doses of ritonavir (RTV) when administered in combination with ABC/3TC (abacavir/lamivudine, Epzicom®) FDC (fixed dose combination) in a once-daily regimen over 96 weeks in ART-naïve, HIV-infected adults
NCT00335270 A Randomized, Prospective Study of the Efficacy, Safety and Tolerability of Two Doses of GW433908Ritonavir Given With Abacavir/Lamivudine Fixed Dose Combination Completed Duke University Phase 4 2006-03-01 The purpose of this study is to evaluate the antiretroviral efficacy, safety, and tolerability of fos-amprenavir boosted with either of two doses of ritonavir (RTV) when administered in combination with ABC/3TC (abacavir/lamivudine, Epzicom®) FDC (fixed dose combination) in a once-daily regimen over 96 weeks in ART-naïve, HIV-infected adults
NCT00337922 Pharmacokinetic Study Of EPZICOM Tablet Completed GlaxoSmithKline Phase 4 2006-07-01 This study was designed to explore the drug levels in the blood in Japanese HIV-infected patients taking EPZICOM tablet at least for 2 weeks prior to administration of the study drug. Pharmacokinetics after administration of EPZICOM tablet will be investigated in a total of 8 subjects.
NCT00544128 Comparison of Epzicom and Truvada for the Initial Once Daily HIV Treatment Completed Ministry of Health, Labour and Welfare, Japan Phase 4 2007-10-01 A non-inferiority randomized control trial in treatment naïve HIV patients to compare virologic effect of two backbone regimens with Epzicom (lamivudine and abacavir) and Truvada (emtricitabine and tenofovir). Both arms are treated with fixed combination of ritonavir boosted atazanavir as key drugs.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Epzicom

Condition Name

Condition Name for Epzicom
Intervention Trials
HIV Infection 5
Infection, Human Immunodeficiency Virus 5
HIV Infections 4
HIV-1 Infection 2
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Condition MeSH

Condition MeSH for Epzicom
Intervention Trials
HIV Infections 15
Immunologic Deficiency Syndromes 6
Acquired Immunodeficiency Syndrome 6
Infection 2
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Clinical Trial Locations for Epzicom

Trials by Country

Trials by Country for Epzicom
Location Trials
United States 110
Canada 8
Germany 6
Italy 4
Spain 4
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Trials by US State

Trials by US State for Epzicom
Location Trials
Florida 7
Texas 7
District of Columbia 6
California 6
Arizona 6
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Clinical Trial Progress for Epzicom

Clinical Trial Phase

Clinical Trial Phase for Epzicom
Clinical Trial Phase Trials
Phase 4 10
Phase 3 6
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for Epzicom
Clinical Trial Phase Trials
Completed 15
Unknown status 3
Recruiting 1
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Clinical Trial Sponsors for Epzicom

Sponsor Name

Sponsor Name for Epzicom
Sponsor Trials
GlaxoSmithKline 9
ViiV Healthcare 5
Gilead Sciences 4
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Sponsor Type

Sponsor Type for Epzicom
Sponsor Trials
Industry 22
Other 11
NIH 3
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Serving leading biopharmaceutical companies globally:

Johnson and Johnson
Mallinckrodt
Express Scripts
Medtronic
McKesson
McKinsey

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