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Last Updated: May 17, 2022

CLINICAL TRIALS PROFILE FOR EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE


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505(b)(2) Clinical Trials for Emtricitabine And Tenofovir Disoproxil Fumarate

This table shows clinical trials for potential 505(b)(2) applications. See the next table for all clinical trials
Trial Type Trial ID Title Status Sponsor Phase Start Date Summary
New Combination NCT00641641 ↗ The Effect of Raltegravir on HIV Decay During Primary and Chronic Infection Completed Merck Sharp & Dohme Corp. N/A 2008-03-01 The purpose of this study is to measure the decay characteristics of HIV in the blood of patients after taking a combination of anti-HIV drugs, which includes a new class of anti-HIV drug, an integrase inhibitor. This study explores how this new combination of therapy reduces virus in various compartments of the body and immune system.
New Combination NCT00641641 ↗ The Effect of Raltegravir on HIV Decay During Primary and Chronic Infection Completed Kirby Institute N/A 2008-03-01 The purpose of this study is to measure the decay characteristics of HIV in the blood of patients after taking a combination of anti-HIV drugs, which includes a new class of anti-HIV drug, an integrase inhibitor. This study explores how this new combination of therapy reduces virus in various compartments of the body and immune system.
New Formulation NCT02583464 ↗ Bioequivalence Study of Two Formulations With the Association of Tenofovir 300 mg and Emtricitabine 200 mg. Completed Laboratorio Elea Phoenix S.A. Phase 1 2014-09-01 Objective: To evaluate the relative bioavailability of a new formulation containing a combination of emtricitabine 200 mg and tenofovir disoproxil fumarate 300 mg (T) and compare this formulation with the branded formulation (R) to meet regulatory criteria for marketing the test product in Argentina.
>Trial Type >Trial ID >Title >Status >Phase >Start Date >Summary

All Clinical Trials for Emtricitabine And Tenofovir Disoproxil Fumarate

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00039741 ↗ Anti-HIV Drug Regimens and Treatment-Switching Guidelines in HIV Infected Children Completed Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) Phase 2/Phase 3 2002-08-01 Little is known about what treatment combinations are best for HIV infected children. This study examined the long-term effectiveness of different anti-HIV drug combinations in children and strategies for switching treatment if the first treatment does not work. The study enrolled children who had not previously taken anti-HIV medication. Participants in this study were recruited in the United States, South America and Europe. Some European children may also enroll in a substudy that will observe changes in body fat in children taking anti-HIV medications.
NCT00039741 ↗ Anti-HIV Drug Regimens and Treatment-Switching Guidelines in HIV Infected Children Completed PENTA Foundation Phase 2/Phase 3 2002-08-01 Little is known about what treatment combinations are best for HIV infected children. This study examined the long-term effectiveness of different anti-HIV drug combinations in children and strategies for switching treatment if the first treatment does not work. The study enrolled children who had not previously taken anti-HIV medication. Participants in this study were recruited in the United States, South America and Europe. Some European children may also enroll in a substudy that will observe changes in body fat in children taking anti-HIV medications.
NCT00039741 ↗ Anti-HIV Drug Regimens and Treatment-Switching Guidelines in HIV Infected Children Completed National Institute of Allergy and Infectious Diseases (NIAID) Phase 2/Phase 3 2002-08-01 Little is known about what treatment combinations are best for HIV infected children. This study examined the long-term effectiveness of different anti-HIV drug combinations in children and strategies for switching treatment if the first treatment does not work. The study enrolled children who had not previously taken anti-HIV medication. Participants in this study were recruited in the United States, South America and Europe. Some European children may also enroll in a substudy that will observe changes in body fat in children taking anti-HIV medications.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Emtricitabine And Tenofovir Disoproxil Fumarate

Condition Name

Condition Name for Emtricitabine And Tenofovir Disoproxil Fumarate
Intervention Trials
HIV Infections 64
Hiv 24
HIV-1 Infection 18
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Condition MeSH

Condition MeSH for Emtricitabine And Tenofovir Disoproxil Fumarate
Intervention Trials
HIV Infections 97
Acquired Immunodeficiency Syndrome 39
Infections 25
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Clinical Trial Locations for Emtricitabine And Tenofovir Disoproxil Fumarate

Trials by Country

Trials by Country for Emtricitabine And Tenofovir Disoproxil Fumarate
Location Trials
United States 904
Canada 86
Spain 52
United Kingdom 47
Germany 44
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Trials by US State

Trials by US State for Emtricitabine And Tenofovir Disoproxil Fumarate
Location Trials
California 65
New York 51
Florida 51
Texas 47
North Carolina 47
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Clinical Trial Progress for Emtricitabine And Tenofovir Disoproxil Fumarate

Clinical Trial Phase

Clinical Trial Phase for Emtricitabine And Tenofovir Disoproxil Fumarate
Clinical Trial Phase Trials
Phase 4 39
Phase 3 54
Phase 2/Phase 3 7
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Clinical Trial Status

Clinical Trial Status for Emtricitabine And Tenofovir Disoproxil Fumarate
Clinical Trial Phase Trials
Completed 129
Active, not recruiting 12
Recruiting 9
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Clinical Trial Sponsors for Emtricitabine And Tenofovir Disoproxil Fumarate

Sponsor Name

Sponsor Name for Emtricitabine And Tenofovir Disoproxil Fumarate
Sponsor Trials
Gilead Sciences 66
National Institute of Allergy and Infectious Diseases (NIAID) 43
AIDS Clinical Trials Group 12
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Sponsor Type

Sponsor Type for Emtricitabine And Tenofovir Disoproxil Fumarate
Sponsor Trials
Other 152
Industry 114
NIH 55
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