MedPath

Study to Evaluate Switching From a TDF-Containing Combination Regimen to a TAF-Containing Fixed Dose Combination (FDC) in Virologically-Suppressed, HIV-1 Positive Participants

Phase 3
Completed
Conditions
HIV
HIV Infections
Interventions
Drug: EFV/FTC/TDF
Drug: ATV
Drug: FTC/TDF
Registration Number
NCT01815736
Lead Sponsor
Gilead Sciences
Brief Summary

The primary objective of this study is to evaluate the non-inferiority of switching to a tenofovir alafenamide (TAF)-containing fixed dose combination (FDC) relative to maintaining tenofovir disoproxil fumarate (TDF)-containing combination regimens in virologically suppressed HIV-infected participants as determined by having HIV-1 RNA \< 50 copies/mL at Week 48.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1443
Inclusion Criteria
  • Ability to understand and sign a written informed consent form, which must be obtained prior to initiation of study procedures
  • Currently receiving antiretroviral therapy consisting of E/C/F/TDF, EFV/FTC/TDF, RTV+ATV+FTC/TDF, or COBI+ATV+FTC/TDF for ≥ 6 consecutive months preceding the final visit in their earlier study
  • Completion of the Week 144 visit in studies GS-US-236-0102, GS-US-236-0103, GS-US-216-0114, or completion of the Week 96 visit in study GS-US-264-0110 (only participants on an EFV-based regimen), or completion of studies GS-US-236-0104, GS-US-216-0105
  • Plasma human immunodeficiency virus type 1-ribonucleic acid (HIV-1 RNA) concentrations at undetectable levels for at least 6 consecutive months prior to the screening visit and have HIV RNA < 50 copies/mL at the screening visit
  • Normal echocardiograph (ECG)
  • Estimated glomerular filtration rate (GFR) ≥ 50 mL/min according to the Cockcroft-Gault formula for creatinine clearance
  • Hepatic transaminases (aspartate aminotransferase [AST] and alanine aminotransferase [ALT]) ≤ 5 × upper limit of the normal range (ULN)
  • Direct bilirubin ≤ 1.5 x ULN
  • Adequate hematologic function
  • Serum amylase ≤ 5 × ULN
  • Females of childbearing potential must agree to utilize highly effective contraception methods or be non-heterosexually active or practice sexual abstinence from screening throughout the duration of study treatment and for 12 weeks following the last dose of study drug if receiving EFV/FTC/TDF regimen, and 30 days for those assigned to all other regimens.
  • Female participants who utilize hormonal contraceptive as one of their birth control methods must have used the same method for at least three months prior to study dosing
  • Female participants who have stopped menstruating for ≥ 12 months but do not have documentation of ovarian hormonal failure must have a serum follicle stimulating hormone (FSH) level at screening within the post-menopausal range based on the Central Laboratory reference range

Key

Exclusion Criteria
  • A new acquired immunodeficiency syndrome (AIDS)-defining condition diagnosed within the 30 days prior to screening
  • Hepatitis B surface antigen position
  • Hepatitis C antibody positive
  • Participants experiencing decompensated cirrhosis
  • Females who are breastfeeding
  • Positive serum pregnancy test
  • Have an implanted defibrillator or pacemaker
  • Current alcohol or substance use judged by the Investigator to potentially interfere with subject study compliance
  • History of malignancy within the past 5 years or ongoing malignancy other than cutaneous Kaposi's sarcoma, basal cell carcinoma, or resected, noninvasive cutaneous squamous carcinoma
  • Active, serious infections (other than HIV-1 infection) requiring parenteral antibiotic or antifungal therapy within 30 days prior to baseline
  • Any other clinical condition or prior therapy that, in the opinion of the Investigator, would make the subject unsuitable for the study or unable to comply with dosing requirements
  • Participation in any other clinical trial without prior approval from the sponsor is prohibited while participating in this trial
  • Participants receiving ongoing therapy with drugs not to be used with elvitegravir (EVG), COBI, FTC, TDF, ATV, RTV, EFV, and TAF or participants with any known allergies to the excipients of E/C/F/TDF, E/C/F/TAF, EFV/FTC/TDF, ATV, COBI, RTV, or FTC/TDF

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Stay on Baseline Treatment Regimen (SBR)E/C/F/TDFRandomized Phase: Participants stayed on their baseline emtricitabine (FTC)/tenofovir disoproxil fumarate (TDF)-containing regimen E/C/F/TDF; efavirenz (EFV)/FTC/TDF; ritonavir (RTV)-boosted atazanavir (ATV)+FTC/TDF; or cobicistat (COBI-boosted ATV+FTC/TDF) administered according to prescribing information for up to 96 weeks. Extension Phase: After completing 96 weeks of randomized treatment (SBR), all participants will be given the opportunity to receive open-label E/C/F/TAF until it becomes commercially available, or until Gilead elects to terminate the development of E/C/F/TAF.
Stay on Baseline Treatment Regimen (SBR)FTC/TDFRandomized Phase: Participants stayed on their baseline emtricitabine (FTC)/tenofovir disoproxil fumarate (TDF)-containing regimen E/C/F/TDF; efavirenz (EFV)/FTC/TDF; ritonavir (RTV)-boosted atazanavir (ATV)+FTC/TDF; or cobicistat (COBI-boosted ATV+FTC/TDF) administered according to prescribing information for up to 96 weeks. Extension Phase: After completing 96 weeks of randomized treatment (SBR), all participants will be given the opportunity to receive open-label E/C/F/TAF until it becomes commercially available, or until Gilead elects to terminate the development of E/C/F/TAF.
Stay on Baseline Treatment Regimen (SBR)ATVRandomized Phase: Participants stayed on their baseline emtricitabine (FTC)/tenofovir disoproxil fumarate (TDF)-containing regimen E/C/F/TDF; efavirenz (EFV)/FTC/TDF; ritonavir (RTV)-boosted atazanavir (ATV)+FTC/TDF; or cobicistat (COBI-boosted ATV+FTC/TDF) administered according to prescribing information for up to 96 weeks. Extension Phase: After completing 96 weeks of randomized treatment (SBR), all participants will be given the opportunity to receive open-label E/C/F/TAF until it becomes commercially available, or until Gilead elects to terminate the development of E/C/F/TAF.
Stay on Baseline Treatment Regimen (SBR)EFV/FTC/TDFRandomized Phase: Participants stayed on their baseline emtricitabine (FTC)/tenofovir disoproxil fumarate (TDF)-containing regimen E/C/F/TDF; efavirenz (EFV)/FTC/TDF; ritonavir (RTV)-boosted atazanavir (ATV)+FTC/TDF; or cobicistat (COBI-boosted ATV+FTC/TDF) administered according to prescribing information for up to 96 weeks. Extension Phase: After completing 96 weeks of randomized treatment (SBR), all participants will be given the opportunity to receive open-label E/C/F/TAF until it becomes commercially available, or until Gilead elects to terminate the development of E/C/F/TAF.
E/C/F/TAFE/C/F/TAFRandomized Phase: Elvitegravir/cobicistat/emtricitabine/tenofovir alafenamide (E/C/F/TAF) for up to 96 weeks. Extension Phase: After completing 96 weeks of randomized treatment, all participants will be given the opportunity to receive open-label E/C/F/TAF until it becomes commercially available, or until Gilead elects to terminate the development of E/C/F/TAF.
Stay on Baseline Treatment Regimen (SBR)COBIRandomized Phase: Participants stayed on their baseline emtricitabine (FTC)/tenofovir disoproxil fumarate (TDF)-containing regimen E/C/F/TDF; efavirenz (EFV)/FTC/TDF; ritonavir (RTV)-boosted atazanavir (ATV)+FTC/TDF; or cobicistat (COBI-boosted ATV+FTC/TDF) administered according to prescribing information for up to 96 weeks. Extension Phase: After completing 96 weeks of randomized treatment (SBR), all participants will be given the opportunity to receive open-label E/C/F/TAF until it becomes commercially available, or until Gilead elects to terminate the development of E/C/F/TAF.
Stay on Baseline Treatment Regimen (SBR)RTVRandomized Phase: Participants stayed on their baseline emtricitabine (FTC)/tenofovir disoproxil fumarate (TDF)-containing regimen E/C/F/TDF; efavirenz (EFV)/FTC/TDF; ritonavir (RTV)-boosted atazanavir (ATV)+FTC/TDF; or cobicistat (COBI-boosted ATV+FTC/TDF) administered according to prescribing information for up to 96 weeks. Extension Phase: After completing 96 weeks of randomized treatment (SBR), all participants will be given the opportunity to receive open-label E/C/F/TAF until it becomes commercially available, or until Gilead elects to terminate the development of E/C/F/TAF.
Primary Outcome Measures
NameTimeMethod
Percentage of Participants With HIV-1 RNA < 50 Copies/mL at Week 48Week 48

The percentage of participants achieving HIV-1 RNA \< 50 copies/mL at Week 48 was analyzed using the snapshot algorithm, which defines a patient's virologic response status using only the viral load at the predefined time point within an allowed window of time, along with study drug discontinuation status.

Secondary Outcome Measures
NameTimeMethod
Percent Change From Baseline in Spine BMD at Week 48Baseline; Week 48

Spine BMD was assessed by DXA scan. BMD is calculated as g/cm\^2; the mean (SD) percentage change is presented.

Change From Baseline in Serum Creatinine at Week 48Baseline; Week 48
Percentage of Participants With HIV-1 RNA < 20 Copies/mL at Week 48Week 48

The percentage of participants achieving HIV-1 RNA \< 20 copies/mL at Week 48 was analyzed using the snapshot algorithm, which defines a patient's virologic response status using only the viral load at the predefined time point within an allowed window of time, along with study drug discontinuation status.

Change From Baseline in CD4 Cell Count at Weeks 96Baseline; Week 96

The analysis of CD4 cell count included values up to 1 day after the last dose date of randomized study drug.The change from baseline in CD4 cell count for the full analysis set was based on observed data (ie, Missing = Excluded) for the total and by the prior treatment regimen.

Percentage of Participants With HIV-1 RNA < 50 Copies/mL at Week 96Week 96

The percentage of participants achieving HIV-1 RNA \< 50 copies/mL at Week 96 was analyzed using the snapshot algorithm, which defines a patient's virologic response status using only the viral load at the predefined time point within an allowed window of time, along with study drug discontinuation status.

Change From Baseline in the Overall EFV-related Symptom Assessment Score at Week 48Baseline; Week 48

The mean (SD) change of the overall EFV-related symptom assessment score is presented. The overall symptom score (ranging from 0 to 20) is the sum of the individual symptom scores ranging from 0 (no symptoms) to 4 (most severe symptoms) from the 5 EFV-related symptom assessments (dizziness, trouble sleeping, impaired concentration, sleepiness, and abnormal or vivid dream). A negative change from baseline indicates improvement.

EFV-Related Symptom Analysis Set: participants who received EFV/FTC/TDF as prior treatment, received at least 1 dose of study drug, and completed EFV-related symptom assessments at the baseline visit and at least 1 postbaseline visit.

Change From Baseline in Cluster Determinant 4 (CD4) Cell Count at Week 48Baseline; Week 48

The analysis of CD4 cell count included values up to 1 day after the last dose date of randomized study drug.The change from baseline in CD4 cell count for the full analysis set was based on observed data (ie, Missing = Excluded) for the total and by the prior treatment regimen.

Percent Change From Baseline in Hip Bone Mineral Density (BMD) at Week 48Baseline; Week 48

Hip BMD was assessed by dual energy x-ray absorptiometry (DXA) scan. BMD is calculated as grams per square centimeter (g/cm\^2); the mean (SD) percentage change is presented.

Percentage of Participants With HIV-1 RNA < 20 Copies/mL at Week 96Week 96

The percentage of participants achieving HIV-1 RNA \< 20 copies/mL at Week 96 was analyzed using the snapshot algorithm, which defines a patient's virologic response status using only the viral load at the predefined time point within an allowed window of time, along with study drug discontinuation status.

Trial Locations

Locations (167)

University of Pennsylvania

🇺🇸

Philadelphia, Pennsylvania, United States

Southwest Infectious Disease Clinical Research, Inc.

🇺🇸

Dallas, Texas, United States

Sunnybrook Health Sciences Centre

🇨🇦

Toronto, Ontario, Canada

Jeffrey Goodman Special Care Clinic

🇺🇸

Los Angeles, California, United States

Anthony Mills MD Inc

🇺🇸

Los Angeles, California, United States

Living Hope Clinical Foundation

🇺🇸

Long Beach, California, United States

AHF Research Center

🇺🇸

Beverly Hills, California, United States

Wohlfeiler, Piperato and Associates, LLC

🇺🇸

Miami Beach, Florida, United States

Therafirst Medical Center

🇺🇸

Fort Lauderdale, Florida, United States

Alameda County Medical Center

🇺🇸

Oakland, California, United States

Midway Immunology and Research Center

🇺🇸

Fort Pierce, Florida, United States

Chelsea Village Medical, PC

🇺🇸

New York, New York, United States

Orange Coast Medical Group

🇺🇸

Newport Beach, California, United States

NorthStar Medical Center

🇺🇸

Chicago, Illinois, United States

Be Well Medical Center

🇺🇸

Berkley, Michigan, United States

Broward Health/Comprehensive Care Center

🇺🇸

Fort Lauderdale, Florida, United States

Gary J. Richmond,M.D.,P.A.

🇺🇸

Fort Lauderdale, Florida, United States

Rosedale Infectious Diseases

🇺🇸

Huntersville, North Carolina, United States

Tarrant County Infectious Disease Associates

🇺🇸

Fort Worth, Texas, United States

New York Hospital Queens

🇺🇸

Flushing, New York, United States

Ottawa Hospital

🇨🇦

Ottawa, Ontario, Canada

Baystate Infectious Diseases Clinical Research

🇺🇸

Springfield, Massachusetts, United States

Saint Michaels Medical Center

🇺🇸

Newark, New Jersey, United States

Summa Health System

🇺🇸

Akron, Ohio, United States

Palmetto Health Richland

🇺🇸

Columbia, South Carolina, United States

AIDS Arms, Inc./ Peabody Health Center

🇺🇸

Dallas, Texas, United States

Carolinas Medical Center-Myers Park

🇺🇸

Charlotte, North Carolina, United States

The Research Institute

🇺🇸

Springfield, Massachusetts, United States

Upstate ID Association

🇺🇸

Albany, New York, United States

Howard Brown Health Center

🇺🇸

Chicago, Illinois, United States

Montefiore Medical Center - AIDS Center

🇺🇸

Bronx, New York, United States

University of NC AIDS Clinical Trials Unit

🇺🇸

Chapel Hill, North Carolina, United States

Beth Israel Medical Center- Division of Infectious Diseases

🇺🇸

New York, New York, United States

Ricky K. Hsu, MD

🇺🇸

New York, New York, United States

ID Care

🇺🇸

Hillsborough, New Jersey, United States

SouthWest CARE Center

🇺🇸

Santa Fe, New Mexico, United States

East Carolina University

🇺🇸

Greenville, North Carolina, United States

East Sydney Doctors

🇦🇺

Darlinghurst, New South Wales, Australia

CHU Saint-Pierre University Hospital

🇧🇪

Brussels, Belgium

Community Research Initiative of New England

🇺🇸

Boston, Massachusetts, United States

Therapeutic Concepts, P.A.

🇺🇸

Houston, Texas, United States

Research Access Network

🇺🇸

Houston, Texas, United States

Peter Shalit, M.D.

🇺🇸

Seattle, Washington, United States

La Playa Medical Group and Clinical Research

🇺🇸

San Diego, California, United States

The Kinder Medical Group

🇺🇸

Miami, Florida, United States

Hennepin County Medical Center

🇺🇸

Minneapolis, Minnesota, United States

Duke University Health System

🇺🇸

Durham, North Carolina, United States

Kaiser Permanente Medical Center, Clinical Trials Unit

🇺🇸

San Francisco, California, United States

Gordon E. Crofoot MD PA

🇺🇸

Houston, Texas, United States

Winnipeg Regional Health Authority - Health Sciences Centre Winnipeg

🇨🇦

Winnipeg, Manitoba, Canada

Albany Medical College

🇺🇸

Albany, New York, United States

Michael Keith Wensley, MD, Inc., A Medical Corporation

🇺🇸

Costa Mesa, California, United States

Kaiser Permanente

🇺🇸

Los Angeles, California, United States

Peter J Ruane, MD, Inc

🇺🇸

Los Angeles, California, United States

Stanford University

🇺🇸

Palo Alto, California, United States

Metropolis Medical Group

🇺🇸

San Francisco, California, United States

Kaiser Permanente Hospital

🇺🇸

San Leandro, California, United States

Whitman Walker Clinic

🇺🇸

Washington, District of Columbia, United States

AIDS Research Consortium of Atlanta

🇺🇸

Atlanta, Georgia, United States

Infectious Disease Specialists of Atlanta

🇺🇸

Decatur, Georgia, United States

Atlanta ID Group, PC

🇺🇸

Atlanta, Georgia, United States

Ruth M. Rothstein CORE Center

🇺🇸

Chicago, Illinois, United States

Mercer University School of Medicine

🇺🇸

Macon, Georgia, United States

University of Hawaii - Hawaii Center for AIDS

🇺🇸

Honolulu, Hawaii, United States

Southampton Healthcare

🇺🇸

Saint Louis, Missouri, United States

Saint Louis University

🇺🇸

Saint Louis, Missouri, United States

South Jersey Infectious Disease

🇺🇸

Somers Point, New Jersey, United States

North Shore University Hospital, Divison of Infectious Diseases

🇺🇸

Manhasset, New York, United States

Garcia's Family Health Group

🇺🇸

Harlingen, Texas, United States

DCOL Center for Clinical Research

🇺🇸

Longview, Texas, United States

Premier Clinical Research

🇺🇸

Spokane, Washington, United States

Clinical Alliance for Research & Education, Infectious Diseases (CARE-ID)

🇺🇸

Annandale, Virginia, United States

Holdsworth House Medical practice

🇦🇺

Darlinghurst, New South Wales, Australia

St Vincent's Hospital, Sydney

🇦🇺

Darlinghurst, New South Wales, Australia

Taylor Square Private Clinic

🇦🇺

Darlinghurst, New South Wales, Australia

Albion Street Centre

🇦🇺

Surry Hills, New South Wales, Australia

SMZ Baumgartner Hoehe - Otto-Wagner-Spital

🇦🇹

Vienna, Austria

São Paulo Secretaria da Saúde - Instituto De Infectologia Emilio Ribas

🇧🇷

Sao Paulo, Brazil

Faculdade de Medicina do ABC

🇧🇷

Santo Andre, Brazil

Instituto De Pesquisa Clinica Evandro Chagas - Fundação Oswaldo Cruz

🇧🇷

Rio de Janeiro, Brazil

São Paulo Secretaria da Saúde - Centro de Referência e Treinamento em DST/AIDS

🇧🇷

Sao Paulo, Brazil

Maple Leaf Research

🇨🇦

Toronto, Ontario, Canada

McGill University Health Centre (MUHC) - Montral Chest Institute

🇨🇦

Montréal, Quebec, Canada

Hôpital de La Croix Rousse

🇫🇷

Lyon, France

CHU Hotel Dieu

🇫🇷

Nantes, France

Archet 1 CHU de Nice - 6ème Niveau

🇫🇷

Nice, France

Hôpital Saint Louis

🇫🇷

Paris, France

Hopital Saint Antoine

🇫🇷

Paris, France

Center for HIV and Hepatogastroenterology

🇩🇪

Duesseldorf, Germany

Centre Hospitalier de Tourcoing

🇫🇷

Tourcoing, France

EPIMED GmbH

🇩🇪

Berlin, Germany

Universitätsklinikum Frankfurt

🇩🇪

Frankfurt am Main, Germany

University of Bonn

🇩🇪

Bonn, Germany

Infektio Research GmbH / Infektiologikum Frankfurt

🇩🇪

Frankfurt am Main, Germany

University Medical Center Hamburg-Eppendorf, Infectious Diseases Unit

🇩🇪

Hamburg, Germany

Universitatsklinikum Freiburg

🇩🇪

Freiburg, Germany

ICH Study Center Hamburg

🇩🇪

Hamburg, Germany

University of Cologne, Department of Internal Medicine

🇩🇪

Köln, Germany

MUC Research GmbH

🇩🇪

München, Germany

Azienda Ospedaliera Luigi Sacco 1° Divisione Malattie Infettive

🇮🇹

Milano, Italy

Fondazione Centro San Raffaele del Monte Tabor

🇮🇹

Milan, Italy

Istituto Nazionale Malattie Infettive "Lazzaro Spallanzani" IRCCS

🇮🇹

Rome, Italy

Comprensorio Amedeo Di Savoia Birago Di Vische

🇮🇹

Torino, Italy

VA Caribbean Healthcare System

🇵🇷

San Juan, Puerto Rico

Hospital Virgen del Rocio

🇪🇸

Sevilla, Spain

Hospital Universitari De Bellvitge

🇪🇸

Barcelona, Spain

Hospital Universitario La Paz

🇪🇸

Madrid, Spain

Centre Hospitalier Universitaire Vaudois

🇨🇭

Lausanne, Switzerland

Brighton and Sussex University Hospitals NHS Trust

🇬🇧

Brighton, United Kingdom

Chelsea and Westminster Hospital Foundation Trust

🇬🇧

London, United Kingdom

Barts and the London NHS Trust

🇬🇧

London, United Kingdom

Courtyard Clinic, St. Georges Hospital

🇬🇧

London, United Kingdom

North Manchester General Hospital

🇬🇧

Manchester, United Kingdom

Epidemiklinikken 5112, Rigshospitalet

🇩🇰

Copenhagen, Denmark

Södersjukhuset

🇸🇪

Stockholm, Sweden

Capital Medical Associates, PC

🇺🇸

Washington, District of Columbia, United States

Greenwich Hospital

🇺🇸

Greenwich, Connecticut, United States

Hospital de Santa Maria

🇵🇹

Lisbon, Portugal

Health for Life Clinic PLLC

🇺🇸

Little Rock, Arkansas, United States

Dupont Circle Physicians Group

🇺🇸

Washington, District of Columbia, United States

Medizinische Universitat Wien

🇦🇹

Vienna, Austria

Antiguo Hospital Civil de Guadalajara "Fray Antonio Alcalde"

🇲🇽

Guadalajara, Mexico

Erasmus MC

🇳🇱

Rotterdam, Netherlands

Servico De Doencas Infecciosas - Hospital De Sao Joao

🇵🇹

Porto, Portugal

HOPE Clinical Research

🇵🇷

San Juan, Puerto Rico

Maharaj Nakorn Chiang Mai University, Faculty of Medicine, Department of Medicine

🇹🇭

Chiang Mai, Thailand

Jacobi Medical Center

🇺🇸

Bronx, New York, United States

Melbourne Sexual Health Clinic

🇦🇺

Carlton, Victoria, Australia

George Washington University Medical Faculty Associates

🇺🇸

Washington, District of Columbia, United States

Hôpital Universitaire Erasme - ULB

🇧🇪

Ghent, Belgium

Ubc Downtown I.D. Clinic

🇨🇦

Vancouver, British Columbia, Canada

Universitätsklinik für Infektiologie, Universitätsspital Bern

🇨🇭

Bern, Switzerland

Medizinische Universität Graz

🇦🇹

Graz, Austria

Clinique medicale l'Actuel

🇨🇦

Montreal, Quebec, Canada

Alfred Hospital

🇦🇺

Melbourne, Victoria, Australia

Northside Clinic

🇦🇺

Melbourne, Victoria, Australia

Clinique Medicale du Quartier Latin

🇨🇦

Montreal, Quebec, Canada

Clinique OPUS

🇨🇦

Montreal, Quebec, Canada

Prahran Market Clinic

🇦🇺

South Yarra, Victoria, Australia

Instituto Dominicano de Estudios Virologicos - IDEV

🇩🇴

Santo Domingo, Dominican Republic

Clinical Research Puerto Rico

🇵🇷

San Juan, Puerto Rico

HIV-NAT, Thai Red Cross AIDS Research Center and Faculty of Medicine Chulalongkorn University

🇹🇭

Bangkok, Thailand

Onze Lieve Vrouwe Gasthuis, Afdeling Infectieziekten

🇳🇱

Amsterdam, Netherlands

University Hospital of Zurich

🇨🇭

Zürich, Switzerland

Ramathibodi Hospital, Mahidol University

🇹🇭

Bangkok, Thailand

Siriraj HospitalDepartment of Preventive and Social Medicine, Faculty of Medicine

🇹🇭

Bangkok, Thailand

Khon Kaen University

🇹🇭

Khon Kaen, Thailand

University of Alabama at Birmingham

🇺🇸

Birmingham, Alabama, United States

Southwest Center for HIV/AIDS

🇺🇸

Phoenix, Arizona, United States

Spectrum Medical Group

🇺🇸

Phoenix, Arizona, United States

Apex Research LLC

🇺🇸

Denver, Colorado, United States

Henry Ford Health System

🇺🇸

Detroit, Michigan, United States

Medical College of Wisconsin

🇺🇸

Milwaukee, Wisconsin, United States

University Health Network, Toronto General Hospital

🇨🇦

Toronto, Ontario, Canada

University of South Florida HIV Clinical Research Unit / Hillsborough County Health Department

🇺🇸

Tampa, Florida, United States

Infectious Disease Research Institute Inc.

🇺🇸

Tampa, Florida, United States

St. Joseph's Comprehensive Research Institute

🇺🇸

Tampa, Florida, United States

East Bay AIDS Center

🇺🇸

Oakland, California, United States

Greiger Clinic

🇺🇸

Mount Vernon, New York, United States

Central West Clinical Research

🇺🇸

Saint Louis, Missouri, United States

University of California, Davis Medical Center

🇺🇸

Sacramento, California, United States

Kaiser Permanente Medical Group

🇺🇸

Sacramento, California, United States

Yale University HIV Clinical Trials Program

🇺🇸

New Haven, Connecticut, United States

Orlando Immunology Center

🇺🇸

Orlando, Florida, United States

IDOCF/ Value Health MD, LLC

🇺🇸

Orlando, Florida, United States

Bichat Hospital

🇫🇷

Paris, France

Thomas Jefferson University

🇺🇸

Philadelphia, Pennsylvania, United States

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