Human Immunodeficiency Virus 
Welcome,         Profile    Billing    Logout  

2679 Trials

   

Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
Human Immunodeficiency Virus
ACTRN12605000661673: Seronegatives And Metabolic Abnormalities Protocol 2 (SAMA 002)

Recruiting
4
50
 
The University of New South Wales, National Heart Lung and Blood Institute, US National Institutes of Health
HIV , Lipid metabolism, Glucose metabolism, Metabolic abnormality, Lipodystrophy, Cardiovascular disease
 
 
ACTRN12612000732886: Rosuvastatin versus Protease Inhibitor Switching for Hypercholesterolaemia in HIV-infected Adults.

Recruiting
4
60
 
St. Vincent's Hospital, Sydney
Hypercholesterolaemia associated with ritonavir-boosted protease inhibitor therapy in of HIV-infected adults
 
 
ACTRN12605000662662: HIV Infection And Metabolic Abnormalities Protocol 1 (HAMA 001)

Recruiting
4
80
 
The University of New South Wales, National Heart Lung and Blood Institute, US National Institutes of Health
HIV , Metabolic abnormality, Lipodystrophy, Cardiovascular disease
 
 
ACTRN12611000816954: A randomised, open-label study to evaluate the efficacy and safety of maraviroc (MVC) as a switch for either nucleoside or nucleotide analogue reverse transcriptase inhibitors (N(t)RTI) or boosted protease inhibitors (PI/r) in HIV-1 infected individuals with stable, well-controlled plasma HIV-RNA while taking their first N(t)RTI + PI/r regimen of combination antiretroviral therapy (cART): MARCH study

Recruiting
4
560
 
University of New South Wales, Kirby Institute, Pfizer Inc., a Delaware Corporation
HIV
 
 
ACTRN12610001098022: ALTAIR - Alternative Antiretroviral Strategies: A Comparison of Three Initial Regimens

Active, not recruiting
4
300
 
The National Centre in HIV Epidemiology and Clinical Research, Gilead Sciences, Inc.
Human Immunodeficiency Virus - HIV, HIV+ treatment-naive patients
 
 
ACTRN12609000881235: A randomised open-label study comparing the safety and efficacy of ritonavir boosted lopinavir and 2-3 nucleoside reverse transcriptase inhibitors (NRTI) backbone versus ritonavir boosted lopinavir and raltegravir in participants virologically failing first-line non-nucleoside reverse transcriptase inhibitors (NNRTI)/2 NRTI therapy (the SECOND-LINE study). This study is for Human Immunodeficiency Virus (HIV) infection.

Active, not recruiting
4
550
 
University of New South Wales/Kirby Institute, University of New South Wales/Kirby Institute, Abbott, Merck Sharpe & Dohme, amfAR
Human Immunodeficiency Virus (HIV) -1 infection
 
 
ACTRN12616001215415: The efficacy of pre-exposure prophylaxis for Human Immunodeficiency Virus (HIV) in high-risk individuals in Victoria, Australia

Recruiting
4
2600
 
The Alfred, Victoria State Government, health and Human Services, The Alfred, Victorian AIDS Council
HIV, Anxiety
 
 
ACTRN12616001387415: NZ PrEP: A study assessing the feasibility,risks and benefits of prescribing daily Truvada in a sample of men who are at high risk of acquiring HIV

Recruiting
4
150
 
Auckland District Health Board, Gilead Sciences
HIV
 
 
ChiCTR-OPC-15006528: Monitoring of Antiviral Therapy Indicators and Optimizing Treatment Management Model

Recruiting
4
250
 
HIV-RNA viral load test (quantitative), immunology, blood routine and hepatorenal function test (quantitative) will be performed 0, 3, 6 and 12 months after treatment initiation respectively. National first-line regimen will be applied: AZT/TDF+3TC+EFV/NVP ;HIV-RNA viral load test (quantitative), immunology, blood routine, and liver and hepatorenal function test (quantitative) will be performed 0, 3, 6 and 12 months after treatment initiation respectively. Optimized regimen will be applied: LPV/r 400/100mg BID+ 3TC 300 mg QD. ;According to current national guideline, HIV-RNA viral load test (quantitative) will be perfomed once a year; immunology, blood routine and hepatorenal function test (quantitative) will be performed 2-4 times each year. National first-line regimen will be applied: AZT/TDF+3TC+EFV/NVP.
8th People's Hospital of Guangzhou; Level of the institution:, Cooperation with Abbvie Pharmaceutical Trading (Shanghai) Co., Ltd. and self-funding
AIDS
 
 
EFV low dose study, ChiCTR-IOR-15007465: A genotype guided low-dose approach to the use of efavirenz in Chinese HIV patients

Recruiting
4
50
 
Efavirenz 400mg orally daily versus 600mg orally daily, in combination with other anti-retrovirals, 4 months
School of Pharmacy, Chinese University of Hong Kong; Dr Leung Wai Shing, Take on all the responsibilities of sponsorship jointly with the primary sponsor, The Chinese University of Hong Kong
HIV infection
 
 
ChiCTR-OPC-16009603: A preliminary study on the delivery of pre-exposure prophylaxis (PrEP) for men who have sex with men (MSM) at high risk of HIV transmission through the application of a self-financed incentivized approach

Recruiting
4
70
 
HIV prevention / Daily pre-exposure prophylaxis / truvada; Truvada tablet (Tenofovir 300 mg / Emtricitabine 200 mg), 1 tablet, 30 weeks, daily
Stanley Ho Centre for Emerging Infectious Diseases; Level of the institution:, Council for the AIDS Trust Fund
HIV infection
 
 
ChiCTR1800016100: Pre-exposure prophylaxis with on-demand versus daily TDF/FTC in men who have sex with men at high risk of HIV infection – a crossover study

Not yet recruiting
4
90
 
Truvada tablet (Tenofovir 300 mg / Emtricitabine 200 mg): 1 tablet daily versus 2 tablets before sex, and 1 tablet at 24 and then 48 hours afterwards, for 16 weeks
Stanley Ho Centre for Emerging Infectious Diseases; Level of the institution:, AIDS Trust Fund
HIV infection
 
 
ChiCTR-TRC-09000407: Antivirus Therapy for Population with HIV, HCV and TB Co-infection Clinical Trial

Completed
4
490
 
PEG-IFN-alpha-2a, ribavirin capsules ;HAART, PEG-IFN-alpha-2a, ribavirin capsules ;HAART, PEG-IFN-alpha-2a, ribavirin capsules ;HAART
Guangzhou 8th People's Hospital; Ministry of Science and Technology People's Republic of China, Ministry of Science and Technology of China
Population with HIV and HCV and TB
 
 
ChiCTR-TRC-11001261: Traditional Chinese medicine for the Herpes Zoster in AIDS patients: a randomized control trial

Completed
4
120
 
Basic treatment ;Basic treatment+TCM
Beijing Ditan Hospital; Beijing Ditan Hospital, The ministry of Finance, China
herpes zoster and AIDS
 
 
ChiCTR-TRC-11001252: Traditional Chinese medicine for the drug eruption caused by anti-HIV medicine: a randomized control trial

Completed
4
175
 
Basic treatment + TCM protocol + TCM protocol ;Basic treatment protocol Aocol A ;Basic treatment protocol B
Beijing Ditan Hospital; Beijing Ditan Hospital, The ministry of Finance, China
AIDS, drug eruption
 
 
ChiCTR-TRC-11001253: Traditional Chinese medicine for the Dyslipidemia caused by highly active antiretroviral therapies (HARRT): a randomized control trial

Completed
4
180
 
Basic treatment+TCM ;Basic treatment
Beijing Ditan Hospital; The Ministry of Health, The Ministry of Finance, China
AIDS, dyslipidemia
 
 
ChiCTR-TRC-11001262: Traditional Chinese medicine for the lung infection in patients with AIDS: a randomized control trial

Completed
4
180
 
Basic treatment+TCM ;Basic treatment
Beijing Ditan Hospital; The ministry of Health, China, The ministry of finance, China
AIDS, lung infection
 
 
ChiCTR-TRC-11001242: Traditional Chinese medicine for the chronic diarrhea in AIDS patients: a randomized double-blinding control trial

Completed
4
300
 
Routine treatment +mimics of Xielikang Capsule+Loperamide ;Routine treatment B+Jianpizhixie recipe+Loperamide mimics ;Routine treatment +mimics of Xielikang Capsule+Loperamide ;Routine treatment+Loperamide
Beijing Ditan Hospital; The Ministry of Health, The Ministry of Finance, The Ministry of Health, China
chronic diarrhea, AIDS
 
 
ChiCTR-TRC-11001243: Traditional Chinese medicine for the HIV associated prurigo: a randomized control trial

Completed
4
360
 
Basic treatment ;Basic treatment+TCM
Beijing Ditan Hospital; The ministry of Health, China, The ministry of Finance, China
AIDS, Prurigo
 
 
ChiCTR-TRC-11001254: Traditional Chinese medicine for the adverse reaction of digestive system caused by highly active antiretroviral therapies (HARRT): a randomized control trial

Completed
4
360
 
Basic treatment ;Basic treatment+TCM
Beijing Ditan Hospital; The ministry of Health, The ministry of finance, China
AIDS
 
 
ChiCTR-TRC-11001260: Traditional Chinese medicine for the hematological toxic reaction caused by highly active antiretroviral therapies (HARRT): a randomized control trial

Completed
4
390
 
Basic treatment+TCM ;Basic treatment
Beijing Ditan Hospital; Beijing Ditan Hospital, The ministry of finance, China
AIDS, hematological toxic reaction
 
 
2010-023245-30: Treatment with Peg-interferon alfa-2a and ribavirin in patients with hepatitis HCV-related, with or without HIV co-infection, and end stage renal disease on dialysis

Ongoing
4
20
Europe
Tablet, Solution for injection, COPEGUS*168CPR RIV 200MG, PEGASYS*SC SIR 0,5ML 180MCG+AG
ISTITUTO NAZIONALE DELLE MALATTIE INFETTIVE LAZZARO SPALLANZANI
Chonic hepatitis HCV-related
 
 
2011-004935-30: Study “before-after”: Adherence Evaluation to antiretroviral therapy administered in two different ways Studio ''before-after'' di valutazione dell'aderenza di due diverse modalita' di somministrazione della terapia antiretrovirale

Ongoing
4
400
Europe
Film-coated tablet, EPIVIR*FL 30CPR RIV 300MG, VIREAD*30CPR 245MG, ZIAGEN*6BLISTER 10CPR 300MG, SUSTIVA*30CPR RIV 600MG BLIST, RETROVIR*60CPR 300MG, TRUVADA*30CPR RIV 200MG/245MG, KIVEXA*BL 30CPR RIV 600MG+300M, COMBIVIR*60CPR RIV 150MG+300MG, ATRIPLA*30CPR RIV600+200+245MG
U.L.S.S. 9 DI TREVISO, studio no profit, farmaci a carico del SSN
HIV infection Infezione da HIV, HIV infection Infezione da HIV, Diseases [C] - Virus Diseases [C02]
 
 
2011-005270-35: Study of the effect of pregnancy on the concentrations of antiretroviral drugs in the blood of women with HIV infection Studio dell'effetto della gravidanza sulle concentrazioni dei farmaci antiretrovirali nel sangue di donne con infezione da HIV

Ongoing
4
120
Europe
Tablet, Capsule, soft, Capsule, hard, Film-coated tablet, VIRAMUNE*60CPR 200MG, COMBIVIR*FL 60CPR RIV, KALETRA*120CPR RIV 200MG+50MG, REYATAZ*60CPS 150MG, TRUVADA*30CPR RIV 200MG/245MG, PREZISTA*60CPR RIV 600MG, ISENTRESS*FL 60CPR RIV 400MG, NORVIR*FL 84CPS MOLLI 100MG
ISTITUTO NAZIONALE DELLE MALATTIE INFETTIVE LAZZARO SPALLANZANI, Istituto Superiore di Sanita'
HIV-1 infection Infezione da HIV-1, HIV infection Infezione da HIV, Diseases [C] - Virus Diseases [C02]
 
 
2011-001982-42: A study of the effect of antiretroviral therapy and immunoglobulin on the HIV reservoir in Acute HIV Infection.

Ongoing
4
10
Europe
Octagam, Solution for infusion, Octagam
Guy's & St. Thomas' NHS Foundation Trust, Guy's & St. Thomas' Charity
Acute HIV Infection, Acute HIV Infection, Diseases [C] - Immune System Diseases [C20]
 
 
2011-005581-37: Efficacy of Switching to Lopinavir/Ritonavir (Kaletra) in Improving Cognitive function in patients treated with Efavirenz (EFV) (SLICE Study)

Ongoing
4
30
Europe
Kaletra, Film-coated tablet, Kaletra
The Newcastle upon Tyne Hospitals NHS Foundation Trust, AbbVie Limited
Cognitive function and sleep pattern in HIV-1 patients, HIV-1 infection, Diseases [C] - Immune System Diseases [C20]
 
 
2010-023625-38: Trial to investigating the effect of Maraviroc on movement of microbes across the gut wall in HIV-1 infected individuals who are receiving antiretroviral therapy

Ongoing
4
10
Europe
Film-coated tablet, Celsentri film-coated tablets
Guy's and St Thomas' NHS Foundation Trust, ViiV Healthcare UK Ltd.
HIV, HIV, Diseases [C] - Immune System Diseases [C20]
 
 
2014-000496-64: Viral suppression in Cerebrospinal Fluid in HIV-1 infected patients receiving Ritonavir-boosted Atazanavir plus lamivudine dual theraphy. SCALA study Supresión viral en el líquido cefalorraquídeo en pacientes con infección por VIH-1 que reciben tratamiento antirretroviral con atazanavir potenciado con ritonavir y lamivudina. Estudio SCALA

Ongoing
4
10
Europe
REYATAZ, NORVIR, LAMIVUDINA EFG
Dr. Daniel Podzamczer Palter. Hospital Univesitari de Bellvitge. Unidad de VIH., Hospital Universitari de Bellvitge - Unidad de VIH
HIV-1 infection Infección por el virus VIH-1, HIV-1 infection Infección por el virus VIH-1, Diseases [C] - Virus Diseases [C02]
 
 
2014-003710-84: The CNS Integrase Inhibitor Study

Ongoing
4
22
Europe
Tivicay, Isentress, Truvada, Film-coated tablet, Tivicay, Isentress, Truvada
Imperial College London
Human Immunodificiency Virus, HIV, Diseases [C] - Virus Diseases [C02]
 
 
2014-004015-36: Role of a switch to an once-daily regimen of antiretroviral therapy on HIV-DNA levels and immune activation. Effetti del passaggio a un regime HAART in unica somministrazione giornaliera sui livelli di HIV-DNA e dei livelli di attivazione immunitaria.

Ongoing
4
30
Europe
STRIBILD, Film-coated tablet, STRIBILD
AZIENDA OSPEDALIERA SAN PAOLO, Gilead Sciences S.r.l.
Human Immunodeficiency Virus (HIV-1) Infection Infezione da virus dell’immunodeficienza umana (HIV1), HIV virus Infection Infezione da virus HIV, Diseases [C] - Virus Diseases [C02]
 
 
2014-002281-70: Immune reconstitution in severely immunosuppressed antiretroviral-naive HIV-1?infected patients (<100 CD4+ T cells/?L) taking antiretroviral regimens based on dolutegravir or ritonavir-boosted darunavir (the AdvanZ-4 Trial). Reconstitución inmune en pacientes con infección por el VIH-1 no tratados previamente y con cifras de linfocitos CD4+ inferiores a 100 céls/mm3 que reciben un régimen de fármacos antirretrovirales basado en dolutegravir o darunavir/ritonavir. Estudio AdvanZ-4.

Ongoing
4
108
Europe
CoatedTablet600 mg de abacavir ( sulfate) 300 mg de lamivudine, PREZISTA 300 mg comprimidos recubiertos con película darunavir, Norvir 100 mg soft tablets, Triumeq, Coated tablet, Capsule, soft, Tablet, KIVEXA( Abacavir 600 mg/ Lamivudine 300 mg) recovered tablets, PREZISTA 300 mg recovered Tablets, NORVIR 100 mg soft Tablets, TRIUMEQ®: Lamivudine(3TC) 300 mg+ Abacavir(ABC) 600 mg + dolutegravir(DGT) 50 mg : 1 comprimido
Fundació Clínic per a la Recerca Biomèdica, ViiV Healthcare UK Limited 980 Great West Road Brentford Middlesex TW8 9GS Reino Unido
tratement HIV infection tratamiento de la infección por HIV, HIV infection infección por HIV, Diseases [C] - Virus Diseases [C02]
 
 
2015-000274-35: clinical trial to assess the safety, tolerability and efficacy of two dolutegravir-based simplification strategies in HIV-infected patients with prolonged virological suppression. ENSAYO CLÍNICO PARA EVALUAR LA SEGURIDAD, TOLERABILIDAD Y EFICACIA DE DOS ESTRATEGIAS DE SIMPLIFICACIÓN BASADAS EN DOLUTEGRAVIR EN PACIENTES INFECTADOS POR VIH CON SUPRESIÓN VIROLÓGICA SOSTENIDA.

Ongoing
4
450
Europe
Lamivudine, Efavirenz, nevirapine, J05AX12, Coated tablet, Capsule, hard, Tablet, Prolonged-release tablet, Tivicay, Stribild, TRUVADA, KIVEXA, ZIAGEN, VIREAD, EMTRIVA, ATRIPLA, EVIPLERA, ISENTRESS, RAYATAZ, PREZISTA, KALETRA, NORVIR, INTELENCE, EDURANT, TRIUMEQ
Fundació Lluita contra la SIDA, Fundació Lluita contra la SIDA
Infection with human immunodeficiency virus (HIV). Infección por el virus de la inmunodeficiencia humana (VIH)., HIV infection Infección por VIH, Diseases [C] - Virus Diseases [C02]
 
 
2013-004809-24: The role of Home packs of HIV PEPSE in High Risk Individuals

Ongoing
4
140
Europe
Film-coated tablet, Celsentri (Trial Arm A), Truvada (Trial Arm A), Celsentri (Trial Arm B), Truvada (Trial Arm B)
Guy's & St. Thomas' NHS Foundation Trust, Viiv Healthcare UK Ltd, Gilead Sciences Ltd
HIV, HIV, Diseases [C] - Virus Diseases [C02]
 
 
2014-002569-32: HIV prevention for men who have sex with men using medication HIV preventie voor mannen die seks hebben met mannen met behulp van medicijnen

Ongoing
4
370
Europe
truvada, Tablet, Truvada
Academic Medical Center, PHSA
prevention of HIV infection HIV infectie preventie, prevention of HIV infection HIV infectie preventie, Health Care [N] - Environment and Public Health [N06]
 
 
2014-004297-42: Effect of changing one medication (Atripla) to another (Eviplera) on functions of the brain and emotions Het effect van wisselen van het ene medicijn (Atripla) naar het andere medicijn (Eviplera) op de functies van de hersenen en emoties

Ongoing
4
60
Europe
Film-coated tablet, Eviplera, Atripla
UMC Utrecht, Gilead Sciences
neurocognitive and emotional functioning in HIV positive men using antiretroviral therapy neurocognitief en emotioneel functioneren bij HIV positieve mannen die antiretrovirale therapie gebruiken, brain functions and emotions with people infected with HIV who use anti-HIV medication. functies van het brein en emoties bij mensen geïnfecteerd met HIV die anti-HIV medicijnen gebruiken., Not possible to specify
 
 
ChiCTR-TRC-14004908: Rilpivirine Versus Efavirenz with Tenofovir and lamivudine's use in treatment-naive adults with HIV-1 infection and injection drug use on Methadone maintenance treatment

Recruiting
4
60
 
taking Rilpivirine RPV+TDF+3TC and methadone ;taking Rilpivirine RPV+TDF+3TC and methadone
Yunnan Provincial Infectious Disease Hospital; Yunnan Provincial Infectious Disease Hospital, Funded by Xian Janssen Pharmaceutical Ltd.
AIDS
 
 
2014-002134-31: Maraviroc and cardiovascular risk in HIV+ patients. Maraviroc e rischio cardiovascolare in pazienti HIV+.

Ongoing
4
40
Europe
NA, NA, Film-coated tablet, Celsentri
Ospedale L. Sacco - Azienda Ospedaliera-Polo Universitario, Ospedale L. Sacco - Azienda Ospedaliera-Polo Universitario
HIV-1 infection. Infezione da HIV-1., HIV-1 HIV-1, Diseases [C] - Virus Diseases [C02]
 
 
NCT01998178: Immune Response and Safety Study of Human Papillomavirus (HPV) Vaccine in HIV-infected Pre-adolescent in Kenya

Active, not recruiting
4
180
RoW
Quadrivalent HPV Vaccine, Gardasil
Kenyatta National Hospital, University of Washington, Merck
Genital Warts, Cervical Cancer
08/15
12/15
ChiCTR-TRC-13003717: Study on Chinese medicine treatment of patients with abnormal lipid metabolism after HAART program

Completed
4
286
 
Highly active antiretroviral therapy in combination lipid particles ;Highly active antiretroviral therapy in combination with placebo
China Academy of Chinese medical Sciences; Capital Medical University, Beijing Ditan Hospital, AIDS and viral hepatitis and other major infectious diseases major science and technology
HIV Acquired Immunodeficiency Syndrome
 
 
2015-004524-65: Efficacy of a vaccine with nine subgroups against human papilloma virus in HIV infected sexually active men who have sex with men. Effekten af en vaccine indeholdende ni undergrupper mod humant papilloma virus hos HIV smittede seksuelt aktive mænd der har sex med mænd.

Ongoing
4
80
Europe
Gardasil 9, Suspension for injection
Department of Infectious Diseases, AIDS- Foundation, Odense University Hospital Research Foundation
The purpose of the study is to investigate the efficacy of a new nonavalent HPV vaccine in sexually active HIV-infected MSM. Formålet med forsøget er at undersøge effekten af en ny ni-valent HPV vaccine hos seksuelt aktive, HIV-smittede MSM., The purpose of the study is to investigate the effect of a new vaccine , which contains nine subgroups against human papilloma virus among sexually active HIV-infected men who have sex with men . Formålet med forsøget er at undersøge effekten af en ny vaccine, som indeholder ni undergrupper mod humant papilloma virus hos seksuelt aktive, HIV-smittede mænd der har sex med mænd., Diseases [C] - Virus Diseases [C02]
 
 
2015-003278-34: A RANDOMIZED BIOEQUIVALENCE STUDY OF EFAVIRENZ GENERIC DRUG AND SUSTIVA® (TABLETS 600 mg) IN PATIENTS WITH HIV-1 STUDIO RANDOMIZZATO PER LA VALUTAZIONE DELLA BIOEQUIVALENZA TRA EFAVIRENZ GENERICO E SUSTIVA® ENTRAMBI IN COMPRESSE DA 600 MG IN PAZIENTI CON HIV-1

Not yet recruiting
4
40
Europe
Efavirenz, SUSTIVA, non applicabile, Film-coated tablet, EFAVIRENZ MYLAN - 600 MG COMPRESSE RIVESTITE CON FILM 30 COMPRESSE IN BLISTER PVC/PVDC/AL, SUSTIVA - 600 MG COMPRESSE FILM RIVESTITE 30 COMPRESSE IN BLISTER USO ORALE
IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI, Mylan S.p.A.
Patients with HIV-1 Pazienti affetti da HIV-1, Patients with HIV-1 Pazienti affetti da HIV-1, Diseases [C] - Virus Diseases [C02]
 
 
2004-002565-20: Food effect on antiviral activity of videx enteric-coated capsules

Ongoing
4
40
Europe
Videx 400, Videx 250, 63305, Videx, Videx
Asociación para el estudio de enfermedades infecciosas
Asymptomatic HIV Infection
 
 
2004-002633-39: Prospective study of switch to 3TC monotherapy with evaluation of replication capacity in patients with virologic failure and 3TC resistance (a multicenter prospective clinical study within the SHCS) SHCS-Projekt Nr. 408

Ongoing
4
5
Europe
Epivir, 3TC, Epivir, Epivir
Prof. Dr. med. Milos Opravil, Universitätsspital Zürich
HIV patients with virological treatment failure due to multi-drug-resistant virus including 3TC resistance
 
 
2004-004802-26: ESTUDIO DE LA INFLUENCIA DE LAS ESTATINAS EN LA REPLICACIÓN PLASMÁTICA DEL VIH EN PACIENTES CON INFECCION POR EL VIH-1 QUE INTERRUMPEN EL TRATAMIENTO ANTIRRETROVIRAL

Ongoing
4
70
Europe
Atorvastatina, Simvastatina,
Fundació Lluita contra la SIDA
Patients HIV infected
 
 
2004-001403-35: Estudio abierto, multicéntrico y aleatorizado sobre la eficacia y seguridad de la reducción de dosis de estavudina en pacientes en tratamiento antirretroviral que incluye estavudina a dosis estándar con buen control virológico e inmunológico.

Ongoing
4
284
Europe
Zerit, Zerit, Zerit, Zerit
Doctor Pere Domingo
AIDS
 
 
2005-000028-17: Eficacia virológica, inmunológica y trascendencia clínica del efecto de la lamivudina en pacientes portadores de la mutación M184V/I con fracaso terapéutico.

Ongoing
4
312
Europe
EPIVIR, COMBIVIR, TRIZIVIR, EPIVIR, COMBIVIR, TRIZIVIR, EPIVIR, COMBIVIR, TRIZIVIR, EPIVIR, COMBIVIR, TRIZIVIR
DAVID DALMAU
HIV INFECTION
 
 
2005-004021-26: Longitudinal relationship between lipodystrophy and adipocyte mitochondria DNA in HIV Patients: comparison between Efavirenz (Sustiva) plus AZT/3TC (Combivir) and a less mitochrondial DNA-toxic regimen - Tenefovir/Emtricitabine (Truvada) plus Efavirenz.

Ongoing
4
60
Europe
Efavirenz, AZT/3TC, emtricitabine/tenofovir, SUSTIVA, COMBIVIR, TRUVADA, SUSTIVA, COMBIVIR, TRUVADA
University Hospital Birmingham
HIV
 
 
2005-004430-41: Effect of food on the pharmacokinetic profile of saquinavir at steady state in HIV-infected patients treated with saquinavir/ritonavir 1000/100 mg b.i.d.

Ongoing
4
24
Europe
Saquinavir mesylate, Ritonavir, n/a, Invirase, Norvir, Invirase, Norvir
St Stephen\'s AIDS Trust
HIV
 
 
2005-003411-75: Estudio sobre la utilización de levetiracetam en monoterapia en pacientes HIV-positivos con epilepsia

Ongoing
4
20
Europe
levetiracetam, ucb-L059, Keppra 500 / 1000 mg comprimidos con cubierta pelicular, Keppra 500 / 1000 mg comprimidos con cubierta pelicular
Fundación para la Investigación Biomédica del Hospital Clínico de San Carlos
Pacientes HIV-positivos con epilepsia
 
 
2006-001243-55: Open, multicenter, phase IV study to evaluate the safety and effectiveness of peginterferon alfa-2a (40 KD) associated with ribavirin for the treatment chronic hepatitis C with persistent normal ALT in HIV coinfected patients

Ongoing
4
230
Europe
Pegasys, Copegus, Pegasys, Copegus, Pegasys, Copegus
Miguel Santin Cerezales
Comparate the safety and effectivenes of the treatment with peginterferon alfa-2a in combination with ribavirin between HIV/HCV coinfected patients with persistent normal ALT levels versus HIV/HCV coinfected patients with high ALT levels
 
 
2006-005609-76: EFFECT OF DIFFERENT MEALS ON THE PHARMACOKINETIC PROFILE OF SAQUINAVIR AT STEADY STATE IN HIV-INFECTED PATIENTS TREATED WITH SAQUINAVIR/RITONAVIR 1000/100 mg BID.

Ongoing
4
24
Europe
Invirse, Norvir, n/a, Norvir, Norvir
St Stephens Aids Trust
HIV
 
 
2006-006174-19: A randomised, open label, phase IV comparative study to determine the effects on renal function of continuing treatment with tenofovir versus replacement with abacavir in HIV positive persons

Ongoing
4
30
Europe
Ziagen, Viread, Truvada, Kivexa, Not appllicable, Not applicable, Not appilcable, Ziagen, Viread, Truvada, Kivexa, Ziagen, Viread, Truvada, Kivexa
St Stephens AIDS Trust
HIV
 
 
2006-006716-30: Randomized, controlled, multicentric trial to evaluate efficacy and safety of the switch from a LPV/r based therapy to an ATV/r or a NVP based treatment in association with ABC/3TC, in HIV patient with undetectable viral load Randomized, controlled, multicentric trial to evaluate efficacy and safety of the switch from a LPV/r based therapy to an ATV/r or a NVP based treatment in association with ABC/3TC, in HIV patient with undetectable viral load

Ongoing
4
200
Europe
VIRAMUNE*60CPR 200MG, REYATAZ*60CPS 150MG, KIVEXA*BL 30CPR RIV 600MG+300M, NORVIR*4FL 84CPS MOLLI 100MG, KALETRA*BLIST 180CPS MOLLI, VIRAMUNE*60CPR 200MG, REYATAZ*60CPS 150MG, KIVEXA*BL 30CPR RIV 600MG+300M, NORVIR*4FL 84CPS MOLLI 100MG, KALETRA*BLIST 180CPS MOLLI
AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI
HIV infection Infezione da HIV
 
 
2006-003425-81: Host genetic factors influencing drug disposition and response to HIV treatment

Ongoing
4
500
Europe
Protease inhibitor, Nucleoside and nucleoside reverse transcriptase inhibitors, Non-nucleoside reverse transcriptase inhibitors, Protease inhibitors, Nucleoside and nucleoside reverse transcriptase inhibitors, Non-nucleoside reverse transcriptase inhibitors, Protease inhibitors, Nucleoside and nucleoside reverse transcriptase inhibitors, Non-nucleoside reverse transcriptase inhibitors
University of Liverpool
Pharmacogeneric study of HIV+ patients receiving antiretroviral therapy. We wish to correlate drug concentration with host genetic patients receiving certain HIV drugs. No dosage modification will be carried out and choice of antiretroviral and their dosing will not be influenced by participation in this study.
 
 
2006-006076-38: The Liverpool HIV TDM Registry: Studying influences upon plasma HIV drug exposure

Ongoing
4
12000
Europe
Protease inhibitor, Nucleoside and nucleoside reverse transcriptase inhibitors, Non-nucleoside reverse transcriptase inhibitors, Protease inhibitors, Nucleoside and nucleoside reverse transcriptase inhibitors, Non-nucleoside reverse transcriptase inhibitors, Protease inhibitors, Nucleoside and nucleoside reverse transcriptase inhibitors, Non-nucleoside reverse transcriptase inhibitors
University of Liverpool, Royal Liverpool & Broadgreen University Hospitals Trust
Pharmacogenetic study of HIV+ patients receiving antiretroviral therapy. We wish to correlate drug concentration with host genetic patients receiving certain HIV drugs. No dosage modification will be carried out and choice of antiretroviral and their dosing will not be influenced by participation in this study.
 
 
2006-006156-36: Papel de los niveles plasmáticos de fitosterol en la predicción del efecto hipolipemiante de la ezetimiba en sujetos infectados por VIH que reciben inhibidores de la proteasa.ROLE OF PHYTOSTEROL PLASMA LEVELS IN PREDICTING THE LIPID LOWERING EFFECT OF EZETIMIBE IN HIV INFECTED SUBJECTS RECEIVING PROTEASE INHIBITORS

Ongoing
4
20
Europe
Ezetrol, Ezetrol
Hospital Clinic, Barcelona
Infección crónica por VIHHipercolesterolemiaChronic HIV infectionhypercholesterolemia
 
 
2006-006297-23: A study of the pharmacokinetics of new formulation lopinavir/ritonavir in the genital tract and plasma of HIV infected women in pregnancy

Ongoing
4
10
Europe
Kaletra 200mg/50mg film coated tablets, NA, Kaletra tablets, Kaletra tablets
Guy\'s & St Thomas\' NHS Foundation Trust
HIV during pregnancy
 
 
2007-000932-19: A phase IV study to assess the feasibility of substituting double ritonavir-boosted protease inhibitors (PI) with ritonavir-boosted darunavir (DRV/r) in HIV-infected individuals with viral suppression on highly active antiretroviral therapy (HAART)

Ongoing
4
20
Europe
Darunavir, Ritonavir, Prezista, Norvir, Prezista, Norvir
St Stephen\'s AIDS Trust
HIV
 
 
2007-007018-12: “Estudio prospectivo, abierto, aleatorizado y cruzado sobre el efecto de la Hidroxicloroquina, 200mg al día, en factores inflamatorios y metabólicos relacionados con la enfermedad cardiovascular en pacientes infectados por el virus de la inmunodeficiencia humana.” \"Open label, prospective, randomized, crossed study of the effect of Hidroxychloroquine, 200 mg QD, on inflammatory and metabolic factors related to cardiovascular disease in human immunodeficiency virus infected patients\"

Ongoing
4
120
Europe
Dolquine, Dolquine
Carlos Alonso-Villaverde Lozano, Hospital Universitari Sant Joan de Reus
Infección por el virus de la inmunodeficiencia adquirida
 
 
2008-002978-35: Intensification of HAART with Maraviroc (MVC) as first line therapy of HIV-1-infected patients to rapidly suppress viral replication and minimize the evolution of drug-resistant variants

Ongoing
4
20
Europe
MARAVIROC,
AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE)
First line therapy of HIV-1-infected patients.
 
 
2008-003635-20: Maraviroc Immune Recovery Study (MIRS):A multicentre, randomized, placebo-controlled, exploratory mechanistic study into the role of Maraviroc on immune recovery

Ongoing
4
130
Europe
Celsentry, Celsentry
Universitair Medisch Centrum Utrecht
HIV-1 infection
 
 
2007-006277-92: Treatment of anal intraepithelial neoplasia in HIV-positive patients, a triple-arm randomized clinical trial

Ongoing
4
150
Europe
Imiquimod, Fluorouracil, Aldara, Efudix, Aldara, Efudix
Academic Medical Center, department of infectious diseases
anal intraepithealial neoplasia in HIV-positive patients
 
 
2008-006371-67: EFFECT OF THIENOPYRIDINE DERIVATIVE (CLOPIDOGREL) ON THE DISPOSITION OF EFAVIRENZ AND NEVIRAPINE IN HIV POSITIVE PATIENTS

Ongoing
4
37
Europe
plavix, Nevirapine, Efavirenz, B01AC04, J05AG03, Plavix (Sanofi Synthelabo, Guildford, United Kingdom), viramune, sustiva;stocrin, Plavix (Sanofi Synthelabo, Guildford, United Kingdom), viramune, sustiva;stocrin
Royal Liverpool and Broadgreen University Hospital, University of Liverpool
To determine whether anti-platelet agent clopidigrel influences the disposition of NNRTIs (efavirenz and nevirapine)
 
 
2009-014694-40: A pilot evaluation of the pharmacokinetics, efficacy and safety of switching from efavirenz to maraviroc administered at 600mg then 300mg twice-daily in patients suppressed on an efavirenz-containing regimen as initial therapy

Ongoing
4
12
Europe
HIV
 
 
2009-011816-39: A randomised, open label, prospective study to assess two different therapeutic strategies following first treatment failure in HIV-1 infected subjects.‘The First Failure Study’ : ‘FAST’

Ongoing
4
44
Europe
Etravirine, Darunavir, Truvada, Ritonavir, Intelence, Prezista, Truvada, Norvir, Intelence, Prezista, Truvada, Norvir
Imperial College London
HIV
 
 
2010-023264-40: Efficacy in the central nervous system (CNS) of two combination regimens with different penetration rank in HIV-positive na�ve patients

Ongoing
4
32
Europe
KALETRA, KIVEXA, REYATAZ, TRUVADA, NORVIR, KALETRA, KIVEXA, REYATAZ, TRUVADA, NORVIR
AZIENDA OSPEDALIERA S. GERARDO DI MONZA
HIV infection
 
 
2010-022120-72: The impact of a new single therapy (Darunavir/ritonavir) on metabolism after successfully suppressing the virus with the normal treatment (Atripla) for HIV-1-infected patients (MIDAs).

Ongoing
4
70
Europe
Prezista, Norvir, Atripla, Prezista, Norvir, Atripla
Guy\'s & St. Thomas\' NHS Foundation Trust, Tibotec (a division of Janssen-Cilag Ltd)
HIV
 
 
2010-023192-26: EFFECT OF SWITCHING FROM NRTIS TO MARAVIROC ON NRTI-ASSOCIATED MITCHONDRIAL TOXICITY AND IMMUNE ACTIVATION Auswirkung des Wechsels von NRTIs zu Maraviroc auf NRTI-assoziierte mitochondriale Toxizität und Immunaktivierung

Ongoing
4
80
Europe
Celcentri, Celcentri, Celcentri
mib Dienstleistungsgesellschaft mbH, ViiV Healthcare GmbH
Increases in inflammatory biomarkers have been associated with various non-AIDS complications such as cardiovascular events. Maraviroc has no known toxic effects on mitochondria and has been shown to reduce immune activation / inflammation in treatment intensification settings. The purpose of this study is to investigate if switching from NRTIs to Maraviroc results in reversal of NRTI-associated mitochondrial toxicity and decreases in markers of immune activation and inflammation.
 
 
2010-022775-57: This is a pilot study to see how giving HIV infected patients, who have Vitamin D deficiency (and are already taking standard therapy) a high dose of vitamin D will affect the levels of vitamin D in their bodies and if this will help them have a better immune response to their infection.

Ongoing
4
40
Europe
Adcal-D3 Lemon Chewable Tablets, Adcal-D3 Lemon Chewable Tablets
Guy\'s and St Thomas\' NHS Foundation Trust, Tibotec (a division of Janssen-Cilag Ltd),
HIV infected patients with vitamin D defficiency
 
 
2011-001463-51: NOT APPLICABLE

Ongoing
4
10
Europe
INTELENCE 100 mg comprimidos, INTELENCE 100 mg comprimidos
Servicio de Enfermedades Infecciosas. Unidad VIH. Hospital Universitari de Bellvitge, HOSPITAL DE BELLVITGE
HIV
 
 
2010-023122-21: This study aims to look at the effect of a high dose of Vitamin D on bone mineral density in HIV patients

Ongoing
4
48
Europe
Dekristol, Dekristol
King\'s College London, Guy\'s and St. Thomas\' NHS Foundation Trust, Viiv Healthcare Ltd
HIV
 
 
2011-003447-21: Randomised controlled trial of the tolerability and completion of maraviroc compared to Kaletra© in combination with Truvada© for HIV post-exposure prophylaxis

Ongoing
4
280
Europe
Maraviroc, Celsentri, Celsentri
Camden Provider Services, Pfizer
Prophylaxis and prevention of HIV Infection.
 
 
2012-000649-11: SSAT046 Addition of Maraviroc to monotherapy Darunavir/Ritonavir study

Ongoing
4
30
Europe
Darunavir, Ritonavir, Maraviroc, Prezista, Norvir, Celsentri, Prezista, Norvir, Celsentri
St Stephen\'s Aids Trust, St Stephen\'s AIDS Trust, Pfizer Inc
HIV
 
 
2012-001142-18: Efficacy and pharmacokinetics of a switch from a regimen consisting of emtricitabine, nevirapine and tenofovir to rilpivirine, emtricitabine and tenofovir in virologically suppressed HIV-1 infected patients. Werkzaamheid en farmacokinetiek van rilpivirine in HIV-1 positieve patiënten waarin het HIV onderdrukt is door een behandeling met emtricitabine, nevirapine en tenofovir en die deze behandeling vervangen door rilpivirine, emtricitabine en tenofovir.

Ongoing
4
50
Europe
Eviplera, J05AR08, Eviplera, Eviplera
Erasmus MC, Gilead
HIVAIDS
 
 
2012-002663-10: Darunavir/ritonavir and rilpivirine in therapy-naïve patients.

Ongoing
4
40
Europe
Edurant (rilpivirine), Prezista (darunavir), Norvir (ritonavir), Edurant, Prezista, Norvir, Edurant, Prezista, Norvir
St Stephen\'s AIDS Trust, Janssen-Cilag Ltd
HIV-1
 
 
2012-003595-39: A clinical trial to compare brain function and neurocognitive performance in antiretroviral treatments with different levels of penetration in the central nervous system. Ensayo clínico para comparar el funcionamiento cerebral y rendimiento neurocognitivo en tratamientos antirretrovirales con distintos niveles de penetracion en el sistema nervioso central.

Ongoing
4
40
Europe
ATAZANAVIR, Reyataz, Norvir, Kivexa, Sustiva, Truvada, Reyataz, Norvir, Kivexa, Sustiva, Truvada
Fundación para la Investigación Biomédica del Hospital Universitario La Paz, Fundacion para la Investigacion Biomédica del Hospital Universitario La Paz
Patients infected with human immunodeficiency virus who have never received antiretroviral treatment. Pacientes infectados con virus de inmunodeficiencia humana que nunca han recibido tratamiento antirretroviral.
 
 
2012-003778-16: The dose and genital tract concentration of Maraviroc needed for protection from HIV infection

Ongoing
4
54
Europe
Celsentri, Celsentri
Guy\'s & St. Thomas\' NHS Foundation Trust, Pfizer Inc
HIV
 
 
2013-002009-70: HPV vaccination after treatment of anal intraepithelial neoplasia HPV vaccinatie na behandeling van anale dysplasie

Ongoing
4
125
Europe
Gardasil, Gardasil
Academic Medical Center, The Netherlands Organisation for Health Research and Development
Intra-anal high-grade anal intraepithelial neoplasia (AIN) (grade 2-3) in HIV+ men that was successfully treated in the past year with conventional cauterization, cryotherapy, or other forms of local treatment.
 
 
2013-003359-39: Treatment with Zoledronic acid or Tenofovir Switching in HIV-Infected Tratamiento con ácido zoledrónico vs sustitución de tenofovir en pacientes infectados por el VIH

Ongoing
4
28
Europe
Aclasta, Aclasta
Fundació Clínic per a la Recerca Biomèdica, St. Vicent's Hospital
low bone mineral density - HIV Baja densidad mineral ósea - VIH
 
 
2013-003704-39: CV risk in HIV patients switching from a boosted PI to DTG

Ongoing
4
112
Europe
Dolutegravir, Darunavir, Atazanavir, Kaletra, Ritonavir, Fosamprenavir, INVIRASE, Tivicay, Prezista, Reyataz, Kaletra, Norvir, Telzir, Invirase, Tivicay, Prezista, Reyataz, Kaletra, Norvir, Telzir, Invirase
St Stephen\'s AIDS Trust, NEAT-ID, Viiv Healthcare Ltd
HIV infection
 
 
ChiCTR-ONRC-13003483: A clinical study of antiviral therapy in adults with early HIV infection

Completed
4
130
 
tenofovir + lamivudine + efavirenz ;no
China Medical University; Level of the institution:, mega-projects of national science research for the 12th Five-Year Plan (2012ZX10001-006)
HIV infection
 
 
2015-005297-37: Bone Evaluation in women over 40 who Switch from Truvada/NNRTI to Triumeq

Ongoing
4
90
Europe
Tenofovir, Lamivudine, Efavirenz, Nevirapine, Etravirine, Rilpivirine, Film-coated tablet, Tablet, Triumeq, Truvada, Atripla, Eviplera
King's College Hospital NHS Foundation Trust, ViiV Healthcare Ltd
Human Immunodeficiency Virus, People infected with Human Immunodeficiency Virus (HIV), Diseases [C] - Immune System Diseases [C20]
 
 
2012-000198-21: A study to assess the efficacy and safety of the withdrawal of nucleos/tide analogues with resistance in multitreated HIV-1-infected subjects with virological suppression ESTUDIO SOBRE LA EFICACIA Y SEGURIDAD DE LA RETIRADA DE ANÁLOGOS DE NUCLEÓS/TIDO CON RESISTENCIA EN SUJETOS CON INFECCIÓN POR VIH-1 MULTITRATADOS Y CON SUPRESIÓN VIROLÓGICA.

Ongoing
4
292
Europe
Epivir, Emtriva, Retrovir, Zerit, Viread, Ziagen, Combivir, Trizivir, Kivexa, Truvada, Videx, Epivir, Emtriva, Retrovir, Zerit, Viread, Ziagen, Combivir, Trizivir, Kivexa, Truvada, Videx
Fundació Lluita contra la SIDA, Ministerio de Sanidad, Política Social e Igualdad (Investigación Independiente)
Infection with human immunodeficiency virus (HIV). Infección por el virus de la inmunodeficiencia humana (VIH).
 
 
2016-001371-69: Tenofovir DP concentrations in seminal cells and semen quality in HIV-1 infected patients receiving a TAF containing regimen Concentraciones de Tenofovir DP en células seminales y calidad del semen en pacientes infectados por el virus VIH-1 que reciben un régimen que contenga TAF

Ongoing
4
15
Europe
Coated tablet, Genvoya
Fundació Lluita contra la SIDA, Gilead Sciences S.L.
HIV-1 positive patients Pacientes VIH-1 positivos, HIV-1 positive patients Pacientes VIH-1 positivos, Diseases [C] - Virus Diseases [C02]
 
 
2016-002006-39: Study on Efficacy and safety of switch ElvitegraviR/cobicistat/emtricitabine/tenofovir alafenamide (E/C/F/TAF) in patients with a HIV infection Studio sull¿ Efficacia e la sicurezza di passaggio a ElvitegraviR/cobicistat/emtricitabina/tenofovir alafenamide (E/C/F/TAF) in pazienti con infettati dal virus HIV

Not yet recruiting
4
30
Europe
Film-coated tablet, Genvoya
ISTITUTO NAZIONALE PER LE MALATTIE INFETTIVE "LAZZARO SPALLANZANI", Gilead Sciences
Treatment of HIV infection Trattamento dell¿ infezione da HIV, Treatment of HIV infection Trattamento dell¿ infezione da HIV, Diseases [C] - Virus Diseases [C02]
 
 
2016-003345-29: Safety of tenofovir alafenamide (TAF) in patients who developed kidney toxicity while receiving tenofovir disoproxil fumarate (TDF)

Ongoing
4
40
Europe
Film-coated tablet, Descovy
Kings College Hospital NHS Foundation Trust, Gilead Sciences
HIV infection, HIV infection, Diseases [C] - Virus Diseases [C02]
 
 
2014-002284-15: A study to assess changes in Central Nervous System (CNS) function where no obvious symptoms exist, when switching from Atripla to Eviplera switch in HIV infected patients

Not yet recruiting
4
40
Europe
Eviplera, Film-coated tablet, Eviplera
St Stephen's AIDS Trust, Gilead Sciences Ltd
HIV, HIV, Diseases [C] - Immune System Diseases [C20]
 
 
2014-004578-40: SSAT 066 Renal Integrase Study

Not yet recruiting
4
60
Europe
Tivicay 50 mg film - coated tablets, Isentress 400 mg Film-coated Tablets, Truvada 200 mg/245 mg film-coated tablets, Stribild 150 mg/150 mg/200 mg/245 mg film-coated tablets, Film-coated tablet, Tivicay 50 mg film-coated tablets, Isentress 400 mg Film-coated Tablets, Truvada 200 mg/245 mg film-coated tablets, Stribild 150 mg/150 mg/200 mg/245 mg film-coated tablets
St Stephen's AIDS Trust, Merck, Sharp & Dohme Limited
HIV
 
 
2016-005078-37: A study to reduce the risk of sexually acquired HIV-1 in adults at high risk.

Ongoing
4
100
Europe
Truvada (emtricitabine and tenofovir disoproxil fumarate), Truvada(emtricitabine&tenofovirdisoproxil fumarate, Film-coated tablet, Truvada
Hellenic Scientific Society for the Study of AIDS and Sexually Transmitted Diseases, Hellenic Scientific Society for the Study of AIDS and Sexually Transmitted Diseases
Healthy volunteers, Healthy volunteers, Diseases [C] - Virus Diseases [C02]
 
 
2016-004646-29: DREAM study Estudio DREAM

Ongoing
4
64
Europe
Triumeq, Genvoya, Tablet, Triumeq, Genvoya
Fundación SEIMC-GESIDA, GILEAD Sciencies S.A.
HIV VIH, HIV VIH, Diseases [C] - Virus Diseases [C02]
 
 
InMIND, NCT02406196: Integrase and Maraviroc Intensification for Neurocognitive Dysfunction

Not yet recruiting
4
186
NA
Placebo for MVC, Maraviroc, MVC, Placebo for DTG, Dolutegravir, DTG
AIDS Clinical Trials Group, National Institute of Allergy and Infectious Diseases (NIAID)
HIV-1 Infection
06/17
06/18
2017-000469-62: Pilot single‐arm clinical trial to evaluate the efficacy, PK interactions and safety of dolutegravir plus 2 NRTIs in HIV‐1‐infected solid organ transplant patients. DGT-SOT Ensayo clínico piloto de un brazo para evaluar la eficacia, las interacciones farmacocinéticas y la seguridad del dolutegravir más 2 inhibidores nucleósidos de la Transcriptasa Inversa (NRTIs en su siglas en inglés) en pacientes trasplantados de órganos sólidos infectados por el VIH-1. DGT-SOT

Ongoing
4
20
Europe
Triumeq 50 mg/600 mg/300 mg comprimidos recubiertos con película dolutegravir/abacavir/lamivudina, Tivicay 50 mg, Truvada comprimidos recubiertos con película., Coated tablet, Tablet, Triumeq®, Dolutegravir 50 mg, 200 mg de emtricitabina y 245 mg de tenofovir disoproxil (equivalente a 300 mg de tenofovir disoproxil fumarato ó 136 mg de tenofovir).
Fundació Clínic per a la Recerca Biomèdica, ViiV Healthcare
HIV-1 infected solid organ transplant patients pacientes trasplantados de órganos sólidos infectados por el VIH-1., HIV-1 infected solid organ transplant patients pacientes trasplantados de órganos sólidos infectados por el VIH-1., Diseases [C] - Virus Diseases [C02]
 
 
2017-002385-49: IN-UK-311-3956: A Feasibility Study of the Switch of Tenofovir disoproxil fumarate to Tenofovir alafenamide fumarate and the Effect on Kidney Function in individuals infected with both Chronic Hepatitis B and HIV.

Not yet recruiting
4
20
Europe
Descovy 200/10mg, Descovy 200/25mg, Film-coated tablet, Descovy 200/10mg, Descovy 200/25mg
King's College Hospital NHS Foundation Trust, Gilead Sciences International Ltd
HIV and Hepatitis B, HIV and Hepatitis B infections, Diseases [C] - Immune System Diseases [C20]
 
 
2017-002855-27: BonE health in ageING Women: Improvement or prevention of changes in Bone MineralDensity by Switching Antiretroviral Agents. Is there an optimal time to intervene? La salute delle ossa nell¿invecchiamento femminile: miglioramento o prevenzione delle variazioni di densit¿ minerale ossea modificando i farmaci antiretrovirali. Esiste un momento ottimale per intervenire?

Not yet recruiting
4
128
Europe
truvada, stribild, eviplera, genvoya, descovy, Odefsey, J05AR03, eviplera, J05AR18, J05AR17, J05AR19, Film-coated tablet, TRUVADA - 30 COMPRESSE RIVESTITE CON FILM IN FLACONE HDPE DA 200 MG/245 MG, STRIBILD - 150MG/150MG/200MG/245MG/ - COMPRESSA RIVESTITA CON FILM - USO ORALE - FLACONE (HDPE) - 30 COMPRESSE, EVIPLERA - 25MG RILPIVIRINA/200MG EMTRICITABINA/245MG TENOFOVIR DISOPROXIL-COMPRESSA RIVESTITA CON FILM-USO ORALE-FLACONE (HDPE) 30 COMPRESSE, GENVOYA - 150 MG / 150 MG / 200 MG /10 MG- COMPRESSA RIVESTITA CON FILM- USO ORALE- FLACONE (HDPE)- 30 COMPRESSE, DESCOVY - 200 MG/10 MG- COMPRESSA RIVESTITA CON FILM- USO ORALE- FLACONE (HDPE)- 30 COMPRESSE, ODEFSEY - 200 MG/25 MG/25 MG- COMPRESSA RIVESTITA- USO ORALE- FLACONE (HDPE) 30 COMPRESSE
UNIVERSITY HEALTH NETWORK, Gilead Sciences, Canadian HIV Trials Network
HIV infection and menopause infezione da HIV e menopausa, HIV infection and menopause infezione da HIV e menopausa, Diseases [C] - Virus Diseases [C02]
 
 
2017-004137-91: A single-arm, open-label, multicenter phase IV trial to evaluate the efficacy and safety of elvitegravir / cobicistat / emtricitabine / tenofovir alfa-namide as first-line treatment in naïve patients with HIV-1 infection with severe immunosuppression Estudio fase IV, abierto, multicéntrico, de un único brazo para evaluar la eficacia y seguridad de elvitegravir/cobicistat/emtricitabina/tenofovir alafenamida como tratamiento de primera línea en pacientes naïve con infección por VIH-1 con inmunosupresión severa

Ongoing
4
50
Europe
Tablet, Genvoya
Fundacion SEIMC-GESIDA, Gilead
AIDS SIDA, AIDS SIDA, Diseases [C] - Virus Diseases [C02]
 
 
2017-004141-24: A study in which people who have HIV and fatty liver disease, who do not drink excessive alcohol, are either asked to take the drug maraviroc on top of their normal anti-HIV medicines or to take their normal anti-HIV medicines alone

Ongoing
4
60
Europe
Celsentri, Film-coated tablet, Celsentri
Brighton and Sussex University Hospitals NHS Trus
Non-alcoholic fatty liver disease in people living with well-controlled HIV-1 infection, A disease of too much fat laid down in the liver in people who have HIV and do not drink over the recommended limit of alcohol, Diseases [C] - Digestive System Diseases [C06]
 
 
2018-000215-24: A trial to evaluate the immunogenicity of vaccine against human papillomavirus in HIV-infected men who have sex with men. GESIDA 10017 Study Ensayo clínico sobre la inmunogenicidad de la vacuna frente al virus del papiloma humano en hombres infectados por el VIH que tienen sexo con hombres. Estudio GESIDA 10017

Ongoing
4
166
Europe
Suspension for injection in pre-filled syringe, Gardasil 9
Fundacion SEIMC-GESIDA, Merck Sharp & Dohme
AIDS SIDA, AIDS SIDA, Diseases [C] - Immune System Diseases [C20]
 
 
2018-001645-14: Study to compare two treatments in patients who have never taken HIV medication randomized in different centers in Spain. (The Symtri study) Estudio para comparar dos tratamientos en pacientes que nunca han tomado medicación para el VIH asignados al azar realizado en diferentes centros de España. (Estudio SYMTRI)

Ongoing
4
316
Europe
Film-coated tablet, Symtuza, Triumeq
Spanish HIV/AIDS Research Networkº, Spanish HIV/AIDS Research Network
HIV infection Infección por VIH, HIV infection Infección por VIH, Diseases [C] - Virus Diseases [C02]
 
 
2016-000437-43: The time to protection and adherence requirements of Raltegravir with or without lamivudine in protection from HIV infection

Not yet recruiting
4
36
Europe
Raltegravir, Lamivudine, Tablet, Film-coated tablet, Raltegravir, Lamivudine
Guy's and St Thomas NHS Foundation Trust, Merck Sharp & Dhome Ltd
HIV, HIV, Diseases [C] - Virus Diseases [C02]
 
 
2017-004750-42: EFFICACY AND SAFETY OF A SIMPLIFICATION TREATMENT BASED ON DOLUTEGRAVIR AND DARUNAVIR / COBICISTAT VS USUAL TREATMENT IN SUPPRESSED HIV-1-INFECTED PATIENTS WITH MULTIDRUG RESISTANCE. Eficacia y seguridad de Dolutegravir más Darunavir/cobicistat como tratamiento de simplificación frente al tratamiento habitual en pacientes infectados por el VIH-1 virológicamente suprimidos y con resistencia a múltiples fármacos.

Ongoing
4
100
Europe
lamivudine, Efavirenz, Nevirapine, Film-coated tablet, Coated tablet, Capsule, hard, Tablet, Rezolsta, Tivicay, Ziagen, EMTRIVA, VIREAD, kivexa, Truvada, Intelence, Edurant, Atripla, Eviplera, Reyataz, Prezista, Kaletra, Norvir, Evotaz, Isentress, Stribild, Triumeq, Genvoya, Celsentri, Descovy
FUNDACIÓ LLUITA CONTRA LA SIDA, ViiV Healthcare
HIV-1 VIH-1, HIV infection Infección por VIH, Diseases [C] - Virus Diseases [C02]
 
 
 

Download Options