- Trials with a EudraCT protocol (2,320)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (44)
2,320 result(s) found for: Virus infection.
Displaying page 1 of 116.
EudraCT Number: 2008-008556-16 | Sponsor Protocol Number: PRADA | Start Date*: 2009-07-13 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: Pharmacokinetic and safety study of RAltegravir and atazanavir in a once DAily dose regimen in HIV-1 in-fected patients (PRADA) | |||||||||||||
Medical condition: HIV infected patients | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003463-31 | Sponsor Protocol Number: P04999 | Start Date*: 2010-08-23 | ||||||||||||||||
Sponsor Name:Schering-Plough Research Institute | ||||||||||||||||||
Full Title: COVER- Registro de observación continua tras exposición Vicriviroc (VCV) | ||||||||||||||||||
Medical condition: Síndrome de inmunodeficiencia adquirida (SIDA) | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000390-59 | Sponsor Protocol Number: P03802 | Start Date*: 2004-07-15 | |||||||||||
Sponsor Name:SCHERING-PLOUGH | |||||||||||||
Full Title: Safety and efficacy of SCH 417690 in HIV-infected treatment-naive subjects | |||||||||||||
Medical condition: HIV-1 infected naive subject | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001111-39 | Sponsor Protocol Number: UMCN-AKF13.03 | Start Date*: 2014-12-08 | ||||||||||||||||
Sponsor Name:Radboud University Nijmegen Medical Center | ||||||||||||||||||
Full Title: Once daily DArunavir/ritonavir in HIV-infected children 6-12 years old: a PHarmacokiNEtic validation of model-based dosing recommendations (DAPHNE) | ||||||||||||||||||
Medical condition: HIV infected children treated with darunavir | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002319-13 | Sponsor Protocol Number: EfaRiLipidomics | Start Date*: 2015-08-28 | |||||||||||
Sponsor Name:Fundació Hospital Vall Hebron Institut de Recerca | |||||||||||||
Full Title: Outcome of plasma lipid profile in patients switching from Atripla® to Eviplera® compared to continuing on Atripla® (EfaRiLipidomics) | |||||||||||||
Medical condition: HIV-1 Infection | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000526-48 | Sponsor Protocol Number: A.S.T.R.A. | Start Date*: 2007-03-06 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Randomized, monocentric trial on sintoms, adherence,toxicity of alternate antiretrovirale regimen | |||||||||||||
Medical condition: PT HIV-1 positive and naive to antiretroviral drug | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001591-33 | Sponsor Protocol Number: DoRSwitch.21 | Start Date*: 2022-10-06 | |||||||||||
Sponsor Name:Fundació Clinic per a la Recerca Biomèdica | |||||||||||||
Full Title: Open-label, single-arm, unicenter and Pilot Study of a Switch strategy from Etravirine (ETR) to Doravirine (DOR) in Virologically-Suppressed HIV-1 Infected Adults With ETR-Resistance | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007018-12 | Sponsor Protocol Number: QUINAVIR | Start Date*: 2008-06-23 | |||||||||||
Sponsor Name:Carlos Alonso-Villaverde Lozano, Hospital Universitari Sant Joan de Reus | |||||||||||||
Full Title: “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... | |||||||||||||
Medical condition: Infección por el virus de la inmunodeficiencia adquirida | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005330-37 | Sponsor Protocol Number: HLS01/2007 | Start Date*: 2008-02-20 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Pharmacokinetics of atazanavir at the dose of 300mg or 400mg in subjects with HIV-1 infection and non-decompensated hepatic cirrhosis (Child-Pugh A o B, Metavir F4), crossover study. | |||||||||||||
Medical condition: HIV-1 Infection | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010912-14 | Sponsor Protocol Number: mi2-maicol-08 | Start Date*: 2009-04-06 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | ||||||||||||||||||
Full Title: MAraviroc In HIV/ HCV Coinfection and Liver fibrosis | ||||||||||||||||||
Medical condition: HIV/ HCV Coinfection | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001058-26 | Sponsor Protocol Number: P04285 | Start Date*: 2006-01-09 | |||||||||||
Sponsor Name:Schering-Plough Research Institute | |||||||||||||
Full Title: Vicriviroc (SCH 417690) in Combination Treatment with Optimized ART Regimen in Experienced Subjects (VICTOR-E2) | |||||||||||||
Medical condition: HIV infection (mixed X4/R5 torpism) with previous therapy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) PT (Prematurely Ended) DE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011273-32 | Sponsor Protocol Number: 149/09 | Start Date*: 2009-05-07 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Pilot study for the evaluation of the safety and the feasibility of treatment simplification to atazanavir/ritonavir + lamivudine in patients on stable treatment with two NRTIs + atazanavir/ritonav... | |||||||||||||
Medical condition: HIV | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005192-14 | Sponsor Protocol Number: HLS03/2012 | Start Date*: 2013-01-31 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Strategic study of dual-therapy with darunavir/ritonavir and rilpivirine QD versus triple-therapy in patients with suppressed viral load: virological efficacy and evaluation of non-HIV related morb... | |||||||||||||
Medical condition: HIV infection. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005786-11 | Sponsor Protocol Number: GS-ES-164-0154 | Start Date*: 2006-03-28 | |||||||||||
Sponsor Name:Gilead Sciences S.L. | |||||||||||||
Full Title: Pilot phase IV, multicenter, randomized, open-label and controlled study to assess the evolution of peripheral body fat distribution after switching from AZT containing backbone to Truvada in HIV-1... | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV-1) infection | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006716-30 | Sponsor Protocol Number: 128/2006/O/Sper | Start Date*: 2006-12-19 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: 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 ... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005057-36 | Sponsor Protocol Number: HCQ-01 | Start Date*: 2008-02-22 | |||||||||||
Sponsor Name:Medical Research Council | |||||||||||||
Full Title: Evaluation of the efficacy of hydroxychloroquine in decreasing immune activation in asymptomatic HIV-infected patients (HCQ-01) | |||||||||||||
Medical condition: HIV infection | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016705-42 | Sponsor Protocol Number: DRV-exp | Start Date*: 2009-11-10 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE DELLE MALATTIE INFETTIVE LAZZARO SPALLANZANI | |||||||||||||
Full Title: Pilot study on efficacy of a simplification strategy from DRV/r 600/100 mg BID to DRV/r 800/100mg QD + OBT in HIV-positive patients HAART-experienced with virological response. | |||||||||||||
Medical condition: HIV infection | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002460-98 | Sponsor Protocol Number: VS411-C201 | Start Date*: 2008-02-07 | |||||||||||
Sponsor Name:VIROSTATICS, SRL | |||||||||||||
Full Title: A randomized double-blind dose-finding multi-centre phase IIa study with VS411 for HIV-1 infection. | |||||||||||||
Medical condition: HIV-1 infection | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002978-35 | Sponsor Protocol Number: HLS05/2008 | Start Date*: 2008-07-24 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: 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 | |||||||||||||
Medical condition: First line therapy of HIV-1-infected patients. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005405-21 | Sponsor Protocol Number: UMCN-AKF 07.06 | Start Date*: 2008-01-21 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: The influence of Raltegravir (MK_0518) on the pharmacokinetics of single-dose Lamotrigine in healthy male subjects (GRANOLA) | |||||||||||||
Medical condition: HIV infection | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
