- Trials with a EudraCT protocol (615)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
615 result(s) found for: - Crohn’s Disease AND HIV Infection.
Displaying page 1 of 31.
| EudraCT Number: 2010-022775-57 | Sponsor Protocol Number: JF002 | Start Date*: 2011-06-09 | ||||||||||||||||||||||||||
| Sponsor Name:Guy's and St Thomas' NHS Foundation Trust | ||||||||||||||||||||||||||||
| Full Title: Effects of Vitamin D supplementation on Vitamin D levels and immune activation in HIV infected individuals on antiretroviral therapy-A pilot study. | ||||||||||||||||||||||||||||
| Medical condition: HIV infected patients with vitamin D defficiency | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| 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 | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022120-72 | Sponsor Protocol Number: JF-001 | Start Date*: 2010-12-17 | ||||||||||||||||||||||||||
| Sponsor Name:Guy's & St. Thomas' NHS Foundation Trust | ||||||||||||||||||||||||||||
| Full Title: The metabolic impact of Darunavir/ritonavir maintenance monotherapy after successful viral suppression with standard Atripla in HIV-1-infected patients (MIDAs). | ||||||||||||||||||||||||||||
| Medical condition: HIV | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
| 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 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) GB (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) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| 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. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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 | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (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 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (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 | ||||||||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-004140-30 | Sponsor Protocol Number: DORAVIPEP | Start Date*: 2020-06-10 | |||||||||||
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
| Full Title: Evaluation of (doravirine / lamivudine / tenofovir disoproxil fumarate) (Delstrigo®) as a New Strategy for non-occupational Post Exposure Prophylaxis, a Prospective Open Label Study. | |||||||||||||
| Medical condition: non-occupational Post Exposure Prophylaxis of HIV | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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 | |||||||||||||
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| 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: 2009-016705-42 | 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 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-011662-28 | Sponsor Protocol Number: ABRACADABRA | Start Date*: 2009-11-26 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | |||||||||||||
| Full Title: Exploratory study on inflammatory immune response related to endothelial dysfunction in HIV-infected na�ve patients treated with abacavir compared to tenofovir-based regimens. | |||||||||||||
| Medical condition: HIV INFECTION | |||||||||||||
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| 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) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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 | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-004120-39 | Sponsor Protocol Number: A5271010 | Start Date*: 2006-02-08 | |||||||||||
| Sponsor Name:Pfizer Pharma GmbH | |||||||||||||
| Full Title: A randomised, double blind, placebo-controlled, multicentre study in asymptomatic HIV infected patients to investigate pharmacodynamics, pharmacokinetics, safety and toleration of UK-453,061 | |||||||||||||
| Medical condition: HIV | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-002661-30 | Sponsor Protocol Number: HLS/MVC01/2008 | Start Date*: 2008-06-13 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
| Full Title: Use of Maraviroc (MVC) in immunogical non-responder HIV-1-infected patients. | |||||||||||||
| Medical condition: HIV-1-infected HAART-treated patients that reached a virologic suppression without a reconstitution of their immune system. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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 | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-001164-32 | Sponsor Protocol Number: KISS | Start Date*: 2005-04-05 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
| Full Title: A RANDOMIZED STUDY, POSPECTIVE, ON THREE DIFFERENT STRATEGY OF HIV POSITIVE NAIVE FOR THE ANTIRETROVIRAL THERAPY | |||||||||||||
| Medical condition: HIV INFECTION CHRONIC AND NAIVE. VIREMIE > 10.000 COPIE/ML AND/OR CD4< 350 CELL/01 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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