- Trials with a EudraCT protocol (753)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (25)
753 result(s) found for: Immunodeficiency.
Displaying page 1 of 38.
EudraCT Number: 2005-000669-21 | Sponsor Protocol Number: ML18243 | Start Date*: 2005-04-26 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: Pilot study of HIV Viral slope in naive patients treated with Enfuvirtide (ENF) based therapy compared to current standard treatment. | |||||||||||||
Medical condition: advanced HIV management | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006522-25 | Sponsor Protocol Number: ZLB06_005CR | Start Date*: 2007-02-01 | |||||||||||
Sponsor Name:CSL Behring AG | |||||||||||||
Full Title: A multicenter study on the efficacy and safety of Vivaglobin® in Previously Untreated Patients (PUPs) with Primary Immunodeficiency (PID) | |||||||||||||
Medical condition: Patients with PID diseases as Common Variable Immunodeficiency (CVID) or X-linked agammaglobulinemia ( XLA), age 1 to 70 years | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Prematurely Ended) BE (Completed) GR (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007882-19 | Sponsor Protocol Number: MI2-STAR2-2006 | Start Date*: 2006-10-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: A pilot, randomized trial to evaluate the lipid profile after antiretroviral regimens including nevirapine or atazanavir boosted with ritonavir in HIV-positive patients naive for antiretrovirals | |||||||||||||
Medical condition: immunodefic syndrome - patients naive antiretroviral therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007934-21 | Sponsor Protocol Number: MI2-INCA-2007 | Start Date*: 2007-06-27 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: Intracellular concentration of Antiretrovirals)INCA STADY | |||||||||||||
Medical condition: HIV -immunodefic syndrome- | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006188-35 | Sponsor Protocol Number: IMMUNEF | Start Date*: 2009-01-29 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | |||||||||||||
Full Title: Immunological efficacy of efavirenz based treatment in HIV-positive naive patients (a pylot study) | |||||||||||||
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: 2005-002818-38 | Sponsor Protocol Number: ML 19326 | Start Date*: 2005-07-21 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: ESPrES 500 - Evaluation of the safety profile of the new 500 mg film-coated tablet (FCT) formulation of boosted saquinavir (Invirase 500 mg) in HIV-1 infected patients | |||||||||||||
Medical condition: HIV-! / AIDS | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002437-13 | Sponsor Protocol Number: TMC114-C226 | Start Date*: 2006-05-09 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals Ltd. | |||||||||||||
Full Title: Early access of TMC114 in combination with low-dose ritonavir (RTV) and other antiretrovirals (ARVs) in highly treatment experienced HIV-1 infected subjects with limited to no treatment options. | |||||||||||||
Medical condition: HIV-1 infected patient | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001681-16 | Sponsor Protocol Number: Break | Start Date*: 2006-06-06 | |||||||||||
Sponsor Name:FONDAZIONE NADIR ONLUS | |||||||||||||
Full Title: A pilot, open label, randomised clinical trial assessing the 12 week immunological response in HIV-1 failing subjects receiving monotherapy with emtricitabine 200 mg once a day or emtricitabine 200... | |||||||||||||
Medical condition: HIV-Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004646-29 | Sponsor Protocol Number: GESIDA9016 | Start Date*: 2017-05-31 | |||||||||||
Sponsor Name:Fundación SEIMC-GESIDA | |||||||||||||
Full Title: A phase IV open- label, randomized and pilot clinical trial, designed to evaluate the potential neurotoxicity of dolutegravir/lamivudine/abacavir in neurosymptomatic HIV patients and their reversi... | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001621-26 | Sponsor Protocol Number: MALINFITA006 | Start Date*: 2006-03-13 | |||||||||||
Sponsor Name:A.U.S.L. RIMINI | |||||||||||||
Full Title: A RANDOMIZED, MULTICENTER STUDY OF USE INTERMITTENT HAART HIGHLY ACTIVE ANTIRETROVIRAL THERAPY THERAPY VERSUS CONTINUATIVE HAART THERAPY IN HIV PATIENTS | |||||||||||||
Medical condition: PATIENTS POSITIVE HIV TO LOW RISK OF DEVELOPMENT OF OPPORTUNISTIC PATHOLOGIES CORRELATED-HIV. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007935-14 | Sponsor Protocol Number: MI2-RIFART-2005 | Start Date*: 2005-03-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: RIFART | |||||||||||||
Medical condition: HIV- TB | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002582-39 | Sponsor Protocol Number: NADIR-02 | Start Date*: 2006-07-10 | |||||||||||
Sponsor Name:FONDAZIONE NADIR ONLUS | |||||||||||||
Full Title: A multicenter, randomized, prospective, controlled study to evaluate the efficacy and the tolerability of a switch to a two different-dosed, nevirapine-based HAARTs in HIV-1 infected patients with ... | |||||||||||||
Medical condition: pazienti HIV-1 positivi | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019518-25 | Sponsor Protocol Number: MENHIR | Start Date*: 2010-06-11 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: (Maraviroc ENHancement of Immunological Response): A pilot study of maraviroc as an add-on in patients with reduced CD4 cell count despite full viral suppression | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000307-26 | Sponsor Protocol Number: CeTMAd-VIH-2014 | Start Date*: 2016-06-09 | |||||||||||
Sponsor Name:Iniciativa Andaluza en Terapias Avanzadas-Fundación Pública Andaluza Progreso y Salud | |||||||||||||
Full Title: Clinical trial Phase I/II, test of concept, double blind, randomized, controlled with placebo, to evalue the safety and efficiency of the treatment with expanded adult mesenchymal stem cells from a... | |||||||||||||
Medical condition: Infection for HIV with controlled viral load and immunological discordant response | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001158-82 | Sponsor Protocol Number: GESIDA10418 | Start Date*: 2018-09-21 | |||||||||||
Sponsor Name:Fundación SEIMC-GESIDA | |||||||||||||
Full Title: Phase IV, Open Label, Randomized, Clinical Trial to Evaluate the Reversibility of abacavir/lamivudine/dolutegravir CNS-Related Neurotoxicity After Switching to tenofovir alafenamide/emtricitabine/d... | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
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: 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: 2012-000240-94 | Sponsor Protocol Number: CLEAR0001 | Start Date*: 2012-05-09 | ||||||||||||||||
Sponsor Name:Aarhus University Hospital | ||||||||||||||||||
Full Title: The Safety and Efficacy of The Histone Deacetylase Inhibitor Panobinostat for Purging HIV-1 from The Latent Reservoir (CLEAR) Study | ||||||||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV) Infection | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
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) |
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