- Trials with a EudraCT protocol (211)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
211 result(s) found for: Human T-lymphotropic virus 2.
Displaying page 3 of 11.
EudraCT Number: 2018-000497-30 | Sponsor Protocol Number: FIS-VED-2017-01 | Start Date*: 2018-05-28 | |||||||||||
Sponsor Name:Fundación Pública Andaluza para la Gestión en Salud de Sevilla (FISEVI) | |||||||||||||
Full Title: Phase II clinical trial to evaluate the safety and efficacy of Vedolizumab combined with antiretroviral treatment to achieve functional healing in people infected with HIV-1 without previous antire... | |||||||||||||
Medical condition: Adult patients infected with HIV and without previous antiretroviral treatment. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004433-18 | Sponsor Protocol Number: PENTA 15 | Start Date*: 2006-02-13 | |||||||||||
Sponsor Name:PENTA | |||||||||||||
Full Title: PLASMA PHARMACOKINETIC STUDY OF ONCE VERSUS TWICE DAILY ABACAVIR AS PART OF COMBINATION ANTIRETROVIRAL THERAPY IN CHILDREN WITH HIV-1 INFECTION AGED 3 MONTHS TO < 36 MONTHS | |||||||||||||
Medical condition: Paediatric HIV infection | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004627-28 | Sponsor Protocol Number: MI2-COAT-2008 | Start Date*: 2009-02-25 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | ||||||||||||||||||
Full Title: Switch from a current boosted rtv PI to ATV/rtv based HAART regimen. Effect on metabolic and hepatic toxicity in HIV/HCV coinfected patients (COAT Study). | ||||||||||||||||||
Medical condition: co-infection HIV-1/HCV | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005023-15 | Sponsor Protocol Number: ANRS HB 04 | Start Date*: 2008-03-10 | |||||||||||
Sponsor Name:ANRS | |||||||||||||
Full Title: ETUDE MULTICENTRIQUE RANDOMISEE, DE PHASE III, COMPARANT L’IMMUNOGENICITE D’UN SCHEMA VACCINAL RENFORCE CONTRE LE VHB (40 µg à S0, S4, et S24), A UN SCHEMA CLASSIQUE (20 µg à S0, S4, et S24), CHEZ ... | |||||||||||||
Medical condition: L'essai ANRS HB 04 B-BOOST compare l’immunogénicité d’un schéma vaccinal renforcé contre le VHB (40 µg à S0, S4, et S24), à un schéma classique (20 µg à S0, S4 et S24), chez des patients infectés p... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000793-45 | Sponsor Protocol Number: TMC114-C209 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals Ltd. | |||||||||||||
Full Title: Open-label safety study of TMC114 in combination with low dose RTV and other ARVs in highly experienced HIV-1 infected patients with limited or no treatment options. | |||||||||||||
Medical condition: HIV-1 infected patient | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002955-85 | Sponsor Protocol Number: AVICCI001 | Start Date*: 2016-01-21 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: A feasibility study to assess the effects of AntiretroViral Intensification with Cenicriviroc for the management of HIV-associated Cognitive Impairment. The AVICCI study | |||||||||||||
Medical condition: Human Immunodeficiency Virus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004331-39 | Sponsor Protocol Number: INDOOR | Start Date*: 2015-01-02 | |||||||||||
Sponsor Name:Fundació Vall Hebron Institut de Recerca | |||||||||||||
Full Title: HIV Reservoir Dynamics After Switching To Dolutegravir in Patients on a PI/r Based Regimen. A Phase IV Open Randomized Trial | |||||||||||||
Medical condition: HIV-1 Infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-018097-64 | Sponsor Protocol Number: 114083 | Start Date*: 2010-03-03 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: Long-term follow-up of study participants from GlaxoSmithKline (GSK) Biologicals’-sponsored clinical trials evaluating Human Immunodeficiency Virus vaccine [F4co (p24-RT-Nef-p17)/AS01B vaccine] (73... | |||||||||||||
Medical condition: ART-treated and ART-naïve HIV-infected adults (ART: anti-retroviral therapy) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003501-10 | Sponsor Protocol Number: 3883 | Start Date*: 2013-04-24 | |||||||||||
Sponsor Name:Vall d'Hebron Institut de Recerca (VHIR) | |||||||||||||
Full Title: Efficacy of dual antiretroviral treatment with maraviroc plus ritonavir-boosted darunavir in early rescue therapy in patients with HIV-1 infection: pilot, multicenter, randomized, controlled and op... | |||||||||||||
Medical condition: Adult patients with HIV-1 infection that present virologic failure to first-line antiretroviral treatment. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000243-50 | Sponsor Protocol Number: INS-2DR | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LE MALATTIE INFETTIVE "LAZZARO SPALLANZANI" | |||||||||||||
Full Title: Understanding the Impact of HIV-DNA resistance mutations detected by NGS in Simplification strategies to 2-Drug Regimens for patients virologically suppressed with previous failures and/or previous... | |||||||||||||
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: 2010-019773-15 | Sponsor Protocol Number: CLI-107-14 | Start Date*: 2010-07-20 | |||||||||||
Sponsor Name:CYTHERIS | |||||||||||||
Full Title: A multicenter, open-labeled, controlled, randomized study of recombinant Interleukin-7 (CYT107) treatment to restore and maintain CD4 T-lymphocyte counts above 500 cells/�L in HIV-infected patients... | |||||||||||||
Medical condition: HIV infected patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004654-28 | Sponsor Protocol Number: GS-ES-164-0151 | Start Date*: 2006-08-28 | |||||||||||
Sponsor Name:Gilead Sciences, S.L. | |||||||||||||
Full Title: Phase IV, multicenter, randomized, open-label pilot study of Truvada or Emtricitabine alone versus HAART interruption in HIV-infected patients who need to interrupt HAART and who are infected with ... | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV-1) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000437-43 | Sponsor Protocol Number: JF-007 | Start Date*: 2017-04-28 | |||||||||||
Sponsor Name:Guy's and St Thomas NHS Foundation Trust | |||||||||||||
Full Title: The time to protection and adherence requirements of Raltegravir with or without lamivudine in protection from HIV infection | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006448-23 | Sponsor Protocol Number: PIVOT | Start Date*: 2008-12-15 | |||||||||||
Sponsor Name:Medical Research Council | |||||||||||||
Full Title: A randomised controlled trial of a strategy of switching to boosted protease inhibitor monotherapy versus continuing combination antiretroviral therapy for the long-term management of HIV-1 infecte... | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003186-28 | Sponsor Protocol Number: BPC01_002 | Start Date*: 2016-01-13 | |||||||||||
Sponsor Name:Bionor Pharma ASA | |||||||||||||
Full Title: BIOSKILL: Studying Vacc-4x, an HIV therapeutic vaccine, an assessment of immune-mediated anti-viral effects, when administered with adjuvant GM-CSF prior to HIV latent reservoir activation by the H... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003163-31 | Sponsor Protocol Number: AI424-328 | Start Date*: 2006-11-28 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: Open-Label, Multiple-Dose, Drug Interaction Study to Assess the Effect of Famotidine with or without Tenofovir on the Pharmacokinetics of Atazanavir when given with Ritonavir in HIV-Infected Subjec... | |||||||||||||
Medical condition: HIV infected Subjects | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002314-39 | Sponsor Protocol Number: Semaglutide2019 | Start Date*: 2021-07-08 | ||||||||||||||||
Sponsor Name:University College Dublin (UCD) | ||||||||||||||||||
Full Title: A randomised, controlled, parallel group, open-label trial evaluating the impact of treatment with the GLP-1 analogue semaglutide on weight loss in people living with HIV and obesity | ||||||||||||||||||
Medical condition: Human immunodeficiency virus (HIV) Infection and Obesity | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001023-23 | Sponsor Protocol Number: CUTHIVAC002 | Start Date*: 2015-08-24 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: A Phase I clinical trial to assess the safety and immunogenicity of HIV DNA-C CN54ENV immunisations administered via the Intramuscular and Intradermal methods with and without electroporation follo... | |||||||||||||
Medical condition: HIV prophylaxis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004476-12 | Sponsor Protocol Number: NCHECR001 | Start Date*: 2007-07-10 | |||||||||||
Sponsor Name:University of New South Wales | |||||||||||||
Full Title: A randomised open-label study comparing the safety and efficacy of three different combination antiretroviral regimens as initial therapy for HIV infection. | |||||||||||||
Medical condition: Chronic HIV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) IE (Completed) DE (Ongoing) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001348-39 | Sponsor Protocol Number: SEM-TAR-01-2014 | Start Date*: 2014-12-03 | ||||||||||||||||
Sponsor Name:Fundación pública andaluza para la gestión de la investigación en salud de Sevilla (FISEVI) | ||||||||||||||||||
Full Title: A Phase II, randomized clinical trial to assess the impact of antiretroviral therapy over viral load in seminal fluid in antiretroviral-naive HIV-positive patients | ||||||||||||||||||
Medical condition: HIV-1 infection | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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