- 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 2 of 11.
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 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014216-35 | Sponsor Protocol Number: PG001 | Start Date*: 2009-10-20 | |||||||||||
Sponsor Name:AZIENDA SANITARIA LOCALE 4 DI TORINO | |||||||||||||
Full Title: REYAGEN study. Optimization of unboosted atazanavir dosing, when associated with tenofovir, guided by pharmacogenetics profile of HIV-patients | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003881-32 | Sponsor Protocol Number: 023-01 | Start Date*: 2007-09-20 | |||||||||||
Sponsor Name:Merck & Co, Inc | |||||||||||||
Full Title: Early Access of MK-0518 in Combination With an Optimized Background Antiretroviral Therapy (OBT) in Highly Treatment Experienced HIV-1 Infected Patients With Limited to No Treatment Options. | |||||||||||||
Medical condition: HIV-1 infected patients | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FI (Completed) ES (Completed) DE (Completed) SE (Prematurely Ended) AT (Completed) NL (Completed) LV (Completed) IT (Completed) EE (Completed) SI (Completed) IE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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 | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004631-37 | Sponsor Protocol Number: TMC114-TiDP29-C230 | Start Date*: 2009-06-25 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals | |||||||||||||
Full Title: A Phase II, open-label trial, to evaluate pharmacokinetics, safety, tolerability and antiviral activity of DRV/rtv once daily in treatment-naïve HIV 1 infected adolescents aged between 12 and < 18 ... | |||||||||||||
Medical condition: HIV-1 | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) FR (Completed) ES (Completed) IT (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002647-25 | Sponsor Protocol Number: TMC278-TiDP6-C215 | Start Date*: 2007-12-18 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals | |||||||||||||
Full Title: A Phase III, randomized, double-blind trial of TMC278 25 mg q.d. versus efavirenz 600 mg q.d. in combination with a background regimen containing 2 nucleoside/nucleotide reverse transcriptase inhib... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) FR (Completed) PT (Completed) GB (Completed) IT (Completed) | |||||||||||||
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: 2021-000738-32 | Sponsor Protocol Number: TMC114FD1HTX1001 | Start Date*: 2022-07-12 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Study to Assess the Acceptability of the Darunavir/Cobicistat (DRV/COBI) Fixed-dose Combination (FDC) Tablet in Human Immunodeficiency Virus (HIV)-1 Infected Children Aged ≥3 Years and Weighing ≥... | |||||||||||||
Medical condition: Human Immunodeficiency Virus-1 | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004358-24 | Sponsor Protocol Number: MV18406 | Start Date*: 2005-05-27 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A phase IIIb/IV randomised, controlled study evaluating an intensification treatment strategy of adding enfuvirtide (ENF) to an oral Highly Active AntiRetroviral Therapy (HAART) in treatment experi... | |||||||||||||
Medical condition: HIV Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001696-30 | Sponsor Protocol Number: TMC278-TiDP38-C213 | Start Date*: 2009-01-21 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals Ltd. | |||||||||||||
Full Title: Ensayo fase II, abierto, de un solo brazo de tratamiento para evaluar la farmacocinética, seguridad, tolerabilidad y actividad antiviral de TMC278 en pacientes adolescentes de entre 12 y 18 años de... | |||||||||||||
Medical condition: HIV-1 Infection | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002070-35 | Sponsor Protocol Number: MUC_NewEra_3.1 | Start Date*: 2009-05-13 | |||||||||||
Sponsor Name:MUC Research GmbH | |||||||||||||
Full Title: NEW ERA STUDY HIV and Eradication: A multicenter, open-label, non-randomized trial to evaluate treatment with multi-drug class (MDC) HAART and its impact on the decay rate of latently infected... | |||||||||||||
Medical condition: Human immuno-deficiency virus [HIV] disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002254-59 | Sponsor Protocol Number: GS-MC-164-0111 | Start Date*: 2005-05-06 | |||||||||||
Sponsor Name:Gilead Sciences Limited | |||||||||||||
Full Title: A phase 3, open label, randomised, parallel group study to compare the effect on prevention and resolution of treatment related adverse events of a simplified, once daily regimen of a fixed dose co... | |||||||||||||
Medical condition: Human immunodeficiency virus (HIV-1) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013795-44 | Sponsor Protocol Number: NCHECR-ENCORE1 | Start Date*: 2012-06-21 | ||||||||||||||||
Sponsor Name:The Kirby Institute (formerly National Centre in HIV Epidemiology and Clinical Research (NCHECR)), University of New Sou | ||||||||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, clinical trial to compare the safety and efficacy of reduced dose efavirenz (EFV) with standard dose EFV plus two nucleotide reverse transcriptase in... | ||||||||||||||||||
Medical condition: Human Immunodeficiency Virus infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001224-21 | Sponsor Protocol Number: MV18220 | Start Date*: 2005-01-14 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A 24 week, open label single arm study to evaluate the safety and efficacy of switching a toxicity causing antiretroviral (ARV) to enfuvirtide (ENF) and to assess resolution or improvement of ARV t... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021209-18 | Sponsor Protocol Number: TMC278-TiDP6-C222 | Start Date*: 2011-03-03 | |||||||||||
Sponsor Name:Janssen R&D Ireland | |||||||||||||
Full Title: An open-label trial with TMC278 25 mg q.d. in combination with a background regimen containing 2 nucleoside/nucleotide reverse transcriptase inhibitors in HIV-1 infected subjects, who participated ... | |||||||||||||
Medical condition: HIV-1 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) GB (Completed) SE (Completed) ES (Completed) IT (Completed) DK (Completed) AT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002008-11 | Sponsor Protocol Number: IMC-M113V-103 | Start Date*: 2021-11-24 | |||||||||||
Sponsor Name:Immunocore Limited | |||||||||||||
Full Title: An open-label dose-escalation study evaluating the safety, pharmacokinetics and antiviral activity of IMC-M113V in HLA-A*02:01-positive subjects with chronic HIV infection who are virologically sup... | |||||||||||||
Medical condition: Chronic HIV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002646-38 | Sponsor Protocol Number: TMC278-TiDP6-C209 | Start Date*: 2008-07-24 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals Limited | |||||||||||||
Full Title: A Phase III, randomized, double-blind trial of TMC278 75 mg q.d. versus efavirenz 600 mg q.d. in combination with a fixed background regimen consisting of tenofovir disoproxil fumarate and emtricit... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) AT (Completed) FR (Completed) DK (Completed) ES (Completed) GB (Completed) PT (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001939-61 | Sponsor Protocol Number: TMC114-TiDP31-C229 | Start Date*: 2008-01-16 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals Ltd. | |||||||||||||
Full Title: A randomized, open-label trial to compare the efficacy, safety and tolerability of DRV/rtv (800/100 mg) q.d. versus DRV/rtv (600/100 mg) b.i.d. in early treatment-experienced HIV-1 infected subjects. | |||||||||||||
Medical condition: HIV-1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) HU (Completed) FR (Completed) AT (Completed) ES (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003955-40 | Sponsor Protocol Number: TMC114FD1HTX1004 | Start Date*: 2022-05-10 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Single-dose, Open-label, Randomized, Crossover Pivotal Bioequivalence Study in Healthy Participants to Assess the Bioequivalence of Darunavir 600 mg in the Presence of Cobicistat 90 mg When Admin... | |||||||||||||
Medical condition: Human Immunodeficiency Virus-1 (Healthy participants) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004728-48 | Sponsor Protocol Number: MK-1439-043 | Start Date*: 2016-11-23 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp, a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Study to Evaluate the Comparative Bioavailability of the Investigational Oral Pediatric Minitablet Formulation of MK-1439 Compared to the Adult Formulation of MK-1439 in Healthy Adult Subjects | |||||||||||||
Medical condition: HIV – Human Immunodeficiency Virus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
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