- 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 6 of 11.
EudraCT Number: 2011-001871-37 | Sponsor Protocol Number: LTN0001 | Start Date*: 2011-06-06 | |||||||||||||||||||||
Sponsor Name:Department of Infectious Diseases - Aarhus University Hospital | |||||||||||||||||||||||
Full Title: Immune Response to Bivalent or Tetravalent Human Papillomavirus Vaccine in HIV infected Adults | |||||||||||||||||||||||
Medical condition: HIV Human Papilloma Virus | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003081-27 | Sponsor Protocol Number: EHVAT01/ANRSVRI05 | Start Date*: 2018-02-19 | |||||||||||
Sponsor Name:Inserm-ANRS | |||||||||||||
Full Title: EHVA T01(European HIV Vaccine Alliance Therapeutic Trial 01)/ANRS VRI05: A Phase I/II randomised therapeutic HIV vaccine trial in individuals who started antiretrovirals during primary or chronic i... | |||||||||||||
Medical condition: Human Immunodeficiency Virus (HIV) infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Prematurely Ended) ES (Prematurely Ended) 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: 2010-024537-23 | Sponsor Protocol Number: AI424-451 | Start Date*: 2011-06-22 | |||||||||||
Sponsor Name:Bristol Myers Squibb International Corporation | |||||||||||||
Full Title: A Prospective Single Arm, Open-Label, International, Multicenter Study to Evaluate the Safety, Efficacy and Pharmacokinetics of Atazanavir (ATV) Powder boosted with Ritonavir (RTV) with an Optimize... | |||||||||||||
Medical condition: HIV in paediatric population | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) PL (Completed) ES (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003614-14 | Sponsor Protocol Number: RAINBOW | Start Date*: 2019-12-16 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LE MALATTIE INFETTIVE "LAZZARO SPALLANZANI" | |||||||||||||
Full Title: Feasibility, efficacy and safety of rapid (within 7 days from HIV diagnosis) antiretroviral initiation strategy based on bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in HIV-infected na... | |||||||||||||
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: 2005-006179-11 | Sponsor Protocol Number: TMC114-C212 | Start Date*: 2006-08-14 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals Ltd. | |||||||||||||
Full Title: A Phase II, open-label trial, to investigate pharmacokinetics, safety, tolerability and antiviral activity of TMC114/rtv b.i.d. in treatment-experienced HIV-1 infected children and adolescents. | |||||||||||||
Medical condition: HIV-1 | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Ongoing) IT (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002385-49 | Sponsor Protocol Number: IN-UK-311-3956 | Start Date*: 2017-11-27 | ||||||||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: IN-UK-311-3956: A Feasibility Study of the Switch of Tenofovir disoproxil fumarate to Tenofovir alafenamide fumarate and the Effect on Glomerular Function in Chronic Hepatitis B and HIV co-infected... | ||||||||||||||||||
Medical condition: HIV and Hepatitis B | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001165-16 | Sponsor Protocol Number: TITAN-001 | Start Date*: 2018-11-28 | |||||||||||
Sponsor Name:Department of infectious Diseases, Aarhus University Hospital | |||||||||||||
Full Title: Combining a TLR9 agonist with broadly neutralizing antibodies for reservoir reduction and immunological control of HIV infection: An investigator-initiated randomized, placebo-controlled, phase IIa... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006873-33 | Sponsor Protocol Number: A4001031 | Start Date*: 2009-02-23 | |||||||||||
Sponsor Name:Pfizer, S.A. | |||||||||||||
Full Title: ENSAYO ABIERTO, MULTICÉNTRICO, DE FARMACOCINÉTICA POR ADMINISTRACIÓN DE DOSIS MÚLTIPLES Y DE SEGURIDAD Y EFICACIA DE 48 SEMANAS DE MARAVIROC EN COMBINACIÓN CON UN TRATAMIENTO DE BASE OPTIMIZADO PAR... | |||||||||||||
Medical condition: Tratamiento VIH | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PT (Completed) IT (Completed) GB (Prematurely Ended) FR (Ongoing) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000446-20 | Sponsor Protocol Number: SPARTAC 04/2/025 | Start Date*: 2006-07-28 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: A multi-centre randomised trial of therapeutic intervention at primary HIV-1 infection | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003951-13 | Sponsor Protocol Number: ANRS177DUETTO | Start Date*: 2021-04-19 | |||||||||||
Sponsor Name:INSERM-ANRS | |||||||||||||
Full Title: Randomized, open-label and multicentric trial evaluating the non-inferiority of antiretroviral dual therapy taken 4 consecutive days per week versus antiretroviral dual therapy 7/7 days per week in... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004553-29 | Sponsor Protocol Number: ML21287 | Start Date*: 2007-10-23 | |||||||||||
Sponsor Name:Roche | |||||||||||||
Full Title: Essai en ouvert, randomisé et multicentrique évaluant l’efficacité et la tolérance de l’association de l’Enfuvirtide en cure d’induction de 3 mois à un traitement optimisé (TO) comprenant au moins ... | |||||||||||||
Medical condition: Patients séropositifs VIH-1 en échec de lignes de traitements antirétroviraux antérieurs | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000360-34 | Sponsor Protocol Number: DUA-1463-SPI-0320-I | Start Date*: 2015-06-26 | |||||||||||
Sponsor Name:Technische Universitaet Muenchen Fakultaet fuer Medizin | |||||||||||||
Full Title: DUALIS A prospective, multicenter, randomized, open-label trial to assess the safety, tolerability and efficacy of dual therapy with boosted Darunavir + Dolutegravir when switching from standard o... | |||||||||||||
Medical condition: HIV-Infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003040-25 | Sponsor Protocol Number: ANRS176 | Start Date*: 2022-09-01 | |||||||||||
Sponsor Name:Inserm-ANRS | |||||||||||||
Full Title: A randomised phase II placebo-controlled trial of ART plus dual long-acting HIV-specific broadly neutralising antibodies (bNAbs) vs ART plus placebo during primary HIV-1 infection to study the impa... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004809-24 | Sponsor Protocol Number: JF006 | Start Date*: 2015-06-05 | ||||||||||||||||
Sponsor Name:Guy's & St. Thomas' NHS Foundation Trust | ||||||||||||||||||
Full Title: The role of Home packs of HIV Post-Exposure Prophylaxis for sexual exposure (PEPSE) to improve the speed and appropriate uptake of PEPSE in high risk individuals | ||||||||||||||||||
Medical condition: HIV | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004160-35 | Sponsor Protocol Number: ISR-003 | Start Date*: 2018-03-13 |
Sponsor Name:Immune System Regulation AB (ISR) | ||
Full Title: A prospective, randomised, controlled, parallel arm, open phase IIa study on the efficacy and safety of the GnRH analogue triptorelin for HIV-1 reservoir reduction in HIV-1 infected male adult pati... | ||
Medical condition: HIV-1 infection | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: SE (Ongoing) DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-003364-19 | Sponsor Protocol Number: AI424376 | Start Date*: 2009-01-09 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Multicenter, Randomized, Open-Label, Active-Controlled Pilot Study to Evaluate the Safety and Antiretroviral Activity of Unboosted Atazanavir BID Plus Raltegravir BID and Boosted Atazanavir QD in... | |||||||||||||
Medical condition: HIV, COMBINATION THERAPY | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-013126-16 | Sponsor Protocol Number: TMC125-TiDP35-C239 | Start Date*: 2009-11-09 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals c/o Tibotec BVBA | |||||||||||||
Full Title: Continued access to etravirine in treatment experienced HIV-1 infected children and adolescents. | |||||||||||||
Medical condition: HIV-1 Infection | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Ongoing) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002880-26 | Sponsor Protocol Number: AI424-128 | Start Date*: 2005-04-06 |
Sponsor Name:Bristol-Myers Squibb International Corporation | ||
Full Title: A Phase IV, Multi-center, Cross-sectional study to evaluate the I50L substitution among subjects experiencing virologic failure on a HAART regimen containing atazanavir (ATV) Protocol: version 2.0... | ||
Medical condition: Subjects experiencing virologic failure after a HAART regimen containing ATV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-015884-15 | Sponsor Protocol Number: IMPAACT-P1066 | Start Date*: 2011-06-30 | |||||||||||
Sponsor Name:The National Institute of Allergy and Infectious Diseases (NIAID) and The Eunice Kennedy Shriver NICHD | |||||||||||||
Full Title: A Phase I/II, Multicenter, Open-Label, Non comparative Study of the International Maternal, Pediatric, Adolescent AIDS Clinical Trials (IMPAACT) Group to Evaluate the Safety, Tolerability, Pharmac... | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
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