- Trials with a EudraCT protocol (125)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
125 result(s) found for: Darunavir.
Displaying page 1 of 7.
EudraCT Number: 2012-000649-11 | Sponsor Protocol Number: SSAT046 | Start Date*: 2012-08-22 |
Sponsor Name:St Stephen's Aids Trust | ||
Full Title: A phase IV, open-label, single centre, single-arm, pilot study to assess Cerebrospinal fluid INflammatory markers after Addition of Maraviroc to MONotherapy darunavir/ritonavir – The CINAMMON Study... | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021159-25 | Sponsor Protocol Number: SILIDAR | Start Date*: 2010-11-08 | |||||||||||
Sponsor Name:Fundació Lluita contra la Sida | |||||||||||||
Full Title: INTERACCIONES FARMACOLÓGICAS ENTRE LA SILIMARINA Y DARUNAVIR/RITONAVIR | |||||||||||||
Medical condition: Infección por el VIH. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000604-88 | Sponsor Protocol Number: SSAT028 | Start Date*: 2008-04-04 |
Sponsor Name:St Stephen's Aids Trust | ||
Full Title: A phase IV, two-arm, open-label, single-centre randomised pilot study to assess the feasibility of immeidate or deferred switching of HIV-infected individuals intolerant of efavirenz, ritonavir-boo... | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000285-30 | Sponsor Protocol Number: TMC114IFD3001 | Start Date*: 2018-01-03 | |||||||||||
Sponsor Name:Janssen Research and Development | |||||||||||||
Full Title: Continued access to darunavir/ritonavir (DRV/rtv) in HIV-1 infected adults, adolescents and children aged 3 years and above. | |||||||||||||
Medical condition: Human Immunodeficiency Virus-1 infection | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002663-10 | Sponsor Protocol Number: SSAT049 | Start Date*: 2012-11-12 |
Sponsor Name:St Stephen's AIDS Trust | ||
Full Title: A phase IV, open-label single-arm study investigating the pharmacokinetics and pharmacodynamics of the antiretroviral combination of rilpivirine and ritonavir-boosted darunavir in therapy-naive HIV... | ||
Medical condition: HIV-1 | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-013265-26 | Sponsor Protocol Number: EQUIDAR | Start Date*: 2009-11-11 | |||||||||||
Sponsor Name:Fundació Lluita contra la Sida | |||||||||||||
Full Title: INTERACCIONES FARMACOLÓGICAS ENTRE ECHINACEA PURPUREA Y DARUNAVIR/RITONAVIR | |||||||||||||
Medical condition: Infección por VIH | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015113-44 | Sponsor Protocol Number: NEAT001 | Start Date*: 2010-05-19 | |||||||||||
Sponsor Name:ANSR | |||||||||||||
Full Title: Ensayo abierto, aleatorizado, de dos años de duración, en el que se comparan dos regímenes de primera línea en sujetos infectados por el VIH que no han recibido tratamiento antirretroviral previo: ... | |||||||||||||
Medical condition: Infección por el virus de la inmunodeficiencia humana | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) FR (Completed) SE (Completed) IE (Completed) DK (Completed) PT (Completed) AT (Completed) DE (Completed) GB (Completed) PL (Completed) IT (Completed) BE (Completed) NL (Completed) HU (Completed) GR (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2011-006272-39 | Sponsor Protocol Number: DRV600 | Start Date*: 2012-04-26 | |||||||||||
Sponsor Name:Fundació Lluita contra la SIDA | |||||||||||||
Full Title: CLINICAL TRIAL TO EVALUATE THE EFFICACY, SAFETY AND ECONOMIC IMPACT OF REDUCING DOSES OF DARUNAVIR IN PATIENTS INFECTED WITH HIV TREATED WITH DARUNAVIR / RITONAVIR ONCE A DAY | |||||||||||||
Medical condition: HIV-infected patients on stable treatment with darunavir / ritonavir 800/100 mg qd plus two transcriptase inhibitors, nucleoside analogs for at least 4 weeks. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002630-36 | Sponsor Protocol Number: P1090 | Start Date*: 2014-02-25 | |||||||||||
Sponsor Name:The National Institute of Allergy and Infectious Diseases (NIAID) [...] | |||||||||||||
Full Title: A PHASE I/II, OPEN-LABEL TRIAL TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND ANTIVIRAL ACTIVITY OF ETRAVIRINE (ETR) IN ANTIRETROVIRAL (ARV) TREATMENT-EXPERIENCED HIV-1 INFECTED INFANT... | |||||||||||||
Medical condition: HIV-1 infection | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001476-37 | Sponsor Protocol Number: PENTA17 | Start Date*: 2015-12-16 | |||||||||||
Sponsor Name:Fondazione PENTA ONLUS | |||||||||||||
Full Title: SMILE: Strategy for Maintenance of HIV suppression with elvitegravir+darunavir/ritonavir in children (PENTA 17) - A two-arm, Phase 2/3 multicentre, open-label, randomised study evaluating safety ... | |||||||||||||
Medical condition: Paediatric HIV-1 Infection | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PT (Completed) GB (GB - no longer in EU/EEA) BE (Completed) DE (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000754-38 | Sponsor Protocol Number: TMC114FD2HTX3001 | Start Date*: 2015-08-19 | |||||||||||
Sponsor Name:Janssen Sciences Ireland UC | |||||||||||||
Full Title: A Phase 3, randomized, active-controlled, double-blind study to evaluate efficacy and safety of darunavir/cobicistat/emtricitabine/tenofovir alafenamide (D/C/F/TAF) once daily fixed dose combinatio... | |||||||||||||
Medical condition: Human Immunodeficiency Virus Type 1 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) GB (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005979-34 | Sponsor Protocol Number: DRV 900100 QD | Start Date*: 2008-01-22 | ||||||||||||||||
Sponsor Name:Fundació Lluita contra la SIDA | ||||||||||||||||||
Full Title: ESTUDIO PILOTO, ABIERTO, COMPARATIVO Y ALEATORIZADO PARA EVALUAR LA EFICACIA Y SEGURIDAD DE DARUNAVIR/RITONAVIR 900/100 MG UNA VEZ AL DIA COMO ESTRATEGIA DE SIMPLIFICACION DEL TRATAMIENTO ANTIRRETR... | ||||||||||||||||||
Medical condition: Pacientes con infección por el VIH. | ||||||||||||||||||
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Population Age: Adults | 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: 2007-000932-19 | Sponsor Protocol Number: SSAT 022 | Start Date*: 2008-02-25 |
Sponsor Name:St Stephen's AIDS Trust | ||
Full Title: A phase IV study to assess the feasibility of substituting double ritonavir-boosted protease inhibitors (PI) with ritonavir-boosted darunavir (DRV/r) in HIV-infected individuals with viral suppress... | ||
Medical condition: HIV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001127-69 | Sponsor Protocol Number: MK-1439-018 | Start Date*: 2015-01-07 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase 3 Multicenter, Double-Blind, Randomized, Active Comparator-Controlled Clinical Trial to Evaluate the Safety and Efficacy of Doravirine (MK-1439) 100 mg Once Daily Versus Darunavir 800 mg On... | |||||||||||||
Medical condition: Human immunodeficiency virus type 1 (HIV-1) infection in antiretroviral naïve HIV-infected patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) GB (GB - no longer in EU/EEA) DE (Completed) DK (Completed) ES (Completed) RO (Ongoing) PT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004544-37 | Sponsor Protocol Number: CREPATS-001 | Start Date*: 2009-03-24 |
Sponsor Name:CREPATS | ||
Full Title: Etude ouverte, non comparative, évaluant chez des patients infectés par le VIH-1, ayant une charge virale indétectable avec un traitement comportant un inhibiteur de la protéase potentialisé par du... | ||
Medical condition: HIV-1 Infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013287-39 | Sponsor Protocol Number: LOPIDAR | Start Date*: 2009-09-25 | |||||||||||
Sponsor Name:Fundació Lluita contra la SIDA | |||||||||||||
Full Title: RANDOMISED AND PROSPECTIVE CLINICAL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF LOPINAVIR/RITONAVIR MONOTHERAPY VS DARUNAVIR/RITONAVIR MONOTHERAPIES AS SIMPLIFICATION SWITCHING STRATEGIES OF PI/NN... | |||||||||||||
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: 2010-021785-30 | Sponsor Protocol Number: A4001095 | Start Date*: 2011-12-07 | |||||||||||
Sponsor Name:ViiV Healthcare UK Limited | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE BLIND, COMPARATIVE TRIAL OF MARAVIROC + DARUNAVIR/RITONAVIR VERSUS EMTRICITABINE/TENOFOVIR + DARUNAVIR/RITONAVIR FOR THE TREATMENT OF ANTIRETROVIRAL NAÏVE HIV INFE... | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) SE (Prematurely Ended) FI (Prematurely Ended) BE (Prematurely Ended) ES (Prematurely Ended) GB (Prematurely Ended) AT (Completed) DK (Prematurely Ended) NL (Completed) PT (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000447-40 | Sponsor Protocol Number: FARM12FEXH(TESS) | Start Date*: 2017-07-12 | ||||||||||||||||
Sponsor Name:ASST SANTI PAOLO E CARLO | ||||||||||||||||||
Full Title: IMPACT ON BONE MINERAL DENSITY (BMD) OF TDF-SPARING ANTIRETROVIRAL REGIMENS IN HIV-POSITIVE MENOPAUSAL WOMEN AFFECTED BY OSTEOPENIA: THE TENOFOVIR SPARING STRATEGY (TESS) STUDY | ||||||||||||||||||
Medical condition: HIV-positive women affected by osteopenia. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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