- Trials with a EudraCT protocol (613)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
613 result(s) found for: - Crohn’s Disease AND HIV Infection.
Displaying page 11 of 31.
EudraCT Number: 2009-017032-41 | Sponsor Protocol Number: AI424-402 | Start Date*: 2011-08-01 | |||||||||||
Sponsor Name:Bristol Myers Squibb International Corporation | |||||||||||||
Full Title: An Open-Label, Randomized Study Evaluating a Switch from a Regimen of Two Nucleoside Reverse Transcriptase Inhibitors plus any Third Agent to either a Regimen of Atazanavir/Ritonavir Once Daily and... | |||||||||||||
Medical condition: HIV-1 infected subjects who are virologically suppressed on a regimen of 2 NRTIs plus any 3rd agent, but experience safety and/or tolerability issues to this regimen. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) ES (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001749-25 | Sponsor Protocol Number: 111474 | Start Date*: 2008-06-18 | |||||||||||
Sponsor Name:Mater Misericordiae University Hospital | |||||||||||||
Full Title: An open label safety study of fosamprenavir/ritonavir (FPV/rtv (Telzir)) administered to HIV/HCV co-infected patients over 96 weeks | |||||||||||||
Medical condition: Antiretroviral - Naive HIV-1 Infected Adults and Antiretroviral Experienced HIV-1 Infected Adults | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002694-13 | Sponsor Protocol Number: COMBOKA-07 | Start Date*: 2009-06-18 | |||||||||||
Sponsor Name:Fundación Biomédica del CHUVI | |||||||||||||
Full Title: Estudio piloto, fase IV para analizar la seguridad de los combos Truvada vs Kivexa como parte de un TARGA basado en Kaletra. Estudio COMBOKA | |||||||||||||
Medical condition: Paciente infectado por el VIH sin tratamiento antirretroviral previo | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003172-32 | Sponsor Protocol Number: MASH | Start Date*: 2018-05-23 |
Sponsor Name:Imperial College London | ||
Full Title: Maraviroc Add-On Therapy for Steatohepatitis in HIV – The MASH Study | ||
Medical condition: Non alcoholic steatohepatitis (NASH) in patients with HIV mono-infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-003160-32 | Sponsor Protocol Number: TMC125-C216 | Start Date*: 2005-12-13 | |||||||||||
Sponsor Name:Tibotec Pharmaceuticals Limited | |||||||||||||
Full Title: A Phase III randomized, double-blinded, placebo-controlled trial to investigate the efficacy, tolerability and safety of TMC125 as part of an ART including TMC114/RTV and an investigator-selected O... | |||||||||||||
Medical condition: HIV-1 infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) PT (Completed) ES (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002077-35 | Sponsor Protocol Number: 111634 | Start Date*: 2012-04-12 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
Full Title: A phase III, open, controlled study in South Africa to assess the immunogenicity, safety and reactogenicity of GSK Biologicals’ 10-valent pneumococcal conjugate vaccine administered as a 3-dose (6,... | ||||||||||||||||||
Medical condition: 3- or 2-dose primary vaccination against Streptococcus pneumoniae together with a 3-dose primary vaccination against diphtheria, tetanus, pertussis, hepatitis B and Haemophilus influenzae type b di... | ||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-002359-18 | Sponsor Protocol Number: PEDVAC | Start Date*: 2008-04-23 | |||||||||||
Sponsor Name:Swedish Institute for Infectious Disease Control | |||||||||||||
Full Title: DNA vaccination in HIV-vertically infected children | |||||||||||||
Medical condition: Pazienti con infezione verticale da HIV di eta' compresa tra 4 -16 anni di ambo i sessi. | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000816-24 | Sponsor Protocol Number: FRAN-03-001 | Start Date*: 2004-10-28 | |||||||||||
Sponsor Name:Abbott France | |||||||||||||
Full Title: A Pilot, Open-Label, Randomized, Comparative Study of the Antiviral Efficacy of Lopinavir/Ritonavir Single-Drug Regimen versus Lopinavir/Ritonavir in Combination with Lamivudine/Zidovudine in Antir... | |||||||||||||
Medical condition: HIV-1 Infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003629-86 | Sponsor Protocol Number: ING114915 | Start Date*: 2012-01-27 | |||||||||||
Sponsor Name:Viiv Healthcare | |||||||||||||
Full Title: A Phase IIIb, randomized, open-label study of the safety and efficacy of GSK1349572 (dolutegravir, DTG) 50 mg once daily compared to darunavir/ritonavir (DRV/r) 800 mg/100 mg once daily each admini... | |||||||||||||
Medical condition: HIV-1 infection in ART-naïve subjects. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005135-10 | Sponsor Protocol Number: 2005-151 | Start Date*: 2006-01-19 |
Sponsor Name:Jeppe Hagstrup Christensen | ||
Full Title: Omacor; omega-3-acid ethyl ester 90 (N-3 PUFA) and risk faktors in HIV infected patients treated with HAART with special focus on lipids | ||
Medical condition: Several investigations show that HIV infected patients have a higher risk for development of heart disease if treated with HAART. The investigation will evaluate the effect of fish oil on blood ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005078-40 | Sponsor Protocol Number: TESEC-05 | Start Date*: 2016-06-03 |
Sponsor Name:Statens Serum Institut | ||
Full Title: A Phase III trial in subjects suspected to have tuberculosis, comparing the diagnostic performance of C-Tb to QuantiFERON®-TB Gold In-Tube, in combination with a double blind randomised splitbody s... | ||
Medical condition: Children (28 days–4 years old) with suspected Mycobacterium tuberculosis infection Participants between 5–65 years old who attended the TB clinic due to suspicion of TB disease (HIV positive and HI... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2005-002849-40 | Sponsor Protocol Number: DermHivImm | Start Date*: 2006-03-29 |
Sponsor Name:Swedish Institute for Infectious Disease Control | ||
Full Title: Active immunotherapy against HIV during highly active anti-retroviral therapy followed by repeated treatment interruptions, VAC 09. | ||
Medical condition: Treatment of HIV infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020983-39 | Sponsor Protocol Number: ING114467 | Start Date*: 2010-12-30 | |||||||||||
Sponsor Name:ViiV Healthcare UK Limited | |||||||||||||
Full Title: A Phase 3, randomized, double-blind study of the safety and efficacy of GSK1349572 plus abacavir/lamivudine fixed-dose combination therapy administered once daily compared to Atripla over 96 weeks ... | |||||||||||||
Medical condition: HIV-1 infected antiretroviral therapy naive adult subjects. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) ES (Completed) GB (Completed) HU (Completed) DK (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000748-14 | Sponsor Protocol Number: M06-802 | Start Date*: 2006-08-14 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Phase 3, Randomized, Open-label Study of Lopinavir/ritonavir Tablets 800/200 mg Once-daily Versus 400/100 mg Twice-daily when Coadministered with Nucleoside/Nucleotide Reverse Transcriptase Inhib... | |||||||||||||
Medical condition: Antiretroviral experienced, HIV-1 Infection. Adequate ICD classification code not available. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) BE (Completed) ES (Completed) DE (Completed) IE (Completed) PT (Completed) GR (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003984-23 | Sponsor Protocol Number: BOC-HIV | Start Date*: 2013-04-19 | ||||||||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||||||||||||||||||
Full Title: A phase III open label study to evaluate safety and efficacy of Boceprevir-response guided therapy in controlled HIV patients with chronic hepatitis C genotype 1 infection who failed previously to ... | ||||||||||||||||||
Medical condition: HCV and HIV seropositive coinfection | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004524-65 | Sponsor Protocol Number: Inf.Q002 | Start Date*: 2015-11-30 | ||||||||||||||||
Sponsor Name:Department of Infectious Diseases | ||||||||||||||||||
Full Title: Efficacy of nonavalent vaccine against human papilloma virus (HPV ) in HIV infected sexually active men who have sex with men (MSM) | ||||||||||||||||||
Medical condition: The purpose of the study is to investigate the efficacy of a new nonavalent HPV vaccine in sexually active HIV-infected MSM. | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001228-32 | Sponsor Protocol Number: COV002 | Start Date*: 2020-05-04 | |||||||||||
Sponsor Name:CTRG | |||||||||||||
Full Title: A phase 2/3 study to determine the efficacy, safety and immunogenicity of the candidate Coronavirus Disease (COVID-19) vaccine ChAdOx1 nCoV-19 | |||||||||||||
Medical condition: SARS-CoV-2 | |||||||||||||
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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: 2019-004195-19 | Sponsor Protocol Number: CREPATS10 | Start Date*: 2020-07-07 | |||||||||||
Sponsor Name:Centre de Recherche et d’Etudes sur la Pathologie Tropicale et le Sida (CREPATS) | |||||||||||||
Full Title: A randomized comparative phase II trial evaluating the capacity of the dual combination doravirine/raltegravir to maintain virological success in HIV-1 infected patients with an HIV-RNA plasma vire... | |||||||||||||
Medical condition: HIV disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015904-24 | Sponsor Protocol Number: UKB-2009-MED-I-JKR-01 | Start Date*: 2010-10-20 |
Sponsor Name:Rheinische Friedrich-Wilhelms-Universität Bonn | ||
Full Title: An open, prospective study to compare the safety and efficacy of raltegravir vs. atazanavir / ritonavir, both in combination with tenofovir DF and emtricitabine, in the treatment of HIV-infection i... | ||
Medical condition: HIV disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004306-50 | Sponsor Protocol Number: A4001050 | Start Date*: 2007-04-23 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A MULTI-CENTER, OPEN LABEL, EXPANDED ACCESS TRIAL OF MARAVIROC | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) BE (Completed) CZ (Completed) DE (Completed) PT (Completed) ES (Completed) NL (Completed) AT (Completed) GR (Completed) IT (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
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