- Trials with a EudraCT protocol (988)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
988 result(s) found for: CD4.
Displaying page 1 of 50.
EudraCT Number: 2012-002418-38 | Sponsor Protocol Number: LUMC2012-01 | Start Date*: 2012-08-21 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Prophylactic infusion of CD4 positive donor lymphocytes early after T-cell depleted allogeneic stem cell transplantation in patients with an unrelated donor | |||||||||||||
Medical condition: Patients with AML, MDS, ALL, CML in accelerated phase or blastic transformation, CLL, MM or aggressive lymphoma, who underwent a (non) myeloablative allo-SCT with an unrelated donor. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001447-19 | Sponsor Protocol Number: LUMCCD4PROTOCOL | Start Date*: 2008-05-27 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Prophylactic infusion of CD4 positive donor lymphocytes early after T-cell depleted stem cell transplantation | ||
Medical condition: Patients with AML, myelodysplasia (MDS), ALL, CML in accelerated phase or blastic transformation, CLL, MM or aggressive lymphoma, who underwent allo SCT (both myeloablative and non-myeloablative). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-005454-19 | Sponsor Protocol Number: 51858 | Start Date*: 2015-03-16 |
Sponsor Name:Erasmus MC | ||
Full Title: The Dolutegravir Antiretroviral Mono-Therapy for HIV Trial | ||
Medical condition: Evaluation of the efficacy and safety of a switch from cART to dolutegravir monotherapy in HIV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007235-40 | Sponsor Protocol Number: 2008-007235 | Start Date*: 2009-06-10 |
Sponsor Name:Department für Pädiatrie, Medizinische Universität Innsbruck | ||
Full Title: Development of Varicella-zoster virus (VZV)-specific CD4+ T cells on primary VZV infection or vaccination in renal transplant (RTX) recipients and healthy donors | ||
Medical condition: Patients (aged 24 months to 80 years) listed for renal transplantation | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2023-000061-14 | Sponsor Protocol Number: BCN04-DASA | Start Date*: 2023-05-26 | |||||||||||
Sponsor Name:Institut de Recerca Germans Trias i Pujol | |||||||||||||
Full Title: Safety and Impact of Dasatinib on Viral Persistence and Inflammation in People with HIV under Antiretroviral Treatment | |||||||||||||
Medical condition: Human immunodeficiency virus (HIV) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012499-28 | Sponsor Protocol Number: HLS01/2009 | Start Date*: 2009-08-07 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Efficacy of the treatment with hydroxychloroquine in non responders HIV-infected HAART-treated patients | |||||||||||||
Medical condition: HIV infection (immunological nonresponders). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000532-85 | Sponsor Protocol Number: T-20 Maint | Start Date*: 2004-11-12 |
Sponsor Name:Penine Acute NHS Trust, North Manchester General Hospital | ||
Full Title: Enfuvirtide induction in heavily drug experienced patients | ||
Medical condition: Heavily drug experienced HIV infected patients at switch of anti- HIV therapy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004747-23 | Sponsor Protocol Number: BPC01-001 | Start Date*: 2014-01-17 | |||||||||||
Sponsor Name:Bionor Pharma ASA | |||||||||||||
Full Title: An Open Phase I/IIa Study to Evaluate the Safety and Effect of Therapeutic HIV-1 Immunization using Vacc-4x + rhuGM-CSF, and HIV-1 Reactivation using Romidepsin, on the Viral Reservoir in Virologic... | |||||||||||||
Medical condition: HIV-infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002344-16 | Sponsor Protocol Number: RR16/209 | Start Date*: 2018-06-28 |
Sponsor Name:University of Leeds | ||
Full Title: Targeted treatment early with etanercept (biosimilar) plus methotrexate or methotrexate with T2T care for DMARD-naïve early RA patients. A prospective, longitudinal cohort study with an embedded pi... | ||
Medical condition: Rheumatoid Arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002268-26 | Sponsor Protocol Number: CTN240 | Start Date*: 2013-01-02 |
Sponsor Name:University Health Network, Toronto General Hospital | ||
Full Title: Valacyclovir in Delaying Antiretroviral Treatment Entry (VALIDATE) | ||
Medical condition: Coinfection of Human Immunodeficiency Virus and Herpes Simplex Virus type 2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-017809-11 | Sponsor Protocol Number: 112673 | Start Date*: 2010-09-27 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A phase I/IIa randomized, observer-blind, placebo-controlled, multicenter study to evaluate the safety and immunogenicity of the GSK Biologicals’ herpes zoster vaccine, gE/AS01B in comparison to pl... | |||||||||||||
Medical condition: Vaccination against herpes zoster (HZ) in adult HIV-infected subjects. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) | |||||||||||||
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: 2018-004557-24 | Sponsor Protocol Number: UKM17_0056 | Start Date*: 2019-07-29 | |||||||||||
Sponsor Name:Westfälische Wilhelms-Universität Münster c/o Universitätsklinikum Münster, Geschäftsbereich Recht u. Drittmittel | |||||||||||||
Full Title: Clarifying the mechanism of action of cladribine in relapsing multiple sclerosis | |||||||||||||
Medical condition: Multiple Sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-006102-23 | Sponsor Protocol Number: ImmuneRaRe_RF-2019-12369708 | Start Date*: 2021-10-13 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: Study of a novel combination of immunovirologic and genetic parameters in early-treated HIV-1 patients undergone to antiretroviral therapy interruption (ATI) aimed at defining an algorithm predicti... | |||||||||||||
Medical condition: HIV-1 positive subjects treated with effective antiretroviral therapy during the acute phase of HIV-1 infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006188-35 | Sponsor Protocol Number: IMMUNEF | Start Date*: 2009-01-29 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | |||||||||||||
Full Title: Immunological efficacy of efavirenz based treatment in HIV-positive naive patients (a pylot study) | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002735-23 | Sponsor Protocol Number: IPROTECT1 | Start Date*: 2013-12-04 | |||||||||||
Sponsor Name:InnaVirVax SA | |||||||||||||
Full Title: Assessment of the therapeutic properties of the VAC-3S immunoprotective vaccine when combined with standard antiretroviral therapy (ART) in the course of HIV-1 infection. A European multicenter, r... | |||||||||||||
Medical condition: Chronically infected HIV-1 patients under viral control on Anti-Retroviral therapy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000199-41 | Sponsor Protocol Number: GESIDA10918 | Start Date*: 2019-07-10 | |||||||||||
Sponsor Name:Fundación SEIMC-GESIDA | |||||||||||||
Full Title: A phase IV, multicenter, open and randomized study to evaluate the impact of the change of antiretroviral treatment from dual therapy to triple therapy on inflammation in patients with type 1 HIV i... | |||||||||||||
Medical condition: HIV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006302-13 | Sponsor Protocol Number: CT-BI Vacc-4x 2007/1 | Start Date*: 2008-06-04 | |||||||||||
Sponsor Name:Bionor Immuno AS | |||||||||||||
Full Title: A Phase II, Randomized, Double-Blind, Multicenter, Immunogenicity Study of Vacc-4x Versus Placebo in Patients Infected with HIV-1 Who Have Maintained an Adequate Response to ART | |||||||||||||
Medical condition: HIV positive subjects who have been clinically stable on antiretroviral therapy for the last six months with a viral load less than 50 copies/mL for the last six months and a CD4 cell count => 400 ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018901-12 | Sponsor Protocol Number: ADPP-002ENM-DA-017 | Start Date*: 2010-10-20 |
Sponsor Name:Medical University Graz, Department of Internal Medicine, Div. Endocrinology and Metabolism [...] | ||
Full Title: Placebo controlled study on effects of vitamin D supplementation in type 1 diabetic subjects on immunological, endocrine and metabolic parameters: Step 2 of the Austrian Diabetes Prevention Program... | ||
Medical condition: To evaluate whether vitamin D supplementation in type 1 diabetic subjects significantly alters the proportion of regulatory T-cells of all circulating CD4 positive T-cells. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002234-53 | Sponsor Protocol Number: eCLEAR-001 | Start Date*: 2016-11-14 | |||||||||||
Sponsor Name:Department of Infectious Diseases, Aarhus University Hospital | |||||||||||||
Full Title: Early administration of anti-latency reversing therapy and broadly neutralizing antibodies to limit the establishment of the HIV-1 reservoir during initiation of antiretroviral treatment - a random... | |||||||||||||
Medical condition: HIV persistence during initiation of antiretroviral therapy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
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