- Trials with a EudraCT protocol (101)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
101 result(s) found for: Immune adherence.
Displaying page 1 of 6.
EudraCT Number: 2004-001098-25 | Sponsor Protocol Number: NAC-E-21 | Start Date*: 2004-08-23 |
Sponsor Name:Zambon SA | ||
Full Title: N-Acetylcisteine (NAC) effect on the inmunologycal system | ||
Medical condition: Postmenopausal health woman aged more than 50 years | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000087-42 | Sponsor Protocol Number: TAISTR_2016 | Start Date*: 2016-05-11 |
Sponsor Name:University College Dublin | ||
Full Title: A multicentre, prospective, single arm, open-label 96 week observational trial of the tolerability, adherence and efficacy of a dolutegravir/abacavir/lamivudine single tablet regimen in HIV-1 antib... | ||
Medical condition: Human Immunodeficiency Virus (HIV) infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-002565-17 | Sponsor Protocol Number: WODDOL | Start Date*: 2021-12-02 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: Multi-center study to evaluate virological efficacy, safety tolerability, drug exposure and patients’ reported outcomes over 48 weeks following randomization to 2-drug therapy with DTG/3TC FDC or c... | |||||||||||||
Medical condition: HIV-1-infected adult women of >18 years of age, without previous virologic failure, currently receiving an effective (HIV-RNA < 50 copies/ml) triple-drug cART, containing tenofovir (TAF or TDF) in ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002070-31 | Sponsor Protocol Number: 1337-EASI-trial | Start Date*: 2019-09-05 |
Sponsor Name:Copenhagen University Hospital Hvidovre | ||
Full Title: Adherence of a 1.600 mg single tablet 5-ASA treatment of Ulcerative colitis (EASI-trial) | ||
Medical condition: Ulcerative colitis (UC) belongs to the group of inflammatory bowel diseases. The disease course is unpredictable and characterised by chronic inflammation of the colonic mucosa, where acute attacks... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002729-21 | Sponsor Protocol Number: VUMC-ARC-GLORIA | Start Date*: 2016-04-25 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: The Glucocorticoid Low-dose Outcome in RheumatoId Arthritis Study Comparing the cost-effectiveness and safety of additional low-dose glucocorticoid in treatment strategies for elderly patients with... | |||||||||||||
Medical condition: Rheumatoid artritis | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) SK (Completed) FI (Prematurely Ended) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003311-19 | Sponsor Protocol Number: AIH-MAB | Start Date*: 2018-01-09 |
Sponsor Name:University Medical Centre Hamburg-Eppendorf | ||
Full Title: Phase IIa proof-of-principle study for the induction treatment of autoimmune hepatitis using infliximab AIH-MAB | ||
Medical condition: Autoimmune Hepatitis (AIH); rare inflammatory liver disease associated with elevated transaminases, elevated Immunoglobulin G, the presence of autoantibodies and interface hepatitis in liver histol... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004137-91 | Sponsor Protocol Number: Gesida92016 | Start Date*: 2018-01-23 | |||||||||||
Sponsor Name:Fundacion SEIMC-GESIDA | |||||||||||||
Full Title: A single-arm, open-label, multicenter phase IV trial to evaluate the efficacy and safety of elvitegravir / cobicistat / emtricitabine / tenofovir alfa-namide as first-line treatment in naïve patien... | |||||||||||||
Medical condition: AIDS | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001919-39 | Sponsor Protocol Number: 48890 | Start Date*: 2014-08-27 |
Sponsor Name:Erasmus MC | ||
Full Title: Lengthening Adalimumab Dosing Interval in IBD patients in long term remission, the LADI study | ||
Medical condition: Inflammatory bowel disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000054-22 | Sponsor Protocol Number: ML28641 | Start Date*: 2013-10-01 |
Sponsor Name:Roche Products Limited | ||
Full Title: OPEN-LABEL, PHASE IIIB STUDY TO EVALUATE THE EFFICACY AND SAFETY OF SUBCUTANEOUS TOCILIZUMAB (MONOTHERAPY OR COMBINATION THERAPY WITH METHOTREXATE OR OTHER DMARDS) IN PATIENTS WITH ACTIVE RHEUMATOI... | ||
Medical condition: Rheumatoid Arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-007935-14 | Sponsor Protocol Number: MI2-RIFART-2005 | Start Date*: 2005-03-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: RIFART | |||||||||||||
Medical condition: HIV- TB | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004354-24 | Sponsor Protocol Number: CSLCT-NHF-05-15 | Start Date*: 2006-10-26 |
Sponsor Name:CSL Limited | ||
Full Title: A Phase IV, Randomised, Observer-Blind,Comparator-Controlled, Single-Centre Study to Evaluate the Immunogenicity, Safety and Tolerability of CSL Influenza Vaccine (Enzira) (2006/2007) in Healthy Ol... | ||
Medical condition: Prophylaxis of influenza | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-004302-10 | Sponsor Protocol Number: Intercept | Start Date*: 2020-08-19 | |||||||||||
Sponsor Name:Västra Götalandsregionen, Sahlgrenska University hospital | |||||||||||||
Full Title: A randomized controlled open-label multi-center study to assess the efficacy of Tocilizumab in treatment of chronic active antibody-mediated rejection in kidney transplant recipients | |||||||||||||
Medical condition: Treatment of chronic active antibody-mediated rejection in kidney transplant recipients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005473-35 | Sponsor Protocol Number: DISCOR-RAL | Start Date*: 2008-11-12 | |||||||||||
Sponsor Name:Fundació Lluita contra la SIDA | |||||||||||||
Full Title: PILOT STUDY TO ASSESS THE ROLE OF IMMUNE ACTIVATION AND APOPTOSIS AS A MARKER FOR TREATMENT INTENSIFICATION WITH RALTEGRAVIR IN HIV-INFECTED PATIENTS ON ANTIRETROVIRAL THERAPY WITH LONG-TERM VIRAL ... | |||||||||||||
Medical condition: Infección VIH-1 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000065-73 | Sponsor Protocol Number: Sobi.Elocta-003 | Start Date*: 2017-08-23 | |||||||||||
Sponsor Name:Swedish Orphan Biovitrum AB (publ) | |||||||||||||
Full Title: A Non-Controlled, Open-Label, Multicenter, Study of Immune Tolerance Induction Performed with rFVIIIFc within a Timeframe of 60 Weeks in Severe Haemophilia A Patients with Inhibitors who have Faile... | |||||||||||||
Medical condition: Severe Haemophilia A Patients with Inhibitors who have Failed Previous Immune Tolerance Induction Therapies | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) IE (Completed) GB (Completed) BE (Completed) FR (Completed) SE (Completed) SI (Completed) IT (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: 2015-003491-69 | Sponsor Protocol Number: CACZ885DCA01 | Start Date*: 2016-04-14 | |||||||||||
Sponsor Name:Novartis Pharmaceuticals | |||||||||||||
Full Title: An Open Label Study to Assess the Safety, Tolerability and Efficacy of Canakinumab (ACZ885) in Patients Aged 4 Years or Older Diagnosed With Cryopyrin-associated Periodic Syndromes (CAPS) in Canada | |||||||||||||
Medical condition: Cryopyrin Associated Periodic Syndrome | |||||||||||||
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Population Age: Children, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016697-32 | Sponsor Protocol Number: INMI/001/09 | Start Date*: 2010-07-29 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE DELLE MALATTIE INFETTIVE LAZZARO SPALLANZANI | |||||||||||||
Full Title: PRotease-Inhibitors MOnotherapy Strategies as maintenance therapy in persons with fully suppressed HIV replication: results from an open-label randomized comparative trial (PRIMO Trial) | |||||||||||||
Medical condition: HIV infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000868-29 | Sponsor Protocol Number: V712-101 | Start Date*: 2021-10-25 | |||||||||||
Sponsor Name:DBV Technologies S.A. | |||||||||||||
Full Title: Epicutaneous Immunotherapy (EPIT) for Peanut Allergy: A Randomized, Double-Blind, Placebo-Controlled Phase I Safety Study in Adult and Pediatric Subjects | |||||||||||||
Medical condition: Peanut allergy | |||||||||||||
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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: 2022-004331-23 | Sponsor Protocol Number: FNO-RS1-TERIFIN | Start Date*: 2023-03-23 | |||||||||||
Sponsor Name:Fakultní nemocnice Ostrava | |||||||||||||
Full Title: The importance of therapeutic monitoring of teriflunomide and fingolimod in the treatment of multiple sclerosis | |||||||||||||
Medical condition: multiple sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002876-26 | Sponsor Protocol Number: 2017-002876-26 | Start Date*: 2018-10-19 | |||||||||||
Sponsor Name:South Tees Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Telomerase ACTivator to reverse Immunosenescence in Acute Coronary Syndrome: a double-blind, phase II, pilot randomised controlled trial (TACTIC) | |||||||||||||
Medical condition: Immunosenescence in patients who have had an acute coronary syndrome diagnosed within the last 6 months. | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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