- Trials with a EudraCT protocol (4,404)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4,404 result(s) found for: - HIV Infection..
Displaying page 133 of 221.
EudraCT Number: 2017-004235-36 | Sponsor Protocol Number: EWO-ISO-2017/2 | Start Date*: 2018-09-27 |
Sponsor Name:Ewopharma AG | ||
Full Title: A phase 4, randomized, open label multi-centre clinical study to evaluate efficacy of Isoprinosine® in female subjects with low-grade cervical dysplasia caused by HrHPV. | ||
Medical condition: Low-grade cervical dysplasia caused by HrHPV | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-004139-11 | Sponsor Protocol Number: VAC52150EBL4001 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Janssen Vaccines & Prevention B.V. | |||||||||||||
Full Title: A Multicountry, Prospective, Clinical Safety Study of Subjects Exposed to the Candidate Ebola Vaccines Ad26.ZEBOV and/or MVA-BN-Filo | |||||||||||||
Medical condition: Ebola | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000842-16 | Sponsor Protocol Number: PIRVACoV | Start Date*: 2021-03-18 | ||||||||||||||||
Sponsor Name:Kristina Jakobsson | ||||||||||||||||||
Full Title: Does PFAS-exposure modify the risk of COVID-19 infection or the immunological response after vaccination against SARS-CoV-2? | ||||||||||||||||||
Medical condition: An observational study in healthy, differently PFAS-exposed subjects to check if PFAS modifies the immunological response to SARS-CoV-2 vaccination. The immunological response is quantified as SARS... | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001849-39 | Sponsor Protocol Number: NETs-C19 | Start Date*: 2020-05-18 |
Sponsor Name:Region Skåne | ||
Full Title: Aerosolized DNase I for the treatment of severe respiratory failure in COVID-19 - a phase 2, randomized controlled trial | ||
Medical condition: SARS-coronavirus-2 infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020551-31 | Sponsor Protocol Number: NBMT-CMV | Start Date*: 2004-09-29 | |||||||||||
Sponsor Name:Nordic Bone and Marrow Transplantation Group | |||||||||||||
Full Title: Randomized study of oral ganciclovir versus i.v. ganciclovir for preemptive therapy of cytomegalovirus infection after stem cell transplantation. | |||||||||||||
Medical condition: First cytomegalovirus DNAemia after stem cell transplantation | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001889-10 | Sponsor Protocol Number: STOIC | Start Date*: 2020-06-02 |
Sponsor Name:University of Oxford, Clinical Trials and Research Governance | ||
Full Title: Use of inhaled corticosteroids as treatment of early COVID-19 infection to prevent clinical deterioration and hospitalisation | ||
Medical condition: COVID 19 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2022-000845-34 | Sponsor Protocol Number: B1851196 | Start Date*: 2022-03-24 |
Sponsor Name:Pfizer Inc. | ||
Full Title: A COHORT STUDY TO EVALUATE IMMUNOGENICITY FOR CHILDREN AGED 5 MONTHS TO ≤60 MONTHS AT THE TIME OF CLINICAL PNEUMONIA DIAGNOSIS | ||
Medical condition: Pneumococcal Infections | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2017-002468-41 | Sponsor Protocol Number: Dial-1 | Start Date*: 2018-06-21 | |||||||||||
Sponsor Name:University Medical Center of the Johannes Gutenberg- University Mainz | |||||||||||||
Full Title: A phase I/II multicenter, open-label Study of DKN-01 to investigate the anti-tumor activity and safety of DKN-01 in Patients with Hepatocellular Carcinoma and WNT signaling Alterations | |||||||||||||
Medical condition: Hepatocellular Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006539-29 | Sponsor Protocol Number: 0 | Start Date*: 2008-03-14 |
Sponsor Name:Dept of Rheumatology, Lund University Hospital, Lund, Sweden | ||
Full Title: Effects of different anti-rheumatic treatments of arthritis on antibody response following pneumococcal vaccination using Prevenar | ||
Medical condition: Patients with rheumatic diseases (rheumatoid arthritis and spondyloarthripaties) who are going to be vaccinated with Prevenar vaccine in order to study the serological responses to two pneumococc... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006083-11 | Sponsor Protocol Number: 110699 to 110704 | Start Date*: 2009-03-23 |
Sponsor Name:GlaxoSmithKline Biologicals | ||
Full Title: An open multicentre, multicountry study to evaluate long-term antibody persistence and immune memory between Years 11 and 15 after the primary study HAB-084 in which healthy adolescents were vaccin... | ||
Medical condition: Adult subjects who received a primary vaccination course with Twinrix Adult following a two-dose schedule or Twinrix Junior following a three-dose schedule as adolescents (12-15 years) approximate... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005627-40 | Sponsor Protocol Number: P12.130 | Start Date*: 2012-09-19 |
Sponsor Name: | ||
Full Title: Comparison of effectiveness of hepatitis B revaccination schemes in healthy non-responders | ||
Medical condition: previous non-response to hepatitis B vaccine (3 vaccinations, standard schedule) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004727-36 | Sponsor Protocol Number: NR 8230-3/2004 | Start Date*: 2005-02-10 |
Sponsor Name:Charles University, 3rd Faculty of Medicine | ||
Full Title: Influence of low-dose i.v. growth hormone treatment together with glutamine supplementation in late-phase critically ill patient after multiple injury. A pilot study. | ||
Medical condition: Prolonged phase of critical illness after severe multiple trauma | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003581-20 | Sponsor Protocol Number: ALPHA | Start Date*: 2023-03-21 |
Sponsor Name:Medical University Vienna | ||
Full Title: Albendazole pharmacokinetics in plasma, intra-cystic fluid, and cystic tissue of human cystic and alveolar echinococcosis | ||
Medical condition: Albendazole is an orally administered broad-spectrum anthelmintic Drug used in treatment of human alveolar and cystic echinococcosis. To date, data on albendazole and tissue pharmacokinetics are li... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001498-63 | Sponsor Protocol Number: BIO101-CL05 | Start Date*: 2020-07-22 | ||||||||||||||||
Sponsor Name:Biophytis S.A. | ||||||||||||||||||
Full Title: Adaptive design phase 2 to 3, randomized, double- blind, multicenter, to evaluate the safety, efficacy, pharmacokinetics and pharmacodynamics of BIO101 in the prevention of the respiratory deterior... | ||||||||||||||||||
Medical condition: Confirmed infection with SARS-CoV-2 (COVID-19) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) BE (Completed) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002694-19 | Sponsor Protocol Number: 62449 | Start Date*: 2018-02-22 |
Sponsor Name:Radboud University Medical Centre | ||
Full Title: Mifepristone and misoprostol versus misoprostol alone for uterine evacuation after early pregnancy failure: a randomized double blind placebo-controlled comparison (M&M trial). | ||
Medical condition: Early pregnancy failure | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-003975-36 | Sponsor Protocol Number: 9766-CL-0107 | Start Date*: 2019-12-13 | |||||||||||
Sponsor Name:Astellas Pharma Global Development, Inc. | |||||||||||||
Full Title: A Phase 2, Open-Label, Non-Comparative, Multicenter Study to Evaluate the Safety and Tolerability, Efficacy and Pharmacokinetics of Isavuconazonium Sulfate for the Treatment of Invasive Aspergillos... | |||||||||||||
Medical condition: Invasive Aspergillosis and Invasive Mucormycosis | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) DE (Completed) ES (Ongoing) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005887-70 | Sponsor Protocol Number: REMED | Start Date*: 2021-01-28 |
Sponsor Name:Fakultní nemocnice Brno | ||
Full Title: Effect of dexamethasone in patients with ARDS and COVID-19 – prospective, multi-centre, open-label, parallel-group, randomized controlled trial | ||
Medical condition: Acute respiratory distress syndrome (ARDS) associated with COVID-19 pneumonia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-011889-28 | Sponsor Protocol Number: AMLSG09-09 | Start Date*: 2010-02-08 |
Sponsor Name:University of Ulm | ||
Full Title: Phase III study of chemotherapy in combination with ATRA with or without gemtuzumab ozogamicin in patients with acute myeloid leukemia and NPM1 gene mutation | ||
Medical condition: adult patients with AML and NPM1 mutation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-005849-16 | Sponsor Protocol Number: KIN001-203 | Start Date*: 2021-03-09 | |||||||||||
Sponsor Name:Kinarus AG | |||||||||||||
Full Title: An 8-week double-blind, randomized, placebo-controlled, phase II study evaluating the effects of oral pamapimod 150 mg with pioglitazone 10 mg daily on COVID-19 development in hospitalized patient... | |||||||||||||
Medical condition: COVID-19 development in hospitalized patients infected with SARS-CoV-2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001156-18 | Sponsor Protocol Number: PanCOVID19 | Start Date*: 2020-03-27 |
Sponsor Name:Fundación para la investigación Biomedica Hospital Universitario La Paz | ||
Full Title: Randomized clinical trial to evaluate the efficacy of different treatments in patients with COVID-19 who require hospitalization | ||
Medical condition: Patients infected with COVID19 | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: View results |
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