- Trials with a EudraCT protocol (44,394)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,394 result(s) found.
Displaying page 2,216 of 2,220.
| EudraCT Number: 2016-000206-10 | Sponsor Protocol Number: HLX02-BC01 | Start Date*: 2017-08-31 | |||||||||||
| Sponsor Name:Shanghai Henlius Biotech Inc. | |||||||||||||
| Full Title: Double-blind, Randomized, Multicenter, Phase III Clinical Study to Compare the Efficacy and to Evaluate the Safety and Immunogenicity of Trastuzumab Biosimilar HLX02 and EU-sourced Herceptin® in Pr... | |||||||||||||
| Medical condition: Previously Untreated Overexpressing metastasic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000319-21 | Sponsor Protocol Number: ClonDO | Start Date*: 2021-12-20 |
| Sponsor Name:Charité – Universitätsmedizin Berlin | ||
| Full Title: Treating Nightmares in Posttraumatic Stress Disorder with the α-adrenergic Agents Clonidine and Doxazosin: A Randomized-Controlled Feasibility Study (ClonDoTrial) | ||
| Medical condition: Posttraumatic Stress Disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-001117-86 | Sponsor Protocol Number: 16/0340 | Start Date*: 2017-07-25 |
| Sponsor Name:University College London | ||
| Full Title: A phase IV, prospective, randomised single-blind UK multicentre non-inferiority trial of low-dose versus standard dose rituximab for prevention of relapses in acquired TTP | ||
| Medical condition: Acquired thrombotic thrombocytopenic purpura | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-004697-25 | Sponsor Protocol Number: V528Nov22 | Start Date*: 2020-09-14 | |||||||||||
| Sponsor Name:The Rotunda Hospital | |||||||||||||
| Full Title: The Home Induction trial: A randomised open-label trial to assess outpatient induction of labour, and compare efficacy of Propess vs Dilapan-S® for induction of labour at 39 weeks’ gestation in nor... | |||||||||||||
| Medical condition: Normal risk nulliparous women who have no pregnancy-related or medical contraindication to Induction of Labour | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000962-14 | Sponsor Protocol Number: CCM-RNT-202101 | Start Date*: 2021-07-02 | |||||||||||
| Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
| Full Title: A Monocenter, Open Label Study to Evaluate the Safety and Efficacy of Daratumumab in Combination with Standard Background Therapy in Participants with Moderate to Severe Systemic Lupus Erythematosus | |||||||||||||
| Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004102-63 | Sponsor Protocol Number: CNS-Lymphoma-Vorax-1 | Start Date*: 2021-05-07 |
| Sponsor Name:Charité Universitätsmedizin Berlin | ||
| Full Title: AN OPEN LABEL, PHASE I/II STUDY TO INVESTIGATE THE USE OF VORAXAZE™ AS INTENDED INTERVENTION IN PATIENTS WITH CENTRAL NERVOUS SYSTEM LYMPHOMA AND WITH IMPAIRED RENAL FUNCTION BEING TREATED WITH HIG... | ||
| Medical condition: CNS lymphoma (CNSL) being treated with HD-MTX in patients with impaired renal function | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-003813-24 | Sponsor Protocol Number: SIFU17 | Start Date*: 2019-11-28 |
| Sponsor Name:Charité-Universitätsmedizin Berlin | ||
| Full Title: A phase I/IIa, prospective, mono-center, randomized, open labeled, controlled study to assess the safety and efficacy of applying Iloprost locally in the fracture site to promote bone healing in pa... | ||
| Medical condition: Proximal humeral fracture | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-004889-35 | Sponsor Protocol Number: UCDCRC/21/10 | Start Date*: 2021-12-08 | ||||||||||||||||
| Sponsor Name:University College Dublin | ||||||||||||||||||
| Full Title: An International Multicentre, Phase 2, Randomised, Adaptive Protocol to determine the need for, optimal timing of and immunogenicity of administering a booster mRNA vaccination dose against SARS-Co... | ||||||||||||||||||
| Medical condition: Severe Acute Respiratory Syndrome Coronavirus 19 (COVID-19/SARS-CoV-2) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IE (Completed) NO (Completed) DE (Completed) ES (Ongoing) BE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-003747-22 | Sponsor Protocol Number: CPHE885B12201 | Start Date*: 2022-08-02 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A Phase 2 study of durcabtagene autoleucel, B-cell maturation Antigen (BCMA)-directed CAR-T Cells in adult participants with relapsed and refractory multiple myeloma | |||||||||||||
| Medical condition: Adult participants with relapsed and refractory multiple myeloma after failure of 3 or more different prior lines of therapy, including failing an immunomodulatory drug (IMiD), a proteasome inhibit... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) ES (Ongoing) FR (Trial now transitioned) IT (Trial now transitioned) GR (Trial now transitioned) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004444-29 | Sponsor Protocol Number: RID-TB:Treat | Start Date*: 2020-11-25 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: An open-label, multi-centre, randomised controlled trial evaluating the effects of short-course rifapentine-based regimens and additional adherence support on LTBI treatment adherence and completio... | |||||||||||||
| Medical condition: Latent Tuberculosis infection (LTBI) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001680-24 | Sponsor Protocol Number: ALiKE | Start Date*: 2018-09-12 |
| Sponsor Name:Medical University of Vienna - Abteilung für Thoraxchirurgie | ||
| Full Title: Combined low-dose everolimus and low-dose tacrolimus after alemtuzumab induction therapy: a randomized prospective trial in lung transplantation | ||
| Medical condition: Lung Transplantation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-004118-12 | Sponsor Protocol Number: NVX_PCV20 | Start Date*: 2023-03-05 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Safety and immunogenicity of concomitant administration of the Novavax vaccine and a 20-valent pneumococcal conjugate vaccine in adults aged ≥60 years: a four-arm, double-blind, non-inferiority trial | ||
| Medical condition: Vaccination is a key strategy for preventing respiratory illnesses. Pneumococcal vaccination is recommended for all adults (age >60 years). Given their wide application, co-administration of pneumo... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-004654-17 | Sponsor Protocol Number: GECP18/03 | Start Date*: 2019-04-02 | |||||||||||
| Sponsor Name:Fundación GECP | |||||||||||||
| Full Title: A phase II open-label study of Atezolizumab in combination with bevacizumab as first line treatment for locally advanced or metastatic high-intermediate tumour mutation burden (TMB) selected non-sq... | |||||||||||||
| Medical condition: Non small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-000222-51 | Sponsor Protocol Number: 06_DOG05_44 | Start Date*: 2007-09-07 |
| Sponsor Name:Southampton University Hospitals NHS Trust | ||
| Full Title: Short CHemo RadioImmunotherapy in Follicular Trial of 90Y Ibritumomab tiuxetan (ZevalinTM) as therapy for first and second relapse in Follicular Lymphoma | ||
| Medical condition: Follicular Lymphoma First and second relapse of Follicular Lymphoma grade 1, 2, 3a. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2026-000081-25 | Sponsor Protocol Number: D5180C00032 | Start Date*: 2026-03-25 |
| Sponsor Name:AstraZeneca AB | ||
| Full Title: A Multicenter, Single-arm, Open-label, Post-Authorization, Phase 4 Effectiveness and Safety Study of Tezepelumab in Adult and Adolescent Participants with Severe Asthma including Several Under-Stud... | ||
| Medical condition: Severe Asthma | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Elderly | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003638-28 | Sponsor Protocol Number: 2015/576 | Start Date*: 2015-09-30 | ||||||||||||||||
| Sponsor Name:Aarhus University Hospital | ||||||||||||||||||
| Full Title: ALOSTRA Alendronate treatment of osteoporosis in rheumatoid arthritis – indication and duration. A randomized, doubleblind, placebocontrolled multi-centre study to evaluate the effects of disconti... | ||||||||||||||||||
| Medical condition: Rheumatoid arthritis and osteoporosis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-001995-13 | Sponsor Protocol Number: BREATH-19 | Start Date*: 2020-05-15 | |||||||||||
| Sponsor Name:Fundación SEIMC-GESIDA | |||||||||||||
| Full Title: A multicentre, open-label clinical trial to evaluate the effectiveness and safety of intravenous tocilizumab for treating patients with COVID-19 pneumonia: the BREATH-19 Study | |||||||||||||
| Medical condition: COVID-19 pneumonia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000612-34 | Sponsor Protocol Number: EpoRepair | Start Date*: 2015-12-15 |
| Sponsor Name:UniversitätsSpital Zürich | ||
| Full Title: Erythropoietin for the repair of cerebral injury in very preterm infants, a randomized, double-blind, placebo-controlled, prospective, and multicenter clinical study | ||
| Medical condition: 1 out of 100 children born extremely early, or more than 8 weeks before the expected date. 20% of these extremely preterm children shows a cerebral hemorrhage at birth, leading to a significantly i... | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004040-30 | Sponsor Protocol Number: EOC.NSI.11.01 | Start Date*: 2013-05-24 |
| Sponsor Name:Ospedale Regionale di Lugano | ||
| Full Title: Natalizumab de-escalation to interferon-beta-1b in patients with relapsing-remitting multiple sclerosis: A multicenter study | ||
| Medical condition: relapse-remitting multiple sclerosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-003244-76 | Sponsor Protocol Number: Prot-HIPEC-Ovar-201201.7 | Start Date*: 2014-07-11 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Feasibility of intraoperative hyperthermic intraperitoneal chemotherapy with carboplatin and paclitaxel in patients with advanced epithelial ovarian cancer – a combined phase I / II trial | ||
| Medical condition: Otherwise treatment-naive patients with epithelial ovarian cancer, FIGO III - IVa | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
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