- Trials with a EudraCT protocol (39,306)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
39,306 result(s) found for: 1.
Displaying page 657 of 1,966.
| EudraCT Number: 2016-004787-20 | Sponsor Protocol Number: MED3-201601 | Start Date*: 2017-10-11 | |||||||||||
| Sponsor Name:Rheinische Friedrich-Wilhelms-Universität Bonn | |||||||||||||
| Full Title: An Open Label, Randomized Phase 2 Clinical Trial of Nivolumab investigating Effiacy and safety of Nivolumab given once prior to, concurrent to the radiotherapy (RT) and as maintenance therapy over ... | |||||||||||||
| Medical condition: Patients with resectable advanced stage HNSCC (T1–T4 N0-N2 M0) with intermediate risk (resection margins > 5 mm, no perineural invasion and no extracapsular evasion) for whom definite RT post surge... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-003949-28 | Sponsor Protocol Number: Inco_Ona1 | Start Date*: 2018-08-07 | |||||||||||
| Sponsor Name:PROF. ANTONELLA GIANNANTONI - CLINICA UROLOGICA - UNIVERSITà DI PERUGIA | |||||||||||||
| Full Title: Incobotulinumtoxin versus Onabotulinumtoxin in the treatment of patients with overactive bladder syndrome | |||||||||||||
| Medical condition: neurogenic overactive bladder | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004351-39 | Sponsor Protocol Number: FARM8MXYFL | Start Date*: 2011-10-28 | |||||||||||||||||||||
| Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||||||||||||
| Full Title: Phase II, randomized, double arm, multi-center study evaluating the efficacy and safety of azithromycin for the long term prophylactic treatment of COPD in primary antibody deficiency patients with... | |||||||||||||||||||||||
| Medical condition: primary immunodefciency patients with COPD and frequent exacerbations | |||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2017-002853-13 | Sponsor Protocol Number: EWALL-BOLD | Start Date*: 2018-03-01 | |||||||||||
| Sponsor Name:Goethe Universität Frankfurt | |||||||||||||
| Full Title: Phase II trial for the treatment of older patients with newly diagnosed CD19 positive, Ph/BCR-ABL negative B-precursor acute lymphoblastic leukemia with sequential dose reduced chemotherapy and Bli... | |||||||||||||
| Medical condition: Patient aged 56 and 74 with CD19 positive, Ph/BCR-ABL negative B-precursor acute lymphoblastic leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000580-17 | Sponsor Protocol Number: TRANSLATE-RE | Start Date*: 2016-07-13 | |||||||||||||||||||||
| Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S.CROCE E CARLE CUNEO | |||||||||||||||||||||||
| Full Title: RESTORE IMMUNE COMPETENCE AGAINST CANCER CELLS IN RENAL CELL CARCINOMA RESISTANT TO STANDARD TREATMENTS TRANSLATE – kidney STUDY | |||||||||||||||||||||||
| Medical condition: metastatic renal cell carcinoma (mRCC) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2016-005145-23 | Sponsor Protocol Number: 53736 | Start Date*: 2017-08-29 | |||||||||||||||||||||
| Sponsor Name:DIPARTIMENTO DI SCIENZE CHIRURGICHE - UNIVERSITà DEGLI STUDI DI TORINO | |||||||||||||||||||||||
| Full Title: Prospective randomized trial comparing corifollitropin alfa (CF-alfa) late start (day 4) vs. CF-alfa standard start (day2) in poor, normal and potential high-responders undergoing IVF/ICSI | |||||||||||||||||||||||
| Medical condition: Women with low reproductive capacity | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2020-002102-58 | Sponsor Protocol Number: TJT2012 | Start Date*: 2020-06-12 | |||||||||||
| Sponsor Name:CHU de Liège | |||||||||||||
| Full Title: Mesenchymal stromal cell therapy for severe COVID-19 infection | |||||||||||||
| Medical condition: Patients with severe COVID-19 infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-002585-33 | Sponsor Protocol Number: PETAL | Start Date*: 2023-01-19 | ||||||||||||||||
| Sponsor Name:FONDAZIONE TOSCANA GABRIELE MONASTERIO | ||||||||||||||||||
| Full Title: A multi-center phase 3 study of 18F-florbetaben positron emission tomography/computed tomography (PET-CT) | ||||||||||||||||||
| Medical condition: cardiac amyloidosis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-002513-36 | Sponsor Protocol Number: ASP-1929-301 | Start Date*: 2019-08-16 | |||||||||||
| Sponsor Name:Rakuten Aspyrian, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Arm, Open-Label, Controlled Trial of ASP-1929 Photoimmunotherapy Versus Physician’s Choice Standard of Care for the Treatment of Locoregional, Recurrent Head and Neck ... | |||||||||||||
| Medical condition: Locoregional, recurrent head and neck squamous cell carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) GR (Completed) BE (Completed) ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-003325-17 | Sponsor Protocol Number: P080403 | Start Date*: 2008-10-24 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Etude ARCTIC Comparaison randomisée 1/ d'un traitement antiplaquettaire ajusté par monitoring à un traitement standard à dose fixe pour stenting coronaire avec DES, et 2/ d'un arrêt versus poursuit... | |||||||||||||
| Medical condition: Patients devant recevoir au moins un stent actif quel que soit le contexte | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-004593-56 | Sponsor Protocol Number: CAVE-2 | Start Date*: 2022-05-19 | |||||||||||
| Sponsor Name:GRUPPO ONCOLOGICO DELL'ITALIA MERIDIONALE | |||||||||||||
| Full Title: A phase II randomized clinical study of the combination of avelumab plus cetuximab as rechallenge strategy in pre-treated RAS/BRAF wild type metastatic colorectal cancer patients | |||||||||||||
| Medical condition: Pre-treated RAS/BRAF wild type metastatic colorectal cancer patients. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005663-31 | Sponsor Protocol Number: 12020 | Start Date*: 2022-10-04 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA ORDINE MAURIZIANO DI TORINO | |||||||||||||
| Full Title: CARotid plaqUe StabilizatiOn and regression with evolocumab) | |||||||||||||
| Medical condition: atherosclerosis desead | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-002251-42 | Sponsor Protocol Number: GZ-2016-11512. | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name: | |||||||||||||
| Full Title: An open-label, single-center study on the safety and efficacy of avalglucosidase alpha in late-onset Pompe patients ≥5 years | |||||||||||||
| Medical condition: Late onset Pompe disease | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-006004-16 | Sponsor Protocol Number: 03PDE2020 | Start Date*: 2021-07-16 |
| Sponsor Name:Celon Pharma S.A. | ||
| Full Title: Phase II, Double blind, Randomized, Placebo controlled, Parallel group, Trial to Explore the Potential Anti-dyskinetic Properties of CPL500036 (PDE10A inhibitor) in Patients with Parkinson's Diseas... | ||
| Medical condition: Levodopa-induced dyskinesia in Parkinson's Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: PL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001438-20 | Sponsor Protocol Number: ASSTBS-FARM-INF_ITL-2021 | Start Date*: 2021-05-10 | ||||||||||||||||
| Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | ||||||||||||||||||
| Full Title: Randomized controlled trial on daily Rifampicin for Four Months Compared with daily Rifampicin/Isoniazid for Three Months for the Treatment of Tuberculosis Infection among migrants: Completion Rate... | ||||||||||||||||||
| Medical condition: Tuberculosis Infection | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-004259-17 | Sponsor Protocol Number: NS3.1 | Start Date*: 2022-03-02 | |||||||||||
| Sponsor Name:OBCTCD-24 Ltd | |||||||||||||
| Full Title: A Phase IIb Randomized, Quadruple-blinded Multicenter, Multinational, Placebo-controlled Study to Evaluate the safety and efficacy of exosomes overexpressing CD24 to prevent clinical deterioration ... | |||||||||||||
| Medical condition: COVID-19 disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-003437-10 | Sponsor Protocol Number: CARTESIO | Start Date*: 2023-04-05 | |||||||||||
| Sponsor Name:Azienda Socio Sanitaria Territoriale di Lodi | |||||||||||||
| Full Title: PILOT STUDY ON THE EFFECTIVENESS OF CHOLINE ALFOSCERATE IN THE UNDER THRESHOLD DEPRESSION OF THE ELDERLY | |||||||||||||
| Medical condition: Under threshold depression of the elderly. | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-003751-42 | Sponsor Protocol Number: ICH-013-UroNEOadI | Start Date*: 2022-01-25 | |||||||||||
| Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | |||||||||||||
| Full Title: Randomized phase III clinical trial of Neo-Adjuvant Intravesical mitomycin C (MMC) treatment in patients with primary treatment-naïve vesical neoplasms. | |||||||||||||
| Medical condition: Patients with primary treatment-naïve vesical neoplasms. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-005478-24 | Sponsor Protocol Number: DYNE251DMD201 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Dyne Therapeutics, Inc | |||||||||||||
| Full Title: A Randomized, Double-Blind, Placebo-Controlled, Multiple Ascending Dose Study Assessing Safety, Tolerability, Pharmacodynamics, Efficacy, and Pharmacokinetics of DYNE-251 Administered to Participan... | |||||||||||||
| Medical condition: Duchenne Muscular Dystrophy | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: IE (Trial now transitioned) BE (Trial now transitioned) ES (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001300-37 | Sponsor Protocol Number: S201.3.125 | Start Date*: 2006-07-11 |
| Sponsor Name:Solvay Pharmaceuticals B.V. | ||
| Full Title: Immunogenicity and reactogenicity of the trivalent influenza subunit vaccine Influvac® for the season 2006/2007. An open, baseline-controlled study in two groups of healthy subjects: adult subjects... | ||
| Medical condition: Prophylaxis of influenza, especially in those who run an increased risk of associated complications. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) BE (Completed) | ||
| Trial results: View results | ||
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