- Trials with a EudraCT protocol (31,658)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31,658 result(s) found for: 0.
Displaying page 744 of 1,583.
| EudraCT Number: 2018-000148-24 | Sponsor Protocol Number: 1 | Start Date*: 2018-06-14 |
| Sponsor Name:Norwegian University of Science and Technology | ||
| Full Title: Safety and efficacy of plasma transfusion from exercise-trained donors in patients with early Alzheimer’s disease: the ExPlas Study | ||
| Medical condition: Early Alzheimer's disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-004539-44 | Sponsor Protocol Number: IRST 153 01 | Start Date*: 2007-10-09 | |||||||||||
| Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI | |||||||||||||
| Full Title: SEQUENTIAL TREATMENT STRATEGY FOR METASTATIC COLORECTAL CANCER: A PHASE III PROSPECTIVE RANDOMIZED MULTICENTER STUDY OF CHEMOTHERAPY (CT) WITH OR WITHOUT BEVACIZUMAB AS FIRST-LINE THERAPY FOLLOWED ... | |||||||||||||
| Medical condition: Diagnosis of Metastatic Colonrectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004947-21 | Sponsor Protocol Number: CLAD19 | Start Date*: 2019-06-26 | |||||||||||
| Sponsor Name:Azienda Ospedaliera Universitaria Integrata Verona | |||||||||||||
| Full Title: Exploring the intrathecal anti-inflammatory effect of cladribine and its relationship with clinical efficacy | |||||||||||||
| Medical condition: highly active relapsing multiple sclerosis | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000295-38 | Sponsor Protocol Number: IMPEDE | Start Date*: 2020-05-27 | |||||||||||
| Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | |||||||||||||
| Full Title: Phase II trial, open label, single-arm, of Immune Checkpoint Inhibitor In High Risk Oral Premalignant Lesions | |||||||||||||
| Medical condition: Clinical and histological evidence of Oral Premalignant Lesions (OPL) with high risk of malignant transformation | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001772-30 | Sponsor Protocol Number: RIDARTII | Start Date*: 2017-09-14 | |||||||||||
| Sponsor Name:FONDAZIONE I.R.C.C.S. POLICLINICO SAN MATTEO | |||||||||||||
| Full Title: Clinical burden of anemia in inflammatory bowel disease: Role of Iron Deficiency And iron Replacement Therapy, therapeutic trial | |||||||||||||
| Medical condition: Anemia in inflammatory bowel disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-003695-31 | Sponsor Protocol Number: FIB | Start Date*: 2017-12-04 | |||||||||||
| Sponsor Name:Ziekenhuis Oost-Limburg | |||||||||||||
| Full Title: Fascia iliaca block for analgesia in unilateral direct anterior approach total hip arthroplasty | |||||||||||||
| Medical condition: Total hip arthroplasty through minimal invasive muscle sparing surgery technique | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-002061-30 | Sponsor Protocol Number: 4.0 | Start Date*: 2016-07-18 | ||||||||||||||||||||||||||
| Sponsor Name:University Hospital Southampton NHS Foundation Trust | ||||||||||||||||||||||||||||
| Full Title: Therapeutic HPV vaccine trial +/- anti-CD40 in HPV-driven squamous cell carcinoma. | ||||||||||||||||||||||||||||
| Medical condition: HPV induced cancers such as Head and Neck Squamous Cell Carcinoma (HNSCC), Anogenital Cancer, Cervical Cancer, Penile Cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2014-005018-47 | Sponsor Protocol Number: 008-IRCC-10IIS-14 | Start Date*: 2015-04-08 | |||||||||||
| Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCCS | |||||||||||||
| Full Title: A PHASE II, RANDOMIZED, MULTICENTER STUDY TO ASSESS THE EFFICACY OF NAB-PACLITAXEL-BASED DOUBLET AS FIRST LINE THERAPY IN PATIENTS WITH CANCER OF UNKNOWN PRIMARY (CUP): the AGNOSTOS trial | |||||||||||||
| Medical condition: Cancers of Unknown Primary (CUP) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-005078-55 | Sponsor Protocol Number: N01183 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:UCB PHARMA | |||||||||||||
| Full Title: Named Patient Program with Levetiracetam Oral Solution, for Pediatric Patients suffering from Epilepsy having previously participated in study N01148 | |||||||||||||
| Medical condition: Epilepsy | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-003275-30 | Sponsor Protocol Number: 011-IRCC-10IIS-15 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCCS | |||||||||||||
| Full Title: Open-label, phase ii study of trastuzumab emtansine in patients with HER2-positive metastatic colorectal cancer progressing after trastuzumab and lapatinib: (HER2 Amplification for Colo-rectaL canc... | |||||||||||||
| Medical condition: metatastatic colorectal carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002173-26 | Sponsor Protocol Number: VX21-CTX001-151 | Start Date*: 2021-10-05 | |||||||||||
| Sponsor Name:VERTEX PHARMACEUTICALS INCORPORATED | |||||||||||||
| Full Title: A Phase 3 Study to Evaluate the Safety and Efficacy of a Single Dose of CTX001 in Pediatric Subjects With Severe Sickle Cell Disease | |||||||||||||
| Medical condition: Severe Sickle Cell Disease (SCD) | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000097-38 | Sponsor Protocol Number: LLB-2016-01 | Start Date*: 2016-02-17 |
| Sponsor Name:Labo'Life | ||
| Full Title: Randomized, double-blind, placebo-controlled study to measure 2L®ALERG (homeopathic drug) efficacy on symptoms of allergic rhinitis and allergic rhinoconjunctivitis in patients with a seasonal alle... | ||
| Medical condition: Patients: Allergic Rhinitis and allergic rhinoconjunctivitis in patients with seasonal allergy to grass pollen | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-004919-11 | Sponsor Protocol Number: FLAIR-i | Start Date*: 2022-05-03 | ||||||||||||||||
| Sponsor Name:Donders Institute for Brain, Cognition and Behaviour, Radboud University | ||||||||||||||||||
| Full Title: The effect of colchicine on Food-reLAted effort-based decision making in brain and behavIouR in overweight and obesity: the FLAIR-i study. | ||||||||||||||||||
| Medical condition: Low-grade inflammation in obesity | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-003091-39 | Sponsor Protocol Number: APHP180158 | Start Date*: 2020-02-10 |
| Sponsor Name:Assistance Publique des Hôpitaux de Paris | ||
| Full Title: To relieve dyspnea with low dose titration of morphine in patients admitted to intensive care for acute respiratory failure: A pilot study - OPIDYS | ||
| Medical condition: Adult patients admitted to intensive care for ARI: severe dyspnea (defined by a visual analogue dyspnea scale (EVA-dyspnea) ≥ 40) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000979-24 | Sponsor Protocol Number: DSIT-2015-02 | Start Date*: 2016-07-06 |
| Sponsor Name:Daiichi Sankyo Italia SpA | ||
| Full Title: Randomized, prospective double-blind placebo controlled study for the evaluation of the number, duration and severity of Upper Respiratory Tract Infections in children with risk of recurrence after... | ||
| Medical condition: upper respiratory tract infections in children at high risk of reccurence. | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001529-24 | Sponsor Protocol Number: MS201944-0170 | Start Date*: 2018-08-31 | |||||||||||
| Sponsor Name:Merck KGaA | |||||||||||||
| Full Title: A Phase IIa, single-arm, multi center study to investigate the clinical activity and safety of avelumab in combination with cetuximab plus gemcitabine and cisplatin in participants with advanced sq... | |||||||||||||
| Medical condition: Non Small Cell Lung Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-001057-40 | Sponsor Protocol Number: 301OTC01 | Start Date*: 2017-03-14 | |||||||||||
| Sponsor Name:Ultragenyx Pharmaceutical, Inc. | |||||||||||||
| Full Title: A Phase 1/2, Open-Label Safety and Dose-Finding Study of Adeno-Associated Virus (AAV) Serotype 8 (AAV8)-Mediated Gene Transfer of Human Ornithine Transcarbamylase (OTC) in Adults with Late-Onset OT... | |||||||||||||
| Medical condition: Ornithine transcarbamylase deficiency | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001774-23 | Sponsor Protocol Number: 020518-1 | Start Date*: 2018-07-19 |
| Sponsor Name:Tampere university hospital | ||
| Full Title: Clinical Drug Trial: Efficacy, safety and pharmacokinetics of tinzaparin during Slow Low Efficient Daily Dialysis in Intensive Care Patients | ||
| Medical condition: Patients with clinical indication for pharmacological thromboprophylaxis and slow low efficient daily dialysis (SLEDD). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-003720-11 | Sponsor Protocol Number: M1084997 | Start Date*: 2006-09-08 | |||||||||||
| Sponsor Name:GE Healthcare Finland Oy | |||||||||||||
| Full Title: Comparison of the quality of anesthesia and intraoperative stress responses to noxious stimulus with high opiate, low hypnotic versus low opiate high hypnotic drug administration during anesthesia ... | |||||||||||||
| Medical condition: Comparing the intra-operative stress responses to noxious stimulus with high opiate, low hypnotic versus low opiate high hypnotic drug administration during anesthesia. Back surgery | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-004627-31 | Sponsor Protocol Number: M15CRI | Start Date*: 2017-06-20 | |||||||||||||||||||||
| Sponsor Name:The Netherlands Cancer Institute | |||||||||||||||||||||||
| Full Title: A multicentre randomised phase II trial of neo-adjuvant chemotherapy followed by surgery vs. neo-adjuvant chemotherapy and subsequent chemoradiotherapy followed by surgery vs. neo-adjuvant chemorad... | |||||||||||||||||||||||
| Medical condition: TNM 7th ed stage IB-IIIC gastric adenocarcinoma (histologically proven); tumour bulk has to be in the stomach but may involve gastro-oesophageal junction | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
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