- 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 1,752 of 2,220.
| EudraCT Number: 2015-003513-24 | Sponsor Protocol Number: IN11004OLE | Start Date*: 2016-05-24 | |||||||||||
| Sponsor Name:Intec Pharma, Ltd. | |||||||||||||
| Full Title: An Open-Label, Multi-Center, Follow-Up Study Designed to Evaluate the Long-Term Effects of AP-CD/LD in Fluctuating Parkinson's Disease Subjects who Completed Study IN 11 004 | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) SK (Prematurely Ended) GB (Prematurely Ended) ES (Prematurely Ended) DE (Completed) BG (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000235-40 | Sponsor Protocol Number: STATIC-2016-000235-40 | Start Date*: 2016-07-29 |
| Sponsor Name:Region Skåne | ||
| Full Title: Stopping anti-TNF treatment in Crohn’s and Colitis patients in remission | ||
| Medical condition: Crohn´s disease Ulcerative colitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002467-34 | Sponsor Protocol Number: AIO-YMO/HEP-0315 | Start Date*: 2017-07-19 | |||||||||||||||||||||||||||||||
| Sponsor Name:AIO-Studien-gGmbH | |||||||||||||||||||||||||||||||||
| Full Title: Nal-IRI with 5-fluorouracil (5-FU) and leucovorin or gemcitabine plus cisplatin in advanced biliary-tract cancer - An open label, non-comparative, randomized, multicenter phase II trial | |||||||||||||||||||||||||||||||||
| Medical condition: Locally advanced or metastatic, non resectable, adenocarcinoma of the biliary tract including intrahepatic and extrahepatic bile duct | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-001193-15 | Sponsor Protocol Number: FASTERCC-001 | Start Date*: 2016-07-06 | |||||||||||||||||||||||||||||||
| Sponsor Name:Department of Oncology, Aarhus University Hospital | |||||||||||||||||||||||||||||||||
| Full Title: Folic acid supplement versus placebo for treating mucositis adverse events in metastatic renal cell carcinoma patients receiving targeted therapy (FASTERCC). A randomized, double-blind, phase II ... | |||||||||||||||||||||||||||||||||
| Medical condition: Mucositis (nasal, oral, pharyngeal, anal, or genital) is often experienced in relation to TKI and mTOR inhibitor treatment of metastatic renal cell carcinoma patients. The present trial will assess... | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-005067-52 | Sponsor Protocol Number: DPCG-01 | Start Date*: 2022-02-10 | ||||||||||||||||
| Sponsor Name:Aalborg University Hospital, Department of Oncology | ||||||||||||||||||
| Full Title: A randomized phase II study of gemcitabine versus reduced-dose combination chemotherapy in fragile patients with non-resectable pancreatic cancer. | ||||||||||||||||||
| Medical condition: Pancreatic Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-002150-12 | Sponsor Protocol Number: DANSVIGT | Start Date*: 2017-10-11 |
| Sponsor Name:Danish Society of Cardiology, Heart Failure Working Group | ||
| Full Title: DanHeart (H-HeFT / Met-HeFT) | ||
| Medical condition: Heart Failure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-005025-25 | Sponsor Protocol Number: NIMAO/2021-1/EB-01 | Start Date*: 2022-06-08 |
| Sponsor Name:CHU DE NIMES | ||
| Full Title: Evaluation de l’efficacité et de la sécurité de la Tamsulosine LP 0,4mg dans le traitement de la dysurie symptomatique de la femme atteinte de sclérose en plaques. Etude contrôlée randomisée en cro... | ||
| Medical condition: Patientes majeures atteintes de sclérose en plaques (EDSS < 7,5) présentant une dysurie modérée à sévère (IPSS>7) par dyssynergie vésico-sphinctérienne authentifiée au bilan urodynamique complet. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002851-92 | Sponsor Protocol Number: AN-EPI3334 | Start Date*: 2016-09-08 |
| Sponsor Name:ANTHERA Pharmaceuticals, Inc. | ||
| Full Title: An Open-Label Study Evaluating the Efficacy and Safety of Liprotamase in Subjects with Exocrine Pancreatic Insufficiency due to Cystic Fibrosis | ||
| Medical condition: Cystic Fibrosis-Related Exocrine Pancreatic Insufficiency | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: HU (Prematurely Ended) CZ (Completed) PL (Prematurely Ended) ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001330-97 | Sponsor Protocol Number: RB16.045 | Start Date*: 2016-11-18 |
| Sponsor Name:CHRU de Brest | ||
| Full Title: Prévention des Fausses Couches Spontanées Répétées par Hydroxychloroquine. Essai thérapeutique multicentrique, randomisé, en double insu, contre placebo. | ||
| Medical condition: fausses couches spontanées | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Suspended by CA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-002197-78 | Sponsor Protocol Number: APHP200011 | Start Date*: 2021-08-19 |
| Sponsor Name:Assistance Publique - Hôpitaux de Paris | ||
| Full Title: Antimicrobial Stewardship For Ventilator Associated Pneumonia in Intensive Care Acronym: ASPIC | ||
| Medical condition: ventilator associated neumonia in intensive care | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-000519-18 | Sponsor Protocol Number: P160906J | Start Date*: 2019-04-09 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: PIMOC : Personalized targeted therapies in inflammatory complex multi organ disease | |||||||||||||
| Medical condition: Patients presenting inflammatory non classified disease targeting at least 2 organs involvement: skin, lymph nodes, hemopoietic system, joints, digestive tract. The disease has been resistant to at... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-003958-23 | Sponsor Protocol Number: 8154 | Start Date*: 2021-10-21 |
| Sponsor Name:Hopitaux Universitaires de Strasbourg | ||
| Full Title: A MULTICENTER, PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF SPIRONOLACTONE FOR THE TREATMENT OF ACTIVE RHEUMATOID ARTHRITIS (RA) | ||
| Medical condition: RHEUMATOID ARTHRITIS | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001030-34 | Sponsor Protocol Number: MC-0241 | Start Date*: 2019-06-12 |
| Sponsor Name:Egis Pharmaceuticals PLC | ||
| Full Title: A Prospective Open-label, Multicentric, Phase IV Trial to Compare the Efficacy of 10-Week Therapy of Ramipril and Indapamide SR Tablets Given Concomitantly with that of the Monotherapy of Ramipril ... | ||
| Medical condition: hypertension | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001885-14 | Sponsor Protocol Number: LOWBACK-SE | Start Date*: 2019-08-06 |
| Sponsor Name:National Research, Development and Innovation Office | ||
| Full Title: The prognostic value of Biomarkers and the Effect of Tolperisone in Acute low back pain and sciatic pain – BETA A Phase 3 investigator initiated study | ||
| Medical condition: Acute low back pain with or withour radicular signs | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-004245-37 | Sponsor Protocol Number: UCDCRC/20/05 | Start Date*: 2020-12-18 | |||||||||||
| Sponsor Name:University College Dublin | |||||||||||||
| Full Title: Randomised Placebo-Controlled Trial of Early Targeted Treatment of Patent Ductus Arteriosus with Paracetamol in Extremely Low Birth Weight Infants (ETAPA) | |||||||||||||
| Medical condition: Patent Ductus Arteriosus | |||||||||||||
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| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Trial now transitioned) CZ (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002016-26 | Sponsor Protocol Number: FBCSG-01-2007 | Start Date*: 2007-08-08 | |||||||||||
| Sponsor Name:Finnish Breast Cancer Group | |||||||||||||
| Full Title: A randomized phase III study comparing trastuzumab plus docetaxel (HT) followed by 5-FU, epirubicin, and cyclophosphamide (FEC) to the same regimen followed by single-agent trastuzumab as adjuvant ... | |||||||||||||
| Medical condition: Invasive early breast cancer that has been removed by surgery. | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: FI (Completed) SE (Completed) GB (GB - no longer in EU/EEA) IS (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004155-37 | Sponsor Protocol Number: A01-115-02-EU | Start Date*: 2020-07-30 | |||||||||||
| Sponsor Name:Aptabio Therapeutics, Inc | |||||||||||||
| Full Title: A randomized, Placebo-controlled, Double-blinded, Multi-centre, Phase 2 Study to Assess Safety, Tolerability and Renal Effects of APX-115 in Subjects with Type 2 Diabetes and Nephropathy | |||||||||||||
| Medical condition: diabetic nephropathy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) HU (Completed) BG (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-002877-27 | Sponsor Protocol Number: CTRIAL-IE-21-29/NRG-GY019 | Start Date*: 2023-07-06 | ||||||||||||||||
| Sponsor Name:Cancer Trials Ireland | ||||||||||||||||||
| Full Title: A Randomized Phase III, Two-Arm Trial of Paclitaxel/Carboplatin/Maintenance Letrozole Versus Letrozole Monotherapy in Patients with Stage II-IV, Primary Low-Grade Serous Carcinoma of the Ovary or P... | ||||||||||||||||||
| Medical condition: Primary low-grade serous carcinoma of the ovary or peritoneum. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: IE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-003218-42 | Sponsor Protocol Number: RC18_0287 | Start Date*: 2019-01-16 |
| Sponsor Name:CHU de Nantes | ||
| Full Title: Phase 2 study evaluating MEchanisms of resistance on tumor tissue and Liquid biopsy in patients with EGFR mutated nonpretreated advanced Lung cancer Receiving OSimErtinib until and beyond radiologi... | ||
| Medical condition: Locally advanced or metastatic Non-small-cell lung carcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001783-28 | Sponsor Protocol Number: BCG-COVID_HU_001 | Start Date*: 2020-05-06 |
| Sponsor Name:National Korányi Institute of Pulmonology | ||
| Full Title: REDUCING ABSENCE FROM WORK OF HEALTHCARE WORKERS DUE TO COVID-19 INFECTION BY BCG (BACILLUS CALMETTE-GUÉRIN) VACCINATION | ||
| Medical condition: healthy volunteers working in the healthcare treating patients with new type of coronavirus (SARS-CoV-2) infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) | ||
| Trial results: (No results available) | ||
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