- Trials with a EudraCT protocol (44,382)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,382 result(s) found.
Displaying page 1,786 of 2,220.
| EudraCT Number: 2020-004784-53 | Sponsor Protocol Number: APHP200002 | Start Date*: 2022-07-19 | |||||||||||
| Sponsor Name:Assistance Publique - Hôpitaux de Paris | |||||||||||||
| Full Title: Rivaroxaban versus standard of care for patients with excessive atrial ectopy or short atrial runs and high embolism risk SHORT RUN AF | |||||||||||||
| Medical condition: excessive atrial ectopy or short atrial runs and high embolism risk | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-005082-47 | Sponsor Protocol Number: HUS/1209/2017 | Start Date*: 2018-09-24 |
| Sponsor Name:Sydän- ja keuhkokeskus, HUS | ||
| Full Title: Repolarization study in LQTS patients | ||
| Medical condition: Long QT syndrome (LQTS) is a hereditary arrhythmia disease. It causes disturbances to the ion flow through cell membranes of cardiomyocytes. These disturbances can sometimes seen in an electrocardi... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-003190-42 | Sponsor Protocol Number: ANZUP1304 | Start Date*: 2014-10-17 | ||||||||||||||||
| Sponsor Name:Cancer Trials Ireland | ||||||||||||||||||
| Full Title: Randomised phase 3 trial of enzalutamide in first line androgen deprivation therapy for metastatic prostate cancer: ENZAMET | ||||||||||||||||||
| Medical condition: Metastatic Prostate Cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: IE (Trial now transitioned) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2019-002240-24 | Sponsor Protocol Number: SIMASPK01b | Start Date*: 2019-06-27 |
| Sponsor Name:Institut klinické a experimentální medicíny | ||
| Full Title: The evolution of advanced microangiopathic diabetic complications before and after simultaneous pancreas and kidney transplantation evaluated with progressive non-invasive methods | ||
| Medical condition: Surgical complications (hernia) after simultaneous pancreas and kidney transplantation | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: CZ (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-003179-33 | Sponsor Protocol Number: BV-2021/06 | Start Date*: 2021-11-29 | |||||||||||
| Sponsor Name:OM Pharma SA | |||||||||||||
| Full Title: A Randomised, Double-Blind, Placebo-controlled, 32-week, Phase IIa trial to investigate the efficacy of OM-85 versus matched placebo in reducing disease severity in children aged 3 to 24 months wit... | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) NL (Prematurely Ended) PL (Prematurely Ended) FR (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-002492-11 | Sponsor Protocol Number: PRECESTO | Start Date*: 2023-09-13 | |||||||||||
| Sponsor Name:NFL BIOSCIENCES SA | |||||||||||||
| Full Title: Phase II Study Assessing Efficacy and Safety of NFL-101 on Reduction of Reinforcing Properties of Cigarettes | |||||||||||||
| Medical condition: Tobacco addiction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000366-18 | Sponsor Protocol Number: 2020/0420/HP | Start Date*: 2022-08-18 | |||||||||||
| Sponsor Name:CHU de ROUEN | |||||||||||||
| Full Title: Efficacy and Tolerance of Baricitinib, a JAK inhibitor, in the treatment of refractory non-infectious uveitis | |||||||||||||
| Medical condition: Active non-anterior non-infectious uveitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000903-19 | Sponsor Protocol Number: UX053-CL101 | Start Date*: 2022-08-24 | |||||||||||
| Sponsor Name:Ultragenyx Pharmaceutical Inc. | |||||||||||||
| Full Title: A Phase 1/2 First-in-human, 2-part Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single Ascending Doses (Part 1: Open-label) and Repeat Doses (Part 2: Randomized, Double-blind... | |||||||||||||
| Medical condition: Glycogen Storage Disease Type III (GSD III) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) IT (Prematurely Ended) ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-000250-35 | Sponsor Protocol Number: WO30070 | Start Date*: 2016-06-16 | |||||||||||
| Sponsor Name:Roche Farma, S.A., que representa en España a F. Hoffmann-La Roche Ltd. | |||||||||||||
| Full Title: A PHASE III, MULTICENTER, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND STUDY OF ATEZOLIZUMAB (ANTI?PD-L1 ANTIBODY) IN COMBINATION WITH GEMCITABINE/CARBOPLATIN VERSUS GEMCITABINE/CARBOPLATIN ALONE I... | |||||||||||||
| Medical condition: Urothelial Carcinoma, locally advanced or metastatic | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) CZ (Completed) EE (Completed) GR (Completed) PL (Completed) SI (Completed) GB (GB - no longer in EU/EEA) FI (Completed) NL (Completed) PT (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-003720-16 | Sponsor Protocol Number: CMIJ821A12201 | Start Date*: 2021-10-15 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A double-blind, placebo-controlled, randomized dose-ranging trial to investigate efficacy and safety of intravenous MIJ821 infusion in addition to comprehensive standard of care on the rapid reduct... | |||||||||||||
| Medical condition: Major Depressive Disorder with suicidal ideation with intent | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SK (Prematurely Ended) NL (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002707-10 | Sponsor Protocol Number: SJ-596 | Start Date*: 2018-04-10 | ||||||||||||||||||||||||||
| Sponsor Name:Regional Dementia Research Centre, Dept of Neurology | ||||||||||||||||||||||||||||
| Full Title: Serum-monitoring of anti-dementia drugs, and the relevance to side-effects, clinical efficacy and compliance | ||||||||||||||||||||||||||||
| Medical condition: Dementia in Alzheimers Disease, Parkinsons Disease and Dementia with Lewy Bodies | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2021-000021-27 | Sponsor Protocol Number: ZN-c3-003 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:K-Group Beta | |||||||||||||
| Full Title: A Phase 1/2 Dose Escalation and Dose Expansion Study of ZN-c3 in Combination with Gemcitabine in Adult and Pediatric Subjects with Relapsed or Refractory Osteosarcoma | |||||||||||||
| Medical condition: Relapsed or Refractory Osteosarcoma | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) ES (Ongoing) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004347-37 | Sponsor Protocol Number: VSV2016b | Start Date*: 2017-01-31 |
| Sponsor Name:Helsinki University Hospital | ||
| Full Title: Femoralblock in endovenous laser | ||
| Medical condition: venous disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-004891-33 | Sponsor Protocol Number: T33/2021 | Start Date*: 2022-04-13 |
| Sponsor Name:Turku University Hospital | ||
| Full Title: COVID-19 vaccine induced immune response in patients with primary antibody deficiency | ||
| Medical condition: COVID-19 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000287-29 | Sponsor Protocol Number: 1 | Start Date*: 2018-03-23 |
| Sponsor Name:Karolinska Institutet | ||
| Full Title: Immediate versus delayed insertion of intrauterine contraception at the time of medical abortion An open-label, randomized, multicenter study | ||
| Medical condition: Post medical abortion contraception | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: SE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-003906-28 | Sponsor Protocol Number: RC31/17/0447 | Start Date*: 2020-02-24 |
| Sponsor Name:CHU de Toulouse | ||
| Full Title: Subcutaneous injections of autologous cultured adipose-derived stroma/stem cells to heal refractory ischemic digital ulcers in patients with scleroderma : a phase II study | ||
| Medical condition: Patients with systemic sclerosis presenting digital ulcer : - located beyond the proximal interphalangeal joint, on finger surface (included periungueal ulcers), - of ischemic origin according to... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-005007-40 | Sponsor Protocol Number: MK-6482-016 | Start Date*: 2021-08-10 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: An Open-label, Multicenter, Phase 2 Study to Evaluate the Efficacy and Safety of Pembrolizumab Plus Lenvatinib in Combination With Belzutifan in Multiple Solid Tumors | |||||||||||||
| Medical condition: HCC, non-microsatellite instability-high (MSI-H)/ deficient mismatch repair (dMMR) CRC, PDAC, and BTC | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) ES (Ongoing) FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004639-35 | Sponsor Protocol Number: 2017/2601 | Start Date*: 2018-10-26 | ||||||||||||||||
| Sponsor Name:Gustave Roussy | ||||||||||||||||||
| Full Title: A Phase III trial of acetylsalicylic acid and atorvastatin in patients with castrate-resistant prostate cancer | ||||||||||||||||||
| Medical condition: castrate-resistant prostate cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2020-001985-12 | Sponsor Protocol Number: BiCAR | Start Date*: 2021-02-08 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:LYSARC | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase II Trial Evaluating Glofitamab, a Bispecific CD3xCD20 Antibody for Relapse/Refractory Lymphomas after CAR T-cells therapy | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Patients who received CAR T-cells therapy for R/R DLBCL (cohort 1) or R/R PMBL, mantle cell lymphoma, t-iNHL or iNHL (cohort 2), at least 1 month ago | ||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-002369-17 | Sponsor Protocol Number: 2021-01 | Start Date*: 2021-07-22 |
| Sponsor Name:GETAID | ||
| Full Title: Management of moderate POstoperative recurrence in Crohn's disease: a randoMizEd contROLled trial, the POMEROL trial. | ||
| Medical condition: Crohn's disease patients having an i2 endoscopic postoperative recurrence 6-12 months after ileocolonic anastomosis. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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