- Trials with a EudraCT protocol (44,394)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,394 result(s) found.
Displaying page 1,786 of 2,220.
| EudraCT Number: 2021-000252-18 | Sponsor Protocol Number: 35RC20_9803_RePERSO | Start Date*: 2021-04-27 | |||||||||||
| Sponsor Name:Rennes University Hospital | |||||||||||||
| Full Title: Evaluation of treatment PERSOnalization based on its therapeutic monitoring in patients with metastatic colorectal cancer treated with regorafenib | |||||||||||||
| Medical condition: metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-000174-25 | Sponsor Protocol Number: 101090401IN | Start Date*: 2023-03-17 | |||||||||||
| Sponsor Name:SANTEN INCORPORATED | |||||||||||||
| Full Title: A Phase IIa, Randomized, Double-Masked, Placebo-Controlled, Parallel-Group, Multicenter Study Assessing the Efficacy and Safety of STN1010904 Ophthalmic Suspension 0.03% and 0.1% Compared with Vehi... | |||||||||||||
| Medical condition: Fuchs Endothelial Corneal Dystrophy (FECD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002588-23 | Sponsor Protocol Number: 2019/0407/HP | Start Date*: 2023-03-13 | ||||||||||||||||
| Sponsor Name:CHU de Rouen | ||||||||||||||||||
| Full Title: Neoadjuvant Chemotherapy for Obstructive Colon cancER first Treated by cOlostomy: A randomized phase III trial - COnCERTO (French 01-18) | ||||||||||||||||||
| Medical condition: Patients first treated by stoma and requiring chemotherapy for obstructive colon cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-005146-15 | Sponsor Protocol Number: NIPIRESCUE_G-113 | Start Date*: 2021-12-22 | |||||||||||
| Sponsor Name:GERCOR | |||||||||||||
| Full Title: Nivolumab and ipilimumab in patients with dMMR and/or MSI metastatic colorectal cancer resistant to anti-PD1 monotherapy: An open-label phase II GERCOR trial (NIPIRESCUE) | |||||||||||||
| Medical condition: dMMR and/or MSI metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-001960-45 | Sponsor Protocol Number: RC18_0206 | Start Date*: 2019-04-15 |
| Sponsor Name:CHU of Nantes | ||
| Full Title: An intensive program with quadruplet induction and consolidation plus tandem autologous stem cell transplantation in Newly Diagnosed High Risk Multiple Myeloma Patients: a phase II study of the Int... | ||
| Medical condition: Young untreated patients with multiple myeloma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-002563-29 | Sponsor Protocol Number: APHP211429 | Start Date*: 2023-04-18 |
| Sponsor Name:Assistance Publique – Hôpitaux de Paris (AP-HP) | ||
| Full Title: Colchicine versus Placebo in Acute Myocarditis Patients to Reduce Late Gadolinium Enhancement Mass on Cardiac Magnetic Resonance and the risk of Clinical Outcomes: The ARGO tria | ||
| Medical condition: NA | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-003318-10 | Sponsor Protocol Number: D20180135 | Start Date*: 2021-08-05 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: Evaluation of MEpolizumab-based regimen Compared to Conventional Therapeutic Strategy For Remission Induction In Patients With Eosinophilic Granulomatosis With Polyangiitis. Prospective, randomized... | |||||||||||||
| Medical condition: Patients with a diagnosis of Eosinophilic Granulomatosis with Polyangiitis (EGPA) with newly-diagnosed disease or with a relapsing disease at the time of screening | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004175-31 | Sponsor Protocol Number: Prucalopride2017 | Start Date*: 2018-04-09 |
| Sponsor Name:TARGID, KU Leuven | ||
| Full Title: A placebo-controlled trial with prucalopride for the treatment of typical reflux symptoms in patients with gastro-esophageal reflux disease with incomplete proton pump inhibitor response | ||
| Medical condition: refractory gastro-esophageal reflux disease | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-001197-42 | Sponsor Protocol Number: 2017-01 | Start Date*: 2017-05-15 |
| Sponsor Name:ASSISATNCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
| Full Title: Evolution of the cardiac function(office) during the follow-up of the anticancer immunotherapy inhibiting PD-1 | ||
| Medical condition: as melanoma, non-small cell lung cancers and kidney cancers | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-001371-24 | Sponsor Protocol Number: 6621 | Start Date*: 2019-01-08 |
| Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
| Full Title: Prospective, randomised, placebo-controlled study of polyvalent intravenous immunoglobulins for the treatment of primary Sjögren's syndrome associated painful sensory neuropathies | ||
| Medical condition: Primary Sjögren's syndrome associated painful sensory neuropathies | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-004633-21 | Sponsor Protocol Number: APHP191047 | Start Date*: 2024-04-29 |
| Sponsor Name:Assistance Publique -Hopitaux de Paris | ||
| Full Title: | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-005508-37 | Sponsor Protocol Number: PI2021_843_0197 | Start Date*: 2021-12-20 |
| Sponsor Name:CHU Amiens-Picardie | ||
| Full Title: Evaluation of plasma concentrations of intravenous lidocaine and epidural ropivacaine when used in combination in major abdominal surgery | ||
| Medical condition: major abdominal surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-002376-14 | Sponsor Protocol Number: ELLOUZE_ORION_2018 | Start Date*: 2019-10-15 |
| Sponsor Name:CHU Dijon Bourgogne | ||
| Full Title: | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-000259-14 | Sponsor Protocol Number: 1/2012AITT | Start Date*: 2012-08-31 |
| Sponsor Name:University of Debrecen, Medical and Health Science Center, Department of Anaesthesiology and Intensive Therapy | ||
| Full Title: Reversal of residual pipecuronium neuromuscular block using sugammadex: a randomized, double-blind, placebo controlled, dosefinding study | ||
| Medical condition: The effect of sugammadex dose on residual neuromuscular blockade will be investigated, therefore patients suffering from various conditions undergoing surgery in general anaesthesia with muscle rel... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: HU (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001965-17 | Sponsor Protocol Number: AITT2013/5 | Start Date*: 2013-09-26 | |||||||||||
| Sponsor Name:Debreceni Egyetem Orvos- és Egészségtudományi Centrum Aneszteziológiai és Intenzív Terápiás Tanszék | |||||||||||||
| Full Title: Incidence of postoperative residual neuromuscular blockade following the administration of rocuronium: A randomized placebo controlled study. | |||||||||||||
| Medical condition: The effect of sugammadex and neostigmin on postoperative residual neuromuscular blockade will be investigated, therefore the patients suffering from various conditions undergoing surgery in general... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-004320-16 | Sponsor Protocol Number: 77242113PSO2002 | Start Date*: 2022-07-05 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A Phase 2b Multicenter, Long-Term Extension, Dose-ranging Study to Evaluate the Efficacy and Safety of JNJ-77242113 for the Treatment of Moderate-to-Severe Plaque Psoriasis | |||||||||||||
| Medical condition: Plaque Psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Ongoing) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003459-12 | Sponsor Protocol Number: RB-NAIT-01-01 | Start Date*: 2020-08-11 | |||||||||||
| Sponsor Name:Rallybio, IPA, LLC | |||||||||||||
| Full Title: A Single-blind, Placebo-controlled, Single-center Study Investigating the Dose of Human Anti-Human Platelet Antigen (HPA)-1a Immune Globulin (NAITgam) Needed to Eliminate HPA-1a Positive Platelets ... | |||||||||||||
| Medical condition: prevention of Fetal Neonatal Alloimmune Thrombocytopenia (FNAIT In mothers negative for HPA-1a antigen, fetal platelets positive for HPA-1a antigen, may enter the mother’s circulation and induce pr... | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004201-33 | Sponsor Protocol Number: IMMU-132-09 | Start Date*: 2019-08-16 | |||||||||||||||||||||
| Sponsor Name:Immunomedics, Inc. | |||||||||||||||||||||||
| Full Title: Phase 3 Study of Sacituzumab Govitecan (IMMU-132) Versus Treatment of Physician's Choice (TPC) in subjects with Hormonal Receptor-Positive (HR+) Human Epidermal Growth Factor Receptor 2 (HER2) Nega... | |||||||||||||||||||||||
| Medical condition: Hormonal Receptor-Positive (HR+) Human Epidermal Growth Factor Receptor 2 (HER2) Negative Metastatic Breast Cancer (MBC) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) DE (Completed) NL (Completed) ES (Ongoing) BE (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2012-002125-30 | Sponsor Protocol Number: 2012LRDVDCM | Start Date*: 2012-10-24 |
| Sponsor Name:UZLeuven | ||
| Full Title: Vitamin D supplementation in cutaneous malignant melanoma outcome | ||
| Medical condition: cutaneous malignant melanoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) HU (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001972-23 | Sponsor Protocol Number: 2015-001972-23 | Start Date*: 2015-06-29 |
| Sponsor Name:Tampere University Hospital | ||
| Full Title: Randomized study to compare vaginal misoprostol to oral misoprostol in inducing labor | ||
| Medical condition: Pregnant women; induction of labor | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
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