- Trials with a EudraCT protocol (44,352)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,352 result(s) found.
Displaying page 2,168 of 2,218.
EudraCT Number: 2020-004606-60 | Sponsor Protocol Number: BP42772 | Start Date*: 2021-06-22 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A 3-ARM, RANDOMIZED, BLINDED, ACTIVE-CONTROLLED, PHASE II STUDY OF RO7121661, A PD1-TIM3 BISPECIFIC ANTIBODY AND RO7247669, A PD1-LAG3 BISPECIFIC ANTIBODY, COMPARED WITH NIVOLUMAB IN PARTICIPANTS W... | |||||||||||||
Medical condition: Advanced or metastatic squamous cell carcinoma of the esophagus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) PL (Trial now transitioned) DK (Trial now transitioned) HU (Trial now transitioned) BE (Completed) FR (Trial now transitioned) IT (Trial now transitioned) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004476-35 | Sponsor Protocol Number: CCFZ533B2201 | Start Date*: 2019-08-19 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A 48-week, 6-arm, randomized, double-blind, placebo-controlled multicenter trial to assess the safety and efficacy of multiple CFZ533 doses administered subcutaneously in two distinct populations o... | |||||||||||||
Medical condition: Sjögren syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) HU (Completed) GB (GB - no longer in EU/EEA) NL (Completed) GR (Completed) FR (Completed) DE (Completed) SE (Completed) AT (Completed) SI (Completed) IT (Completed) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004130-24 | Sponsor Protocol Number: M15-572 | Start Date*: 2017-07-27 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Subjects with Active Psoriatic Arthritis Who Have a History of Inadequate Response to at ... | |||||||||||||
Medical condition: Moderately to Severely Active Psoriatic Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) BE (Completed) DE (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) GR (Completed) NL (Completed) PT (Completed) EE (Completed) LV (Completed) LT (Completed) SI (Completed) HU (Completed) ES (Ongoing) HR (Completed) BG (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001514-41 | Sponsor Protocol Number: G040188 | Start Date*: 2005-07-06 |
Sponsor Name:The Cardiovascular Research Foundation | ||
Full Title: A dual arm factorial randomized trial in patients with ST segment elevation AMI to compare the results of using either anticoagulation with unfractionated heparin plus routine GP IIb/IIIa inhibitio... | ||
Medical condition: The medical condition for this clinical trial is Acute Myocardial Infarction (AMI). AMI is defined as death or necrosis of myocardial cells. It is a diagnosis at the end of the spectrum of myocardi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) SE (Prematurely Ended) ES (Completed) DE (Completed) GB (Completed) DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003212-65 | Sponsor Protocol Number: ASF-1075-205 | Start Date*: 2007-09-05 | |||||||||||
Sponsor Name:Astion Pharma A/S | |||||||||||||
Full Title: Efficacy and safety of ASF-1075 cream 5% on pruritus in adult patients with atopic dermatitis. A multi-centre, randomised, double-blind, vehicle-controlled, parallel groups, proof of concept study. | |||||||||||||
Medical condition: Caucasian male and female patients 18-65 years of age with mild to moderate atopic dermatitis and experiencing moderate to severe pruritus. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000436-25 | Sponsor Protocol Number: RC3600 | Start Date*: 2012-12-05 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Frederiksberg University Hospital | ||||||||||||||||||||||||||||||||||||||
Full Title: Randomized, double-blinded and placebo-controlled clinical trial of the Rauvolfia-Citrus decoction in patients with type II diabetes | ||||||||||||||||||||||||||||||||||||||
Medical condition: Non-insulin dependent diabetes mellitus | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-004167-25 | Sponsor Protocol Number: NKI-AVLM22TGA | Start Date*: 2023-05-04 |
Sponsor Name:Department of Medical Oncology and Clinical Pharmacology, The Netherlands Cancer Institute - Antoni van Leeuwenhoek Hosp | ||
Full Title: Phase I/II study with galunisertib combined with capecitabine in patients with advanced chemotherapy resistant colorectal cancer with peritoneal metastases | ||
Medical condition: Advanced colorectal cancer with peritoneal metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002784-34 | Sponsor Protocol Number: NL69665.091.19 | Start Date*: 2020-01-08 | ||||||||||||||||
Sponsor Name:Radboudumc [...] | ||||||||||||||||||
Full Title: Deferoxamine in Aneurysmal Subarachnoid Hemorrhage pilot trial | ||||||||||||||||||
Medical condition: patients with aneurysmal subarachnoid hemorrhage | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000794-20 | Sponsor Protocol Number: 20160218 | Start Date*: 2016-08-30 | |||||||||||
Sponsor Name:Radboud University Medical Center | |||||||||||||
Full Title: Visualizing beta cells in patients with a history of gestational diabetes | |||||||||||||
Medical condition: Gestational diabetes | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003324-20 | Sponsor Protocol Number: STOPFOP1 | Start Date*: 2020-01-08 | |||||||||||
Sponsor Name:VU University Medical Center | |||||||||||||
Full Title: Saracatinib trial TO Prevent FOP | |||||||||||||
Medical condition: Fibrodyplasia Ossificans Progressiva (FOP) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002372-36 | Sponsor Protocol Number: 2022-16039 | Start Date*: 2024-01-02 |
Sponsor Name:Wageningen Research Stichting | ||
Full Title: The CanISleepinMS Study: Effect of cannabidiol (CBD) on sleep quality in patients with multiple sclerosis, a series of 15 randomised, placebo controlled N-of-1 trials | ||
Medical condition: Insomnia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002145-15 | Sponsor Protocol Number: NOK0023 | Start Date*: 2023-10-31 |
Sponsor Name:Nederlandse Obesitas Kliniek | ||
Full Title: Applying Mysimba in patients with weight regain after bariatric surgery | ||
Medical condition: Weight regain post bariatric surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002493-13 | Sponsor Protocol Number: M16BRC | Start Date*: 2016-09-15 | |||||||||||
Sponsor Name:NKI-AVL | |||||||||||||
Full Title: Substantially improving the cure rate of high-risk BRCA1-like breast cancer patients with personalized therapy | |||||||||||||
Medical condition: High risk breast cancer (stage III), BRCA1-like | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000070-29 | Sponsor Protocol Number: 74668 | Start Date*: 2022-09-15 |
Sponsor Name:VU University Medical Center | ||
Full Title: A Proof-of-Concept Study to Explore the Potential Efficacy of Deferiprone in Patients With Pelizaeus-Merzbacher disease (PMD) | ||
Medical condition: Pelizaeus-Merzbacher disease | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000689-79 | Sponsor Protocol Number: 50364 | Start Date*: 2015-10-13 |
Sponsor Name:Vrije Universiteit Medical Center | ||
Full Title: Rectal preserving treatment for early rectal cancer. A multi-centred randomised trial of radical surgery versus adjuvant chemoradiotherapy after local excision for early rectal cancers. | ||
Medical condition: Patients with a margin free (at least 1 mm) endoluminal local excision (by TEM, TAMIS, TSPM, EMR/ESD or polypectomy) of an early rectal cancer (below 10 cm). According to current guidelines these ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004588-11 | Sponsor Protocol Number: ABR64005 | Start Date*: 2019-09-10 |
Sponsor Name:University Maastricht | ||
Full Title: Control Crohn Safe Trial: Long term efficacy and safety of periodic treatment with adalimumab versus standard step-care for newly diagnosed Crohn's disease. | ||
Medical condition: The chronic inflammatory bowel disease Crohn's disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003012-27 | Sponsor Protocol Number: 18062020 | Start Date*: 2021-01-12 |
Sponsor Name:Canisius Wilhelmina Ziekenhuis | ||
Full Title: Impact of peri-operative tEstosterone levels oN Functional and oncological Outcomes following RadiCal prostatEctomy | ||
Medical condition: Late-onset hypogonadism | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000837-17 | Sponsor Protocol Number: NL80854.018.22 | Start Date*: 2022-12-07 |
Sponsor Name:Amsterdam UMC | ||
Full Title: Subcutaneous vedolizumab drug de-escalation using therapeutic drug monitoring in inflammatory bowel disease: a randomized controlled pilot study | ||
Medical condition: Inflammatory bowel diseases (Crohn's disease, ulcerative colitis) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005933-34 | Sponsor Protocol Number: SFHI01 | Start Date*: 2021-08-09 | |||||||||||
Sponsor Name:Sorin CRM SAS (Microport CRM) | |||||||||||||
Full Title: Evaluation of a modified Anti-Platelet Therapy associated with low-dose rapamycin DES Firehawk in Acute Myocardial Infarction Patients treated with complete revascularization strategy | |||||||||||||
Medical condition: Patients with clinically stable, low to moderate complexity acute Myocardial Infarction (MI; troponine-positive Non-ST-Elevation MI or ST-Elevation MI) requiring primary Percutaneous Coronary Inte... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) NL (Trial now transitioned) ES (Ongoing) IT (Ongoing) PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005633-33 | Sponsor Protocol Number: 202000842 | Start Date*: 2021-06-02 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Prediction of ECT treatment response and reduction of Cognitive Side-effects using EEG and Rivastigmine | ||
Medical condition: A depressive disorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
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