- Trials with a EudraCT protocol (3)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3 result(s) found for: Learning algorithms.
Displaying page 1 of 1.
| EudraCT Number: 2021-005919-30 | Sponsor Protocol Number: AK_NEN_DOTA-FDG_21 | Start Date*: 2022-09-21 | ||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Department of Clinical Physiology and Nuclear Medicine, Rigshospitalet | ||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Dual 64Cu-DOTATATE and 18F-FDG PET/CT Imaging of Patients with Neuroendocrine Neoplasms | ||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Neuroendocrine neoplasms | ||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2019-004613-14 | Sponsor Protocol Number: VERITA_PALG-CLL5 | Start Date*: 2021-10-31 | |||||||||||
| Sponsor Name:POLISH ADULT LEUKEMIA GROUP | |||||||||||||
| Full Title: A prospective, multicenter, phase II trial to assess the efficacy and safety of MRD-driven treatment with VEnetoclax and RItuximab combination in previously unTreated pAtients with chronic lymphocy... | |||||||||||||
| Medical condition: Chronic lymphocytic leukemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000239-34 | Sponsor Protocol Number: PONTIACII | Start Date*: 2015-12-30 |
| Sponsor Name:Medizinische Universität Wien | ||
| Full Title: NT-proBNP Selected PreventiOn of cardiac eveNts in a populaTion of dIabetic patients without A history of Cardiac disease; a prospective randomized trial | ||
| Medical condition: The purpose of this study is to evaluate the effect of high dose Renin-Angiotensin System (RAS)-antagonists and beta-blocker treatment for the primary prevention of cardiac events in a population o... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) NL (Ongoing) GB (GB - no longer in EU/EEA) ES (Ongoing) HU (Completed) | ||
| Trial results: (No results available) | ||
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