- Trials with a EudraCT protocol (31)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31 result(s) found for: Clinical Trials Directive.
Displaying page 2 of 2.
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EudraCT Number: 2014-000845-64 | Sponsor Protocol Number: CCR4085 | Start Date*: 2014-12-17 | |||||||||||
Sponsor Name:The Royal Marsden NHS Foundation Trust | |||||||||||||
Full Title: A multicentre randomised phase II study of aflibercept plus chemotherapy in patients with colorectal liver-only metastases deemed to be inoperable or unsuitable for upfront liver resection | |||||||||||||
Medical condition: colorectal cancer with liver metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002169-30 | Sponsor Protocol Number: 3804 | Start Date*: 2014-10-08 |
Sponsor Name:The Royal Marsden NHS Foundation Trust | ||
Full Title: Planning treatment for oesophago-gastric cancer: a randomised maintenance therapy trial (PLATFORM Trial) | ||
Medical condition: Oesophago-gastric adenocarcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023001-36 | Sponsor Protocol Number: BAY86-4875/14607 | Start Date*: 2011-04-26 | |||||||||||
Sponsor Name:Bayer Health Care AG | |||||||||||||
Full Title: Multicenter, open-label study to evaluate the safety and efficacy (by blinded reading) of contrast-enhanced magnetic resonance angiography (MRA) after a single intravenous injection of 0.1 mmol/k... | |||||||||||||
Medical condition: Subjects with known or suspected vascular disease of the supra-aortic vessels | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) SE (Completed) FR (Completed) IT (Completed) PL (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023002-13 | Sponsor Protocol Number: BAY 86-4875/91759 | Start Date*: 2011-05-11 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: Multicenter, open-label study to evaluate the safety and efficacy (by blinded reading) of Gadobutrol-enhanced magnetic resonance angiography (MRA) after a single injection of 0.1 mmol/kg of Gadobut... | |||||||||||||
Medical condition: Subjects with known or suspected renal artery disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003005-25 | Sponsor Protocol Number: RADIANCE | Start Date*: 2019-12-17 | ||||||||||||||||
Sponsor Name:University Hospital Frankfurt, Goethe University | ||||||||||||||||||
Full Title: Radiochemotherapy +/- Durvalumab for locally-advanced Anal Carcinoma A multicenter, randomized, phase II trial of the German Anal Cancer Study Group | ||||||||||||||||||
Medical condition: anal cancer (UICC-Stage IIB-IIIC, incl. T2>4cm Nany ) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003763-22 | Sponsor Protocol Number: BAY73-4506/15984 | Start Date*: 2014-07-02 | ||||||||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||||||||||||
Full Title: A combined Phase IIa / IIb study of the efficacy, safety, and tolerability of repeated topical doses of regorafenib eye drops, in treatment-naïve subjects with neovascular age related macular degen... | ||||||||||||||||||||||||||||
Medical condition: neovascular age related macular degeneration | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: HU (Prematurely Ended) DE (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004146-18 | Sponsor Protocol Number: CCR3549 | Start Date*: 2011-11-09 | |||||||||||
Sponsor Name:The Royal Marsden NHS Foundation Trust | |||||||||||||
Full Title: Cyclophosphamide, doxorubicin, vincristine and prednisolone (CHOP) versus gemcitabine, cisplatin and methyl prednisolone (GEM-P) in the first line treatment Of T-cell Lymphoma, a multicentre rando... | |||||||||||||
Medical condition: T-cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020121-41 | Sponsor Protocol Number: 11728 | Start Date*: 2011-01-17 | |||||||||||
Sponsor Name:Bayer Health Care AG, D-51368 Leverkusen | |||||||||||||
Full Title: An uncontrolled, open-label, phase II study in subjects with metastatic adenocarcinoma of the colon or rectum who are receiving first line chemotherapy with mFOLFOX6 (oxaliplatin/ folinic acid/5-fl... | |||||||||||||
Medical condition: Metastatic adenocarcinoma of the colon or rectum (metastatic CRC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004484-39 | Sponsor Protocol Number: BAY1895344/18594 | Start Date*: 2017-07-18 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: An open-label, first-in-human, dose-escalation study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and maximum tolerated dose and / or recommended Phase II dose of the A... | |||||||||||||
Medical condition: Part A+A.1: Histologically confirmed solid tumors or NHL Part A J-arm : Advanced solid tumors Part B: a) DDR deficient advanced solid tumors: i) CRPC; ii) HER2- negative BC (estrogen-receptor posit... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001605-14 | Sponsor Protocol Number: CCR4309 | Start Date*: 2015-07-21 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:The Royal Marsden NHS Foundation Trust | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Randomised, double-blind, placebo controlled, multi-centre phase II study to assess the Efficacy and safety of 2nd line Olaparib in combination with Paclitaxel, in Western patients with advanced ... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Advanced Gastric and Gastro-oesophageal cancer | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015878-35 | Sponsor Protocol Number: BAY63-2521/14308 | Start Date*: 2010-03-22 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: Randomized, double blind, placebo controlled, parallel group, multi-center study to evaluate the hemodynamic effects of Riociguat (BAY 63-2521) as well as safety and kinetics in patients with pulmo... | |||||||||||||
Medical condition: Pacientes sintomáticos con una hipertensión pulmonar asociada a una disfunción del ventrículo izquierdo (PH-sLVD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Trial now transitioned) NL (Completed) BE (Completed) AT (Completed) FR (Completed) GB (Completed) IT (Trial now transitioned) DK (Completed) CZ (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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