- Trials with a EudraCT protocol (44,336)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,336 result(s) found.
Displaying page 786 of 2,217.
EudraCT Number: 2008-002152-26 | Sponsor Protocol Number: ISRCTN86894066 | Start Date*: 2009-01-20 | |||||||||||
Sponsor Name:The Royal Marsden Foundation Trust and The Institute of Cancer Research | |||||||||||||
Full Title: Randomised double-blind controlled phase III trial of hyperbaric oxygen therapy in patients suffering long-term adverse effects of radiotherapy for pelvic cancer | |||||||||||||
Medical condition: Chronic radiation-induced gastrointestinal symptoms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001069-18 | Sponsor Protocol Number: 12/0533 | Start Date*: 2013-07-11 | |||||||||||
Sponsor Name:University College London (UCL) | |||||||||||||
Full Title: MINeralocorticoid receptor antagonist pretreatment to MINIMISE reperfusion injury after ST-Elevation Myocardial Infarction(STEMI). | |||||||||||||
Medical condition: Cardiovascular disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000004-33 | Sponsor Protocol Number: IPR/18 | Start Date*: 2008-10-13 | |||||||||||
Sponsor Name:MOLMED | |||||||||||||
Full Title: NGR012: A phase II study of NGR-hTNF administered in combination with doxorubicin every 3 weeks in patients affected by advanced or metastatic ovarian cancer | |||||||||||||
Medical condition: Patients affected by advanced or metastatic ovarian cancer previously treated with platinum regimens (cis or carboplatin) plus paclitaxel | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003162-41 | Sponsor Protocol Number: ET2012000058 | Start Date*: 2013-01-21 | |||||||||||
Sponsor Name:Centre Léon Bérard | |||||||||||||
Full Title: A randomized, multicenter, open-label, phase II study of the optimal scheme of administration of pazopanib in thyroid carcinoma | |||||||||||||
Medical condition: Iodine refractory Differentiated Thyroid Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001596-21 | Sponsor Protocol Number: POL7080-003 | Start Date*: 2013-08-19 |
Sponsor Name:Polyphor Ltd | ||
Full Title: A phase II, open-label, multi-center study to assess pharmacokinetics (PK), safety and efficacy of POL7080 co-administered with standard of care (SoC) treatment in patients with ventilator- associa... | ||
Medical condition: Ventilator- associated pneumonia due to suspected or documented Pseudomonas aeruginosa infection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000144-21 | Sponsor Protocol Number: UCL/10/0299 | Start Date*: 2011-10-05 | |||||||||||||||||||||
Sponsor Name:University College London | |||||||||||||||||||||||
Full Title: ION– Is ablative radiOiodine Necessary for low risk differentiated thyroid cancer patients | |||||||||||||||||||||||
Medical condition: Patients with differentiated thyroid cancer who are classed as low risk | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005151-13 | Sponsor Protocol Number: MEM-COUGH-01 | Start Date*: 2012-05-17 | |||||||||||
Sponsor Name:University of Manchester [...] | |||||||||||||
Full Title: Open-label Pilot Study of Memantine in Chronic Cough Patients Attending a Specialist Clinic | |||||||||||||
Medical condition: Idiopathic and treatment resistant Chronic Cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005129-57 | Sponsor Protocol Number: KCT02/2012-VICTORY | Start Date*: 2013-02-21 | ||||||||||||||||
Sponsor Name:Krka, d.d., Novo mesto | ||||||||||||||||||
Full Title: The Efficacy and Safety of Valsartan and Combination of Valsartan and Hydrochlorothiazide in the Treatment of Patients with mild to moderate Arterial Hypertension. | ||||||||||||||||||
Medical condition: Patients with mild to moderate arterial hypertension. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SI (Completed) CZ (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003835-40 | Sponsor Protocol Number: RG12-024 | Start Date*: 2012-12-10 |
Sponsor Name:University of Birmingham | ||
Full Title: A multicentre, phase II randomised controlled trial evaluating cabazitaxel versus docetaxel re-challenge for the treatment of metastatic Castrate Refractory Prostate Cancer, previously treated with... | ||
Medical condition: Metastatic Castrate Refractory Prostate Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000640-10 | Sponsor Protocol Number: 2012/VCC/0009 | Start Date*: 2012-12-13 | ||||||||||||||||
Sponsor Name:Velindre NHS Trust | ||||||||||||||||||
Full Title: A randomised Phase II study of two pre-operative chemoradiotherapy regimes (oxaliplatin and capecitabine followed by radiotherapy with either oxaliplatin and capecitabine or paclitaxel and carbopla... | ||||||||||||||||||
Medical condition: Histologically confirmed operable oesophageal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-001456-36 | Sponsor Protocol Number: EGF100151 | Start Date*: 2004-09-06 | |||||||||||
Sponsor Name:GLAXO SMITHKLINE | |||||||||||||
Full Title: A phase III, randomized, open-label, multicenter study comparing GW572016 and Capecitabile (Xeloda) versus Capecitabile in women with refractory advanced or metastatic breast cancer. | |||||||||||||
Medical condition: Solid tumor treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002762-12 | Sponsor Protocol Number: MESOT-TREM-2012 | Start Date*: 2012-06-29 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | ||||||||||||||||||
Full Title: A SECOND-LINE, SINGLE ARM, PHASE II CLINICAL STUDY WITH TREMELIMUMAB, A FULLY HUMANIZED ANTI-CTLA-4 MONOCLONAL ANTIBODY, AS MONOTHERAPY IN PATIENTS WITH UNRESECTABLE MALIGNANT MESOTHELIOMA | ||||||||||||||||||
Medical condition: Patients affected by advanced malignant mesothelioma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001881-14 | Sponsor Protocol Number: GIFT/1 | Start Date*: 2013-03-01 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: A phase II clinical trial to evaluate the safety and efficacy of interferon gamma in elevating frataxin levels in Friedreich ataxia patients | |||||||||||||
Medical condition: Friedreich's Ataxia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004423-20 | Sponsor Protocol Number: V00498TA301 | Start Date*: 2013-01-10 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: STUDY OF EFFICACY AND SAFETY OF V0498 VERSUS PLACEBO IN ACUTE SORE THROAT PAIN | |||||||||||||
Medical condition: Acute sore throat | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) LV (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005486-21 | Sponsor Protocol Number: GA1102 | Start Date*: 2012-01-26 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare (UK) Ltd. | |||||||||||||
Full Title: A multicentre, randomised, double-blind, two arm, parallel group, placebo controlled, pilot study to assess the effect of Gaviscon Advance as add-on therapy in GORD patients with inadequate respons... | |||||||||||||
Medical condition: Gastro Oesophageal Reflux Disease (GORD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000333-40 | Sponsor Protocol Number: 11-534 | Start Date*: 2012-07-30 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Towards plannable breast surgery: diagnostic accuracy of microbubble enhanced Iodine-125 seed localization of the sentinel lymph node (MIB study) | ||
Medical condition: Patient with breast cancer with an indication for sentinel lymph node biopsy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001738-17 | Sponsor Protocol Number: GIMEMALAL0904 | Start Date*: 2004-11-08 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL'ADULTO | |||||||||||||
Full Title: Evaluation of the intensification of post-remissional therapy in the treatment of high-risks adult Acute Lymphoblastic Leukemia and monitoring of the minimal residual disease | |||||||||||||
Medical condition: Patients with T- and B-ALL; Age >14 and <61 years | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005589-37 | Sponsor Protocol Number: RMRHS0095 | Start Date*: 2013-03-08 | ||||||||||||||||
Sponsor Name:University of Warwick | ||||||||||||||||||
Full Title: select-d: Anticoagulation Therapy in SELECTeD Cancer Patients at Risk of Recurrence of Venous Thromboembolism | ||||||||||||||||||
Medical condition: Venous Thromboembolism and Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022899-32 | Sponsor Protocol Number: TH0918 | Start Date*: 2011-01-19 | |||||||||||
Sponsor Name:Celerion | |||||||||||||
Full Title: An open label, randomised, single dose, 5 way cross over study to compare the rate and extent of absorption of a 8.75mg Flurbiprofen lozenge with flavour and excipient base variants of a 8.75mg Fl... | |||||||||||||
Medical condition: Sore throat | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004795-11 | Sponsor Protocol Number: 26866138-MMY-3033 | Start Date*: 2013-02-20 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Randomized, Controlled Phase 3 Study to Evaluate Optimized Retreatment and Prolonged Therapy with Bortezomib (Velcade) in Patients with Multiple Myeloma in First or Second Relapse | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) BE (Completed) IT (Completed) PT (Completed) PL (Completed) FI (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
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