- Trials with a EudraCT protocol (28,504)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
28,504 result(s) found for: - Crohn’s Disease.
Displaying page 567 of 1,426.
EudraCT Number: 2009-013128-22 | Sponsor Protocol Number: HE 42/09 | Start Date*: 2010-06-29 | |||||||||||
Sponsor Name:Hellenic Cooperative Oncology Group | |||||||||||||
Full Title: Lapatinib and Whole Brain Radiotherapy for patients with brain metastases from lung and breast tumors. A phase II study of the Hellenic Cooperative Oncology Group (HeCOG). | |||||||||||||
Medical condition: Patients with brain metastases from lung and breast tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010756-10 | Sponsor Protocol Number: Index-CSBTE-01-09 | Start Date*: 2009-05-19 | |||||||||||
Sponsor Name:InDex Pharmaceuticals AB | |||||||||||||
Full Title: Effect of an additional single dose of Kappaproct to corticosteroid treated patients with brain edema caused by brain tumor | |||||||||||||
Medical condition: Patients with increasing clinical symptoms of brain edema caused by brain tumor or brain metatstasis, on maximum dose of corticosteroids will be asked to participate in the study. The brain edema m... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002914-12 | Sponsor Protocol Number: 0018 | Start Date*: 2005-04-13 | |||||||||||
Sponsor Name:Theravance Inc. | |||||||||||||
Full Title: A phase 3, Randomized, Double-Blind, Multinational Trial of Intravenous Televancin Versus Vancomycin for Treatment of Complicated Gram-positive Skin and Skin Structure Infections with a focus on Pa... | |||||||||||||
Medical condition: Complicated Gram-Positive Skin and Skin Structure Infections With a Focus on Patients With Infections Due to Methicillin-Resistant Staphylococcus aureus. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005670-71 | Sponsor Protocol Number: ML18792/GOIRC | Start Date*: 2006-02-09 | |||||||||||
Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA | |||||||||||||
Full Title: Dose-finding and Phase II study of the Combination of Bevacizumab rhuMAb VEGF plus low- dose Immunotherapy and Chemotherapy in patients with metastatic Renal Cell Cancer. | |||||||||||||
Medical condition: Patients with metastatic Renal Cell Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002817-37 | Sponsor Protocol Number: PIX200701 | Start Date*: 2008-07-29 | |||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO "CARLO BESTA" | |||||||||||||
Full Title: A PHASE II, PLACEBO CONTROLLED, DOSE FINDING PILOT STUDY OF PIXANTRONE EFFICACY ADMINISTERED INTRAVENOUSLY IN PATIENTS AFFECTED WITH MYASTHENIA GRAVIS | |||||||||||||
Medical condition: Patients affected with MG showing clinically meaningful improvement after therapeutic plasmapheresis. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003844-41 | Sponsor Protocol Number: 2719 | Start Date*: 2007-03-02 |
Sponsor Name:Royal Marsden NHS Trust | ||
Full Title: Feasibility study of R-CHOP plus bevacizumab in patients with diffuse large B cell lymphoma (DLBCL) | ||
Medical condition: Previously untreated diffuse large B-cell non-Hodgkin's lymphoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-003983-73 | Sponsor Protocol Number: C-2006-009 | Start Date*: 2007-01-17 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: A Phase IIa Multicenter, Randomized, Double-Blind, Placebo -Controlled, Parallel Group Study of RWJ-445380 Cathepsin-S Inhibitor in Patients with Active Rheumatoid Arthritis Despite Methotrexate Th... | |||||||||||||
Medical condition: Rheumatoid arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003651-20 | Sponsor Protocol Number: V211-017 | Start Date*: 2007-06-04 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Phase III Clinical Trial to Evaluate the Safety, Tolerability, and Immunogenicity of Zoster Vaccine Live (Oka/Merck) in Patients on Chronic/Maintenance Corticosteroids | |||||||||||||
Medical condition: Zoster Vaccine | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) BE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017869-27 | Sponsor Protocol Number: TERSSC-001 incl. Amendment 1 | Start Date*: 2010-09-23 | |||||||||||
Sponsor Name:University Hospital Zurich | |||||||||||||
Full Title: A dual-center, open-label Proof of Concept study to evaluate the efficacy of Terguride for the treatment of fibrosis in patients with systemic sclerosis. | |||||||||||||
Medical condition: Diffuse scleroderma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017437-22 | Sponsor Protocol Number: CCPS5959 | Start Date*: 2010-02-24 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PERUGIA | |||||||||||||
Full Title: MANAGEMENT OF PRIMARY AND SECUNDARY PERITONEAL CARCINOMATOSIS FROM COLO-RECTAL CANCER, RECURRENT OVARIAN CANCER AND ABDOMINAL SARCOMATOSIS BY CYTOREDUCTIVE SURGERY PLUS HYPERTHERMIC INTRAPERITONEAL... | |||||||||||||
Medical condition: Peritoneal carcinomatosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004934-26 | Sponsor Protocol Number: N/A | Start Date*: 2008-11-26 | ||||||||||||||||
Sponsor Name:UMCG | ||||||||||||||||||
Full Title: Pharmacokinetics and –dynamics of intrathecal baclofen therapy in patients with spasticity | ||||||||||||||||||
Medical condition: Spasticity of varying origin (i.e. MS, spinal cord injury), which doesn't respond on treatment with oral medication | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007604-15 | Sponsor Protocol Number: STH14971 | Start Date*: 2009-03-03 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: A Pilot Study of the Effect of Glucocorticoid Receptor Antagonism in Patients with Sub-Clinical Cushing's Syndrome | |||||||||||||
Medical condition: Sub Clinical Cushing's Syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001236-13 | Sponsor Protocol Number: 2008-001236-13 | Start Date*: 2007-12-01 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PADOVA | |||||||||||||
Full Title: Sperimental controlled and randomized in singol blind study. Use of continuous epidural ketamina in patients submitted to toracotomy for pulmonary resection. | |||||||||||||
Medical condition: pulmonary resection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011637-27 | Sponsor Protocol Number: CHARTT-001 | Start Date*: 2010-08-24 |
Sponsor Name:Hull and East Yorkshire NHS Hospital Trust | ||
Full Title: Clopidogrel versus Aspirin in Chronic Heart Failure | ||
Medical condition: Heart Failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-000222-51 | Sponsor Protocol Number: 06_DOG05_44 | Start Date*: 2007-09-07 |
Sponsor Name:Southampton University Hospitals NHS Trust | ||
Full Title: Short CHemo RadioImmunotherapy in Follicular Trial of 90Y Ibritumomab tiuxetan (ZevalinTM) as therapy for first and second relapse in Follicular Lymphoma | ||
Medical condition: Follicular Lymphoma First and second relapse of Follicular Lymphoma grade 1, 2, 3a. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000440-24 | Sponsor Protocol Number: SDX-101-03 | Start Date*: 2004-08-24 |
Sponsor Name:Cephalon UK Limited | ||
Full Title: A Randomized, Multi-Center, Phase II Study to Investigate the Safety and Efficacy of SDX-101 (R-etodolac) in Combination with Chlorambucil, and that of Chlorambucil alone, in Patients with Chronic ... | ||
Medical condition: Chronic Lymphocytic Leukemia (CLL) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-000649-20 | Sponsor Protocol Number: STAR-03 | Start Date*: 2012-06-11 | |||||||||||
Sponsor Name:FONDAZIONE DELL'ISTITUTO TOSCANO TUMORI | |||||||||||||
Full Title: Phase II study of pre-operative treatment with external radiotherapy plus panitumumab in operable locally advanced rectal cancer (favourable and intermediate prognostic group) (RaP Study/STAR-03) | |||||||||||||
Medical condition: Operable locally advanced rectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001462-16 | Sponsor Protocol Number: 26866138-CAN-2002, VEL-04-118 | Start Date*: 2006-03-14 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: A phase II Study of Bortezomib (Velcade), a proteasome Inhibitor, in treating patients with idiopathic Myelofibrosis (IM) randomized to receive new investigational drugs. | |||||||||||||
Medical condition: idiopathic myelofibrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002179-32 | Sponsor Protocol Number: CT/12.05 | Start Date*: 2012-07-24 |
Sponsor Name:Hellenic Oncology Research Group (H.O.R.G.) | ||
Full Title: A Multicenter, Phase II, Single-Arm Clinical Trial of nab-Paclitaxel as salvage treatment for patients with Locally Advanced or Metastatic Adenocarcinomas of the Stomach and Gastro-esophageal junction | ||
Medical condition: Patients with Locally Advanced or Metastatic Adenocarcinomas of the Stomach and Gastro-esophageal junction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005357-23 | Sponsor Protocol Number: 01 | Start Date*: 2013-01-27 | |||||||||||
Sponsor Name:AUSL VITERBO | |||||||||||||
Full Title: Preventing injection pain by Clostridium Histolyticum Collagenase Administration for teatment of Dupuytrens contracture | |||||||||||||
Medical condition: Dupuytren s Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
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