- Trials with a EudraCT protocol (128)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
128 result(s) found for: Thalidomide.
Displaying page 1 of 7.
EudraCT Number: 2005-003931-40 | Sponsor Protocol Number: BRD/05/95 | Start Date*: 2006-04-20 |
Sponsor Name:University College London | ||
Full Title: Phase ll Trial of Fludarabine & Cyclophosphamide followed by Thalidomide for Angioimmunoblastic Lymphoma | ||
Medical condition: Angioimmunoblastic T-cell lymphoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023828-24 | Sponsor Protocol Number: 09107 | Start Date*: 2011-06-09 |
Sponsor Name:University of Nottingham | ||
Full Title: The effect of Thalidomide on sputum biomarkers in IPF cough. | ||
Medical condition: Cough in Idiopathic Pulmonary fibrosis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-000371-18 | Sponsor Protocol Number: 220105 | Start Date*: 2005-09-23 |
Sponsor Name:Portsmouth Hospitals Trust | ||
Full Title: The use of Thalidomide as a treatment for the cachexia of incurable upper gastrointestinal adenocarcinomas:a randomised, double-blinded, placebo controlled trial. | ||
Medical condition: The cachexia associated with terminal gastrointestinal adenocarcinomas | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004007-34 | Sponsor Protocol Number: HOVON87MM/NMSG18 | Start Date*: 2008-11-20 | |||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||
Full Title: Randomized phase III trial in elderly patients with previously untreated symptomatic Multiple Myeloma comparing MP-Thalidomide (MP-Thal) followed by thalidomide maintenance versus MP-Lenalidomide (... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) SE (Completed) DK (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002749-23 | Sponsor Protocol Number: AGMT_MM-1/EMN-13 | Start Date*: 2015-01-19 |
Sponsor Name:AGMT gGmbH | ||
Full Title: Ixazomib in combination to thalidomide - dexamethasone for patients with relapsed and/or refractory multiple myeloma | ||
Medical condition: refractory and/or relapsed multiple myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) CZ (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014922-40 | Sponsor Protocol Number: PT-171-503 | Start Date*: 2010-07-07 |
Sponsor Name:Erasmus MC | ||
Full Title: Carfilzomib in combination with Thalidomide and Dexamethasone for remission induction and consolidation of Multiple Myeloma at first presentation | ||
Medical condition: Multiple myeloma at first presentation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001426-24 | Sponsor Protocol Number: P02470 | Start Date*: 2004-11-23 |
Sponsor Name:Prof. Heinz Ludwig, MD, Wilhelminenspital, First Department of Medicine and Medical Oncology | ||
Full Title: Multicenter, open, randomized study for first-line treatment of multiple myeloma: thalidomide/dexamethasone vs. MP for induction therapy and thalidomide/Intron A vs. Intron A for maintenance therapy | ||
Medical condition: First line treatment of multiple myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-007939-29 | Sponsor Protocol Number: CLBH589BIT01T | Start Date*: 2008-03-06 | |||||||||||
Sponsor Name:FONDAZIONE NEOPLASIE SANGUE ONLUS | |||||||||||||
Full Title: A PHASE II,MULTI-CENTER, OPEN LABEL STUDY OF ORAL LBH589 PLUS MELPHALAN, PREDNISONE AND THALIDOMIDE (LB-MPT)IN ADVANCED, REFRACTORY MULTIPLE MYELOMA PATIENTS. | |||||||||||||
Medical condition: Patients with refractory or advanced Multiple Myeloma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000786-24 | Sponsor Protocol Number: NET-2013-02355002 | Start Date*: 2017-03-07 | |||||||||||
Sponsor Name:IRCCS Burlo Garofolo | |||||||||||||
Full Title: Thalidomide, a novel immunological treatment to modify the natural history of paediatric Crohn's disease: a new proposal from a well-established paediatric research network | |||||||||||||
Medical condition: Crohn's Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005414-20 | Sponsor Protocol Number: 14/05 | Start Date*: 2006-03-06 | |||||||||||
Sponsor Name:ISTITUTO PER L INFANZIA BURLO GAROFOLO | |||||||||||||
Full Title: Randomized controlled double-blind Vs. placebo multicentre study on the safety and effectiveness of thalidomide in the treatment of refractory Crohn s disease and ulcerative colitis. | |||||||||||||
Medical condition: Inflammatory Bowel Disease Crohn Disease, Ulcerative Colitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004096-36 | Sponsor Protocol Number: THALI-HHT | Start Date*: 2011-10-11 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: Efficacy of thalidomide in the treatment of severe recurrent epistaxis in hereditary hemorrhagic telangiectasia (HHT) | |||||||||||||
Medical condition: Severe recurrent epistaxis in hereditary hemorrhagic telangiectasia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001628-35 | Sponsor Protocol Number: X05140 | Start Date*: 2006-01-31 |
Sponsor Name:EBMT - CLWP | ||
Full Title: A randomized controlled study of Velcade (Bortezomib) plus Thalidomide plus Dexamethasone compared to Thalidomide plus Dexamethasone for the treatment of myeloma patients progressing or relapsing a... | ||
Medical condition: multiple myeloma patients in progression or relapse after autologous transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) DE (Completed) GB (Completed) CZ (Completed) AT (Completed) HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-005164-25 | Sponsor Protocol Number: 04.09 | Start Date*: 2005-04-14 |
Sponsor Name:Odense University Hospital | ||
Full Title: Phase II study of thalidomide in combination with temozolomide in metastatic malignant melanoma with brain metastases | ||
Medical condition: Advanced metastic malignant melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-005166-20 | Sponsor Protocol Number: 04.10 | Start Date*: 2005-04-14 |
Sponsor Name:Odense University Hospital | ||
Full Title: Phase II study of first-line therapy with Thalidomide in combination with Peg-introna and decrescendo IL-2 in patients with metastatic malignant melanoma | ||
Medical condition: Metastatic malignant melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000427-42 | Sponsor Protocol Number: LT 2005 XX | Start Date*: 2005-04-15 |
Sponsor Name:UK Children’s Cancer Study Group | ||
Full Title: SIOPEL 5 (HCC-1) trial on the hepatocellular carcinoma family of tumours in children/adolescents and young adults | ||
Medical condition: Hepatocellular carcinoma | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-010956-93 | Sponsor Protocol Number: HM09/8885 | Start Date*: 2009-09-17 | |||||||||||
Sponsor Name:University of Leeds [...] | |||||||||||||
Full Title: Randomised comparisons, in myeloma patients of all ages, of thalidomide, lenalidomide, carfilzomib and bortezomib induction combinations, and of lenalidomide and combination lenalidomide vorinostat... | |||||||||||||
Medical condition: Newly diagnosed patients with symptomatic myeloma | |||||||||||||
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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: 2005-004937-16 | Sponsor Protocol Number: THA PH INT 2005 CL 001 | Start Date*: 2006-02-17 | |||||||||||
Sponsor Name:Celgene International Sarl | |||||||||||||
Full Title: Randomised, Controlled, Open-Label, Multi-Centre Comparison of Thalidomide Versus High-Dose Dexamethasone for the Treatment of Relapsed Refractory Multiple Myeloma | |||||||||||||
Medical condition: Multiple myeloma (MM) is a malignant, lymphoproliferative disease of the B-cell system. The incidence is approximately 4 per 100,000 and it is age-dependent, with an increase in incidence of approx... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) CZ (Completed) GB (Completed) SK (Completed) PT (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004823-39 | Sponsor Protocol Number: CC-5013-MM-020/IFM 07-01 | Start Date*: 2008-04-03 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A PHASE III, RANDOMIZED, OPEN-LABEL, 3-ARM STUDY TO DETERMINE THE EFFICACY AND SAFETY OF LENALIDOMIDE (REVLIMID) PLUS LOW-DOSE DEXAMETHASONE WHEN GIVEN UNTIL PROGRESSIVE DISEASE OR FOR 18 FOUR-WEEK... | |||||||||||||
Medical condition: Previously untreated multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) IE (Prematurely Ended) IT (Completed) AT (Completed) ES (Completed) SE (Completed) BE (Completed) PT (Completed) DE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004928-21 | Sponsor Protocol Number: Auto-Allo-TSCTinMM | Start Date*: 2008-06-27 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: Autologous-Allogeneic Tandem Stem Cell Transplantation and Maintenance Therapy with Thalidomide / DLI for patients with Multiple Myeloma (MM) and age <= 60 years: A phase II-study | |||||||||||||
Medical condition: Multiple Myeloma Stage II or III according to Salmon and Durie | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003174-27 | Sponsor Protocol Number: RC13-0284 | Start Date*: 2014-06-12 |
Sponsor Name:CHU de Nantes | ||
Full Title: A PHASE III STUDY OF VELCADE (BORTEZOMIB) THALIDOMIDE DEXAMETHASONE (VTD) VERSUS VELCADE (BORTEZOMIB) CYCLOPHOSPHAMIDE DEXAMETHASONE (VCD) AS AN INDUCTION TREATMENT PRIOR TO AUTOLOGOUS STEM CELL TR... | ||
Medical condition: Young untreated patients with Multiple myeloma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: View results |
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