- Trials with a EudraCT protocol (602)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
602 result(s) found for: Myeloma.
Displaying page 1 of 31.
EudraCT Number: 2016-004282-31 | Sponsor Protocol Number: V14-11056 | Start Date*: 2017-03-15 | ||||||||||||||||
Sponsor Name:Vivolux AB | ||||||||||||||||||
Full Title: VLX1570 and Low-Dose Dexamethasone in Relapsed or Relapsed and Refractory Multiple Myeloma: A Clinical and Correlative Phase 1/2 Study | ||||||||||||||||||
Medical condition: Multiple Myeloma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000987-31 | Sponsor Protocol Number: 35RC17_8825_IMMUNO-MYELO | Start Date*: 2021-04-23 | |||||||||||
Sponsor Name:CHU Rennes | |||||||||||||
Full Title: Immunomonitoring and multiple myeloma: impact of lenalidomide on immune checkpoint expression | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001292-11 | Sponsor Protocol Number: NMSG 17/07 | Start Date*: 2007-08-05 | |||||||||||
Sponsor Name:Nordic Myeloma Study Group | |||||||||||||
Full Title: Talidomid vs Velcade vid melfalanrefraktärt myelom | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003752-30 | Sponsor Protocol Number: 088 | Start Date*: 2008-11-27 | |||||||||||
Sponsor Name:Merck & Co., Inc | |||||||||||||
Full Title: Estudio internacional, multicéntrico, aleatorizado, doble ciego de Vorinostat (MK-0683) o placebo en combinación con bortezomib en pacientes con mieloma multiple An International, Multicenter, Ran... | |||||||||||||
Medical condition: mieloma múltiple multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) DE (Prematurely Ended) BE (Completed) FR (Completed) AT (Completed) CZ (Completed) PT (Prematurely Ended) HU (Prematurely Ended) IT (Completed) BG (Prematurely Ended) GB (Completed) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003856-35 | Sponsor Protocol Number: Uni-Koeln-3946 | Start Date*: 2020-12-18 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Daratumumab for first line treatment of transplant-ineligible myeloma patients followed by daratumumab re-treatment at first relapse (GMMG-DADA) | |||||||||||||
Medical condition: multiple myeloma (untreated) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003599-39 | Sponsor Protocol Number: AMD3100-3102-DE | Start Date*: 2005-12-02 | |||||||||||
Sponsor Name:AnorMED Corp. | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, comparative trial of AMD3100 (240 mcg/kg) plus G-CSF (10 mcg/kg) versus G-CSF (10 mcg/kg) plus placebo to mobilize and collect greater than or equal ... | |||||||||||||
Medical condition: Mobilization of stem cells prior to autologous stem cell transplantation in patients with multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022029-13 | Sponsor Protocol Number: CBHQ880A2204 | Start Date*: 2011-08-11 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A single-arm, open-label, phase 2 clinical trial evaluating disease response following treatment with intravenous BHQ880, a fully human, anti-Dickkopf1 (DKK1) neutralizing antibody in previously un... | |||||||||||||
Medical condition: Adults diagnosed with high-risk Smoldering Multiple Myeloma (SMM) and who have not received any previous antimyeloma treatment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002675-41 | Sponsor Protocol Number: CRAD001C2455 | Start Date*: 2007-05-22 | |||||||||||
Sponsor Name:Universitaetsklinikum Schleswig-Holstein | |||||||||||||
Full Title: A non-randomised, multi-center Phase I/II trial of safety, tolerability and efficacy of Everolimus (RAD001) in relapsed or refractory Multiple Myeloma | |||||||||||||
Medical condition: Multiple Myeloma (Salmon-Durie stage II or III, Relapsed or refractory disease after failure of two or more treatment regimens) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001416-20 | Sponsor Protocol Number: DSC/07/2357/29 | Start Date*: 2009-05-19 | |||||||||||
Sponsor Name:ITALFARMACO | |||||||||||||
Full Title: Phase II High Pulse Dose Clinical Trial of Orally Administered ITF 2357 In Patients with Relapsed/Refractory Multiple Myeloma | |||||||||||||
Medical condition: Patients with Relapsed/Refractory Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005425-30 | Sponsor Protocol Number: AURA-6202-011 | Start Date*: 2008-04-17 | |||||||||||
Sponsor Name:Nerviano Medical Sciences S.r.l. | |||||||||||||
Full Title: An Exploratory Phase II Study of PHA-739358 in Patients with Multiple Myeloma Harbouring the t (4;14) translocation with or without FGFR3 Expression | |||||||||||||
Medical condition: Multiple Myeloma Harbouring the t (4;14) translocation with or without FGFR3 Expression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003926-10 | Sponsor Protocol Number: CHUBX2017/32 | Start Date*: 2019-02-13 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Prospective comparison of 18F-choline PET/CT and 18F-FDG PET/CT in the initial work-up of Multiple Myeloma | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002557-38 | Sponsor Protocol Number: Allo-MM-PostCy-Study | Start Date*: 2018-02-13 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: Cyclophosphamide as graft-versus-host prophylaxis after allogeneic stem cell transplantation for multiple myeloma. A phase II study. | |||||||||||||
Medical condition: Multiple myeloma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001013-89 | Sponsor Protocol Number: DAMTE | Start Date*: 2018-08-28 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA "BIANCHI-MELACRINO-MORELLI" | ||||||||||||||||||
Full Title: Double ASCT in MM: phase III study comparing between melphalan based regimen vs a new regimen consisting of melphalan and thiotepa | ||||||||||||||||||
Medical condition: multiple myeloma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005103-32 | Sponsor Protocol Number: H9S-MC-JDCG | Start Date*: 2012-08-13 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo Controlled Phase 2 Study of LY2127399 in Combination with Bortezomib and Dexamethasone in Patients with Previously Treated Multiple Myeloma | |||||||||||||
Medical condition: Previously Treated Multiple Myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) GR (Completed) PL (Completed) DE (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005638-56 | Sponsor Protocol Number: 0805603 | Start Date*: 2009-02-16 | ||||||||||||||||
Sponsor Name:CHU de TOULOUSE | ||||||||||||||||||
Full Title: Protocole IFM 2008 : Primo-traitement des patients de moins de 65 ans atteints de myélome | ||||||||||||||||||
Medical condition: Myelome, Myelome multiple | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004580-19 | Sponsor Protocol Number: REVIR | Start Date*: 2008-10-14 | |||||||||||
Sponsor Name:CHU DE POITIERS | |||||||||||||
Full Title: PHARMACOKINETICS, SAFETY AND EFFICACY OF LENALIDOMIDE (REVLIMID®) IN COMBINATION WITH DEXAMETHASONE IN PATIENTS WITH MULTIPLE MYELOMA AND IMPAIRED RENAL FONCTION | |||||||||||||
Medical condition: multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001175-29 | Sponsor Protocol Number: MM-FOT-08 | Start Date*: 2008-04-02 | |||||||||||
Sponsor Name:OSPEDALE POLICLINICO S. MATTEO | |||||||||||||
Full Title: Phase II trial evaluating fotemustine (Muphoran) treatment in patients with refractory or relapsing multiple myeloma | |||||||||||||
Medical condition: multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004815-24 | Sponsor Protocol Number: FM-MYEL-06-01 | Start Date*: 2006-12-05 | |||||||||||
Sponsor Name:FONDAZIONE MICHELANGELO - AVANZAMENTO DELLO STUDIO E CURA DEI TUMORI | |||||||||||||
Full Title: Bortezomib and dexamethasone treatment before donor lymphocyte infusions for myeloma patients progressing or relapsing after allogeneic transplantation of hematopoietic cells | |||||||||||||
Medical condition: Myeloma patients progressing or relapsing after allogeneic transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003891-39 | Sponsor Protocol Number: HOVON 76 MM | Start Date*: 2007-05-22 | |||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||
Full Title: Lenalidomide maintenance following tandem autologous stem cell and non myeloablative allogeneic transplantation for patients with multiple myeloma <= 66 years who have been treated in or according... | |||||||||||||
Medical condition: multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005709-62 | Sponsor Protocol Number: GEN503 | Start Date*: 2012-08-01 | |||||||||||
Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
Full Title: An Open label, International, Multicenter, Dose Escalating Phase 1/2 Trial Investigating the Safety of Daratumumab in Combination with Lenalidomide and Dexamethasone in Patients with Relapsed or Re... | |||||||||||||
Medical condition: Relapsed or Relapsed and Refractory Multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DK (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
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