- Trials with a EudraCT protocol (48)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
48 result(s) found for: Macroglobulinemia.
Displaying page 1 of 3.
EudraCT Number: 2005-000174-52 | Sponsor Protocol Number: FCR-1-WM | Start Date*: 2005-01-11 | |||||||||||
Sponsor Name:ASSOCIAZIONE MALATTIE SANGUE | |||||||||||||
Full Title: Phase II multicenter study of immuno-chemotherapy with fludarabine, cyclophosphamide and rituximab (FCR) for symptomatic Waldenstrom's macroglobulinemia | |||||||||||||
Medical condition: Waldenstrom's macroglobulinemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002388-25 | Sponsor Protocol Number: 703 | Start Date*: 2014-04-01 | |||||||||||
Sponsor Name:Azienda Ospedaliera Ospedali Riuniti Marche Nord | |||||||||||||
Full Title: Phase II study to evaluate the safety and the efficacy of rituximab, cyclophosphamide, non-pegylated liposomal doxorubicin, vincristine and prednisolone (R-COMP 14) as front-line therapy for patien... | |||||||||||||
Medical condition: Active and untreated Waldenstrom Macroglobulinemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005129-22 | Sponsor Protocol Number: FIL_BRB | Start Date*: 2014-06-09 | |||||||||||
Sponsor Name:Fondazione Italiana Linfomi | |||||||||||||
Full Title: FASE II STUDY WITH BORTEZOMIB, RITUXIMAB AND BENDAMUSTIN –BRB- FOR NON-HODGKIN LYMPHOPLASMACYTIC LYMPHOMA/WALDENSTROM MACROGLOBULINEMIA’S PATIENTS AT FIRST RELAPSE | |||||||||||||
Medical condition: NON-HODGKIN LYMPHOPLASMACYTIC LYMPHOMA/WALDENSTROM MACROGLOBULINEMIA’S PATIENTS | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003526-88 | Sponsor Protocol Number: CZAR-1 | Start Date*: 2020-12-15 | |||||||||||
Sponsor Name:University Hospital Ulm | |||||||||||||
Full Title: Efficacy and safety of Carfilzomib in combination with Ibrutinib vs. Ibrutinib alone in Waldenström’s Macroglobulinemia (CZAR-1) | |||||||||||||
Medical condition: Waldenström's Macroglobulinemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) GR (Trial now transitioned) AT (Trial now transitioned) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020868-38 | Sponsor Protocol Number: RV-WM-PI-0548 | Start Date*: 2011-06-14 | |||||||||||
Sponsor Name:U.O.C. EMATOLOGIA - OSP. S. EUGENIO - ASL RM C | |||||||||||||
Full Title: (A Phase 2) STUDY TO DETERMINE THE EFFICACY AND SAFETY OF LENALIDOMIDE AND LOW-DOSE DEXAMETHASONE (Rd) FOLLOWED BY RITUXIMAB, AUTOGRAFT AND LENALIDOMIDE MAINTENANCE IN NEWLY DIAGNOSED WALDESTROM MA... | |||||||||||||
Medical condition: Waldenstr�m`s Macroglobulinemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003563-31 | Sponsor Protocol Number: 26866138CAN 2021 | Start Date*: 2007-03-09 | |||||||||||
Sponsor Name:European Myeloma Network | |||||||||||||
Full Title: Phase II Study of Combination Bortezomib (VELCADE, PS-341), Dexamethasone, and Rituximab (MabThera) (BDR) in Patients with previously untreated Waldenstrom’s Macroglobulinemia (WM). | |||||||||||||
Medical condition: Newly diagnosed Waldenstrom's macroglobulinemia (WM) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) NL (Ongoing) ES (Ongoing) FR (Ongoing) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005053-20 | Sponsor Protocol Number: ML39235 | Start Date*: 2018-02-06 | |||||||||||
Sponsor Name:Polish Myeloma Consortium | |||||||||||||
Full Title: A multicenter, single-arm, phase II study to evaluate a safety and efficacy of obinutuzumab induction followed by 2 years of maintenance in patients with relapsed/refractory Waldenström Macroglobul... | |||||||||||||
Medical condition: Waldenström's macroglobulinemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000506-37 | Sponsor Protocol Number: ECWM-1 | Start Date*: 2014-10-31 |
Sponsor Name:University Hospital Ulm | ||
Full Title: Efficacy of first line Dexamethasone, Rituximab and Cyclophosphamide (DRC) +/- Bortezomib for patients with Waldenström's Macroglobulinemia | ||
Medical condition: Waldenström's Macroglobulinemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) IT (Ongoing) PT (Prematurely Ended) SE (Completed) GR (Completed) ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2011-005156-34 | Sponsor Protocol Number: UCL/11/0353 | Start Date*: 2012-08-09 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Subcutaneous Bortezomib, Cyclophosphamide and Rituximab (BCR) versus Fludarabine, Cyclophosphamide and Rituximab (FCR) for initial therapy of Waldenstrőm macroglobulinaemia: a randomised phase II s... | |||||||||||||
Medical condition: Waldenstrom's macroglobulinaemia (WM) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004218-42 | Sponsor Protocol Number: P060207 | Start Date*: 2008-01-30 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Essai thérapeutique de phase IIA évaluant l'efficacité du Bortezomib (velcade) chez les patients atteints de la maladie de Waldenstrom en phase avancée | |||||||||||||
Medical condition: Maladie de Waldenstrom réfractaire ou en rechute après une ou deux lignes de traitement ayant comporté des alkylants et/ou des analogues de purine et/ou un anticorps monoclonal seul ou en association. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001767-23 | Sponsor Protocol Number: UCL/18/0131 | Start Date*: 2019-03-12 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: A phase II trial to investigate the safety and efficacy of rituximab and pembrolizumab in relapsed/refractory Waldenström’s macroglobulinaemia | |||||||||||||
Medical condition: Relapsed and refractory Waldenström's Macroglobulinaemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002980-33 | Sponsor Protocol Number: BGB-3111-302 | Start Date*: 2017-02-21 | |||||||||||
Sponsor Name:BeiGene Ltd. c/o BeiGene USA Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Open-Label, Multicenter Study Comparing the Efficacy and Safety of the Bruton’s Tyrosine Kinase (BTK) Inhibitors BGB-3111 and Ibrutinib in Subjects with Waldenström’s Macr... | |||||||||||||
Medical condition: Subjects with Waldenström’s Macroglobulinemia (WM) who require therapy according to the consensus panel criteria from the 7th International Workshop on Waldenström’s Macroglobulinemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) SE (Completed) ES (Completed) NL (Completed) PL (Completed) GR (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005297-10 | Sponsor Protocol Number: DCL-16-001 | Start Date*: 2021-05-19 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Cellectar Biosciences, Inc. | |||||||||||||||||||||||||||||||||||||||||||
Full Title: An Open-Label, Multicenter, Phase 2 Study of CLR 131 in Patients with Relapsed or Refractory (R/R) Select B-Cell Malignancies (CLOVER-1) and Expansion Cohort in Patients with Waldenstrom Macroglobu... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Part A: MM (multiple myeloma), CLL/SLL(chronic lymphocytic leukemia/small lymphocytic lymphoma), LPL/WM(lymphoplasmacytic lymphoma/ Waldenstrom's Macroglobulinemia), MZL(marginal zone lymphoma), MC... | |||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: CZ (Completed) GR (Trial now transitioned) FR (Trial now transitioned) ES (Ongoing) FI (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004362-95 | Sponsor Protocol Number: ECWM-2 | Start Date*: 2019-04-12 | |||||||||||
Sponsor Name:University Hospital Ulm | |||||||||||||
Full Title: Efficacy of first line Bortezomib, Rituximab, Ibrutinib (B-RI) for patients with treatment naive Waldenström’s Macroglobulinemia | |||||||||||||
Medical condition: Waldenström's Macroglobulinemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005478-22 | Sponsor Protocol Number: PCYC-1127-CA | Start Date*: 2014-07-04 | |||||||||||
Sponsor Name:Pharmacyclics, Incorporated | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study of Ibrutinib or Placebo in Combination With Rituximab in Subjects with Previously Treated Waldenstrom’s Macroglobulinemia | |||||||||||||
Medical condition: Relapsed or refractory Waldenstrom’s Macroglobulinemia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) ES (Completed) GR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000108-41 | Sponsor Protocol Number: 062-HEM-102 | Start Date*: 2019-02-06 | |||||||||||||||||||||
Sponsor Name:Sunesis Pharmaceuticals, Inc. | |||||||||||||||||||||||
Full Title: A Phase 1b/2 Dose-Escalation and Cohort-Expansion Study of the Noncovalent, Reversible Bruton’s Tyrosine Kinase Inhibitor, SNS 062, in Patients With B-Lymphoid Malignancies | |||||||||||||||||||||||
Medical condition: Male or female adult patients with an advanced B-Lymphoid malignancies that have relapsed/progressed after appropriate prior therapy and have resistance and/or mutations that may respond to subsequ... | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-004356-38 | Sponsor Protocol Number: M19-388 | Start Date*: 2021-08-03 | |||||||||||||||||||||||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||||||||||||||||||||||
Full Title: An Extension Study of Venetoclax for Subjects Who Have Completed a Prior Venetoclax Clinical Trial | |||||||||||||||||||||||||||||||||
Medical condition: Chronic lymphocytic leukemia; Non-Hodgkin's lymphoma; Multiple Myeloma; T prolymphocytic leukemia; Chronic myeloid leukemia; Waldenstrom's macroglobulinemia lymphoma and Relapsed/refractory pediatr... | |||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) GB (GB - no longer in EU/EEA) PL (Trial now transitioned) PT (Completed) SE (Completed) BE (Trial now transitioned) GR (Trial now transitioned) DK (Trial now transitioned) AT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005338-13 | Sponsor Protocol Number: ONC-2011-004 | Start Date*: 2013-08-17 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Istituto Clinico Humanitas - Humanitas Cancer Center | ||||||||||||||||||||||||||||||||||||||
Full Title: OFATUMUMAB-BENDAMUSTINE FOR RELAPSED/REFRACTORY INDOLENT LYMPHOMA: A MULTICENTER PHASE 2 TRIAL | ||||||||||||||||||||||||||||||||||||||
Medical condition: Non-Hodgkin's Follicular and Non-Follicular indolent lymphomas, relapsed/refractory | ||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006370-15 | Sponsor Protocol Number: WM RV 0426 (2008_15/0837) | Start Date*: 2009-01-23 | ||||||||||||||||
Sponsor Name:CHRU de Lille | ||||||||||||||||||
Full Title: A multicenter phase I/II dose excalation study of lenalidomide in relapse/refractory Waldenström macroglobulinemia | ||||||||||||||||||
Medical condition: Maladie de Waldenstöm rédicivante ou réfractaire | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003212-36 | Sponsor Protocol Number: ACE-WM-001 | Start Date*: 2014-12-09 | ||||||||||||||||
Sponsor Name:Acerta Pharma BV | ||||||||||||||||||
Full Title: An Open-label, Phase 1b/2 Study of ACP-196 in Subjects with Waldenström Macroglobulinemia | ||||||||||||||||||
Medical condition: Waldenström Macroglobulinemia | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) GB (GB - no longer in EU/EEA) ES (Ongoing) FR (Trial now transitioned) GR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
