- Trials with a EudraCT protocol (256)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
		
	   		
	   		    
                    
                   	
                   	    256 result(s) found for: T-cell lymphoma.
                    
                
			
   			
		
		Displaying page 1 of 13.
	
	
	| EudraCT Number: 2010-023040-32 | Sponsor Protocol Number: ROMI-ADVM-004 | Start Date*: 2011-05-05 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Celgene Corporation | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A phase IV, Open-Label, Single-Arm ROLLOVER STUDY FOR SUBJECTS WHO PARTICIPATED IN OTHER ROMIDEPSIN PROTOCOLS. Estudio de extensión de fase IV, abierto, de un solo brazo para pacientes que hayan p... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Rollover study supporting all indications from prior Romidepsin protocols eligible for participation in this study. Estudio de extensión que recoge todas las indicaciones de protocolos anteriores d... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: ES (Prematurely Ended) GB (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-003526-80 | Sponsor Protocol Number: CLSG-PTCL-CHEPA | Start Date*: 2021-12-16 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Kooperativní lymfomová skupina, z.s. | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase II Open Label Study of Brentuximab Vedotin in combination with CHEP in Patients with Previously Untreated CD30-expressing Peripheral T-cell Lymphomas. | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Peripheral T-cell lymphomas (PTCL) | |||||||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: CZ (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-004146-18 | Sponsor Protocol Number: CCR3549 | Start Date*: 2011-11-09 | |||||||||||
| Sponsor Name:The Royal Marsden NHS Foundation Trust | |||||||||||||
| Full Title: Cyclophosphamide, doxorubicin, vincristine and prednisolone (CHOP) versus gemcitabine, cisplatin and methyl prednisolone (GEM-P) in the first line treatment Of T-cell Lymphoma, a multicentre rando... | |||||||||||||
| Medical condition: T-cell Lymphoma | |||||||||||||
| 
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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: 2019-003983-28 | Sponsor Protocol Number: SGN35-028 | Start Date*: 2020-11-27 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:SEAGEN INC. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A phase 2, multicenter, single-arm study of retreatment with brentuximab vedotin in subjects with relapsed or refractory classic Hodgkin lymphoma (cHL) or CD30-expressing peripheral T cell lymphoma... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: - classic Hodgkin lymphoma (cHL) - Systemic anaplastic large cell lymphoma (sALCL) - CD30-expressing peripheral T cell lymphoma (PTCL) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2019-003982-17 | Sponsor Protocol Number: SGN35-015 | Start Date*: 2020-10-21 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:SEATTLE GENETICS, INC. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A phase 2 open-label study of brentuximab vedotin in front-line therapy of Hodgkin lymphoma (HL) and CD30-expressing peripheral T-cell lymphoma (PTCL) in older patients or patients with significant... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: • Hodgkin lymphoma (HL) • CD30-expressing peripheral T-cell lymphoma (PTCL) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2021-006229-23 | Sponsor Protocol Number: PTCLS-IDE | Start Date*: 2022-04-07 | |||||||||||
| Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
| Full Title: Pilot phase II study of Selinexor in combination with Ifosfamide, Etoposide and Dexamethasone (SIDE) in patients with relapsed or refractory Peripheral T-cell Lymphomas. | |||||||||||||
| Medical condition: peripheral T Cell lymphoma | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-000243-23 | Sponsor Protocol Number: Hx-CD4-109 | Start Date*: 2004-08-03 | |||||||||||
| Sponsor Name:Genmab A/S | |||||||||||||
| Full Title: An Open-Label Therapeutic Exploratory Clinical Trial of HuMax-CD4, a Fully Human Monoclonal Anti-CD4 Antibody, in Patients with refractory or relapsed Non-Cutaneous CD4+ T-Cell Lymphoma | |||||||||||||
| Medical condition: The mature non-cutaneous T-cell lymphomas expressing the CD4 molecule are the object of this protocol. 1.Peripheral T-cell lymphoma (PTCL) unspecified 2.Angioimmunnoblastic T-cell lymphoma 3.Anapl... | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022036-36 | Sponsor Protocol Number: A8641014 | Start Date*: 2011-02-15 | |||||||||||||||||||||
| Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||||||||||||
| Full Title: A Phase 1 trial of pf‑03084014 in patients with advanced solid tumor malignancy and t‑cell acute lymphoblastic leukemia/lymphoblastic lymphoma | |||||||||||||||||||||||
| Medical condition: advanced solid tumor malignancies or relapsed or refractory acute T-cell lymphoblastic leukemia/lymphoblastic lymphoma (T-ALL/LBL). | |||||||||||||||||||||||
| 
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2006-004234-33 | Sponsor Protocol Number: PTCL-06 | Start Date*: 2006-10-06 | |||||||||||
| Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
| Full Title: Intensive chemo-immunotherapy as first-line treatment in adult patients with peripheral T-cell Lymphoma PTCL | |||||||||||||
| Medical condition: Non Hodgkin peripheral T-cell lymphomas | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024215-14 | Sponsor Protocol Number: C25001 | Start Date*: 2012-11-06 | |||||||||||
| Sponsor Name:Millennium Pharmaceuticals, Inc | |||||||||||||
| Full Title: A Randomized, Open-Label, Phase 3 Trial of brentuximab vedotin (SGN-35) Versus Physician's Choice (Methotrexate or Bexarotene) in Patients With CD30-Positive Cutaneous T-Cell Lymphoma | |||||||||||||
| Medical condition: CD30-Positive Cutaneous T-Cell Lymphoma | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Completed) ES (Completed) DE (Completed) AT (Completed) IT (Completed) PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-004675-11 | Sponsor Protocol Number: 133/2004/U | Start Date*: 2004-09-14 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
| Full Title: Clinical trial of phase II for the a front line treatment of the non-Hodgkin lymphomas of derivation lymphocyte T Gemcitabine and Oxaliplatin GEMOX | |||||||||||||
| Medical condition: Non Hodgkin s disease of lymphocyte T derivation | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-003879-12 | Sponsor Protocol Number: MK-0683 042-00 | Start Date*: 2007-03-23 | |||||||||||
| Sponsor Name:Merck & Co., Inc. | |||||||||||||
| Full Title: Compassionate Use of Vorinostat (MK-0683) for the Treatment of Patients with Advanced Cutaneous T-Cell Lymphoma | |||||||||||||
| Medical condition: Cutaneous T-cell lymphoma (CTCL) | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) IE (Completed) DK (Completed) FI (Completed) SI (Completed) IT (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-002336-74 | Sponsor Protocol Number: SGN35-032 | Start Date*: 2020-12-08 | |||||||||||
| Sponsor Name:Seattle Genetics, Inc. | |||||||||||||
| Full Title: A dual-cohort, open-label, phase 2 study of brentuximab vedotin and CHP (A+CHP) in the frontline treatment of subjects with peripheral T-cell lymphoma (PTCL) with less than 10% CD30 expression | |||||||||||||
| Medical condition: Non-sALCL PTCL and CD30 expression <10% | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-000306-36 | Sponsor Protocol Number: 2008-000306-36 | Start Date*: 2009-04-16 | ||||||||||||||||||||||||||
| Sponsor Name:Region Skåne | ||||||||||||||||||||||||||||
| Full Title: Nexavar in Relapsed Peripheral T-cell Non-Hodgkins Lymphoma | ||||||||||||||||||||||||||||
| Medical condition: Patients >18 years with relapsed or resitant peripheral T-cell lymphoma, defined as having progressed on 1st or 2nd line therapy. | ||||||||||||||||||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: SE (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2006-006130-17 | Sponsor Protocol Number: NordicLymphomaGroup | Start Date*: 2007-09-05 | |||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||
| Full Title: ACT-1 (younger patients) A randomized phase III study to evaluate the efficacy of chemoimmunotherapy with the monoclonal antibody Campath-1H (Alemtuzumab) given in combination with 2-weekly CHOP v... | |||||||||||||
| Medical condition: Patients 18 - 65 years old with newly diagnosed non-cutanous, non leukemic Peripheral T- cell lymphoma, except alk-protein positive and negative anaplastic large cell lymphoma. | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) FI (Completed) PT (Completed) DE (Completed) SE (Completed) NL (Completed) AT (Completed) PL (Completed) CZ (Completed) BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001164-24 | Sponsor Protocol Number: PTCL01 | Start Date*: 2006-11-14 | |||||||||||
| Sponsor Name:G.I.S.L. - GRUPPO ITALIANO STUDIO LINFOMI | |||||||||||||
| Full Title: MAINTENANCE TREATMENT WITH ALEMTUZUMAB Campath AS AN ALTERNATIVE TO ALLOGENIC TRANSPLANTATION IN PATIENTS WITHOUT COMPATIBLE DONOR IN PATIENTS WITH PERIPHERAL T CELL LYMPHOMA | |||||||||||||
| Medical condition: patients with Perpheral T cell Lymphoma | |||||||||||||
| 
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022230-81 | Sponsor Protocol Number: PDX-017 | Start Date*: 2011-04-05 | |||||||||||
| Sponsor Name:Allos Therapeutics, Inc. | |||||||||||||
| Full Title: A Multi-center, Randomized, Phase 3 Study of Sequential Pralatrexate Versus Observation in Patients with Previously Undiagnosed Peripheral T-cell Lymphoma Who Have Achieved an Objective Response Fo... | |||||||||||||
| Medical condition: Patients with previously undiagnosed peripheral T-cell lymphoma who have achieved an objective response following initial treatment with CHOP-based chemotherapy | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) CZ (Completed) IE (Completed) ES (Completed) BE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001396-11 | Sponsor Protocol Number: PXD101-CLN-6 | Start Date*: 2007-09-18 | |||||||||||
| Sponsor Name:CuraGen Corporation | |||||||||||||
| Full Title: A Phase II Clinical Trial of PXD101 in Patients with Recurrent or Refractory Cutaneous and Peripheral T-Cell Lymphomas | |||||||||||||
| Medical condition: T-cell Lymphoma | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004516-51 | Sponsor Protocol Number: GEN112 | Start Date*: 2006-11-20 | |||||||||||
| Sponsor Name:Genmab A/S | |||||||||||||
| Full Title: A multicentre open-label, dose-escalation, trial of zanolimumab in combination with CHOP chemotherapy in subjects with CD4 positive non-cutaneous peripheral T-Cell Lymphoma with nodal involvement | |||||||||||||
| Medical condition: CD4 positive non-cutaneous peripheral T-Cell Lymphoma with nodal involvement | |||||||||||||
| 
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) DE (Completed) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000433-30 | Sponsor Protocol Number: UCL/17/0053 | Start Date*: 2018-05-23 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: Phase II Trial of Pembrolizumab and Radiotherapy in Cutaneous T cell lymphoma | |||||||||||||
| Medical condition: Cutaneous T cell lymphoma | |||||||||||||
| 
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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) | |||||||||||||
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