- Trials with a EudraCT protocol (107)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
107 result(s) found for: Chromosome 11.
Displaying page 4 of 6.
EudraCT Number: 2021-003410-39 | Sponsor Protocol Number: D8242C00001 | Start Date*: 2023-01-19 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Modular Phase I/II, Open-label, Dose Escalation and Expansion, Multicentre Study to Assess the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of AZD0466 as Monotherapy or in Com... | |||||||||||||
Medical condition: Advanced Non-Hodgkin Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) FR (Completed) IT (Prematurely Ended) PT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002918-41 | Sponsor Protocol Number: IJB-EBC-Decrescendo-2020 | Start Date*: 2021-08-25 | |||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||
Full Title: De-Escalation of neoadjuvant ChemotheRapy in HER2-positive, EStrogen reCEptor-negative, Node-negative early breast cancer patients who achieved pathological complete response after neoadjuvant chem... | |||||||||||||
Medical condition: HER2-positive, estrogen receptor (ER)-negative/progesterone receptor (PR)-negative, node-negative early breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) IT (Prematurely Ended) IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004336-30 | Sponsor Protocol Number: CYTB323A12101 | Start Date*: 2020-04-07 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: Phase I/II, open label, multicenter study of rapcabtagene autoleucel in adult patients with CLL/SLL, 3L+ DLBCL, r/r ALL and 1L HR LBCL. | ||
Medical condition: ALL, CLL/SLL and DLBCL and High-Risk LBCL. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) DE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000832-13 | Sponsor Protocol Number: 14/P/153 | Start Date*: 2015-09-30 | |||||||||||
Sponsor Name:University Hospitals Plymouth NHS Trust | |||||||||||||
Full Title: Randomised, open label study of rituximab/ibrutinib vs rituximab/chemotherapy in older patients with untreated mantle cell lymphoma | |||||||||||||
Medical condition: Untreated symptomatic Mantle Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) SE (Trial now transitioned) DK (Trial now transitioned) FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001594-24 | Sponsor Protocol Number: CABL001E2201 | Start Date*: 2018-10-17 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A phase 2, multi-center, open-label, randomized study of oral asciminib added to imatinib versus continued imatinib versus switch to nilotinib in patients with CML-CP who have been previously treat... | |||||||||||||
Medical condition: Chronic Myelogenous Leukemia in chronic phase (CML-CP), previously treated with imatinib and have not achieved deep molecular response | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) PT (Completed) GB (GB - no longer in EU/EEA) DE (Completed) PL (Completed) DK (Completed) FR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002117-28 | Sponsor Protocol Number: ACE-LY-004 | Start Date*: 2015-05-06 | |||||||||||
Sponsor Name:Acerta Pharma B.V. | |||||||||||||
Full Title: An Open-label, Phase 2 Study of ACP-196 in Subjects with Mantle Cell Lymphoma | |||||||||||||
Medical condition: Mantle Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) BE (Completed) CZ (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004928-38 | Sponsor Protocol Number: GEICAM/2012-07 | Start Date*: 2013-02-19 | |||||||||||
Sponsor Name:GEICAM (Fundación Grupo Español de Investigación en Cáncer de Mama) | |||||||||||||
Full Title: A phase III clinical trial to evaluate patient´s preference of subcutaneous trastuzumab (SC) versus intravenous (IV) administration in patients with HER2 positive Advanced Breast Cancer (ABC) who ... | |||||||||||||
Medical condition: Patients with HER2 positive Advanced Breast Cancer receiving trastuzumab with or without CT or HT therapy for at least four months without evidence of disease progression and a life expectancy of a... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005906-38 | Sponsor Protocol Number: 0811001 | Start Date*: 2009-02-09 | |||||||||||
Sponsor Name:CHU de Toulouse | |||||||||||||
Full Title: Détermination de biomarqueurs associés à la réponse au Natalizumab dans la Sclérose en plaques | |||||||||||||
Medical condition: sclérose en plaques | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000679-16 | Sponsor Protocol Number: EORTC 06023 | Start Date*: 2005-05-17 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Randomized phase II trial with infliximab (Remicade) in patients with myelodysplastic syndrome and a relatively low risk of developing acute leukemia | |||||||||||||
Medical condition: myelodysplastic syndrome (MDS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001706-42 | Sponsor Protocol Number: JCAR015-ALL-001 | Start Date*: 2016-11-16 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A Phase 2, Open-Label, Multiple Cohort, Single-Arm, Multi-Center Trial To Determine The Safety, Feasibility, And Efficacy Of JCAR015 In Adult Subjects With B-Cell Acute Lymphoblastic Leukemia | |||||||||||||
Medical condition: B-cell Acute Lymphoblastic Leukemia (ALL) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002153-30 | Sponsor Protocol Number: MO40628 | Start Date*: 2018-10-24 | |||||||||||
Sponsor Name:Roche Farma S.A.(Soc Uni) que realiza el ensayo en España y que actúa como representante de F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A randomized, multicenter, open-label cross-over study to evaluate patient preference and satisfaction of subcutaneous administration of the fixed-dose combination of pertuzumab and trastuzumab in ... | |||||||||||||
Medical condition: Human epidermal growth factor receptor 2 (HER2)-positive Early Breast Cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PT (Completed) SE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004540-29 | Sponsor Protocol Number: Pona-CELL | Start Date*: 2020-10-06 | |||||||||||
Sponsor Name:Ústav hematologie a krevní transfuze | |||||||||||||
Full Title: Ponatinib plus reduced-intensity chemotherapy in the first-line treatment of adult patients with Ph-positive acute lymphoblastic leukemia | |||||||||||||
Medical condition: NEWLY DIAGNOSED PHILADELPHIA CHROMOSOME-POSITIVE ACUTE LYMPHOBLASTIC LEUKEMIA | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005208-26 | Sponsor Protocol Number: P13/12 | Start Date*: 2016-02-22 | |||||||||||
Sponsor Name:Centre Hospitalier de Versailles | |||||||||||||
Full Title: CANDIDATE THERAPIES IN COMBINATION OR SEQUENTIALLY WITH TYROSINE KINASE INHIBITORS IN CHRONIC PHASE CHRONIC MYELOGENOUS LEUKAEMIA (CP-CML) PATIENTS IN COMPLETE CYTOGENETIC RESPONSE WITHOUT ACHIEVIN... | |||||||||||||
Medical condition: CHRONIC PHASE CHRONIC MYELOGENOUS LEUKAEMIA (CP-CML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003069-39 | Sponsor Protocol Number: VARIANT | Start Date*: 2023-06-01 | |||||||||||
Sponsor Name:Friedrich-Schiller-Universität Jena | |||||||||||||
Full Title: Venetoclax after TKI to target persisting stem cells in CML | |||||||||||||
Medical condition: Chronic Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001438-16 | Sponsor Protocol Number: OBI-822-011 | Start Date*: 2022-01-25 | |||||||||||
Sponsor Name:OBI Pharma, Inc. | |||||||||||||
Full Title: The GLORIA Study: A Phase 3, Randomized, Open-Label Study of the Anti-Globo H Vaccine Adagloxad Simolenin (OBI-822)/OBI-821 in the Adjuvant Treatment of Patients with High-Risk, Early-Stage Globo H... | |||||||||||||
Medical condition: Triple Negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002181-12 | Sponsor Protocol Number: STEP | Start Date*: 2019-09-30 | |||||||||||
Sponsor Name:ISTITUTI FISIOTERAPICI OSPITALIERI | |||||||||||||
Full Title: EXPLORING OPTIMAL SEQUENCE TREATMENT IN HER2+ PERTUZUMAB PRE- TREATED ADVANCED BREAST CANCER PATIENTS. THE STEP TRIAL. | |||||||||||||
Medical condition: HER2 POSITIVE METASTATIC BREAST CANCER | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004796-23 | Sponsor Protocol Number: REP0114 | Start Date*: 2015-07-06 | |||||||||||
Sponsor Name:Dompé Farmaceutici s.p.a. | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled phase 2 study of paclitaxel in combination with reparixin compared to paclitaxel alone as front-line therapy for Metastatic Triple-Negative Breast Can... | |||||||||||||
Medical condition: Metastatic triple negative Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) IT (Completed) ES (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014295-21 | Sponsor Protocol Number: 998HB102 | Start Date*: 2010-05-06 | |||||||||||
Sponsor Name:Biogen Idec Hemophilia Inc. | |||||||||||||
Full Title: B-LONG: An Open-label, Multicenter Evaluation of the Safety, Pharmacokinetics, and Efficacy of Recombinant, Long-acting Coagulation Factor IX Fc fusion protein (rFIXFc) in the Prevention and Treat... | |||||||||||||
Medical condition: The medical condition to be investigated is Hemophilia B, or Christmas disease. Hemophilia B is a deficiency in the clotting FIX and is a recessively inherited coagulation disorder due to an X-chro... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) DE (Completed) FR (Completed) PL (Completed) BE (Completed) IT (Completed) NL (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003076-36 | Sponsor Protocol Number: 9HB02PED | Start Date*: 2012-05-29 | |||||||||||
Sponsor Name:Biogen Idec Research Ltd | |||||||||||||
Full Title: Open-label, Multicenter Evaluation of Safety, Pharmacokinetics, and Efficacy of Recombinant Coagulation Factor IX Fc Fusion Protein, BIIB029, in the Prevention and Treatment of Bleeding Episodes in... | |||||||||||||
Medical condition: The medical condition to be investigated is Hemophilia B, or Christmas disease. Hemophilia B is a deficiency in the clotting FIX and is a recessively inherited coagulation disorder due to an X-chro... | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) IE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004189-27 | Sponsor Protocol Number: WO30085 | Start Date*: 2016-10-21 | |||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||
Full Title: A RANDOMIZED, MULTICENTER, DOUBLE-BLIND, PLACEBO-CONTROLLED PHASE II STUDY OF THE EFFICACY AND SAFETY OF TRASTUZUMAB EMTANSINE IN COMBINATION WITH ATEZOLIZUMAB OR ATEZOLIZUMAB-PLACEBO IN PATIENTS W... | |||||||||||||||||||||||
Medical condition: Unresectable locally advanced or metastatic breast cancer (MBC). | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
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