- Trials with a EudraCT protocol (5,029)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5,029 result(s) found for: Chronic diseases.
Displaying page 1 of 252.
EudraCT Number: 2018-001334-18 | Sponsor Protocol Number: CarPAs | Start Date*: 2020-09-10 | ||||||||||||||||
Sponsor Name:Associazione Italiana Pazienti Leucemia Mieloide Cronica (AIPLMC) | ||||||||||||||||||
Full Title: Cardiovascular assessment of Ponatinib as treatment option in chronic phase chronic myeloid leukemia after failure of Imatinib and Bosutinib (CarPAs) | ||||||||||||||||||
Medical condition: Chronic Myeloid Leukemia (CML) in Chronic Phase (CP) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004347-12 | Sponsor Protocol Number: ICT-10 | Start Date*: 2016-03-05 | |||||||||||
Sponsor Name:Hybrigenics SA | |||||||||||||
Full Title: Exploratory Study of Inecalcitol in Imatinib-Treated Residual Chronic Myeloid Leukaemia: INIM Study | |||||||||||||
Medical condition: Residual disease in Chronic Myeloid Leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000899-28 | Sponsor Protocol Number: CAMN107CNL08T | Start Date*: 2018-09-04 | |||||||||||||||||||||
Sponsor Name:Albert Schweitzer Hospital | |||||||||||||||||||||||
Full Title: Dipeptidylpeptidase IV (CD26) on Philadelphia-positive leukemic stem cells (LSC) as marker and novel therapeutic target in chronic myeloid leukemia (CML). | |||||||||||||||||||||||
Medical condition: Chronic myeloid leukemia | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000597-22 | Sponsor Protocol Number: GIMEMACML0307 | Start Date*: 2007-06-20 | |||||||||||
Sponsor Name:G.I.M.E.M.A. GRUPPO ITALIANO MALATTIE EMATOLOGICHE DELL'ADULTO | |||||||||||||
Full Title: The protein tyrosine kinase inhibitor nilotinib as first-line treatment of Ph+ chronic myeloid leucemia (CML) in early chronic phase: a Phase II exploratory, multicenter study | |||||||||||||
Medical condition: Ph+ CML in early chronic phase | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001603-42 | Sponsor Protocol Number: AIL0115 | Start Date*: 2015-09-22 | |||||||||||
Sponsor Name:AIL CATANIA ASSOCIAZIONE ITALIANA CONTRO LEUCEMIE-LINFOMI E MIELOMA ONLUS | |||||||||||||
Full Title: “Arrest Imatinib or Dasatinib in CML patients with Deep Molecular Responses” (AID MORE) | |||||||||||||
Medical condition: Chronic phase CML patients with BCR-ABL/ABLIS transcript levels below MR3 (<0.1%) and above MR4.5 (>0.0032%) at the time of accrual. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003780-50 | Sponsor Protocol Number: B1871008 | Start Date*: 2008-07-30 | |||||||||||
Sponsor Name:Wyeth Pharmaceuticals Inc, a wholly owned subsidiary of Pfizer Inc, 500 Arcola Road, Collegeville, PA 19426 USA | |||||||||||||
Full Title: A Phase 3 Randomized, Open-Label Study of Bosutinib Versus Imatinib in Subjects With Newly Diagnosed Chronic Phase Philadelphia Chromosome Positive Chronic Myelogenous Leukemia | |||||||||||||
Medical condition: Chronic myelogenous leukemia (CML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) GB (Completed) BE (Completed) ES (Completed) LV (Completed) LT (Completed) FR (Completed) IT (Completed) SI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001380-61 | Sponsor Protocol Number: CSTI5710102E2 | Start Date*: 2005-04-15 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An extension to a phase II open label study to determine the safety and anti-leukemic effects of STI571 in patients with Philadelphia chromosome positive chronic myeloid leukemia in myeloid blast c... | |||||||||||||
Medical condition: Ph+ CML in myeloid blast crisis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018339-16 | Sponsor Protocol Number: CSTI571ADE75T-GMIHO-005/2009 | Start Date*: 2010-07-19 | |||||||||||
Sponsor Name:GMIHO mbH | |||||||||||||
Full Title: CRESCENDO (Compliance: Role Emerges for Success in CML: Evaluation aND Optimisation): A prospective, multi-center, phase IV study to assess the compliance in patients with Philadelphia chromosome-p... | |||||||||||||
Medical condition: CML - chronic myelogenous leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001381-14 | Sponsor Protocol Number: CSTI5710109E2 | Start Date*: 2005-08-02 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: An extension to a phase II study to determine the safety and the anti- leukemic effects of STI571 in adults patients with Philadelphia chromosome positive leukemia including acute lymphoblastic le... | |||||||||||||
Medical condition: Philadelphia chromosome positive leukemia including acute lymphoblastic leukemia, acute myeloid leukemia and accelerate phase myeloid leukemia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002850-26 | Sponsor Protocol Number: NL72928.078.20 | Start Date*: 2020-07-20 | |||||||||||||||||||||
Sponsor Name:Albert Schweitzer Hospital | |||||||||||||||||||||||
Full Title: Vaccination response to pneumococcal antigen as novel predictor for successful tyrosine kinase inhibitor discontinuation in chronic myeloid leukemia: the vaccinSTOP study. | |||||||||||||||||||||||
Medical condition: Chronic myeloid leukemia | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003502-16 | Sponsor Protocol Number: DasaHIT | Start Date*: 2016-08-11 | |||||||||||
Sponsor Name:Friedrich-Schiller-Universität Jena | |||||||||||||
Full Title: Treatment optimization for patients with chronic myeloid leukemia (CML) with treatment naïve disease (1st line) and patients with resistance or intolerance against alternative Abl-Kinase Inhibitors... | |||||||||||||
Medical condition: Chronic Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000602-17 | Sponsor Protocol Number: CABL001A2001B | Start Date*: 2021-08-10 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: An open label, multi-center asciminib roll-over study to assess long-term safety in patients who have completed a Novartis sponsored asciminib study and are judged by the investigator to benefit fr... | |||||||||||||
Medical condition: CML-CP (at the end of parent study) who are currently participating in an asciminb Novartis sponsored study (parent study) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) CZ (Trial now transitioned) ES (Ongoing) DE (Ongoing) BG (Trial now transitioned) IT (Trial now transitioned) PT (Trial now transitioned) DK (Trial now transitioned) PL (Trial now transitioned) AT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004707-32 | Sponsor Protocol Number: IMPROVE(PS-CLL-002) | Start Date*: 2017-05-10 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: A Multi-Center, Open Label, Uncontrolled, Phase 2a Clinical Trial Evaluating the Safety and Efficacy of the Addition of Ibrutinib to Venetoclax through a MRD-guided Approach in Relapsed/Refractory ... | |||||||||||||
Medical condition: Relapsed or Refractory Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003079-32 | Sponsor Protocol Number: CC-5013-CLL-008 | Start Date*: 2009-06-19 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: ESTUDIO FASE 3, MULTICÉNTRICO, ALEATORIZADO, ABIERTO Y DE GRUPOS PARALELOS PARA VALORAR LA EFICACIA Y SEGURIDAD DE LENALIDOMIDA (REVLIMID®) FRENTE A CLORAMBUCILO COMO TERAPIA DE PRIMERA LÍNEA EN PA... | |||||||||||||
Medical condition: TERAPIA DE PRIMERA LÍNEA EN PACIENTES ANCIANOS CON LEUCEMIA LINFOCÍTICA CRÓNICA DE CÉLULAS B NO TRATADOS PREVIAMENTE (FIRST-LINE THERAPY FOR PREVIOUSLY UNTREATED ELDERLY PATIENTS WITH B-CELL CHRON... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) AT (Completed) BE (Completed) PT (Completed) CZ (Completed) GB (Completed) HU (Completed) IT (Completed) FR (Completed) NL (Completed) DK (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000606-29 | Sponsor Protocol Number: M13-641 | Start Date*: 2012-05-30 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: An Extension Study of Navitoclax (ABT-263) in Subjects with Chronic Lymphocytic Leukemia (CLL) | |||||||||||||
Medical condition: Chronic Lymphocytic Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002563-23 | Sponsor Protocol Number: CD-RI-MEDI8968-1103 | Start Date*: 2012-03-15 | |||||||||||
Sponsor Name:MedImmune Limited | |||||||||||||
Full Title: A Phase 2 Double-blind, Placebo-controlled Study to Evaluate the Efficacy of MEDI8968 in Chronic Obstructive Pulmonary Disease | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) LV (Completed) CZ (Completed) LT (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021786-78 | Sponsor Protocol Number: V1_30.4.2010 | Start Date*: 2010-11-11 | |||||||||||
Sponsor Name:Medizinische Universität Wien | |||||||||||||
Full Title: Treatment of chronic lymphocytic leukemia with the use of an antiviral compound - a proof of principle study | |||||||||||||
Medical condition: Chronic lymphocytic leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001099-49 | Sponsor Protocol Number: CLOSE(PS-CLL-001) | Start Date*: 2018-07-12 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: Clonal evolution in progressive CLL patients harboring subclonal TP53 aberrations treated with ibrutinib first-line | |||||||||||||
Medical condition: Chronic Lymphocytic Leukemia (CLL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004508-37 | Sponsor Protocol Number: BY217/M2-128 | Start Date*: 2007-01-08 | |||||||||||
Sponsor Name:Nycomed GmbH | |||||||||||||
Full Title: Effect of roflumilast in COPD patients treated with tiotropium. A 24-week, double-blind study with 500 µg roflumilast once daily versus placebo. | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) AT (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006057-21 | Sponsor Protocol Number: CABL001A2302 | Start Date*: 2021-09-17 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A phase 3b, multi-center, open-label, treatment optimization study of oral asciminib in patients with Chronic Myelogenous Leukemia in chronic phase (CML-CP) previously treated with 2 or more tyrosi... | |||||||||||||
Medical condition: Chronic Myelogenous Leukemia in chronic phase (CML-CP) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) DE (Trial now transitioned) IT (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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