- Trials with a EudraCT protocol (84)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
84 result(s) found for: Acute promyelocytic leukemia.
Displaying page 4 of 5.
EudraCT Number: 2013-001570-14 | Sponsor Protocol Number: GO28852 | Start Date*: 2013-09-20 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | ||||||||||||||||||
Full Title: A phase IB/II study to evaluate the safety and efficacy of vismodegib in relapsed/refractory acute myelogenous leukemia (AML) and relapsed/refractory high-risk myelodysplastic syndrome (MDS). | ||||||||||||||||||
Medical condition: Adult patients with acute myelogenous leukemia (AML) or myelodysplastic syndrome (MDS). | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003107-19 | Sponsor Protocol Number: CHDM201A2101 | Start Date*: 2019-03-13 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: A phase I/II multi-center study of HDM201 added to chemotherapy in adult subjects with relapsed/refractory (R/R) or newly diagnosed acute myeloid leukemia (AML) | ||
Medical condition: Relapsed refractory (R/R) or newly diagnosed acute myeloid leukemia (AML) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-004287-98 | Sponsor Protocol Number: TCD17197 | Start Date*: 2022-03-16 | |||||||||||||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Developpement | |||||||||||||||||||||||
Full Title: An open-label, first-in-human, dose-escalation/expansion study of SAR443579 administered as single agent by intravenous infusion in patients with relapsed or refractory acute myeloid leukemia (R/R ... | |||||||||||||||||||||||
Medical condition: Relapsed or refractory acute myeloid leukemia (R/R AML), B-cell acute lymphoblastic leukemia (B-ALL) or high risk-myelodysplasia (HR-MDS) | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006799-32 | Sponsor Protocol Number: CHR-2797-038 | Start Date*: 2009-12-11 | |||||||||||
Sponsor Name:Chroma Therapeutics Ltd | |||||||||||||
Full Title: The OPAL Study: A Phase II Single Arm Study to Evaluate the Efficacy, Safety and Tolerability of Tosedostat (CHR-2797) in Elderly Subjects with Treatment Refractory or Relapsed Acute Myeloid Leukemia | |||||||||||||
Medical condition: Treatment Refractory or Relapsed Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004661-15 | Sponsor Protocol Number: CLI-037 | Start Date*: 2005-05-17 |
Sponsor Name:Vion Pharmaceuticals, Inc. | ||
Full Title: A Phase III Randomized Study of CLORETAZINE™ (VNP40101M) and Cytosine Arabinoside (AraC) in Patients with Acute Myeloid Leukemia in First Relapse | ||
Medical condition: Acute Myeloid Leukemia (AML) in First Relapse | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) DE (Temporarily Halted) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003836-22 | Sponsor Protocol Number: FLG-V001 | Start Date*: 2019-12-11 | |||||||||||
Sponsor Name:HUS Helsinki University Hospital | |||||||||||||
Full Title: TWO-STAGE, TWO-ARM, OPEN-LABEL PHASE II STUDY OF VENETOCLAX IN COMBINATION WITH AZACYTIDINE IN ACUTE MYELOID LEUKEMIA PATIENTS SELECTED USING EX VIVO DRUG SENSITIVITY SCREENING | |||||||||||||
Medical condition: Acute myeloid leukemia in patients who are non-fit for standard induction therapy (except acute promyelocytic leukemia) and present with de novo, secondary, released or refractory AML | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001494-91 | Sponsor Protocol Number: CCRG12-001 | Start Date*: 2012-10-11 | ||||||||||||||||
Sponsor Name:Antwerp University Hospital | ||||||||||||||||||
Full Title: Wilms’ tumor (WT1) antigen-targeted dendritic cell vaccination to prevent relapse in adult patients with acute myeloid leukemia: a multicenter randomized phase II trial | ||||||||||||||||||
Medical condition: Adult patients with acute myeloid leukemia in complete remission | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001308-31 | Sponsor Protocol Number: PALG-AML1/2016 | Start Date*: 2017-06-27 |
Sponsor Name:Polish Adult Leukaemia Group (PALG) | ||
Full Title: A Polish Adult Leukemia Group (PALG) prospective, multicenter clinical trial to compare the efficacy of two standard induction therapies (DA-90 vs DAC) and two standard salvage regimens (FLAG-IDA ... | ||
Medical condition: The study will include newly diagnosed AML patients (other than acute promyelocytic leukemia); age 18-60 years, who are eligible for standard induction chemotherapy. The patients will be randomized... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002675-17 | Sponsor Protocol Number: NCT-2017-0545 | Start Date*: 2019-12-20 |
Sponsor Name:Ruprecht-Karls-University of Heidelberg Medical Faculty represented in law by Heidelberg University Hospital | ||
Full Title: Quizartinib and High-dose Ara-C plus Mitoxantrone in Relapsed/Refractory AML with FLT3-ITD | ||
Medical condition: Relapsed/Refractory AML with FLT3-ITD | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2014-001233-89 | Sponsor Protocol Number: SGI-110-04 | Start Date*: 2015-05-15 | |||||||||||
Sponsor Name:Astex Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Open-label, Randomized Study of SGI-110 versus Treatment Choice (TC) in Adults with Previously Untreated Acute Myeloid Leukemia (AML) Who Are Not Considered Candidates for I... | |||||||||||||
Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SE (Completed) BE (Completed) HU (Completed) DE (Completed) GB (Completed) NL (Completed) FI (Completed) CZ (Completed) AT (Completed) ES (Completed) PL (Completed) FR (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018699-26 | Sponsor Protocol Number: CLBH589BDE05T | Start Date*: 2010-10-25 |
Sponsor Name:Goethe Universität Frankfurt | ||
Full Title: Phase I/II study with oral panobinostat maintenance therapy following allogeneic stem cell transplantation in patients with high risk MDS or AML (PANOBEST) | ||
Medical condition: MDS and AML in patients with high risk features after hemapoietic stem cell transplantation with reduced conditioning | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023436-16 | Sponsor Protocol Number: HOVON 107 | Start Date*: 2011-05-31 | |||||||||||||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||||||||||||
Full Title: The feasibility and efficacy of subcutaneous and intravenous Plerixafor for mobilization of peripheral blood stem cells in allogeneic HLA–identical sibling donors: a randomized phase II study. | |||||||||||||||||||||||
Medical condition: stem cell mobilization | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) DE (Restarted) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005256-97 | Sponsor Protocol Number: SGI-110-06 | Start Date*: 2017-06-19 | |||||||||||
Sponsor Name:Astex Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Open-Label Study of Guadecitabine (SGI-110) versus Treatment Choice in Adults with Previously Treated Acute Myeloid Leukemia | |||||||||||||
Medical condition: Acute Myeloid Leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) HU (Completed) ES (Completed) GB (Completed) FR (Completed) PL (Completed) SE (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005023-36 | Sponsor Protocol Number: PALM | Start Date*: 2021-12-21 |
Sponsor Name:Akershus University Hospital | ||
Full Title: Precision therapy versus standard therapy in Acute Myeloid Leukaemia and Myelodysplastic syndrome in elderly (PALM) | ||
Medical condition: Acute myeloid leukemia and severe myelodysplastic syndrome and chronic myelomonocytic leukemia | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002104-12 | Sponsor Protocol Number: FP2CLI004 | Start Date*: 2021-09-08 | |||||||||||
Sponsor Name:Faron Pharmaceuticals Ltd. | |||||||||||||
Full Title: A Phase I/II Open-Label Study to Assess the Safety, Tolerability and Preliminary Efficacy of the Clever-1 Antibody Bexmarilimab in Combination with Standard of Care Therapy in Patients with Myelody... | |||||||||||||
Medical condition: -Myelodysplastic Syndrome -Chronic Myelomonocytic Leukemia -Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004583-26 | Sponsor Protocol Number: LV2020-001 | Start Date*: 2022-03-08 |
Sponsor Name:LAVA Therapeutics N.V. | ||
Full Title: A Phase 1 and 2a open-label study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, immunogenicity and antitumor activity of LAVA-051 in patients with relapsed or refractory... | ||
Medical condition: Relapsed/refractory chronic lymphocytic leukemia (CLL), multiple myeloma (MM), or acute myeloid leukemia (AML) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) IT (Prematurely Ended) ES (Completed) FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-005158-12 | Sponsor Protocol Number: NCT-2017-0530 | Start Date*: 2019-04-01 |
Sponsor Name: Ruprecht-Karls-University Heidelberg Medical Faculty, University Hospital | ||
Full Title: TEAM-Trial: Targeting Epigenetic therapy resistance in AML with Bortezomib: A multi-centre matched threshold crossing phase II approach | ||
Medical condition: Patients with confirmed diagnosis of Acute Myeloid Leukemia (AML)according to WHO-2016 classification (except acute promyelocytic leukemia) either de novo AML, AML after preceding myelodysplastic o... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014445-80 | Sponsor Protocol Number: CP4055-306 | Start Date*: 2010-06-23 | |||||||||||
Sponsor Name:Clavis Pharma | |||||||||||||
Full Title: A Randomised Phase III Study of Elacytarabine vs. Investigator’s Choice in Patients with Late Stage Acute Myeloid Leukaemia | |||||||||||||
Medical condition: Late Stage Acute Myeloid Leukaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) DE (Completed) ES (Ongoing) BE (Completed) PL (Completed) IT (Ongoing) GB (Completed) IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003285-12 | Sponsor Protocol Number: BGB-11417-103 | Start Date*: 2022-05-17 |
Sponsor Name:BeiGene, Ltd. | ||
Full Title: A Phase 1b/2, Open-Label, Dose Finding, and Expansion Study of the Bcl-2 Inhibitor BGB-11417 in Patients With Myeloid Malignancies | ||
Medical condition: Myeloid malignancies (acute myeloid leukemia [AML], myelodysplastic syndromes [MDS], and myelodysplastic syndrome/myeloproliferative neoplasms [MDS/MPN]) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000749-19 | Sponsor Protocol Number: SPON934-11 | Start Date*: 2011-06-29 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: Bloodwise and NCRI Working Group Pick a Winner Programme (LI-1) Trial | |||||||||||||
Medical condition: Acute myeloid leukemia and high-risk myelodysplastic syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DK (Completed) | |||||||||||||
Trial results: View results |
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