- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: Histone deacetylase.
Displaying page 1 of 2.
EudraCT Number: 2016-000782-22 | Sponsor Protocol Number: SAHA-Pilot-2016 | Start Date*: 2017-01-03 |
Sponsor Name:Medical University of Graz | ||
Full Title: A pilot study of peroral Vorinostat (Zolinza) in patients with refractory histone deacetylase-positive uterine sarcoma. | ||
Medical condition: Uterine sarcoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-003344-62 | Sponsor Protocol Number: mitHDAC | Start Date*: 2005-11-15 |
Sponsor Name:Imperial College | ||
Full Title: Effect of theophylline on histone deacetylase activity: enhancement of in-vitro glucocorticoid function in patients with COPD. | ||
Medical condition: Chronic Obstructive Lung Disease (COPD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001907-36 | Sponsor Protocol Number: 0683 013-02 | Start Date*: 2005-03-18 |
Sponsor Name:Merck Sharp & Dohme Limited | ||
Full Title: A Phase II Clinical Trial of Oral Suberoylanilide Hydroxamic Acid (L-001079038) in Patients with Relapsed Diffuse Large B-Cell Lymphoma (DLBCL) | ||
Medical condition: Relapsed Diffuse Large B-Cell Lymphoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004480-21 | Sponsor Protocol Number: DSC/07/2357/28 | Start Date*: 2007-11-30 | |||||||||||
Sponsor Name:ITALFARMACO | |||||||||||||
Full Title: A phase IIA study of the histone-deacetylase inhibitor ITF2357 in patients with JAK-2 V617F positive chronic myeloproliferative diseases | |||||||||||||
Medical condition: chronic myeloproliferative diseases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001489-85 | Sponsor Protocol Number: FRM-0334-002 | Start Date*: 2015-02-23 | |||||||||||
Sponsor Name:FORUM Pharmaceuticals Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Dose-Escalating, Phase 2a Safety, Tolerability, and Pharmacodynamic Study of Two Doses of an Histone Deacetylase Inhibitor (FRM-0334) in Subjects wit... | |||||||||||||
Medical condition: Prodromal to Moderate Frontotemporal Dementia with Granulin Mutation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) NL (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004747-23 | Sponsor Protocol Number: BPC01-001 | Start Date*: 2014-01-17 | |||||||||||
Sponsor Name:Bionor Pharma ASA | |||||||||||||
Full Title: An Open Phase I/IIa Study to Evaluate the Safety and Effect of Therapeutic HIV-1 Immunization using Vacc-4x + rhuGM-CSF, and HIV-1 Reactivation using Romidepsin, on the Viral Reservoir in Virologic... | |||||||||||||
Medical condition: HIV-infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002395-41 | Sponsor Protocol Number: 309100 | Start Date*: 2004-12-03 |
Sponsor Name:Schering AG | ||
Full Title: Phase II study of MS-275, a histone deacetylase inhibitor, comparing 2 dosage schedules in patients with metastatic melanoma | ||
Medical condition: Metastatic malignant melanoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003554-15 | Sponsor Protocol Number: 18031977 | Start Date*: 2006-11-09 |
Sponsor Name:National Cancer Institute | ||
Full Title: The histone deacetylase inhibitor (HDAC) valproic acid as second line treatment for hormone refractory metastatic prostate cancer. A phase II. study. | ||
Medical condition: hormone refractory metastatic prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-009916-33 | Sponsor Protocol Number: 00332/AMLSG14-09 | Start Date*: 2011-05-13 | |||||||||||
Sponsor Name:University Medical Center Freiburg | |||||||||||||
Full Title: Prospective randomized multicenter phase II trial of low-dose decitabine (DAC) administered alone or in combination with the histone deacetylase inhibitor valproic acid (VPA) and all-trans retinoic... | |||||||||||||
Medical condition: Patients older than 60 years with acute myeloid leukemia according to WHO (≥ 20 % blasts in the peripheral blood (pB) or bone marrow (BM)) not qualifying for, or not consenting to, standard remissi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001770-42 | Sponsor Protocol Number: 4745 | Start Date*: 2018-10-24 | |||||||||||||||||||||
Sponsor Name:The Royal Marsden NHS Foundation Trust | |||||||||||||||||||||||
Full Title: A multicenter phase II non-randomised trial assessing the efficacy of Domatinostat plus avelumab in patients with previously treated advanced mismatch repair proficient oesophagogastric and colore... | |||||||||||||||||||||||
Medical condition: Advanced gastrooesophageal and colorectal cancer | |||||||||||||||||||||||
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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: 2011-002744-27 | Sponsor Protocol Number: CR01849 | Start Date*: 2011-11-01 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: Pharmacodynamic Studies of a Histone Deacetylase Inhibitor in FRDA | |||||||||||||
Medical condition: Friedreich’s ataxia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001076-18 | Sponsor Protocol Number: 26481585LYM2001 | Start Date*: 2011-09-20 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2, Single-arm, Open-label, Multicenter Study of the Histone Deacetylase Inhibitor (HDACi) JNJ-26481585 in Subjects With Previously Treated Stage Ib-IVa Cutaneous T-cell Lymphoma | |||||||||||||
Medical condition: Stage Ib-IVa Cutaneous T-cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Completed) PT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007139-26 | Sponsor Protocol Number: S075LBH501 | Start Date*: 2008-04-17 | |||||||||||
Sponsor Name:SENDO TECH | |||||||||||||
Full Title: A phase II study of the histone deacetylase inhibitor Panobinostat (LBH589) in patients with advanced Small Cell Lung Cancer (SCLC) | |||||||||||||
Medical condition: SCLC patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) GR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007091-41 | Sponsor Protocol Number: DSC/07/2357/31 | Start Date*: 2008-01-19 | |||||||||||
Sponsor Name:ITALFARMACO | |||||||||||||
Full Title: Phase II Trial of the Histone-Deacetylase Inhibitor ITF2357 Followed by Mechlorethamine in Relapsed/Refractory Hodgkins Lymphoma Patients | |||||||||||||
Medical condition: Hodgkin's lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010982-22 | Sponsor Protocol Number: DSC/08/2357/38 | Start Date*: 2009-04-20 | |||||||||||
Sponsor Name:ITALFARMACO | |||||||||||||
Full Title: Phase II study of the histone-deacetylase inhibitor GIVINOSTAT (ITF2357) in combination with hydroxyurea in patients with JAK2V617F positive Polycythemia Vera non-responder to hydroxyurea monotherapy | |||||||||||||
Medical condition: Polycythemia Vera | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005465-19 | Sponsor Protocol Number: DSC/06/2357/21 | Start Date*: 2007-02-09 | |||||||||||
Sponsor Name:ITALFARMACO | |||||||||||||
Full Title: Open label, uncontrolled, pilot, phase II study of histone-deacetylase inhibitor ITF2357 administered orally to subjects with chronic lynphocytic leukemia (CLL) refractory/relapsed after convention... | |||||||||||||
Medical condition: Chronic lynphocytic leukemia (CLL) refractory/relapsed after conventional chemotherapy or relapsed after autologous bone marrow transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002113-12 | Sponsor Protocol Number: DSC/05/2357/17 | Start Date*: 2006-09-19 | |||||||||||
Sponsor Name:ITALFARMACO | |||||||||||||
Full Title: Open label, uncontrolled, pilot, phase II study of histone-deacetylase inhibitor ITF2357 administered orally to subjects aged over 60 years with primary or secondary DLBCL refractory/ relapsed afte... | |||||||||||||
Medical condition: Primary or secondary DLBCL refractory/relapsed after conventional chemotherapy | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001084-56 | Sponsor Protocol Number: DSC/04/2357/10 | Start Date*: 2005-05-27 | |||||||||||
Sponsor Name:ITALFARMACO | |||||||||||||
Full Title: Phase II Multiple-Dose Clinical Trial of Oral ITF 2357 In Patients with Advanced Multiple Myeloma | |||||||||||||
Medical condition: multiple myeloma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002281-23 | Sponsor Protocol Number: Spon1345-14 | Start Date*: 2016-06-13 | |||||||||||
Sponsor Name:Cardiff University | |||||||||||||
Full Title: A phase 2 study of the monocyte-targeted histone deacetylase inhibitor tefinostat (CHR-2845) in chronic myelomonocytic leukaemia (CMML) | |||||||||||||
Medical condition: Chronic myelomonocytic leukaemia (CMML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000049-36 | Sponsor Protocol Number: DSC/07/2357/26 | Start Date*: 2007-05-07 | |||||||||||
Sponsor Name:ITALFARMACO | |||||||||||||
Full Title: Phase II study of the histone-deacetylase inhibitor ITF2357 in very high-risk relapsed/refractory Hodgkin's lymphoma patients | |||||||||||||
Medical condition: Hodgkin's lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
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