- Trials with a EudraCT protocol (1,193)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
1,193 result(s) found for: Hematologic Disease.
Displaying page 32 of 60.
EudraCT Number: 2015-004066-28 | Sponsor Protocol Number: AMLSG2415 | Start Date*: 2018-04-04 |
Sponsor Name:University Hospital Ulm | ||
Full Title: A Phase II Study with a Safety Run-in Phase Evaluating Vosaroxin With Azacitidine in Older Patients with Newly Diagnosed Acute Myeloid Leukemia and Intermediate/Adverse Genetic Risk or Myelodysplas... | ||
Medical condition: Patients with confirmed diagnosis of acute myeloid leukemia (WHO 2016) and intermediate or adverse genetic risk (according to 2017 ELN recommendations); or patients with myelodysplastic syndrome wi... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-004429-26 | Sponsor Protocol Number: Atu027-I-02 | Start Date*: 2013-02-25 | ||||||||||||||||
Sponsor Name:Silence Therapeutics GmbH | ||||||||||||||||||
Full Title: A Phase Ib/IIa study of combination therapy with Gemcitabine and Atu027 in subjects with locally advanced or metastatic pancreatic adenocarcinoma | ||||||||||||||||||
Medical condition: Locally advanced or metastatic pancreatic adenocarcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-024298-37 | Sponsor Protocol Number: ESOT/1/2010 | Start Date*: 2011-03-28 | |||||||||||
Sponsor Name:Dipartimento Integrato di Oncologia, Ematologia e Patologie dell'Apparato Respiratorio | |||||||||||||
Full Title: Early strong opiod treatment in cancer pain -Morphine vs weak opiods | |||||||||||||
Medical condition: Tumor Pain, mild-moderate intensity (VAS 3-7) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005087-25 | Sponsor Protocol Number: NeoPAN01-2013 | Start Date*: 2014-04-01 | |||||||||||
Sponsor Name:FUNDACION HOSPITAL DE MADRID | |||||||||||||
Full Title: Gemcitabine plus nab-paclitaxel versus folfirinox as neoadjuvant treatment in patients with potentially resectable pancreatic carcinoma. NeoPAN Study | |||||||||||||
Medical condition: Potentially resectable pancreatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001534-13 | Sponsor Protocol Number: JAN13004-30 | Start Date*: 2015-10-02 | |||||||||||
Sponsor Name:SPHERIUM BIOMED S.L. | |||||||||||||
Full Title: Phase IB-II clinical trial of melatonin oral gel for the prevention and treatment of oral mucositis in patients with head and neck cancer undergoing chemoradiation. | |||||||||||||
Medical condition: Oral mucositis in patients with head and neck cancer undergoing chemoradiation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001721-13 | Sponsor Protocol Number: TAK-013/EC-302 | Start Date*: 2005-01-24 | |||||||||||
Sponsor Name:Takeda Europe R&D Center Ltd | |||||||||||||
Full Title: A Phase III, multi-center, randomized, double-blind study to evaluate the efficacy and safety of 50 mg and 100 mg of sufugolix (TAK-013) tablets administered twice daily versus placebo for 12 weeks... | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000783-16 | Sponsor Protocol Number: ML21531 | Start Date*: 2008-06-18 | ||||||||||||||||
Sponsor Name:ROCHE SAS | ||||||||||||||||||
Full Title: Multicenter, phase II trial assessing the efficacy and safety of bevacizumab (Avastin®) combined to trastuzumab (Herceptin®) based chemotherapy in patients with primary inflammatory HER2+ breast ca... | ||||||||||||||||||
Medical condition: Primary inflammatory HER2+ breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002480-15 | Sponsor Protocol Number: M14REP | Start Date*: 2014-10-15 | ||||||||||||||||
Sponsor Name:The Dutch Working Group on Immunotherapy of Oncology (WIN-O) | ||||||||||||||||||
Full Title: A Phase II, Open-Label, Multicenter Study of Vemurafenib plus Cobimetinib (GDC-0973) in Unresectable Stage IIIc or Metastatic Melanoma; Response Monitoring and Resistance Prediction with Positron E... | ||||||||||||||||||
Medical condition: BRAFV600-mutation positive patients with unresectable stage IIIc or IV melanoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001720-21 | Sponsor Protocol Number: TAK-013/EC301 | Start Date*: 2004-12-24 | |||||||||||
Sponsor Name:Takeda Europe R&D Centre Ltd | |||||||||||||
Full Title: A Phase III, multi-center, randomized, double-blind comparator study to evaluate the efficacy and safety of 50 mg and 100 mg of TAK-013 tablets administered twice daily versus 3.75mg of Leuprolide ... | |||||||||||||
Medical condition: Endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001746-32 | Sponsor Protocol Number: EORTC 21012 | Start Date*: 2005-08-31 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Phase II clinical trial with Caelyx mono-chemotherapy in patients with advanced Mycosis fungoides stage IIb, IVa and IVb with or without previous chemotherapy | |||||||||||||
Medical condition: patients with refractory or relapsed advanced stages of mycosis fungoides (stage IIb, IVa, or Ivb) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001645-26 | Sponsor Protocol Number: TMZ-FTM.CB.1 | Start Date*: 2008-06-01 | |||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO "CARLO BESTA" | |||||||||||||
Full Title: Phase II study: Systemic treatment with alternating weekly regimen of temozolomide and monthly fotemustine combination in recurrent glioblastoma patients. | |||||||||||||
Medical condition: Glioblastoma recurrent | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005190-36 | Sponsor Protocol Number: 20050252 | Start Date*: 2015-01-22 | ||||||||||||||||||||||||||
Sponsor Name:Amgen Inc | ||||||||||||||||||||||||||||
Full Title: A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of Panitumumab in Children with Solid Tumors | ||||||||||||||||||||||||||||
Medical condition: Solid Tumours | ||||||||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000171-24 | Sponsor Protocol Number: GCTSK004 | Start Date*: 2016-07-12 |
Sponsor Name:Národný onkologický ústav | ||
Full Title: Phase II study of gemcitabine, carboplatin and VELIPARIB (ABT-888) in refractory testicular germ cell cancer. | ||
Medical condition: Refractory histologically confirmed extracranial primary germ cell cancer, seminoma, or nonseminoma germ cell tumours | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004987-21 | Sponsor Protocol Number: ONO-7579-01 | Start Date*: 2017-09-13 | |||||||||||
Sponsor Name:Ono Pharmaceutical Co., Ltd. | |||||||||||||
Full Title: An open-label, multi-center, dose-escalation and expansion study to evaluate the safety and efficacy of ONO-7579 in patients with advanced solid tumors/ NTRK gene fusion positive advanced solid tumors | |||||||||||||
Medical condition: Advanced solid tumors and Neurotrophic receptor tyrosine kinase (NTRK) gene fusion positive advanced solid tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006197-88 | Sponsor Protocol Number: FANCOSTEM-1 | Start Date*: 2012-03-22 | |||||||||||
Sponsor Name:Cristina Díaz de Heredia Rubio | |||||||||||||
Full Title: Clinical Phase II Trial to evaluate efficacy and safety of CD34+ cells mobilization and collection after treatment with plerixafor and filgrastim in patients with Fanconi anemia for subsequent tra... | |||||||||||||
Medical condition: Fanconi anemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002768-15 | Sponsor Protocol Number: GS-US-401-2076 | Start Date*: 2018-02-26 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Prospective, Open-Label, Multicenter, Phase 2 Trial to Evaluate the Safety and Efficacy of the Combination of Tirabrutinib (GS-4059) and Entospletinib with and without Obinutuzumab in Subjects wi... | |||||||||||||
Medical condition: Adults with relapsed or refractory chronic lymphocytic leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004165-58 | Sponsor Protocol Number: GO39590 | Start Date*: 2017-02-21 | |||||||||||
Sponsor Name:Genentech, Inc | |||||||||||||
Full Title: A PHASE II, MULTICENTER, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND STUDY OF MOXR0916 IN COMBINATION WITH ATEZOLIZUMAB VERSUS ATEZOLIZUMAB ALONE IN PATIENTS WITH UNTREATED LOCALLY ADVANCED OR ME... | |||||||||||||
Medical condition: Advanced or Metastatic Urothelial Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) PT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002856-26 | Sponsor Protocol Number: ADO-EP02(ML29328) | Start Date*: 2016-12-19 | |||||||||||
Sponsor Name:SRH Wald-Klinikum Gera GmbH | |||||||||||||
Full Title: A PHASE II, SINGLE-ARMED, MULTICENTER TRIAL OF NEOADJUVANT VISMODEGIB IN PATIENTS WITH LARGE AND/OR RECURRENT RESECTABLE BASAL CELL CARCINOMA | |||||||||||||
Medical condition: Patients with large and/or recurrent resectable basal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000469-35 | Sponsor Protocol Number: GO29227 | Start Date*: 2014-08-12 | ||||||||||||||||
Sponsor Name:Genentech, Inc. | ||||||||||||||||||
Full Title: A RANDOMIZED, PHASE II, MULTICENTER, PLACEBO-CONTROLLED STUDY OF IPATASERTIB (GDC-0068), AN INHIBITOR OF AKT, IN COMBINATION WITH PACLITAXEL AS FRONT-LINE TREATMENT FOR PATIENTS WITH METASTATIC TRI... | ||||||||||||||||||
Medical condition: Inoperable locally advanced or metastatic triple negative breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Completed) BE (Completed) ES (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003909-42 | Sponsor Protocol Number: GS-US-401-1958 | Start Date*: 2016-09-20 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Prospective, Open-Label, Multicenter, Phase 2 Trial to Evaluate the Safety and Efficacy of the Combination of Tirabrutinib (GS-4059) and Idelalisib with and without Obinutuzumab in Subjects with... | |||||||||||||
Medical condition: Adults with relapsed or refractory chronic lymphocytic leukemia (CLL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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