- Trials with a EudraCT protocol (2,679)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (78)
2,679 result(s) found for: Clinical Oncology.
Displaying page 1 of 134.
EudraCT Number: 2019-004753-87 | Sponsor Protocol Number: BBI608-901 | Start Date*: 2020-03-18 |
Sponsor Name:Sumitomo Dainippon Pharma Oncology, Inc. | ||
Full Title: A Rollover Study to Provide Continued Access to Napabucasin for Patients Enrolled in Sumitomo Dainippon Pharma Oncology, Inc. sponsored Napabucasin Protocols | ||
Medical condition: Metastatic Pancreatic Adenocarcinoma and Metastatic Colorectal Cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000974-44 | Sponsor Protocol Number: D910CC00001 | Start Date*: 2019-10-25 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase 1b/2, Open-label, Multicenter Study of Novel Oncology Therapies in Combination with Chemotherapy and Bevacizumab as First-line Therapy in Metastatic Microsatellite-stable Colorectal Cancer ... | |||||||||||||
Medical condition: Metastatic Microsatellite-Stable Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002540-25 | Sponsor Protocol Number: CSTI571A2406 | Start Date*: 2013-02-19 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An open label, multi-center imatinib roll-over protocol for patients who have completed a previous Novartis sponsored imatinib study and are judged by the investigator to benefit from continued ima... | ||
Medical condition: Male and female patients who are currently enrolled in a Novartis-sponsored, Oncology OGD&GMA imatinib study, are benefiting from treatment with imatinib and have fulfilled all their requirements ... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) GB (GB - no longer in EU/EEA) FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003844-11 | Sponsor Protocol Number: ML29242 | Start Date*: 2015-04-27 |
Sponsor Name:Department of Oncology, Linköping University Hospital, Linköping, Sweden | ||
Full Title: Continous treatment with bevacizumab in elderly patients with mCRC: an open label, single arm, prospective phase IV trial to evaluate outcome and safety of continuous bevacizumab treatment in combi... | ||
Medical condition: Metastatic colorectal cancer | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-004981-14 | Sponsor Protocol Number: OOI/KEMB/2006-2 | Start Date*: 2006-12-20 |
Sponsor Name:National Institute of Oncology, Budapest, Hungary | ||
Full Title: Phase II., non randomized, open study: inoperable gall bladder or biliary tract EGFR expressing carcinoma treatment with Erbitux and 5-fluorouracil, epiadriamycin, mitomycin containing combination ... | ||
Medical condition: Irresectable biliary tract cancer where palliation is the aim. It could be locally extanded and also metastatic cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006755-12 | Sponsor Protocol Number: COU-AA-001Ext | Start Date*: 2007-03-06 | |||||||||||
Sponsor Name:Janssen Oncology, Inc. | |||||||||||||
Full Title: An Expanded Access Open Label Study of CB7630 (Abiraterone Acetate) in Patients with Advanced Prostate Cancer Who Have Completed CB7630 Clinical Study COU-AA-001 | |||||||||||||
Medical condition: Hormone refractory prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003564-72 | Sponsor Protocol Number: | Start Date*: 2012-01-13 |
Sponsor Name:Aarhus University Hospital [...] | ||
Full Title: A Randomised phase II study with the combination of Xeloda (Capecitabine) plus Navelbine Oral ( Vinorelbine) day 1 and day 8 every 3. week versus Xeloda plus Navelbine Oral given metronimic as 1. o... | ||
Medical condition: Patient with relapse of breast cancer will be randomised for two different chemotherapy regimes ( 2 treatments arms) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002210-22 | Sponsor Protocol Number: COU-AA-003-EXT | Start Date*: 2008-09-25 | |||||||||||
Sponsor Name:Janssen Oncology, Inc. | |||||||||||||
Full Title: An Extended Study of CB7630 (Abiraterone Acetate) in Patients with Advanced Prostate Cancer Who Have Failed Androgen Deprivation and Docetaxel-Based Chemotherapy and Completed Clinical Study COU-AA... | |||||||||||||
Medical condition: Hormone refractory prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001533-28 | Sponsor Protocol Number: AAML0531 | Start Date*: 2016-05-03 |
Sponsor Name:Children's Oncology Group | ||
Full Title: A Phase III Randomized Trial of Gemtuzumab Ozogamicin (Mylotarg) Combined With Conventional Chemotherapy for De Novo Acute Myeloid Leukemia (AML) in Children, Adolescents, and Young Adults | ||
Medical condition: Acute myeloid leukaemia | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2012-001049-42 | Sponsor Protocol Number: | Start Date*: 2012-07-05 |
Sponsor Name:Department of Oncology, Rigshospitalet | ||
Full Title: MRI-perfusion and FLT- and FET-PET during bevacizumab monotherapy for patients with recurrent Glioblastoma Multiforme | ||
Medical condition: Recurrent Glioblastoma multiforme | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001545-41 | Sponsor Protocol Number: KO-MEN-001 | Start Date*: 2021-09-09 | |||||||||||
Sponsor Name:Kura Oncology, Inc. | |||||||||||||
Full Title: A Phase 1/2 First in Human Study of the Menin-MLL(KMT2A) Inhibitor KO-539 in Patients with Relapsed or Refractory Acute Myeloid Leukemia | |||||||||||||
Medical condition: Relapsed and/or refractory Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004281-10 | Sponsor Protocol Number: PT/11/2017 | Start Date*: 2018-01-10 | |||||||||||||||||||||
Sponsor Name:Department of Pediatric oncology, Aarhus University hospital | |||||||||||||||||||||||
Full Title: Pharmacokinetics and pharmacodynamics of Piperacillin-Tazobactam (PT) in pediatric oncology patients with fever and neutropenia | |||||||||||||||||||||||
Medical condition: Pediatric oncology patients with fever | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000494-20 | Sponsor Protocol Number: ABC-SE | Start Date*: 2016-07-03 | |||||||||||
Sponsor Name:Skåne University Hospital, Department of Oncology | |||||||||||||
Full Title: A Clinical Trial to Compare Efficacy and Tolerability of Atorvastatin in Addition to Endocrine Based Treatment with Focus on Mechanisms of Resistance to Endocrine Based Treatment (fulvestrant/aroma... | |||||||||||||
Medical condition: Estrogen receptor positive metastatic or locally advanced inoperable breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002968-10 | Sponsor Protocol Number: 024 | Start Date*: 2008-01-17 |
Sponsor Name:Department of Medicine I, Clinical Dep. f. Oncology, University Hospital, | ||
Full Title: Treatment of Patients Suffering from Tumour Cachexia with Dronabinol (tetrahydrocannabinol) or Placebo Comparison of individually optimised dosages in a double blind, randomised parallel design | ||
Medical condition: tumour cachexia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001396-69 | Sponsor Protocol Number: KO-TIP-002 | Start Date*: 2016-10-27 |
Sponsor Name:Kura Oncology Inc., | ||
Full Title: An Open Label Phase II Study of Tipifarnib in Subjects with Relapsed or Refractory Peripheral T-Cell LymphomaLymphoma | ||
Medical condition: Subjects with Relapses and Refractory Peripheral T-Cell Lymphoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2022-001811-16 | Sponsor Protocol Number: PS21GAP | Start Date*: 2022-12-19 | |||||||||||
Sponsor Name:Princess Maxima Center for pediatric oncology | |||||||||||||
Full Title: 68Ga-SATO in pediatric neuroblastoma patient; exploratory, safety, non-randomized, open label, comparative study | |||||||||||||
Medical condition: Neuroblastoma | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004362-26 | Sponsor Protocol Number: I3Y-MC-JPCF | Start Date*: 2017-08-14 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Open-Label, Phase 3 Study of Abemaciclib Combined with Standard Adjuvant Endocrine Therapy versus Standard Adjuvant Endocrine Therapy Alone in Patients with High-Risk, Node-Positive, ... | |||||||||||||
Medical condition: Node Positive, Early Stage, Hormone Receptor Positive, Human Epidermal Receptor 2 Negative, Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) NL (Trial now transitioned) HU (Ongoing) GB (GB - no longer in EU/EEA) BE (Ongoing) DK (Trial now transitioned) FI (Trial now transitioned) PL (Trial now transitioned) GR (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) CZ (Ongoing) FR (Ongoing) PT (Trial now transitioned) IT (Ongoing) RO (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004796-40 | Sponsor Protocol Number: 2018_58 | Start Date*: 2020-06-11 |
Sponsor Name:CHU de Lille | ||
Full Title: Multicenter Phase II study with dose-light escalation, intraoperative glioblastoma photodynamic therapy | ||
Medical condition: Glioblastoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) BE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000878-11 | Sponsor Protocol Number: OMO1.01.02 | Start Date*: 2017-06-08 | |||||||||||
Sponsor Name:OCTIMET Oncology NV | |||||||||||||
Full Title: A modular, multi-arm, multi-part, first time in patient study to evaluate the safety and tolerability of OMO-1, alone and in combination with anti-cancer treatments, in patients with locally advanc... | |||||||||||||
Medical condition: Locally advanced, unresectable or metastatic solid malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) NL (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005070-11 | Sponsor Protocol Number: M13-694 | Start Date*: 2015-07-08 |
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | ||
Full Title: A Phase 3 Placebo-Controlled Study of Carboplatin/Paclitaxel With or Without Concurrent and Continuation Maintenance Veliparib (PARP inhibitor) in Subjects with Previously Untreated Stages III or I... | ||
Medical condition: Newly diagnosed, untreated Stage III or IV high-grade serous epithelial ovarian, fallopian tube, or primary peritoneal cancer | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DK (Completed) ES (Restarted) PL (Completed) | ||
Trial results: (No results available) |
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