- Trials with a EudraCT protocol (7,029)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (712)
7,029 result(s) found for: cancer.
Displaying page 291 of 352.
EudraCT Number: 2020-005106-25 | Sponsor Protocol Number: D8241C00001 | Start Date*: 2021-11-15 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Modular Phase I/II, Open-Label, Multi-Centre Study to Assess the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of AZD0466 Monotherapy or in Combination in Patients with Advanced... | |||||||||||||
Medical condition: Advanced Haematological Malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002688-77 | Sponsor Protocol Number: D9720C00001 | Start Date*: 2021-06-15 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Modular Phase I/IIa, Open-label, Multicentre Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of Ascending Doses of AZD5305 as Monotherapy and... | |||||||||||||
Medical condition: Advanced Solid Tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001671-51 | Sponsor Protocol Number: SGN35-023 | Start Date*: 2016-06-15 | ||||||||||||||||
Sponsor Name:Seattle Genetics, Inc. | ||||||||||||||||||
Full Title: A RANDOMIZED, OPEN LABEL, PHASE 2 STUDY OF RITUXIMAB AND BENDAMUSTINE WITH OR WITHOUT BRENTUXIMAB VEDOTIN FOR RELAPSED OR REFRACTORY CD30-POSITIVE DIFFUSE LARGE B CELL LYMPHOMA | ||||||||||||||||||
Medical condition: i) Relapsed or Refractory CD30-Positive Diffuse Large B-Cell Lymphoma ii) follicular non-Hodgkin lymphoma (NHL) grade 3b | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) CZ (Completed) FR (Completed) ES (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000144-26 | Sponsor Protocol Number: ABI-007-PST-001 | Start Date*: 2013-09-17 | |||||||||||
Sponsor Name:Abraxis BioScience, LLC, a wholly-owned subsidiary Celgene Corporation | |||||||||||||
Full Title: A Phase 1/2, multicenter, open-label, dose-finding study to assess the safety, tolerability, and preliminary efficacy of weekly nab-paclitaxel in pediatric patients with recurrent or refractory s... | |||||||||||||
Medical condition: recurrent or refractory solid tumor | |||||||||||||
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Population Age: Infants and toddlers, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) GB (Completed) FR (Completed) ES (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003990-89 | Sponsor Protocol Number: Uni-Koeln-1707 | Start Date*: 2015-05-12 | |||||||||||
Sponsor Name:University of Cologne | |||||||||||||
Full Title: Brentuximab vedotin or B-CAP in the treatment of older patients with newly diagnosed classical Hodgkin Lymphoma – a GHSG-NLG Intergroup Phase II trial – | |||||||||||||
Medical condition: Treatment of older patients with newly diagnosed classical Hodgkin lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NO (Completed) SE (Completed) DK (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004770-22 | Sponsor Protocol Number: TAS-117-201 | Start Date*: 2021-04-01 | |||||||||||
Sponsor Name:Taiho Oncology, Inc. | |||||||||||||
Full Title: A Phase 2 Study of TAS-117 in Patients with Advanced Solid Tumors Harboring Germline PTEN Inactivating Mutations | |||||||||||||
Medical condition: Advanced Solid Tumors Harboring Germline PTEN Inactivating Mutations | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) AT (Prematurely Ended) IT (Prematurely Ended) ES (Prematurely Ended) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004482-14 | Sponsor Protocol Number: CEGF816X2101 | Start Date*: 2014-08-15 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase I/II, multicenter, open-label study of EGFRmut–TKI EGF816,administered orally in adult patients with EGFRmut solid malignancies | |||||||||||||
Medical condition: Solid tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Temporarily Halted) FR (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004677-20 | Sponsor Protocol Number: Gemtax IV | Start Date*: 2006-03-17 |
Sponsor Name:University of Heidelberg, Klinikum Mannheim, Dep Surgery/Thoracical Oncology | ||
Full Title: Randomised Phase II/III Study on Sectional Single Agent Gemcitabine and Docetaxel Versus Carboplatine / Gemcitabine Doublet Therapy, both combined Cetuximab in the Treatment of Advanced NSCLC (Stag... | ||
Medical condition: Lung cancer remains the leading cause of cancer-related death in men and has increased its incidence in women over the past decades (protocol page 9). Data from both meta-analysis and clinical tria... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) LT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-022968-13 | Sponsor Protocol Number: ET-B-031-10 | Start Date*: 2011-03-16 | |||||||||||
Sponsor Name:Pharma Mar, S.A. Sociedad Unipersonal | |||||||||||||
Full Title: Multicenter, Open-Label, Phase II Study of Trabectedin (Yondelis®) in Patients with Hormonal Receptors Positive, HER2 Negative, Advanced Breast Carcinoma, Overexpressing or Underexpressing Xeroderm... | |||||||||||||
Medical condition: Advanced Breast Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000811-12 | Sponsor Protocol Number: ST03 | Start Date*: 2008-01-31 | ||||||||||||||||
Sponsor Name:Medical Research Council Clinical Trials Unit | ||||||||||||||||||
Full Title: A Randomised Phase II/III trial of peri-operative Chemotherapy with or without Bevacizumab in Operable Oesophagogastric Adenocarcinoma and A Feasibility Study Evaluating Lapatinib in HER-2 Positive... | ||||||||||||||||||
Medical condition: Patients with histologically verfied lower oesophageal, Siewert Type I, II or III oesophagogastric junction or gastric adenocarcinoma. Type III or gastric tumours should be stage 1b (T1N1, T2a/bN0... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002234-14 | Sponsor Protocol Number: OR2805-101 | Start Date*: 2023-06-07 |
Sponsor Name:OncoResponse, Inc. | ||
Full Title: A Phase 1-2 Study of OR2805 Alone and in Combination with other Anti-cancer Agents in Subjects with Advanced Malignancies | ||
Medical condition: Solid tumor cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004165-13 | Sponsor Protocol Number: IJB-LBC-NEOCHECKRAY-2018 | Start Date*: 2019-06-06 | |||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||
Full Title: Neo-adjuvant chemotherapy combined with SBRT to the primary tumour +/- durvalumab (MEDI4736), +/- oleclumab in luminal B breast cancer: a phase ll randomized trial | |||||||||||||
Medical condition: Luminal B Breast Cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003949-42 | Sponsor Protocol Number: 208471 | Start Date*: 2019-12-11 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Phase 1b/2a Pilot Randomized Study to Evaluate the Safety and Tolerability of Autologous T-Cells Expressing Enhanced TCRs (T-Cell Receptors) Specific for NY-ESO-1/LAGE-1a (GSK3377794) Alone, or i... | |||||||||||||
Medical condition: Stage IIIb or Stage IV Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003958-67 | Sponsor Protocol Number: CAAA405A12302 | Start Date*: 2022-04-06 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: Phase II/III study for evaluation of the diagnostic performance of [18F]CTT1057 PET imaging for the detection of PSMA positive tumors using histopathology as a standard of truth (GuideView) | |||||||||||||
Medical condition: Untreated high risk prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) ES (Ongoing) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001626-56 | Sponsor Protocol Number: MK-3475-01A | Start Date*: 2020-09-06 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc | |||||||||||||
Full Title: Substudy 1: A Phase 2, Umbrella Study with Rolling Arms of Investigational Agents with Pembrolizumab in Combination with Chemotherapy in Treatment Naive Patients with Advanced Non-small Cell Lung C... | |||||||||||||
Medical condition: Non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011925-14 | Sponsor Protocol Number: 1199.37 | Start Date*: 2009-08-24 | |||||||||||
Sponsor Name:Boehringer Ingelheim | |||||||||||||
Full Title: A multicenter, open label, phase I / II study to evaluate safety, pharmacokinetics and efficacy of BIBF 1120 in comparison with oral sorafenib for advanced hepatocellular carcinoma patients. | |||||||||||||
Medical condition: Histologically or cytologically confirmed hepatocellular carcinoma not amenable to local therapy with adequate renal, hematological and liver paramenters with Child-Pugh score 7 or less, in 1st lin... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) AT (Completed) DE (Completed) SK (Completed) HU (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004231-25 | Sponsor Protocol Number: MS201923_0050 | Start Date*: 2024-05-21 | |||||||||||
Sponsor Name:Merck Healthcare KGaA | |||||||||||||
Full Title: A Phase II, open-label, single-arm study of berzosertib (M6620) in combination with topotecan in participants with relapsed platinum-resistant small-cell lung cancer | |||||||||||||
Medical condition: Relapsed platinum resistant small-cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Completed) ES (Temporarily Halted) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005822-27 | Sponsor Protocol Number: BLU-945-1101 | Start Date*: 2021-10-22 | |||||||||||
Sponsor Name:Blueprint Medicines Corporation | |||||||||||||
Full Title: A Phase 1/2 Study Targeting Acquired Resistance Mechanisms in Patients with EGFR Mutant Non-Small Cell Lung Cancer | |||||||||||||
Medical condition: EGFR Mutant Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) NL (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005336-27 | Sponsor Protocol Number: FRX106365 | Start Date*: 2006-04-21 |
Sponsor Name:GlaxoSmithKline Research & Development Limited | ||
Full Title: The INPACT study (Improving with Nadroparin the Prognosis in Advanced Cancer Treatment) A randomized, controlled trial to evaluate the effects of nadroparin on survival and disease progression in ... | ||
Medical condition: Advanced malignancies of the lung, pancreas, or prostate. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) BE (Completed) IT (Completed) SI (Completed) HU (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000394-21 | Sponsor Protocol Number: A6301094 | Start Date*: 2016-07-20 | |||||||||||
Sponsor Name:Pfizer Inc | |||||||||||||
Full Title: A THREE MONTH PROSPECTIVE OPEN LABEL STUDY OF THERAPY WITH FRAGMIN® (DALTEPARIN SODIUM INJECTION) IN CHILDREN WITH VENOUS THROMBOEMBOLISM WITH OR WITHOUT MALIGNANCIES. | |||||||||||||
Medical condition: Acute treatment and secondary prophylaxis of recurrent VTE (venous thromboembolism) in children with or without cancer. | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SI (Completed) PL (Completed) GB (Completed) DE (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
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