- Trials with a EudraCT protocol (50)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
50 result(s) found for: Cancer genomics.
Displaying page 1 of 3.
EudraCT Number: 2017-003684-35 | Sponsor Protocol Number: R2810-ONC-1763 | Start Date*: 2018-07-10 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Open-Label Study of Combinations of Standard and High Dose REGN2810 (Cemiplimab; Anti-PD-1 Antibody) and Ipilimumab (Anti-CTLA-4 Antibody) in the Second-Line Treatment of Patients wit... | |||||||||||||
Medical condition: Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) FR (Completed) PL (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004860-12 | Sponsor Protocol Number: ERCAVATAR2015 | Start Date*: 2016-02-24 | |||||||||||
Sponsor Name:Centro Nacional Investigaciones Oncológicas (CNIO) | |||||||||||||
Full Title: Integrated Genomics and Avatar Mouse Models for Personalized Treatment of Pancreatic Cancer | |||||||||||||
Medical condition: Metastatic pancreatic cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004603-35 | Sponsor Protocol Number: REACH | Start Date*: 2009-04-28 | |||||||||||||||||||||
Sponsor Name:University of Heidelberg | |||||||||||||||||||||||
Full Title: Radiotherapy (IMRT), Erbitux And Chemotherapy For Unresectable Carcinomas Of Head and Neck. REACH-Study | |||||||||||||||||||||||
Medical condition: Histologically confirmed locally advanced (stage III or IV), non-metastatic squamous cell carcinoma of oro-, hypopharynx or larynx (T2-4, NX, M0). | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-000476-26 | Sponsor Protocol Number: N14DAR | Start Date*: 2020-07-13 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Netherlands Cancer Institute | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Dynamics of Androgen Receptor genomics and transcriptomics after neoadjuvant androgen ablation (DARANA) | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Prostate cancer | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007943-29 | Sponsor Protocol Number: EFC6521 | Start Date*: 2008-07-29 |
Sponsor Name:sanofi-aventis recherche & développement | ||
Full Title: A multinational, randomized, double blind, placebo-controlled study to evaluate the efficacy and safety of AVE5026 in the prevention of venous thromboembolism (VTE) in cancer patients at high risk ... | ||
Medical condition: The subjects who will participate to this clinical trial are cancer patients (i.e. patients with metastatic or locally advanced tumor of the lung, pancreas, stomach, colon/ rectum, bladder or ovary... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) HU (Completed) FR (Completed) AT (Completed) LV (Completed) EE (Completed) SE (Completed) SK (Completed) NL (Completed) PT (Completed) LT (Completed) BE (Completed) DK (Completed) CZ (Completed) FI (Completed) SI (Completed) IT (Completed) BG (Completed) ES (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000469-35 | Sponsor Protocol Number: CL03-ORY-1001SCLC | Start Date*: 2018-10-10 | |||||||||||
Sponsor Name:Oryzon Genomics S. A. | |||||||||||||
Full Title: A pilot study to assess the safety, tolerability, dose finding and efficacy ORY-1001 in combination with platinum-etoposide chemotherapy in patients with relapsed, extensive-stage disease small cel... | |||||||||||||
Medical condition: Relapsed, extended-stage disease small cell lung cancer (ED SCLC). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000809-12 | Sponsor Protocol Number: PREDIXLumA | Start Date*: 2014-11-17 | ||||||||||||||||||||||||||
Sponsor Name:Karolinska University Hospital | ||||||||||||||||||||||||||||
Full Title: PREDIX Luminal A - Neoadjuvant response-guided treatment of slowly proliferating hormone receptor positive tumors. Part of a set of translational phase II trials based on molecular subtypes | ||||||||||||||||||||||||||||
Medical condition: Primary breast cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000167-25 | Sponsor Protocol Number: UC-0110/1201 | Start Date*: 2012-05-29 | |||||||||||
Sponsor Name:UNICANCER | |||||||||||||
Full Title: A multicentric randomized phase II study evaluating dual targeting of the EGFR using the combination of cetuximab and afatinib versus cetuximab alone in patients with chemotherapy refractory wtKRAS... | |||||||||||||
Medical condition: Refractory wtKRAS metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001321-14 | Sponsor Protocol Number: INCB54828-201 | Start Date*: 2017-01-12 | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 2, Open-Label, Single-Agent, Multicenter Study to Evaluate the Efficacy and Safety of INCB054828 in Subjects With Metastatic or Surgically Unresectable Urothelial Carcinoma Harboring FGF/FG... | |||||||||||||
Medical condition: Subjects with metastatic or surgically unresectable urothelial cancer (may include primary site from ureters, upper tract, renal pelvis, and bladder) with an FGF/FGFR alteration, who failed at leas... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) FR (Completed) ES (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002608-16 | Sponsor Protocol Number: NVALT-8B | Start Date*: 2009-07-13 |
Sponsor Name:UMCG | ||
Full Title: A randomized phase III study of adjuvant chemotherapy with or without low-molecular weight heparin in patients with high risk for recurrence and completely resected non-small-cell lung cancer: NVAL... | ||
Medical condition: This is a randomized multicenter phase III study. Patient with a high SUVof the primary tumor prior to surgery will be randomised to four cycles of pemetrexed and cisplatin with or without nadropar... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002644-21 | Sponsor Protocol Number: NVALT-8A | Start Date*: 2009-07-13 |
Sponsor Name:UMCG | ||
Full Title: A randomized phase III study of adjuvant chemotherapy in patients with completely resected Non-Small-Cell Lung Cancer and low-risk for recurrence: NVALT-8A | ||
Medical condition: This is a randomized multicenter phase III study. Patient with a low SUV of the primary tumor prior to surgery will be randomised to four cycles of cisplatin-based chemotherapy or observation in a ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000482-36 | Sponsor Protocol Number: CL02-ORY-1001AML | Start Date*: 2018-09-07 | |||||||||||
Sponsor Name:Oryzon Genomics S. A. | |||||||||||||
Full Title: A pilot study to assess the safety, tolerability, dose finding and efficacy of ORY-1001 in combination with azacitidine in older patients with AML in first line therapy. | |||||||||||||
Medical condition: Patients with acute mieloyd leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003192-18 | Sponsor Protocol Number: NCT-PMO-1602 | Start Date*: 2021-07-08 | |||||||||||
Sponsor Name:German Cancer Research Center | |||||||||||||
Full Title: Continuous ReAssessment with Flexible ExTension in Rare Malignancies – CRAFT: The NCT PMO-1602 Phase II Trial | |||||||||||||
Medical condition: Metastatic or locally advanced malignancies | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000649-39 | Sponsor Protocol Number: EMR62202-502 | Start Date*: 2004-12-01 |
Sponsor Name:Merck KGaA | ||
Full Title: A randomized, controlled, multicenter, phase I/II study of cetuximab plus irinotecan investigating the pharmacodynamics, genomics and -genetics as well as the safety and efficacy of a dose escalat... | ||
Medical condition: Metastatic colorectal cancer refractory to irinotecan treatment | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) AT (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003298-24 | Sponsor Protocol Number: R4018ONC1721 | Start Date*: 2020-06-11 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 1/2 Study of REGN4018 (A MUC16xCD3 Bispecific Antibody) Administered Alone or in Combination with Cemiplimab in Patients with Recurrent Ovarian Cancer or Other Recurrent MUC16+ Cancers | ||||||||||||||||||
Medical condition: Recurrent Ovarian Cancer Recurrent Fallopian Tube Cancer Recurrent Primary Peritoneal Cancer Recurrent Endometrial Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: BE (Trial now transitioned) ES (Ongoing) NL (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001309-22 | Sponsor Protocol Number: 2593957 | Start Date*: 2021-03-29 | |||||||||||
Sponsor Name:IQVIA Commercial GmbH & Co. OHG | |||||||||||||
Full Title: Evaluation of immunological effects of the hedgehog inhibitors on basal cell carcinoma - An open label, prospective, observational biomarker study of the DeCOG. | |||||||||||||
Medical condition: Basal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001908-38 | Sponsor Protocol Number: R5093-ONC-1863 | Start Date*: 2020-09-28 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: A PHASE 1/2 STUDY OF REGN5093 IN PATIENTS WITH MET-ALTERED ADVANCED NON-SMALL CELL LUNG CANCER | |||||||||||||
Medical condition: Non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000808-10 | Sponsor Protocol Number: PREDIX-HER2 | Start Date*: 2014-11-12 | ||||||||||||||||||||||||||
Sponsor Name:Karolinska University Hospital | ||||||||||||||||||||||||||||
Full Title: PREDIX HER2 - Neoadjuvant response-guided treatment of HER2 positive breast cancer. Part of a platform of translational phase II trials based on molecular subtypes | ||||||||||||||||||||||||||||
Medical condition: Primary breast cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000987-80 | Sponsor Protocol Number: ET19036 | Start Date*: 2019-10-15 | |||||||||||
Sponsor Name:Centre Léon Bérard | |||||||||||||
Full Title: COTESARC - A multicentre Phase I-II study evaluating the combination of a MEK inhibitor and a PDL1 inhibitor in pediatric and adult patients with locally advanced and/or metastatic soft tissue sarc... | |||||||||||||
Medical condition: advanced/metastatic soft tissu sarcoma | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001455-32 | Sponsor Protocol Number: WIN001 | Start Date*: 2017-12-15 |
Sponsor Name:Worldwide Innovative Network Association | ||
Full Title: A proof of concept study to explore safety and efficacy of tri-therapy approach in advanced/metastatic NSCLC and retrospectively assess the ability of integrated genomics and transcriptomics to mat... | ||
Medical condition: Patients with advanced/metastatic non-small cell lung cancer (NSCLC) with no documented targetable alterations (EGFR mutation, ALK translocation, ROS1 mutation if available or MET exon 14 skipping ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: View results |
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