- Trials with a EudraCT protocol (695)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
695 result(s) found for: Oxaliplatin.
Displaying page 1 of 35.
EudraCT Number: 2015-002202-37 | Sponsor Protocol Number: 2015-115 | Start Date*: 2016-01-06 |
Sponsor Name:radboudumc | ||
Full Title: Pilot study: Is concomitant administration of lidocaine during oxaliplatin infusion able to prevent pain as a result of oxaliplatin induced acute neuropathy? | ||
Medical condition: Acute oxaliplatin induced neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001018-76 | Sponsor Protocol Number: CA209-649 | Start Date*: 2016-10-10 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Randomized, Multicenter, Open-Label, Phase 3 Study of Nivolumab Plus Ipilimumab versus Oxaliplatin plus Fluoropyrimidine in Subjects with Previously Untreated Advanced or Metastatic Gastric or Ga... | ||||||||||||||||||
Medical condition: Gastric or Gastroesophageal Junction Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) GR (Completed) PL (Completed) HU (Completed) DE (Completed) PT (Completed) FR (Completed) CZ (Completed) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005088-25 | Sponsor Protocol Number: 01234 | Start Date*: 2006-11-15 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Phase I/II study of oxaliplatin combined with melphalan in isolated hepatic perfusion for the treatment of liver metastases. | ||
Medical condition: Patients with isolated hepatic metastases of histologically confirmed colorectal adenocarcinoma and for the phase I study also isolated hepatic metastases of all other solid tumors. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002576-27 | Sponsor Protocol Number: ICM-URC2016/27 | Start Date*: 2017-03-01 | |||||||||||
Sponsor Name:Institut régional du Cancer de Montpellier | |||||||||||||
Full Title: Lean body mass normalization of oxaliplatin based chemotherapy for stage III colon cancer patients treated in adjuvant satting: Impact on Oxaliplatin induced sensitive neurotoxicity. A multicenter ... | |||||||||||||
Medical condition: colon 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: 2006-001097-24 | Sponsor Protocol Number: OE7-432-LOR-0033-I | Start Date*: 2007-07-19 |
Sponsor Name:Technische Universitaet Muenchen, Medizinische Fakultaet | ||
Full Title: Phase I/II study of continous infusion with 5-FU and weekly Oxaliplatin / Cetuximab combined with concurrent radiation as neoadjuvant treatment in locally advanced oesophageal squamous cell carcinoma. | ||
Medical condition: Locally advanced oesophageal squamous cell carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003187-32 | Sponsor Protocol Number: etoxel-01-2005 | Start Date*: 2005-12-19 |
Sponsor Name:Department of Oncology, Rigshospitalet | ||
Full Title: A phase II study of etoposide, oxaliplatin and capecitabine in patients with advanced hepatocellular carcinoma | ||
Medical condition: Advanced Hepatocellular carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001959-38 | Sponsor Protocol Number: 2005-001959-38 | Start Date*: 2005-07-07 |
Sponsor Name:Gedske Daugaard | ||
Full Title: Fase II trial with gemcitabine and oxaliplatin in patients with unknown primary tumours | ||
Medical condition: To test the effect of Gemcitabine and axaliplatin in patients with unknown primary tumours and performance 2 or age 66 to 75 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005289-11 | Sponsor Protocol Number: oxaliplatine 1 | Start Date*: 2008-10-08 |
Sponsor Name:Institut Jules Bordet | ||
Full Title: A non randomized , stratified phase II trial evaluating efficacy and safety of oxaliplatin in combination with 5-Fluorouracil in patients with platinum-sensitive and platinum-resistant recurrent ov... | ||
Medical condition: ovarian carcinoma in relapse | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-005169-36 | Sponsor Protocol Number: NKV110721 | Start Date*: 2008-02-07 |
Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
Full Title: NKV110721, A Study of Single Dose Intravenous Casopitant in Combination with Ondansetron and Dexamethasone for the Prevention of Oxaliplatin-Induced Nausea and Vomiting | ||
Medical condition: Prevention of nausea and vomiting due to first cycle of oxaliplatin based chemotherapy in patients with colorectal cancer receiving a combination with 5-fluorouracil and leucovorin, or in combinati... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) CZ (Completed) DE (Completed) HU (Completed) IT (Completed) SK (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001333-88 | Sponsor Protocol Number: ACTION | Start Date*: 2014-10-16 |
Sponsor Name:Academic Medical Center | ||
Full Title: A phase Ib/II study on the addition of Nab-paclitaxel (Abraxane) to capecitabine and oxaliplatin in the first-line treatment of metastastasized oesophagogastric carcinoma | ||
Medical condition: Metastasized oesophagogastric carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-012040-16 | Sponsor Protocol Number: EMR62242–004 | Start Date*: 2009-10-06 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: An open-label, randomized, controlled, multi-center, Phase I/II trial investigating 2 EMD 525797 doses in combination with cetuximab + irinotecan versus cetuximab + irinotecan alone, as second-line... | |||||||||||||
Medical condition: Subjects with k-ras WT, metastatic colorectal cancer who have failed a fist line chemotherapy with an oxaliplatin-containing regimen will be eligible for this trial. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) BE (Completed) CZ (Completed) GB (Completed) HU (Completed) GR (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005675-34 | Sponsor Protocol Number: CS1008-A-E203 | Start Date*: 2009-07-01 | |||||||||||
Sponsor Name:Daiichi Sankyo Development Ltd | |||||||||||||
Full Title: A PHASE 2 OPEN-LABEL RANDOMISED, TRIAL OF CS-1008 IN COMBINATION WITH IRINOTECAN VS IRINOTECAN ALONE IN SUBJECTS WITH METASTATIC COLORECTAL CARCINOMA WHO FAILED FIRST LINE OXALIPLATIN BASED CHEMOTH... | |||||||||||||
Medical condition: Second-line therapy for previously-treated advanced or metastatic colorectal adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012151-23 | Sponsor Protocol Number: SPON 671-09 | Start Date*: 2009-11-11 |
Sponsor Name:Cardiff University | ||
Full Title: A randomised phase II study of Irinotecan, 5-Fluorouracil and Folinic Acid (FOLFIRI) with or without the addition of an endothelin receptor antagonist in patients with metastatic colorectal cancer ... | ||
Medical condition: Metastatic Colorectal Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000048-89 | Sponsor Protocol Number: AFLIBL06266 | Start Date*: 2012-05-23 | |||||||||||
Sponsor Name:sanofi-aventis France | |||||||||||||
Full Title: A Multicenter, Single arm, Open Label Clinical Trial Evaluating Safety and Health-Related Quality of Life of Aflibercept in Combination with Irinotecan/5FU chemotherapy (FOLFIRI) in Patients with ... | |||||||||||||
Medical condition: Colorectal Neoplasms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003898-86 | Sponsor Protocol Number: HL BOR 001 | Start Date*: 2005-03-07 | |||||||||||
Sponsor Name:Institut jules Bordet | |||||||||||||
Full Title: EVALUATION OF THE TREATMENT OF PERITONEAL CARCINOMATOSIS OF COLORECTAL ORIGIN THROUGH COMPLETE RESECTION AND HYPERTHERMIC INTRA-PERITONEAL PEROPERATIVE CHEMOTHERAPY (HIPEC) WITH OXALIPLATIN | |||||||||||||
Medical condition: Peritoneal carcinomatosis secondary to a carcinoma of colorectal or appendicular origin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000945-36 | Sponsor Protocol Number: XALIP_C_02090 | Start Date*: 2007-09-18 | |||||||||||
Sponsor Name:sanofi-aventis groupe | |||||||||||||
Full Title: A multicenter, randomized, double blind, placebo controlled Phase III study to assess the efficacy of xaliproden in patients with oxaliplatin-induced peripheral sensory neuropathy (PSN) following a... | |||||||||||||
Medical condition: Patient with oxaliplatin-induced peripheral sensory neuropathy after having completed an oxaliplatin-containing chemotherapy regimen post complete surgical removal of primary colorectal tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Completed) IT (Prematurely Ended) GB (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000192-17 | Sponsor Protocol Number: GO-80, V1 18 Mar 05 | Start Date*: 2005-05-18 |
Sponsor Name:Barts & The London NHS Trust | ||
Full Title: Gemcitabine and Oxaliplatin in the treatment of locally advanced or metastatic transitional cell carcinoma of the urinary tract in patients with impaired renal function and patients who have progr... | ||
Medical condition: Locally advanced or metastatic transitional cell carcinoma of the urinary tract | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001834-34 | Sponsor Protocol Number: 4919 | Start Date*: 2006-03-14 |
Sponsor Name:Oxford Radcliffe Hospitals NHS Trust | ||
Full Title: Phase 2 trial of neo-adjuvant Oxaliplatin and 5-fluorouracil in oesophageal cancer | ||
Medical condition: Operable oesophageal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005666-12 | Sponsor Protocol Number: IMA910-101 | Start Date*: 2008-04-15 |
Sponsor Name:immatics biotechnologies GmbH | ||
Full Title: An open label, multicenter Phase 1-2 study to investigate the effectiveness, safety and immunogenicity of a monotherapy with intradermal IMA910 plus GM-CSF following pre-treatment with low-dose cyc... | ||
Medical condition: Adult HLA-A*02-positive patients who have been diagnosed with unresectable, locally advanced and/or metastatic colorectal cancer before first-line chemotherapy. Patients must have completed a 12 we... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) HU (Completed) BE (Completed) GB (Completed) LV (Completed) BG (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-000820-42 | Sponsor Protocol Number: EFC10262 | Start Date*: 2008-06-24 | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: A Multinational, Randomized, Double-blind Study, Comparing the Efficacy of Aflibercept Once Every 2 Weeks versus Placebo in Patients with Metastatic Colorectal Cancer (MCRC) Treated with Irinotecan... | |||||||||||||
Medical condition: Patients with metastatic colorectal cancer (MCRC) treated with irinotecan/5FU combination (FOLFIRI) after failure of an oxaliplatin based regimen. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) GR (Completed) NL (Completed) CZ (Completed) EE (Completed) ES (Completed) DK (Completed) SE (Completed) BE (Completed) GB (Completed) IT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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