- Trials with a EudraCT protocol (124)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
124 result(s) found for: Cancer pharmacogenomics.
Displaying page 1 of 7.
EudraCT Number: 2006-004016-40 | Sponsor Protocol Number: 13570 | Start Date*: 2006-11-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA OSPEDALI RIUNITI UMBERTO I - G.M.LANCISI - G.SALESI | |||||||||||||
Full Title: APPLICATION OF PHARMACOGENOMICS IN THE TREATMENT OF ELDERLY PATIENTS WITH ADVANCED COLORECTAL CANCER | |||||||||||||
Medical condition: ELDERLY PATIENTS WITH METASTATIC COLORECTAL CANCER | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000095-28 | Sponsor Protocol Number: H3E-MC-JMHW | Start Date*: 2017-03-02 |
Sponsor Name:Eli Lilly and Company | ||
Full Title: A Phase II Study of Pemetrexed in Children with Recurrent Malignancies | ||
Medical condition: Recurrent Malignancies (recurrent solid tumors): Target tumor types were osteosarcoma, Ewing sarcoma/peripheral PNET, rhabdomyosarcoma, neuroblastoma (measurable disease), neuroblastoma (metaiodob... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2005-000586-19 | Sponsor Protocol Number: 307971 | Start Date*: 2005-07-25 |
Sponsor Name:Bayer Schering Pharma AG | ||
Full Title: Phase-II study to investigate the efficacy and safety of ZK 219477 as second-line therapy in patients with Stage IIIB or Stage IV non-small-cell lung cancer (NSCLC) | ||
Medical condition: Non small cell lung cancer (NSCLC) stage IIIB or stage IV | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-004321-83 | Sponsor Protocol Number: GEFCAPI04 | Start Date*: 2014-01-27 |
Sponsor Name:Institut Català d'Oncologia (ICO) | ||
Full Title: A randomised phase III trial comparing a strategy based on molecular analysis to the empiric strategy in patients with carcinoma of an unknoun primary (CUP) | ||
Medical condition: Carcinomas of an unknown primary site (CUP) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002808-28 | Sponsor Protocol Number: OZM-061 | Start Date*: 2017-12-29 | |||||||||||
Sponsor Name:Princess Margaret Cancer Centre | |||||||||||||
Full Title: Olala Trial: A Retrospective/Prospective Analysis of Characterization of the Long-Term Responders on Olaparib in Solid Tumours | |||||||||||||
Medical condition: epithelial ovarian cancer (including fallopian tube or peritoneal cancer) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000548-25 | Sponsor Protocol Number: PM1183-B-004-13 | Start Date*: 2013-06-11 | |||||||||||
Sponsor Name:Pharma Mar S.A. Sociedad Unipersonal | |||||||||||||
Full Title: A Randomized-Controlled Three-arm Phase II Study of Lurbinectedin (PM01183) Alone or In Combination with Gemcitabine and a control arm with Docetaxel as Second-Line Treatment in Unresectable Non-Sm... | |||||||||||||
Medical condition: Unresectable Non-Small Cell Lung Cancer (NSCLC). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005276-16 | Sponsor Protocol Number: ET743-OVA-301 | Start Date*: 2005-10-27 | |||||||||||
Sponsor Name:Pharma Mar S.A. | |||||||||||||
Full Title: An open-label multicenter randomized Phase 3 study comparing the combination of DOXIL®/CAELYX® and YONDELIS® with DOXIL®/CAELYX® alone in subjects with advanced relapsed ovarian cancer. | |||||||||||||
Medical condition: Advanced relapsed ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) DE (Completed) ES (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005251-39 | Sponsor Protocol Number: PM1183-C-004-14 | Start Date*: 2015-06-15 | ||||||||||||||||
Sponsor Name:Pharma Mar S.A., Sociedad Unipersonal | ||||||||||||||||||
Full Title: Phase III Randomized Clinical Trial of Lurbinectedin (PM01183) versus Pegylated Liposomal Doxorubicin or Topotecan in Patients with Platinum-resistant Ovarian Cancer (CORAIL Trial) | ||||||||||||||||||
Medical condition: Platinum-resistant ovarian cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: HU (Completed) ES (Completed) CZ (Completed) AT (Completed) BE (Completed) GB (Completed) FR (Completed) DE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000879-26 | Sponsor Protocol Number: 311602-Amendment 1 | Start Date*: 2008-08-07 | ||||||||||||||||
Sponsor Name:Bayer Schering Pharma AG | ||||||||||||||||||
Full Title: (REASON) double-blind, Randomized phase II study to Evaluate the safety and efficacy of Acetyl-l-carnitine in the prevention of SagOpilone-induced peripheral Neuropathy. | ||||||||||||||||||
Medical condition: - Advanced refractory or relapsed ovarian cancer - Patients with metastatic hormone-refractory prostate cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) NL (Completed) BE (Completed) GB (Completed) DE (Completed) ES (Prematurely Ended) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000120-33 | Sponsor Protocol Number: C-550-01 | Start Date*: 2018-11-19 | |||||||||||||||||||||
Sponsor Name:Agenus Inc., | |||||||||||||||||||||||
Full Title: A Phase 1/2, Open-Label, Multi-Arm Trial to Investigate the Safety, Tolerability, Pharmacokinetics, Biological, and Clinical Activity of AGEN1884 in Combination with AGEN2034 in Subjects with Metas... | |||||||||||||||||||||||
Medical condition: Phase 1 – Part A dose escalation in patients with locally advanced, recurrent and/or metastatic solid tumor for which no standard therapy exists or standard therapy has failed. Phase 2 - Part B adv... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) PL (Completed) ES (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005661-11 | Sponsor Protocol Number: XELOXART | Start Date*: 2006-03-30 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA "S. GIOVANNI BATTISTA DI TORINO" | |||||||||||||
Full Title: PHASE II STUDY OF NEOADJUVANT CHEMORADIOTHERAPY IN LOCALLY ADVANCED RECTAL CANCER | |||||||||||||
Medical condition: rectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000992-28 | Sponsor Protocol Number: KCT04/2015-DORETAonko/SI | Start Date*: 2015-07-15 | |||||||||||
Sponsor Name:Krka, d.d., Novo mesto | |||||||||||||
Full Title: A comparison of the severity of acute pain and the frequency of chronic pain after post-operative analgesia of lower and higher intensity following surgical emptying of the axillary gland in breast... | |||||||||||||
Medical condition: Acute pain after surgical emptying of the axillary gland in breast cancer patients. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001552-44 | Sponsor Protocol Number: TRIO 015 | Start Date*: 2008-09-29 | |||||||||||
Sponsor Name:Cancer International research Group | |||||||||||||
Full Title: A MULTICENTER OPEN LABEL PHASE II STUDY OF THE EFFICACY AND SAFETY OF AMG 479, A FULLY HUMAN MONOCLONAL ANTIBODY AGAINST INSULIN-LIKE GROWTH FACTOR TYPE 1 RECEPTOR (IGF-1R) AS SECOND LINE THERAPY I... | |||||||||||||
Medical condition: Recurrent Platinum-sensitive ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Prematurely Ended) IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006413-33 | Sponsor Protocol Number: 3206K2-104-WW | Start Date*: 2008-02-14 |
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc | ||
Full Title: A Phase 1/2 Dose Escalation Study of TRU-015 in Subjects with Relapsed or Refractory B-cell Non-Hodgkin's Lymphoma | ||
Medical condition: Relapsed or refractory B-cell Non Hodgkin's Lymphoma. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2008-001551-22 | Sponsor Protocol Number: TRIO 014 | Start Date*: 2008-10-21 | |||||||||||
Sponsor Name:Cancer International Research Group | |||||||||||||
Full Title: A randomized, double-blind, placebo controlled, multicenter, phase II study of adding AMG 479, a fully human monoclonal antibody against insulin-like growth factor type 1 receptor (IGF-1R) to first... | |||||||||||||
Medical condition: Optimally debulked epithelial ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) ES (Completed) IE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022163-35 | Sponsor Protocol Number: EFC11785 | Start Date*: 2011-04-04 |
Sponsor Name:sanofi-aventis R&D | ||
Full Title: Randomized, Open Label Multi-Center Study Comparing Cabazitaxel at 20 mg/m² and at 25 mg/m² Every 3 Weeks in Combination with Prednisone for the Treatment of Metastatic Castration Resistant Prostat... | ||
Medical condition: metastatic Castration Resistant Prostate Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Completed) HU (Completed) BE (Completed) ES (Completed) GB (Completed) FR (Completed) DE (Completed) PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-016846-16 | Sponsor Protocol Number: OCTO-16 | Start Date*: 2010-12-14 | ||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||
Full Title: Phase II Clinical Trial of 6-Mercaptopurine(6MP)and low-dose Methotrexate In Patients With Known BRCA Defective Tumours. | ||||||||||||||||||
Medical condition: Advanced or metastatic breast or ovarian cancer. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000015-25 | Sponsor Protocol Number: 3066A1-303-WW | Start Date*: 2004-07-16 |
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc. Clinical Research and Development | ||
Full Title: A phase 3 randomized, placebo-controlled, double-blind study of oral CCI-779 administered in combination with letrozole vs. letrozole alone as first line hormonal therapy in postmenopausal women wi... | ||
Medical condition: locally advanced or metastatic breast cancer (stage 3B or 4) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SK (Completed) LV (Completed) LT (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-022064-12 | Sponsor Protocol Number: EFC11784 | Start Date*: 2011-03-23 | |||||||||||
Sponsor Name:sanofi-aventis R&D | |||||||||||||
Full Title: Randomized, Open Label, Multi-Center Study comparing Cabazitaxel at 25 mg/m2 and at 20 mg/m² in Combination with Prednisone Every 3 Weeks to Docetaxel in Combination with Prednisone in Patients wit... | |||||||||||||
Medical condition: metastatic Castration Resistant Prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) ES (Completed) FI (Completed) DK (Completed) PT (Completed) IT (Completed) DE (Completed) RO (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002534-23 | Sponsor Protocol Number: 3124001 | Start Date*: 2018-02-08 | |||||||||||
Sponsor Name:Orion Corporation Orion Pharma | |||||||||||||
Full Title: SAFETY AND PHARMACOKINETICS OF ODM-208 IN PATIENTS WITH METASTATIC CASTRATION-RESISTANT PROSTATE CANCER | |||||||||||||
Medical condition: Metastatic castration-resistant prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FI (Trial now transitioned) FR (Trial now transitioned) GB (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
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