- Trials with a EudraCT protocol (5,819)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5,819 result(s) found for: Chemotherapy.
Displaying page 89 of 291.
| EudraCT Number: 2016-005115-41 | Sponsor Protocol Number: TG4010.24 | Start Date*: 2017-11-29 | |||||||||||
| Sponsor Name:Transgene S.A. | |||||||||||||
| Full Title: A phase II study evaluating the efficacy and the safety of first-line chemotherapy combined with TG4010 and nivolumab in patients with advanced non-squamous Non-Small-Cell Lung Cancer (NSCLC) | |||||||||||||
| Medical condition: Stage IIIB-IV non small cell lung cancer (NSCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) HU (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000217-35 | Sponsor Protocol Number: EpSSG RMS 2005 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Rikshospitalet-Radiumhospitalet HF | ||
| Full Title: EpSSG RMS 2005 a protocol for non metastatic rhabdomyosarcoma | ||
| Medical condition: Rhabdomyosarkom (RMS) er en kreftform utgående fra muskelvev. RMS kan oppstå hvor som helst i kroppen og rammer folk i alle aldre. Behandlingen av RMS består av cellegift, operasjon og/eller strål... | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: NO (Ongoing) NL (Completed) BE (Completed) IT (Ongoing) GB (GB - no longer in EU/EEA) IE (Completed) ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-005197-10 | Sponsor Protocol Number: VT3996-202 | Start Date*: 2021-10-01 | |||||||||||
| Sponsor Name:Viracta Therapeutics, Inc. | |||||||||||||
| Full Title: An Open-Label, Phase 2 Trial of Nanatinostat in Combination with Valganciclovir in Patients with Epstein-Barr Virus-Positive (EBV+) Relapsed/Refractory Lymphomas (NAVAL-1) | |||||||||||||
| Medical condition: Epstein-Barr Virus-Positive (EBV+) Relapsed/Refractory Lymphomas | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001975-17 | Sponsor Protocol Number: N/A | Start Date*: 2022-03-08 | |||||||||||
| Sponsor Name:Queen Mary University of London | |||||||||||||
| Full Title: A randomised phase II study comparing 3 vs 6 cycles of platinum-based chemotherapy prior to maintenance avelumab in advanced urothelial cancer | |||||||||||||
| Medical condition: Unresectable locally advanced or metastatic urothelial carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004906-79 | Sponsor Protocol Number: ESPAC-6 | Start Date*: 2021-10-08 | ||||||||||||||||
| Sponsor Name:Ruprecht-Karls-University Heidelberg, Medical Faculty represented by Universitätsklinikum Heidelberg | ||||||||||||||||||
| Full Title: An open labelled phase III adjuvant trial of disease-free survival in patients with resected pancreatic ductal adenocarcinoma randomized to allocation of oxaliplatin- or gemcitabine-based chemother... | ||||||||||||||||||
| Medical condition: Resected pancreatic ductal adenocarcinoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) SE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2012-004418-32 | Sponsor Protocol Number: TestisCAB | Start Date*: 2016-03-16 | |||||||||||
| Sponsor Name:Oslo University Hospital - Cancer Department | |||||||||||||
| Full Title: Cabazitaxel as salvage treatment for cisplatin-resistant germ cell cancer. | |||||||||||||
| Medical condition: Cisplatin-resistant germ cell cancer of the testicle or extragonadal GCC originating from retroperitoneum or mediastinum. | |||||||||||||
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| Population Age: Adults | Gender: Male | ||||||||||||
| Trial protocol: IT (Completed) DK (Completed) SE (Ongoing) NO (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-005305-58 | Sponsor Protocol Number: H6Q-MC-S023 | Start Date*: 2007-04-12 | |||||||||||
| Sponsor Name:Eli Lilly and Company limited | |||||||||||||
| Full Title: A Randomized, Double-Blind, Phase 2 Trial of Fulvestrant Plus Enzastaurin versus Fulvestrant Plus Placebo in Aromatase Inhibitor-Resistant Metastatic Breast Cancer | |||||||||||||
| Medical condition: metastatic breast cancer, resistant to aromatase inhibitors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: NL (Completed) FR (Completed) DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001701-26 | Sponsor Protocol Number: C-III-001 | Start Date*: 2006-02-23 | |||||||||||
| Sponsor Name:CESAR Central European Society for | |||||||||||||
| Full Title: First- Line Treatment of Postmenopausal Patients with Endocrine Responsive Metastatic Breast Cancer. A Randomized, Multicenter Study Comparing Letrozole Combined with Standard Chemotherapy Vs Letro... | |||||||||||||
| Medical condition: hormone-receptor-positive metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: AT (Completed) CZ (Prematurely Ended) HU (Prematurely Ended) SI (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-018015-11 | Sponsor Protocol Number: IMCLCP15-0805 | Start Date*: 2010-10-20 | |||||||||||
| Sponsor Name:ImClone LLC | |||||||||||||
| Full Title: A Randomized Phase 2 Study of Human Anti-PDGFRα Monoclonal Antibody IMC-3G3 plus Mitoxantrone plus Prednisone or Mitoxantrone plus Prednisone in Metastatic Castration-Refractory Prostate Cancer (CR... | |||||||||||||
| Medical condition: Metastatic Castration-Refractory Prostate Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) ES (Completed) CZ (Completed) IT (Completed) HU (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024394-39 | Sponsor Protocol Number: CBEZ235B2201 | Start Date*: 2011-05-06 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A Phase II study of orally administered BEZ235 monotherapy in patients with hormone receptor positive, HER2 negative, metastatic breast cancer, with or without PI3K activated pathway | |||||||||||||
| Medical condition: Patients who have experienced progression of disease after first-line antineoplasic treatment of advanced endometrial carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) GB (Prematurely Ended) BE (Prematurely Ended) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003984-20 | Sponsor Protocol Number: LSK-AM301 | Start Date*: 2017-12-11 |
| Sponsor Name:Elevar Therapeutics, Inc | ||
| Full Title: A Prospective, Randomized, Double-Blinded, Placebo-Controlled, Multinational, Multicenter, Parallel-group, Phase III Study to Evaluate the Efficacy and Safety of Apatinib plus Best Supportive Care ... | ||
| Medical condition: Advanced or Metastatic Gastric Cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) PL (Completed) FR (Completed) IT (Completed) RO (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-003702-41 | Sponsor Protocol Number: IDR-OM-02 | Start Date*: 2018-07-03 |
| Sponsor Name:Soligenix UK Limited | ||
| Full Title: A Pivotal, Double-Blind, Randomized, Placebo-Controlled, Multinational Study of SGX942 (Dusquetide) for the Treatment of Oral Mucositis in Patients Being Treated With Concomitant Chemoradiation for... | ||
| Medical condition: Oral Mucositis in Patients Being Treated with Concomitant Chemoradiation for the Treatment of Squamous Cell Carcinoma of the Head and Neck | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) FR (Ongoing) ES (Completed) HU (Completed) PL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-006326-24 | Sponsor Protocol Number: D699BC00001 | Start Date*: 2012-11-07 |
| Sponsor Name:AstraZeneca AB | ||
| Full Title: A Randomised, Double-blind, Parallel-group, Multicentre, Phase III Study to Compare the Efficacy and Tolerability of Fulvestrant (FASLODEX) 500 mg with Anastrozole (ARIMIDEX) 1 mg as Hormonal Treat... | ||
| Medical condition: hormone receptor positive breast cancer, hormone naive, breast, cancer, neoplasm breast cancer, metastatic, tumour, neoplasm | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) CZ (Completed) SK (Completed) IT (Completed) PL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-000528-39 | Sponsor Protocol Number: TAK-676-1002 | Start Date*: 2023-03-20 | |||||||||||
| Sponsor Name:Takeda Development Center Americas, Inc. (TDC Americas) | |||||||||||||
| Full Title: An Open-label, Dose Escalation, Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of TAK-676 as a Single Agent and in Combination With Pembrolizumab in Ad... | |||||||||||||
| Medical condition: Solid Neoplasms | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021082-74 | Sponsor Protocol Number: U31287-A-U201 | Start Date*: 2011-01-21 | |||||||||||||||||||||
| Sponsor Name:DAIICHI SANKYO DEVELOPMENT LTD. | |||||||||||||||||||||||
| Full Title: RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLIND PHASE 1B/2 STUDY OF U3-1287 (AMG 888) IN COMBINATION WITH ERLOTINIB IN EGFR TREATMENT NAÏVE SUBJECTS WITH ADVANCED NON-SMALL CELL LUNG CANCER (NSCLC) WH... | |||||||||||||||||||||||
| Medical condition: Treatment for advanced or metastatic NSCLC in combination with erlotinib in subjects who are epidermal growth factor receptor (EGFR) treatment naïve after failure of at least one prior chemotherapy... | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) BE (Completed) LT (Completed) HU (Completed) GB (Completed) BG (Completed) AT (Completed) SI (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2008-002819-40 | Sponsor Protocol Number: TDM4450g | Start Date*: 2009-03-02 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A randomized, multicenter, Phase II study of the efficacy and safety of trastuzumab-MCC-DM1 vs. trastuzumab (Herceptin®) and docetaxel (Taxotere®) in patients with metastatic HER2-positive breast c... | |||||||||||||
| Medical condition: HER2-positive metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) AT (Completed) BE (Completed) HU (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-016019-39 | Sponsor Protocol Number: TPU-S1303 | Start Date*: 2011-02-14 | |||||||||||
| Sponsor Name:Taiho Oncology, Inc. | |||||||||||||
| Full Title: AN OPEN-LABEL, MULTICENTER, RANDOMIZED, PHASE 3 STUDY OF S-1 AND CISPLATIN COMPARED WITH 5-FU AND CISPLATIN IN PATIENTS WITH METASTATIC DIFFUSE GASTRIC CANCER PREVIOUSLY UNTREATED WITH CHEMOTHERAPY | |||||||||||||
| Medical condition: Metastatic Diffuse Gastric Cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) HU (Completed) GB (Completed) ES (Completed) PT (Completed) EE (Completed) IT (Prematurely Ended) BG (Completed) LT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-005887-97 | Sponsor Protocol Number: MO19390 | Start Date*: 2006-07-06 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: Open-label study of bevacizumab (AVASTIN®) in combination with platinum-containing chemotherapy as first-line treatment of patients with advanced or recurrent non-squamous non-small cell lung cancer | |||||||||||||
| Medical condition: Advanced or recurrent non-squamous non-small cell lung cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SI (Completed) FI (Completed) SE (Completed) ES (Completed) NL (Completed) AT (Completed) CZ (Completed) EE (Completed) DE (Completed) LT (Completed) HU (Completed) SK (Completed) GB (Completed) PT (Completed) DK (Completed) LV (Completed) IS (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003707-19 | Sponsor Protocol Number: MS200647_0047 | Start Date*: 2019-04-15 | ||||||||||||||||||||||||||
| Sponsor Name:Merck KGaA | ||||||||||||||||||||||||||||
| Full Title: A Phase II, Multicenter, Open label Study to Investigate the Clinical Efficacy of M7824 Monotherapy in Participants With Locally Advanced or Metastatic Biliary Tract Cancer Who Fail or are Intolera... | ||||||||||||||||||||||||||||
| Medical condition: Biliary Tract Cancer | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Completed) DE (Completed) GB (GB - no longer in EU/EEA) ES (Ongoing) IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-003520-37 | Sponsor Protocol Number: RG_18-220 | Start Date*: 2020-02-07 | |||||||||||
| Sponsor Name:University of Birmingham | |||||||||||||
| Full Title: A multi-stage randomised trial of durvalumab (Medi4736) with chemoradiotherapy with 5-fluorouracil and mitomycin C in patients with muscle-invasive bladder cancer | |||||||||||||
| Medical condition: Muscle invasive bladder cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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