- Trials with a EudraCT protocol (155)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
155 result(s) found for: Alternative cancer treatments.
Displaying page 1 of 8.
EudraCT Number: 2014-003389-26 | Sponsor Protocol Number: RG14-093 | Start Date*: 2015-01-12 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: Phase III randomised controlled trial Comparing Alternative Regimens for escalating treatment of intermediate and high-risk oropharyngeal cancer | |||||||||||||
Medical condition: Oropharyngeal Cancer | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Temporarily Halted) IE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003158-24 | Sponsor Protocol Number: | Start Date*: 2011-09-22 | |||||||||||
Sponsor Name:Pia Österlund and Helena Isoniemi | |||||||||||||
Full Title: A population-based prospective study to evaluate clinical behaviour, resectability and survival in metastatic colorectal cancer patients in Finland | |||||||||||||
Medical condition: Metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003889-12 | Sponsor Protocol Number: 3 | Start Date*: 2022-01-20 |
Sponsor Name:Consorcio Centro de Investigacion Biomedica en Red, M.P. (CIBER) | ||
Full Title: Prospective, multicenter and open study to evaluate the efficacy of esmolol in the early identification of cardiovascular disorders induced by cirrhosis, diabetes mellitus and cardiotoxic treatments. | ||
Medical condition: Cardiovascular disorders induced by cirrhosis, diabetes mellitus and cardiotoxic treatments. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000469-35 | Sponsor Protocol Number: GO29227 | Start Date*: 2014-08-12 | ||||||||||||||||
Sponsor Name:Genentech, Inc. | ||||||||||||||||||
Full Title: A RANDOMIZED, PHASE II, MULTICENTER, PLACEBO-CONTROLLED STUDY OF IPATASERTIB (GDC-0068), AN INHIBITOR OF AKT, IN COMBINATION WITH PACLITAXEL AS FRONT-LINE TREATMENT FOR PATIENTS WITH METASTATIC TRI... | ||||||||||||||||||
Medical condition: Inoperable locally advanced or metastatic triple negative breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Completed) BE (Completed) ES (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-001203-32 | Sponsor Protocol Number: DEDALUS | Start Date*: 2021-10-25 | |||||||||||
Sponsor Name:FONDAZIONE I.R.C.C.S. POLICLINICO SAN MATTEO | |||||||||||||
Full Title: An open-label, multi-center, phase 2 study of chemo-immunotherapy followed by reduced-dose hypo-fractionated RT and maintenance immunotherapy for stage III unresectable Non –small-cell lung carcino... | |||||||||||||
Medical condition: stage III unresectable non-small cell lung cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004212-23 | Sponsor Protocol Number: DMM1-TGF-03 | Start Date*: 2005-02-03 | |||||||||||
Sponsor Name:Unidad Integral de Investigación en Oncología, S.L. | |||||||||||||
Full Title: Randomized study with oral tegafur versus capecitabina in the treatment of advanced politreated breast cancer and refractory, resistant or in progression to the standard chemotherapeutic treatment | |||||||||||||
Medical condition: breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2019-002192-33 | Sponsor Protocol Number: TRADEhypo | Start Date*: 2020-02-06 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH | ||||||||||||||||||||||||||||||||||||||
Full Title: Thoracic Radiotherapy plus Durvalumab in Elderly and/or frail NSCLC stage III patients unfit for chemotherapy- Employing optimized (hypofractionated) radiotherapy to foster durvalumab efficacy | ||||||||||||||||||||||||||||||||||||||
Medical condition: unresectable stage III NSCLC (Non–small-cell lung cancer) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003971-37 | Sponsor Protocol Number: PRIMUS004 | Start Date*: 2020-08-19 | |||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde Health Board [...] | |||||||||||||
Full Title: PRIMUS 004: A multi-arm non-comparative signal seeking phase II platform trial of biomarker-directed novel second-line treatments in metastatic pancreatic cancer | |||||||||||||
Medical condition: Pancreatic 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) |
EudraCT Number: 2006-005485-40 | Sponsor Protocol Number: LipoGem-PII-1L-Pancr | Start Date*: 2009-05-29 | |||||||||||
Sponsor Name:Regulon Α.Ε. | |||||||||||||
Full Title: Multicenter Phase II/III Clinical Study of Lipoplatin plus Gemcitabine as First-Line Treatment in Inoperable, Locally Advanced or Metastatic Pancreatic Cancer. | |||||||||||||
Medical condition: locally advanced or metastatic inoperable adenocarcinoma of the pancreas with no prior chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prohibited by CA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004061-13 | Sponsor Protocol Number: ESR21-21165 | Start Date*: 2022-06-09 | ||||||||||||||||
Sponsor Name:VHIO Vall d’Hebron Institute of Oncology | ||||||||||||||||||
Full Title: Single cell characterization of persistent cells upon treatment with durvalumab (MEDI4736) with or without tremelimumab in MSS and MSI colorectal and endometrial tumors | ||||||||||||||||||
Medical condition: MSS and MSI colorectal and endometrial tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001321-68 | Sponsor Protocol Number: B1761026 | Start Date*: 2018-05-22 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: Gemtuzumab Ozogamicin (mylotarg (registered)) Expanded Access Protocol For Treatment Of Patients In The United States With Relapsed/refractory Acute Myelogenous Leukemia Who May Benefit From Treatm... | |||||||||||||
Medical condition: Acute Myelogenous Leukemia, including myelodysplastic syndrome and acute promyelocytic leukemia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001005-85 | Sponsor Protocol Number: ATX-NS-001 | Start Date*: 2021-07-06 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Achilles Therapeutics UK Limited | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: An open label, multi-centre, phase I/IIa study evaluating the safety and clinical activity of neoantigen reactive T cells in patients with 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: DE (Trial now transitioned) FR (Trial now transitioned) NL (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005581-36 | Sponsor Protocol Number: 309821 | Start Date*: 2006-05-24 |
Sponsor Name:Schering AG | ||
Full Title: Randomized phase II study to investigate the efficacy, safety and tolerability of ZK 230211 (25 mg vs. 100 mg) as second-line endocrine therapy for postmenopausal women with hormone receptor-positi... | ||
Medical condition: Metastatic breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Prematurely Ended) GB (Completed) DE (Prematurely Ended) ES (Completed) IT (Prematurely Ended) FI (Prematurely Ended) SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2018-002220-16 | Sponsor Protocol Number: D4194C00006 | Start Date*: 2019-02-01 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Phase II, Open-Label, Multi-Centre, International Safety Study of Durvalumab Following Sequential Chemotherapy and Radiation Therapy in Patients with Stage III, Unresectable Non-Small Cell Lung C... | |||||||||||||
Medical condition: Patients with unresectable Stage III non-small cell lung cancer (NSCLC), who have not progressed following platinum-based sequential chemoradiation therapy (sCRT) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) ES (Ongoing) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003399-36 | Sponsor Protocol Number: MK-4214-008 | Start Date*: 2011-10-28 | |||||||||||||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||||||||||||
Full Title: A Phase III Randomized, Double-Blind, Active-Controlled Clinical Trial to Study the Efficacy and Safety of MK-4214 (filgrastim) and Neupogen™ as an Adjunct to Combination Chemotherapy with Doxorubi... | |||||||||||||||||||||||
Medical condition: Breast Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: LV (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-003408-33 | Sponsor Protocol Number: ESR-21-21536 | Start Date*: 2023-04-25 | |||||||||||
Sponsor Name:TheraOp gGmbH | |||||||||||||
Full Title: PACCELIO - FDG-PET based small volume accelerated immuno chemoradio-therapy in locally advanced NSCLC | |||||||||||||
Medical condition: Locally advanced, unresectable non-small-cell lung cancer (NSCLC) (Stage III) with a PD-L1-expression of ≥ 1% | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2023-000156-38 | Sponsor Protocol Number: 20230123SE | Start Date*: 2023-05-04 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Semmelweis University, Department of Internal Medicine and Oncology | ||||||||||||||||||||||||||||||||||||||
Full Title: Value-based health economic comparative study of subcutaneous and intravenous trastuzumab-pertuzumab for HER-2 positive metastatic breast cancer based on patient reported outcomes. | ||||||||||||||||||||||||||||||||||||||
Medical condition: HER-2 positive advanced breast cancer, locally unresectable or metastatic breast cancer | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004586-67 | Sponsor Protocol Number: CBYL719X2402 | Start Date*: 2017-07-13 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A phase II, multicenter, open-label, two-cohort, noncomparative study to assess the efficacy and safety of alpelisib plus fulvestrant or letrozole in patients with PIK3CA mutant, hormone receptor (... | |||||||||||||
Medical condition: Hormone receptor positive, HER2-negative advanced breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) GB (GB - no longer in EU/EEA) FR (Completed) BE (Completed) NL (Completed) DK (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004758-39 | Sponsor Protocol Number: ESR-18-13485 | Start Date*: 2019-06-12 | |||||||||||
Sponsor Name:AZIENDA UNITÀ SANITARIA LOCALE DELLA ROMAGNA | |||||||||||||
Full Title: A PHASE II STUDY OF CAPECITABINE PLUS CONCOMITANT RADIATION THERAPY FOLLOWED BY DURVALUMAB (MEDI4736) AS PREOPERATIVE TREATMENT IN RECTAL CANCER | |||||||||||||
Medical condition: Locally advanced (T3-4 N0-1) rectal cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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