- Trials with a EudraCT protocol (596)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (101)
596 result(s) found for: Doxorubicin.
Displaying page 1 of 30.
EudraCT Number: 2006-001443-63 | Sponsor Protocol Number: 01062 | Start Date*: 2006-07-10 |
Sponsor Name:European Lung Cancer Working Party | ||
Full Title: A phase II study assessing the activity of valproate acid plus doxorubicin in refractory or recurrent malignant mesothelioma. | ||
Medical condition: This is a prospective phase II study investigating well-known antimetabolite (doxorubicin) and antiepileptic (valproate) drugs, in combination, for the treatment of refractory or recurrent malignan... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-004927-11 | Sponsor Protocol Number: INNO-206-P2-STS-01 | Start Date*: 2012-03-02 | |||||||||||
Sponsor Name:CytRx Corporation | |||||||||||||
Full Title: A Multicenter, Randomized, Open-Label Phase 2b Study to Investigate the Preliminary Efficacy and Safety of INNO-206 (Doxorubicin-EMCH) Compared to Doxorubicin in Subjects with Metastatic, Locally A... | |||||||||||||
Medical condition: Metastatic, Locally Advanced, or Unresectable Soft Tissue Sarcoma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003324-36 | Sponsor Protocol Number: NT14035-3/2013 | Start Date*: 2013-11-07 |
Sponsor Name:Charles University in Prague, Faculty of Medicine in Hradec Králové | ||
Full Title: Kinetically guided removal of plazma pegylated liposomal doxorubicin to enhance the benefit of cytostatic therapy of patients with ovarian cancer. | ||
Medical condition: Primary aim: enhanced therapeutic benefit of liposomal doxorubicin - a drug indicated for ovarian cancer resistant to chemotherapy with the first line drugs. This approach can be considered a model... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: CZ (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001244-56 | Sponsor Protocol Number: LiCTOP-C-001 | Start Date*: 2013-07-23 | |||||||||||
Sponsor Name:Department of Pharmacy, Uppsala University | |||||||||||||
Full Title: An open, multicenter, single dose, parallel study, evaluating the pharmacokinetics of doxorubicin and its active metabolite (doxorubicinol) after a hepatic intra-arterial injection of either a lipi... | |||||||||||||
Medical condition: Intermediate hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000163-25 | Sponsor Protocol Number: HE2006 | Start Date*: 2005-08-04 |
Sponsor Name:Research and Enterprise, University of Birmingham | ||
Full Title: Proteomics and Pharmacokinetics of Adriamycin Following Different Techniques for Chemoembolisation of Hepatocellular Carcinoma (PPATCH) Trial | ||
Medical condition: Hepatocellular cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004060-40 | Sponsor Protocol Number: AGO15 | Start Date*: 2008-03-13 |
Sponsor Name:Studienzentrale AGO Austria | ||
Full Title: Phase II multicenter trial of the Austrian AGO of the combination of liposomal Doxorubicin (Myocet®) and Carboplatin in primary advanced or metastatic and recurrent endometrial cancer | ||
Medical condition: primary advanced or recurrent/metastatic endometrial cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000547-14 | Sponsor Protocol Number: BGOG-cx3 | Start Date*: 2017-08-30 | |||||||||||
Sponsor Name:BGOG-UZLeuven | |||||||||||||
Full Title: BGOG-cx3: Prospective randomized Phase II trial comparing doxorubicin alone versus doxorubicin and atezolizumab in recurrent cervical cancer | |||||||||||||
Medical condition: recurrent cervical cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000366-36 | Sponsor Protocol Number: TLK286.3025 | Start Date*: 2006-06-07 | |||||||||||
Sponsor Name:Telik, Inc. | |||||||||||||
Full Title: Phase 3 randomized study of TLK286 (Telcyta™) in combination with liposomal doxorubicin (Doxil®/Caelyx®) versus liposomal doxorubicin (Doxil®/Caelyx®) as second-line therapy in platinum refractory ... | |||||||||||||
Medical condition: platinum refractory or resistant ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001770-40 | Sponsor Protocol Number: 11546 | Start Date*: 2005-06-03 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A randomized controlled study of BAY 43-9006 in combination with doxorubicin versus doxorubicin in patients with advanced hepatocellular carcinoma. | |||||||||||||
Medical condition: advanced hepatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002625-35 | Sponsor Protocol Number: CALGB80802 | Start Date*: 2013-09-23 |
Sponsor Name:All Ireland Co-operative Oncology Research Group (ICORG) | ||
Full Title: Phase III Randomized Study Of Sorafenib Plus Doxorubicin Versus Sorafenib In Patients With Advanced Hepatocellular Carcinoma (HCC) | ||
Medical condition: Advanced or Metastatic Hepatocellular Carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-003145-17 | Sponsor Protocol Number: TH-CR-406/SARC021 | Start Date*: 2012-02-28 | |||||||||||
Sponsor Name:Threshold Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized Phase 3, Multicenter, Open-Label Study Comparing TH-302 in Combination with Doxorubicin vs. Doxorubicin Alone in Subjects with Locally Advanced Unresectable or Metastatic Soft Tissue S... | |||||||||||||
Medical condition: Locally Advanced Unresectable or Metastatic Soft Tissue Sarcoma | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) HU (Completed) PL (Prematurely Ended) BE (Completed) IT (Completed) AT (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000134-30 | Sponsor Protocol Number: I5B-MC-JGDJ | Start Date*: 2015-09-22 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial of Doxorubicin plus Olaratumab versus Doxorubicin plus Placebo in Patients with Advanced or Metastatic Soft Tissue Sarcoma | |||||||||||||
Medical condition: Advanced or Metastatic Soft Tissue Sarcoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) HU (Completed) DE (Completed) ES (Ongoing) AT (Completed) FR (Completed) SE (Ongoing) FI (Completed) BE (Completed) NL (Ongoing) PL (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003091-77 | Sponsor Protocol Number: B9991009 | Start Date*: 2016-03-16 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Open-Label Study of Avelumab (MSB0010718C) Alone or in Combination with Pegylated Liposomal Doxorubicin versus Pegylated Liposomal Doxorubicin Alone to In Patien... | |||||||||||||
Medical condition: Ovarian Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) HU (Completed) AT (Completed) ES (Completed) GR (Completed) IE (Completed) NL (Completed) FR (Completed) PL (Completed) DK (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002399-40 | Sponsor Protocol Number: | Start Date*: 2005-05-11 |
Sponsor Name:Rigshospitalet | ||
Full Title: Carboplatin + paclitaxel vs carboplatin + stealth liposomal doxorubicin. A randomised multicentre trial. | ||
Medical condition: Recurrent ovarian cancer Cytologic / histologic diagnosis of stage IC-IV ovarian cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001783-75 | Sponsor Protocol Number: SATCG-4 | Start Date*: 2008-03-31 |
Sponsor Name:Department of Oncology, Lund University Hospital | ||
Full Title: Phase 2 trial with Avastin and Doxorubicin postoperatively for patients with anaplastic thyroid carcinoma | ||
Medical condition: Patients that suffer from anaplastic thyroid cancer and have completed our "standard" initial therapy with radiotherapy and chemotherapy, and has been macroscopical radically resected after complet... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000915-80 | Sponsor Protocol Number: NB 2006 05 | Start Date*: 2005-09-06 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: A phase II study of Topotecan-Vincristine-Doxorubicin (TVD) in children with stage 4 neuroblastoma failing to respond to COJEC | |||||||||||||
Medical condition: Neuroblastoma | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004088-77 | Sponsor Protocol Number: BA2006/03/03 | Start Date*: 2007-12-03 |
Sponsor Name:BioAlliance Pharma | ||
Full Title: Doxorubicin-Transdrug® in Advanced HepatoCellular Carcinoma A Randomized, Multicenter Phase 2-3 Study. | ||
Medical condition: Advanced hepatocarcinoma (HCC) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-005862-36 | Sponsor Protocol Number: mammatherm | Start Date*: 2007-07-16 |
Sponsor Name:Klinikum der Universität München Innenstadt, I. Frauenklinik | ||
Full Title: Prospectively Randomized Phase I/II Trial of Liposomal-encapsulated Doxorubicin and Cisplatin +/- Locoregional Hyperthermia in patients with Metastatic Breast Cancer | ||
Medical condition: This is an open-label, multicenter, randomized controlled, Phase I/II study comparing the time to progressive disease after randomisation in patients treated with 6 cycles of liposomal-encapsulated... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003648-55 | Sponsor Protocol Number: EZH-301 | Start Date*: 2020-08-17 | ||||||||||||||||
Sponsor Name:Epizyme, Inc. | ||||||||||||||||||
Full Title: A Phase 1b/3 Global, Randomized, Double-blind, Placebo-Controlled Trial of Tazemetostat in Combination With Doxorubicin as Frontline Therapy for Advanced Epithelioid Sarcoma | ||||||||||||||||||
Medical condition: Phase 1b: Have histologically confirmed Soft tissue sarcoma (STS). Phase 3: Morphology and immunophenotypic panel consistent with epithelioid sarcoma (eg, CD34, epithelial membrane antigen [EMA], ... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) BE (Completed) PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004822-19 | Sponsor Protocol Number: ICORG 05-11/NSABP B-38 | Start Date*: 2006-02-15 |
Sponsor Name:ICORG the all Ireland Co-operative Oncology Research Group | ||
Full Title: A Phase III, adjuvant trial comparing three chemotherapy regimens in women with node positive breast cancer: Docetaxel/Doxorubicin/Cyclophosphamide (TAC); Dose-Dense (DD) Doxorubicin/Cyclophosphami... | ||
Medical condition: Early stage node positive breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
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