- Trials with a EudraCT protocol (35)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
35 result(s) found for: X-ray tube.
Displaying page 1 of 2.
EudraCT Number: 2008-008746-20 | Sponsor Protocol Number: AGO 10 | Start Date*: 2010-01-28 |
Sponsor Name:Studienzentrale AGO Austria | ||
Full Title: Randomized Phase II AGO-Study comparing combined liposomal doxorubicin (Myocet) and gemcitabine (Gemzar) with liposomal doxorubicin (Myocet) monotherapy in platinum-refractory and platinum-resistan... | ||
Medical condition: platinum-refractory and platinum-resistant epithelial cancer of the ovary, fallopian tube, and the peritoneum | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-001551-39 | Sponsor Protocol Number: 53718678RSV2005 | Start Date*: 2019-11-14 | |||||||||||
Sponsor Name:Janssen Sciences Ireland UC | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Clinical Outcomes, Antiviral Activity, Safety, Tolerability, Pharmacokinetics, and Pharmacokinetics/Pharmacodynamics of JNJ-5371... | |||||||||||||
Medical condition: Respiratory Syncytial Virus | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (GB - no longer in EU/EEA) DE (Completed) ES (Completed) SE (Completed) BE (Completed) BG (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021186-70 | Sponsor Protocol Number: 10089DMCA-CS | Start Date*: 2010-10-01 |
Sponsor Name:Belfast Health and Social Care Trust | ||
Full Title: Keratinocyte growth factor in Acute lung injury to REduce pulmonary dysfunction – a randomised placebo controlled trial (KARE) | ||
Medical condition: Acute Lung Injury | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023603-10 | Sponsor Protocol Number: S52762 | Start Date*: 2011-01-18 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: Ilaris (Canakinumab) in the Schnitzler syndrome | |||||||||||||
Medical condition: Schnitzler syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000897-39 | Sponsor Protocol Number: GS-US-373-1499 | Start Date*: 2017-01-09 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: Evaluation of the Efficacy and Safety of GS-5745 as Add-On Therapy to a Tumor Necrosis Factor Inhibitor and Methotrexate Regimen in Subjects with Moderate to Severe Rheumatoid Arthritis. | |||||||||||||
Medical condition: Rheumatoid Arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) DE (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002348-27 | Sponsor Protocol Number: PH2/052 | Start Date*: 2007-10-26 |
Sponsor Name:Cancer Research UK | ||
Full Title: A Cancer Research UK Phase II Proof of Principle Trial of the activity of the PARP-1 inhibitor, AG-014699, in known carriers of a BRCA 1 or BRCA 2 mutation with locally advanced or metastatic breas... | ||
Medical condition: advanced or metastatic breast or ovarian carcinoma (proven carrier of a mutation in BRCA1 or 2 gene) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-021166-30 | Sponsor Protocol Number: 2010-SS-Canakinumab | Start Date*: 2010-11-25 |
Sponsor Name:Radboud University Nijmegen Medical Centre | ||
Full Title: Efficacy and safety of canakinumab in Schnitzler syndrome | ||
Medical condition: Schnitzler syndrome is an acquired autoinflammatory syndrome characterized by urticaria and monoclonal gammopathy, accompanied by intermittent fever, arthralgia or arthritis, bone pain and lymphade... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004562-40 | Sponsor Protocol Number: GOG-0146Q | Start Date*: 2008-01-14 | |||||||||||
Sponsor Name:Gynecologic Oncology Group | |||||||||||||
Full Title: A PHASE II EVALUATION OF TOPOTECAN ADMINISTERED WEEKLY IN THE TREATMENT OF RECURRENT PLATINUM-SENSITIVE OVARIAN, FALLOPIAN TUBE, OR PRIMARY PERITONEAL CANCER | |||||||||||||
Medical condition: Patients with recurrent ovarian, fallopian tube, or primary peritoneal cancers. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002801-30 | Sponsor Protocol Number: ABA-01 | Start Date*: 2006-12-14 |
Sponsor Name:MENARINI RICERCHE S.p.A | ||
Full Title: A RANDOMIZED, DOUBLE BLIND, PLACEBO CONTROLLED, MULTICENTRE TRIAL OF ABAGOVOMAB MAINTENANCE THERAPY IN PATIENTS WITH EPITHELIAL OVARIAN CANCER AFTER COMPLETE RESPONSE TO FIRST LINE CHEMOTHERAPY | ||
Medical condition: Epithelial Ovarian Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) CZ (Completed) HU (Completed) DE (Prematurely Ended) IT (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004125-24 | Sponsor Protocol Number: AGO-OVAR2.21 | Start Date*: 2013-04-10 | ||||||||||||||||
Sponsor Name:AGO Research GmbH | ||||||||||||||||||
Full Title: A prospective, randomized Phase III trial of carboplatin/gemcitabine/bevacizumab vs. carboplatin/pegylated liposomal doxorubicin/bevacizumab in patients with platinum-sensitive recurrent ovarian ca... | ||||||||||||||||||
Medical condition: Evaluation of the best therapeutic index for patients with platinum-sensitive ovarian cancer when treatment with bevacizumab and gemcitabine/carboplatin or with bevacizumab and PLD/carboplatin. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Completed) AT (Completed) BE (Completed) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-005479-82 | Sponsor Protocol Number: CACZ885G2301 | Start Date*: 2009-06-12 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A. | |||||||||||||
Full Title: Estudio doble ciego, randomizado, controlado con placebo, con diseño de retirada en la prevención de brotes con canakinumab (ACZ885) en pacientes con artritis idiopática juvenil sistémica y manifes... | |||||||||||||
Medical condition: Artritis idiopática juvenil sistémica y manifestaciones sistémicas activas. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) NO (Ongoing) FR (Completed) HU (Completed) BE (Completed) DE (Completed) SE (Completed) IT (Completed) GB (Completed) DK (Prematurely Ended) AT (Completed) GR (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001054-17 | Sponsor Protocol Number: PHRN15-SE/AMIKINHAL | Start Date*: 2017-01-27 | |||||||||||
Sponsor Name:CHRU de Tours | |||||||||||||
Full Title: Double-blinded multicenter randomized controlled trial comparing inhaled amikacin versus placebo to prevent ventilator associated pneumonia | |||||||||||||
Medical condition: Patient with mechanical ventilation through an endotracheal tube | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005476-27 | Sponsor Protocol Number: CACZ885G2305 | Start Date*: 2009-05-14 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A. | |||||||||||||
Full Title: Estudio randomizado, doble ciego, controlado con placebo, a dosis única para evaluar la eficacia inicial de canakinumab (ACZ885) respecto a los Criterios ACR 30 Pediátricos Adaptados en pacientes c... | |||||||||||||
Medical condition: Artritis idiopática juvenil sistémica y manifestaciones sistémicas activas. | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) NO (Ongoing) FR (Completed) HU (Completed) DE (Completed) BE (Completed) SE (Completed) IT (Completed) GB (Completed) DK (Completed) GR (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002862-11 | Sponsor Protocol Number: CXA-NP-11-04 | Start Date*: 2015-07-27 | |||||||||||
Sponsor Name:Cubist Pharmaceuticals GmbH | |||||||||||||
Full Title: A Prospective, Randomized, Double-Blind, Multicenter, Phase 3 Study to Assess the Safety and Efficacy of Intravenous Ceftolozane/tazobactam Compared With Meropenem in Adult Patients with Ventilated... | |||||||||||||
Medical condition: Ventilated Nosocomial Pneumonia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) EE (Completed) DE (Completed) BE (Completed) LV (Completed) CZ (Completed) HU (Completed) SK (Completed) AT (Completed) GR (Completed) PT (Completed) HR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000850-36 | Sponsor Protocol Number: 201600136 | Start Date*: 2017-05-01 |
Sponsor Name:Archivel Farma S.L. | ||
Full Title: Double-Blind, Randomized, Placebo-Controlled Phase IIa Clinical Trial to Investigate the Safety and Immunogenicity of RUTI® Therapeutic Vaccination in Patients with Multi-Drug Resistant Tuberculos... | ||
Medical condition: The medical condition to be investigated is culture-confirmed Multidrug-resistant tuberculosis, i.e. tuberculosis resistant to the two first-line drugs Rifampicin and Isoniazid | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002213-18 | Sponsor Protocol Number: EDP938-103 | Start Date*: 2020-11-05 | |||||||||||
Sponsor Name:Enanta Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Effects of EDP-938 in Adult Hematopoietic Cell Transplant Recipients With Acute Respiratory Syncytial Virus Infection o... | |||||||||||||
Medical condition: Respiratory syncytial virus (RSV) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Prematurely Ended) BE (Completed) PL (Prematurely Ended) GR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004440-19 | Sponsor Protocol Number: CLAM320B2202 | Start Date*: 2016-03-01 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 30-month multicenter, phase 2b/3, randomized, open label trial to evaluate the efficacy and safety of clofazimine administered orally in addition to background regimen compared to background regi... | |||||||||||||
Medical condition: Treatment of multidrug-resistant pulmonary tuberculosis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Prematurely Ended) LT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003964-38 | Sponsor Protocol Number: IRFMN-OVA-7289 | Start Date*: 2017-03-21 | ||||||||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | ||||||||||||||||||
Full Title: The BAROCCO study (Best Approach in Recurrent-Ovarian-Cancer-with Cediranib-Olaparib): an Italian multicenter randomized phase II study of weekly paclitaxel vs. Cediranib-Olaparib with continuous ... | ||||||||||||||||||
Medical condition: resistant high grade epithelial ovarian, fallopian tube, or primary peritoneal cancer. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-002324-41 | Sponsor Protocol Number: PH2/051 | Start Date*: 2006-11-30 | |||||||||||
Sponsor Name:Cancer Research UK | |||||||||||||
Full Title: A Cancer Research UK Randomised Multicentre Phase II Trial of the DNA-hypomethylating Agent, 5-Aza-2'-deoxycytidine(Decitabine) given intravenously in Combination with Carboplatin, versus Carboplat... | |||||||||||||
Medical condition: Progressive, advanced ovarian cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001493-29 | Sponsor Protocol Number: CVC-for-COVID-19 | Start Date*: 2020-05-11 |
Sponsor Name:Charité - Universitaetsmedizin Berlin | ||
Full Title: Charité trial of Cenicriviroc (CVC) treatment for COVID-19 patients | ||
Medical condition: SARS-CoV-2 infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
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