- Trials with a EudraCT protocol (11,926)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
11,926 result(s) found for: II.
Displaying page 96 of 597.
EudraCT Number: 2015-002799-26 | Sponsor Protocol Number: | Start Date*: 2015-10-27 |
Sponsor Name:Papworth Hospital NHS Foundation Trust | ||
Full Title: TRANSFORM-UK: A Therapeutic Open Label Study of Tocilizumab in the Treatment of Pulmonary Arterial Hypertension | ||
Medical condition: Pulmonary arterial hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-003728-36 | Sponsor Protocol Number: 21012 | Start Date*: 2004-12-10 |
Sponsor Name:E.O.R.T.C. - EUROPEAN ORGANIZATION FOR RESEARCH AND TREATMENT OF CANCER | ||
Full Title: PHASE II CLINICAL TRIAL WITH CAELYX MONO-CHEMOTHERAPY IN PATIENTS WITH ADVANCED MYCOSIS FUNGOIDES STAGE IIb, IVa AND IVb WITH OR WITHOUT PREVIOUS CHEMOTHERAPY. | ||
Medical condition: ADVANCED STAGE CUTANEOUS T CELL LYMPHOMA. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-013103-63 | Sponsor Protocol Number: 1884 | Start Date*: 2011-12-14 | |||||||||||
Sponsor Name:Asklepios Kliniken Hamburg GmbH | |||||||||||||
Full Title: Pilot study investigating the effect of intra-coronary and intra-myocardial application of enriched CD133pos autologous bone marrow derived stem cells for improving left ventricular function in chr... | |||||||||||||
Medical condition: Patients with chronic ischemic cardiomyopathy with an LVEF ≤45% and symptomatic heart failure NYHA ≥ II under optimal therapy and drug treatment according to the current ESC heart failure guidelines. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000924-42 | Sponsor Protocol Number: LAPADO-Study | Start Date*: 2007-06-06 |
Sponsor Name:Sana Klinikum Lichtenberg | ||
Full Title: Phase I/II-Studie zur neoadjuvanten Chemotherapie mit nicht-pegyliertem liposomalem Doxorubicin, Paclitaxel und Lapatinib bei Patientinnen mit HER2-überexprimierenden, primärem Mammakarzinomen | ||
Medical condition: Im Rahmen der klinischen Studie soll eine Chemotherapie, die aus den Medikamenten nicht-pegyliertes liposomales Doxorubicin, Paclitaxel und Lapatinib besteht, verabreicht werden. Das Ziel dieser kl... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000823-15 | Sponsor Protocol Number: NEUPRODEX | Start Date*: 2013-12-23 |
Sponsor Name:Charité – Universitätsmedizin Berlin | ||
Full Title: Neuroprotection with Dexmedetomidine in patients undergoing elective cardiac or abdominal surgery | ||
Medical condition: The drug Dexmedetomidine will be investigated in patients (men and women) undergoing elective cardiac or abdominal surgery. The study medication will be administered perioperatively by intravenous ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-001362-40 | Sponsor Protocol Number: CSTI571BIT15 | Start Date*: 2004-07-22 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: PHASE II STUDY OF IMATINIB MESYLATE IN CHORDOMA | |||||||||||||
Medical condition: Treatment of advanced or unresectable chordoma | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021410-34 | Sponsor Protocol Number: EOC-2-Opht-2010 | Start Date*: 2010-08-12 | ||||||||||||||||
Sponsor Name:Medical Centre Haaglanden | ||||||||||||||||||
Full Title: A double blind randomized study on the efficacy of cyclopentolate 1% and cyclopentolate 1% with tropicamide 1% in children | ||||||||||||||||||
Medical condition: Depth of cycloplegia; changes of astigmatism; recuperation from cycloplegia and mydriasis | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002117-30 | Sponsor Protocol Number: 000010/BT | Start Date*: 2016-02-16 | |||||||||||
Sponsor Name:Bone Therapeutics S.A. | |||||||||||||
Full Title: A Two-stage 6-month, Multicentre, Randomised, Double-blind, Controlled Study on the Safety and Efficacy of a Single Intra-articular Administration of JTA-004 in Patients with Symptomatic Knee Osteo... | |||||||||||||
Medical condition: Symptomatic osteoarthritis of the knee with Kellgren-Lawrence grade II and III | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001415-21 | Sponsor Protocol Number: MRI-R-USPIO-05-2005 | Start Date*: 2005-07-20 |
Sponsor Name:Institut für Röntgendiagnostik der Technischen Universität München | ||
Full Title: Phase II Studie zur Evaluierung der SH U 555 C unterstützten Magnetresonanztomographie der arteriosklerotischen Karotisstenose bei Patienten vor Thrombendarteriektomie | ||
Medical condition: Arteriosklerotische Karotisstenose | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001754-92 | Sponsor Protocol Number: AAE581C2201 | Start Date*: 2005-02-14 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A phase II, 12-month, double-blind, placebo-controlled, dose-finding, multicenter study to evaluate the safety, tolerability, and disease modifying efficacy of daily oral AAE581 (10, 25 and 50 mg t... | ||
Medical condition: Osteoarthritis (OA) is a disease with a complex pathophysiology leading to the degeneration of articular cartilage and bone. It is characterized by pain, biochemical and enzymatic changes, cartilag... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004449-32 | Sponsor Protocol Number: AR II 01-2005 | Start Date*: 2006-01-12 |
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALI RIUNITI DI BERGAMO A.O. DI RILIEVO NAZIONALE | ||
Full Title: EFFECTIVENESS OF THE LEVOSIMENDAN IN THE THERAPY OF DIASTOLIC DYSFUNCTION OF CARDIAC SURGERY | ||
Medical condition: DIASTOLIC DYSFUNCTION OF CARDIAC SURGERY TREATMENT BEFORE SURGERY | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-007056-18 | Sponsor Protocol Number: 3403 | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:The Newcastle upon tyne Hospitals NHS Trust | |||||||||||||
Full Title: The Discoid Lupus Research Project | |||||||||||||
Medical condition: Discoid lupus erythematosus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007974-45 | Sponsor Protocol Number: EKZ-AMC001 | Start Date*: 2009-07-16 |
Sponsor Name:AMC | ||
Full Title: Phase II trial of the combination of gemcitabine and 131I-MIBG therapy in paediatric patients with relapsed or progressive neuroblastoma | ||
Medical condition: relapsed or progressive neuroblastoma in pediatric patients of 1 to 18 years | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000233-18 | Sponsor Protocol Number: AIO KRK 0205 | Start Date*: 2008-04-09 | |||||||||||
Sponsor Name:Universität zu Köln | |||||||||||||
Full Title: Phase I/II Studie zum Einsatz von Capecitabin und Oxaliplatin (XELOX) in Kombination mit Bevacizumab und Imatinib in der Erstlinientherapie von Patienten mit fortgeschrittenem kolorektalem Karzinom | |||||||||||||
Medical condition: fortgeschrittenes kolorektalen Karzinom mit inoperablen Metastasen | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016317-20 | Sponsor Protocol Number: SCA_LITIO_12 | Start Date*: 2009-10-26 | |||||||||||
Sponsor Name:UNIVERSITA` DEGLI STUDI DI NAPOLI FEDERICO II | |||||||||||||
Full Title: PILOT STUDY TO ASSESS SAFETY AND TOLERABILITY OF LITHIUM ON SPINOCEREBELLAR ATAXIA OF TYPE 2 | |||||||||||||
Medical condition: Spinocerebellar ataxia type 2 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007241-12 | Sponsor Protocol Number: PH-L19SIPI131-07/07 | Start Date*: 2008-10-06 | |||||||||||
Sponsor Name:Philogen S.p.A. | |||||||||||||
Full Title: A PHASE I/II DOSE FINDING AND EFFICACY STUDY OF THE TUMOUR TARGETING HUMAN 131I-L19SIP MONOCLONAL ANTIBODY IN PATIENTS WITH CANCER | |||||||||||||
Medical condition: Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024018-71 | Sponsor Protocol Number: 2010-024018-71 | Start Date*: 2011-03-31 |
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | ||
Full Title: PREMEDICATION IN CHILDREN: CLONIDINE VERSUS MELATONIN | ||
Medical condition: HEALTHY CHILDREN UNDERGOING ELECTIVE MINOR SURGERY | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002689-30 | Sponsor Protocol Number: MedOPP107 | Start Date*: 2017-03-16 | |||||||||||
Sponsor Name:Medica Scientia Innovation Research (MedSIR ARO) | |||||||||||||
Full Title: Multicenter open-label, phase II trial, to evaluate the efficacy and safety of nal-IRI for progressing brain metastases in patients with HER2-negative breast cancer | |||||||||||||
Medical condition: Progressing brain metastases in patients with HER2-negative breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001261-33 | Sponsor Protocol Number: | Start Date*: 2019-11-05 |
Sponsor Name:University College London | ||
Full Title: Randomised phase II/III study of Rituximab and Ibrutinib (RI) versus Dexamethasone, Rituximab and Cyclophosphamide (DRC) as initial therapy for Waldenström's macroglobulinaemia | ||
Medical condition: Waldenström's macroglobulinaemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2008-005506-40 | Sponsor Protocol Number: CLDE225B2203 | Start Date*: 2009-08-06 |
Sponsor Name:Novartis Pharma | ||
Full Title: A double-blind, randomized, vehicle-controlled Proof of Concept (PoC) study, to evaluate the safety, local tolerability, pharmacokinetics and pharmacodynamics of multiple topical administrations of... | ||
Medical condition: Gorlin syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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