- Trials with a EudraCT protocol (44,352)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,352 result(s) found.
Displaying page 33 of 2,218.
EudraCT Number: 2007-005953-49 | Sponsor Protocol Number: 26866138MMY 2051 | Start Date*: 2009-06-18 | |||||||||||
Sponsor Name:Prof. M.A. Dimopoulos | |||||||||||||
Full Title: A Prospective, Multicenter, Non-comparative, Open-label, Phase II Study to Evaluate the Effects of the Combination of Bortezomib/Dexamethasone/Zoledronic Acid on Bone Mineral Density, Bone Metaboli... | |||||||||||||
Medical condition: This will be a Phase II, prospective, non-comparative, multicenter, open-label study of the effects of the combination of Bortezomib/Dexamethasone/Zoledronic acid on bone mineral density, skeletal ... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005977-67 | Sponsor Protocol Number: GIR1 | Start Date*: 2008-02-12 | |||||||||||
Sponsor Name:CONSORZIO ONCOTECH | |||||||||||||
Full Title: SUNITINIB EITHER BEFORE OR AFTER CYTOREDUCTIVE NEPHRECTOMY A PHASE II TRIAL IN PATIENTS WITH METASTATIC RENAL CELL CARCINOMA | |||||||||||||
Medical condition: Patients with metastatic Renal Cell Carcinoma not previously treated with nephrectomy and systemic therapy. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006084-73 | Sponsor Protocol Number: VIAjectTM-07J | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:BIODEL Inc | |||||||||||||
Full Title: An Open Label, Multi-Center, Follow-on Study Examining the Long-Term Safety and Efficacy of Insulin VIAjectTM in Subjects with Type 1 Diabetes Mellitus | |||||||||||||
Medical condition: Diabetes Mellitus Type 1 | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002210-22 | Sponsor Protocol Number: COU-AA-003-EXT | Start Date*: 2008-09-25 | |||||||||||
Sponsor Name:Janssen Oncology, Inc. | |||||||||||||
Full Title: An Extended Study of CB7630 (Abiraterone Acetate) in Patients with Advanced Prostate Cancer Who Have Failed Androgen Deprivation and Docetaxel-Based Chemotherapy and Completed Clinical Study COU-AA... | |||||||||||||
Medical condition: Hormone refractory prostate cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002009-31 | Sponsor Protocol Number: EB069 | Start Date*: 2007-06-13 |
Sponsor Name:Emotional Brain BV | ||
Full Title: A double blind randomized placebo controlled cross-over study to validate the distinction between women with different levels of attention and valence direction for erotic stimuli, in relation with... | ||
Medical condition: Hypoactive sexual desire disorder and female sexual arousal disorder | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007208-28 | Sponsor Protocol Number: TROPISMVC | Start Date*: 2009-05-06 |
Sponsor Name:Asociación para el Estudio de las Enfermedades Infecciosas | ||
Full Title: Estudio comparativo de dos métodos para predecir el uso de co-receptores por el virus de la inmunodeficiencia 1 (HIV-1): el ensayo fenotípico (Trofile ESTA®) y la respuesta virológica a corto plazo... | ||
Medical condition: Infección por el Virus de la Inmunodeficiencia Humana tipo-1 (VIH-1). El antirretroviral maraviroc pertenece a un grupo de medicamentos llamados antagonistas del CCR5 e impide la entrada del VIH-1 ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004970-24 | Sponsor Protocol Number: NHL-14 | Start Date*: 2008-01-17 | |||||||||||
Sponsor Name:AGMT - Arbeitsgemeinschaft Medikamentöse Tumortherapie Gemeinnützige GmbH | |||||||||||||
Full Title: Multizentrische Studie über die Cardiotoxizität von R-CHOP (Rituximab, Cyclophosphamid, Doxorubicin, Vincristin und Prednisolon) v. R-COMP (Rituximab, Cyclophosphamid, liposomalem Doxorubicin, Vinc... | |||||||||||||
Medical condition: Diffus großzelliges B-Zell Lymphom | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004980-23 | Sponsor Protocol Number: P05134 | Start Date*: 2008-05-05 | |||||||||||
Sponsor Name:Schering-Plough Farma, Lda. | |||||||||||||
Full Title: Double-Blind evaluation of the safety and efficacy of Quadriderme cream (betamethasone dipropionate, clotrimazole and gentamicin sulphate ) compare with betamethasone dipropionate combined with gen... | |||||||||||||
Medical condition: Impetiginous Eczema | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004985-41 | Sponsor Protocol Number: DYSK-PD-2007 | Start Date*: 2007-11-29 |
Sponsor Name:Department of Neuroscience, neurology | ||
Full Title: Different dyskinesias in Parkinson's disease and their relation to levodopa pharmacokinetics | ||
Medical condition: Parkinson's disease, G20.9. Different dyskinesias related to advanced Parkinson's disease will be investigated. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004994-25 | Sponsor Protocol Number: CSMS995A2101 | Start Date*: 2008-02-04 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo-controlled, crossover study in women with irritable bowel syndrome to evaluate feasibility and reproducibility of barostat assessments of colorecta... | |||||||||||||
Medical condition: Irritable Bowel Syndrom | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002335-32 | Sponsor Protocol Number: AN08/8505 | Start Date*: 2008-11-28 |
Sponsor Name:The University of Leeds | ||
Full Title: Does concentration affect the ED50 of bupivacaine for supraclavicular brachial plxus block? | ||
Medical condition: Not applicable | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002343-16 | Sponsor Protocol Number: 1014/05 | Start Date*: 2006-01-05 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Postoperative nausea and vomiting: acupuncture effect on postoperative prevention | |||||||||||||
Medical condition: Postoperative nausea and vomiting laparoscopic cholecistectomy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000526-48 | Sponsor Protocol Number: A.S.T.R.A. | Start Date*: 2007-03-06 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Randomized, monocentric trial on sintoms, adherence,toxicity of alternate antiretrovirale regimen | |||||||||||||
Medical condition: PT HIV-1 positive and naive to antiretroviral drug | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001465-14 | Sponsor Protocol Number: CSLCT-NHF-06-30 | Start Date*: 2007-05-17 |
Sponsor Name:CSL Limited | ||
Full Title: A Single Centre, Open-Label Study to Evaluate the Immunogenicity and Safety of Enzira Vaccine in Healthy Adults aged ≥ 18 to < 60 years and in Healthy Older Adults aged ≥ 60 years for the 2007/2008... | ||
Medical condition: Prophylaxis of Influenza | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-001187-78 | Sponsor Protocol Number: 112897 | Start Date*: 2008-01-02 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: The 3Mg Trial: A randomised controlled trial of intravenous or nebulised magnesium sulphate versus standard therapy for acute severe asthma | |||||||||||||
Medical condition: Acute severe asthma | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001206-24 | Sponsor Protocol Number: 16901 | Start Date*: 2007-07-31 |
Sponsor Name:UMCG | ||
Full Title: Effect of selective COX-2 inhibition on neuroinflammation in Parkinson's disease | ||
Medical condition: Parkinson's disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002109-32 | Sponsor Protocol Number: CORL2007 | Start Date*: 2007-05-10 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO | |||||||||||||
Full Title: USE OF FENOLDOPAM TO IMPROVE GLOMERULAR FILTRATION RATE IN EARLY RENAL DYSFUNCTION AFTER LIVER TRANSPLANTATION | |||||||||||||
Medical condition: Adult liver transplanted patients age > 18 years , with pre-transplantation normal renal function creatinine clearance 1ml/kg/min | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002120-14 | Sponsor Protocol Number: 3074K4-2207-WW | Start Date*: 2008-10-29 | |||||||||||||||||||||
Sponsor Name:Wyeth Research Division of Wyeth Pharmaceutical Inc. | |||||||||||||||||||||||
Full Title: A Multicenter, Open-Label, Ascending Multiple-Dose Study to Assess the Pharmacokinetics, Safety, and Tolerability of Tigecycline in Patients 8 to 11 Years of Age With Selected Serious Infections | |||||||||||||||||||||||
Medical condition: Complicated intra-abdominal infections (cIAI), complicated skin and skin structure infections (cSSSI), community-acquired pneumonia (CAP). | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) GB (Completed) Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-001160-36 | Sponsor Protocol Number: 2008-1 | Start Date*: 2009-06-04 | ||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||
Full Title: A trial of Guanfacine, an alpha 2 adrenergic agonist, for Spatial Neglect and Impaired Vigilance following Stroke and Focal Brain Damage | ||||||||||||||||||
Medical condition: Spatial Neglect following Hemispheric stroke and focal brain injury | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-006405-17 | Sponsor Protocol Number: FDM-study | Start Date*: 2009-02-25 | |||||||||||
Sponsor Name:Kuopio University Hospital | |||||||||||||
Full Title: Finnish Dyspepsia Management -study | |||||||||||||
Medical condition: Tutkimukseen rekrytoidaan n. 400 dyspepsiaoireiden vuoksi erikoissairaanhoitoon lähetettyä alle 60-vuotiasta potilasta, joiden vaiva tutkimusten jälkeen todetaan toiminnalliseksi. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
