- Trials with a EudraCT protocol (57)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1,140)
57 result(s) found for: Rad.
Displaying page 1 of 3.
EudraCT Number: 2017-003169-82 | Sponsor Protocol Number: rAd-IFN-MM-301 | Start Date*: 2019-01-30 | |||||||||||
Sponsor Name:Trizell Ltd | |||||||||||||
Full Title: A Phase III, Open Label, Randomized, Parallel Group Study to Evaluate the Efficacy and Safety of Intrapleural Administration of Adenovirus-Delivered Interferon Alpha-2b (rAd-IFN) in Combination wit... | |||||||||||||
Medical condition: Malignant Pleural Mesothelioma | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) FR (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001473-25 | Sponsor Protocol Number: CRAD001A2401 | Start Date*: 2005-01-27 |
Sponsor Name:Novartis Pharmaceuticals Corporation | ||
Full Title: A facilitated access program to provide Everolimus (RAD) for maintenance for patients completing therapy in RAD trials in solid organ transplantation. | ||
Medical condition: Solid Organ Transplant - maintenace phase | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-001545-25 | Sponsor Protocol Number: CHDR1409 | Start Date*: 2014-07-02 | ||||||||||||||||
Sponsor Name:Centre for Human Drug Research | ||||||||||||||||||
Full Title: Randomized, double-blind, placebo-controlled, three way crossover, double dummy, single centre study evaluating the effect of haloperidol 2 mg and lorazepam 1 mg on posturography and underlying sys... | ||||||||||||||||||
Medical condition: Healthy volunteers (balance disorders) | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002725-74 | Sponsor Protocol Number: COU-AA-004 | Start Date*: 2007-07-16 | |||||||||||
Sponsor Name:Cougar Biotechnology, Inc | |||||||||||||
Full Title: A Phase II Open Label Study of CB7630 (Abiraterone Acetate) and Prednisone in Patients with Advanced Prostate Cancer Who Have Failed Androgen Deprivation and Docetaxel-Based Chemotherapy | |||||||||||||
Medical condition: HRPC (Hormone refractory prostate cancer) refractory to androgen deprivation and Docetaxel based chemotherapy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001499-20 | Sponsor Protocol Number: RV-MM-GMSG-392 | Start Date*: 2014-09-30 | |||||||||||
Sponsor Name:Meletios-Athanasios Dimopoulos | |||||||||||||
Full Title: A phase II open label, non comparative, non randomized study for the assessment of the efficacy and safety of lenalidomide + adriamycine and low dose dexamethasone combination (RAD) in newly diagno... | |||||||||||||
Medical condition: Newly Diagnosed multiple myeloma | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000222-22 | Sponsor Protocol Number: 2004/045 | Start Date*: 2005-04-25 |
Sponsor Name:OLV-ziekenhuis | ||
Full Title: Prospective Open Single-Centre Study on the Effect of Initiation of RAD and CNI minimalisation on renal function in heart transplant patients | ||
Medical condition: heart transplant patients with impaired renal function under treatment of CNI | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003035-78 | Sponsor Protocol Number: 72/2006/U/Sper | Start Date*: 2006-07-11 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: SICUREZZA ED EFFICACIA DI CICLOSPORINA A BASSE DOSI IN ASSOCIAZIONE AD EVEROLIMUS NEL PROTEGGERE LA FUNZIONE RENALE NEI PAZIENTI CON TRAPIANTO DI CUORE | |||||||||||||
Medical condition: Heart transplant | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001712-31 | Sponsor Protocol Number: | Start Date*: 2005-01-24 |
Sponsor Name:Lothian Health - University Hospitals Division | ||
Full Title: A study to evaluate the biological effects of RAD001 on invasive breast cancer | ||
Medical condition: Breast Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-016616-21 | Sponsor Protocol Number: DSMMXIV | Start Date*: 2011-10-20 | |||||||||||
Sponsor Name:Wuerzburg University Hospital | |||||||||||||
Full Title: Lenalidomide, Adriamycin, Dexamethasone (RAD) Versus Lenalidomide, Bortezomib, Dexamethasone (VRD) for Induction in Newly Diagnosed Multiple Myeloma followed by Response-adapted Consolidation and ... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004004-60 | Sponsor Protocol Number: Rad-HCC | Start Date*: 2017-03-02 | |||||||||||
Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | |||||||||||||
Full Title: Prospective study of anti-inflammatory therapy post interventional radiological treatment of HCC in the cirrhotic patient. | |||||||||||||
Medical condition: patients with HCC in the setting of cirrhosis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004908-36 | Sponsor Protocol Number: RAD001A B253 E03 | Start Date*: 2007-01-10 |
Sponsor Name:Novartis Farmaceútica S.A | ||
Full Title: Extension E-03 al Protocolo nº RAD001AB253 Estudio de seguimiento de 2 años para obtener datos especificos de la evolución de los pacientes de novo trasplantados cardíacos que discontinuaron la med... | ||
Medical condition: Trasplante cardiaco de novo | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-006795-30 | Sponsor Protocol Number: Satauni | Start Date*: 2009-01-16 | |||||||||||
Sponsor Name:Institute of Clinical Medicine, Family Medicine, University of Turku | |||||||||||||
Full Title: Controlled-release melatonin in fast withdrawal of temazepam, zopiclone or zolpidem in elderly persons with insomnia | |||||||||||||
Medical condition: Individuals over 55 years with primary insomnia and DDD need of temazepam, zopiclone or zolpidem | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004098-24 | Sponsor Protocol Number: GEP 04/0606 | Start Date*: 2008-01-14 | |||||||||||
Sponsor Name:FNCLCC | |||||||||||||
Full Title: A phase II, randomized, multi-center study, assessing value of adding RAD 001 to Trastuzumab as preoperative therapy of HER-2 positive primary breast cancer amenable to surgery | |||||||||||||
Medical condition: HER-2 overexpressing primary operable breast cancer | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023345-30 | Sponsor Protocol Number: RAD-IPMT | Start Date*: 2010-11-18 | |||||||||||
Sponsor Name:U.L.S.S. 9 DI TREVISO | |||||||||||||
Full Title: Prospective spontaneous cross-over study on pancreatic T1/T2 enhancement in patients with IPMT: comparison Omniscan-Dotarem | |||||||||||||
Medical condition: Pancreatic intraductal papillary mucinous tumor | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005255-17 | Sponsor Protocol Number: | Start Date*: 2014-09-05 |
Sponsor Name:University of Leeds | ||
Full Title: Chronotherapeutic lifestyle intervention for diabetes and obesity to reset the circadian rhythm and improve cardiometabolic risk in the European population | ||
Medical condition: first-degree relatives of individuals with type 2 diabetes. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004183-21 | Sponsor Protocol Number: 2858 | Start Date*: 2013-01-25 |
Sponsor Name:North Bristol NHS Trust | ||
Full Title: A randomized, double blind, placebo controlled, cross over trial of Melatonin for the treatment of nocturia in adults with progressive multiple sclerosis, with an open label, single-arm extension s... | ||
Medical condition: Nocturia; Multiple Sclerosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012449-48 | Sponsor Protocol Number: ALS-8-09-A-101 | Start Date*: 2009-11-09 |
Sponsor Name:Air Liquide Santé International | ||
Full Title: „Sympathetic neural outflow during Xenon anesthesia in humans“ | ||
Medical condition: We would like to frame the thesis, that a general, inhalative Xenon anesthesia (1 MAC) does not effect the sympathetic outflow and the sympathetic baroreflex reagibility under spontaneous breathing... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000007-28 | Sponsor Protocol Number: DSMMXII | Start Date*: 2009-05-22 | |||||||||||
Sponsor Name:Universitaetsklinikum Wuerzburg | |||||||||||||
Full Title: Lenalidomide (Revlimid®), Adriamycin and Dexamethasone (RAD) as an Induction Therapy in Newly Diagnosed Multiple Myeloma Followed by a Risk-Defined Transplant Strategy and Lenalidomide Maintenance ... | |||||||||||||
Medical condition: Multiple Myeloma | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004048-50 | Sponsor Protocol Number: 3-062-18 | Start Date*: 2019-02-14 | |||||||||||
Sponsor Name:University of Aberdeen [...] | |||||||||||||
Full Title: Double blind randomised controlled trial of exogenous administration of melatonin in chronic pain (DREAM-CP) | |||||||||||||
Medical condition: Sleep disturbance in patients with chronic pain | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000629-30 | Sponsor Protocol Number: 06022013 | Start Date*: 2013-04-09 | |||||||||||
Sponsor Name:Department of surgery, Herlev Hospital | |||||||||||||
Full Title: The sun protective effect of melatonin: a randomized, placebo-controlled, double-blinded study on healthy volunteers. | |||||||||||||
Medical condition: Erythema after sun exposure in healthy volunteers | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
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. |
