- Trials with a EudraCT protocol (44,380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,380 result(s) found.
Displaying page 214 of 2,219.
| EudraCT Number: 2009-012270-12 | Sponsor Protocol Number: BC22419 | Start Date*: 2010-05-21 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
| Full Title: Effects of 150 μg aleglitazar on renal function in patients with Type 2 diabetes and moderate renal impairment, as compared to Actos® | |||||||||||||
| Medical condition: Type 2 diabetes with moderate renal function impairment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) HU (Completed) SK (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005491-14 | Sponsor Protocol Number: P05225 | Start Date*: 2008-07-16 | |||||||||||
| Sponsor Name:SCHERING-PLOUGH | |||||||||||||
| Full Title: TEMOZOLOMIDE IN METASTATIC BREAST CANCER PATIENTS AT HIGH RISK OF BRAIN RECURRENCE: IMPACT ON THE INCIDENCE OF BRAIN METASTASES | |||||||||||||
| Medical condition: pazienti | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-018092-14 | Sponsor Protocol Number: CRAD001RDE35T | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:Krankenhaus Nordwest GmbH | ||||||||||||||||||
| Full Title: A randomized, double-blind, multi-center phase III study evaluating paclitaxel with and without RAD001 in patients with gastric carcinoma who have progressed after therapy with a fluoropyrimidine/p... | ||||||||||||||||||
| Medical condition: advanced (i.e. inoperable, recurrent or metastatic) gastric cancer or adenocarcinoma of the esophagogastric junction | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-018101-52 | Sponsor Protocol Number: V72P13E2 | Start Date*: 2010-05-18 |
| Sponsor Name:Novartis Vaccines and Diagnostics S.r.l | ||
| Full Title: Title of the trial: A Phase 3, Open-Label, Multi-Center, Extension Study of V72P13E1 to Assess Antibody Persistence at One Year After a Fourth Dose Boost or Two Catch-Up Doses of Novartis Meningoco... | ||
| Medical condition: Groups 1a, 1b, 2a and 2b: From the last study visit in V72P13E1 to the start of the study V72P13E2 (Day 1):assessment of immunogenicity or safety Group 3: From birth to the start of the study V7... | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: FI (Completed) CZ (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-019014-25 | Sponsor Protocol Number: Istrokepilot | Start Date*: 2010-07-27 |
| Sponsor Name:Karolinska University Hospital | ||
| Full Title: A PROSPECTIVE, RANDOMISED, OPEN, BLINDED EVALUATION, ASCENDING-DOSE, PILOT TRIAL OF IMATINIB IN ACUTE ISCHAEMIC STROKE (I-STROKE/pilot) | ||
| Medical condition: Acute ischaemic stroke | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-004429-45 | Sponsor Protocol Number: CHORUS | Start Date*: 2008-02-04 | |||||||||||||||||||||
| Sponsor Name:Medical Research Council | |||||||||||||||||||||||
| Full Title: A randomised trial to determine the impact of timing of surgery and chemotherapy in newly diagnosed patients with advanced epithelial ovarian, primary peritoneal or fallopian tube carcinoma | |||||||||||||||||||||||
| Medical condition: Women with newly diagnosed, suspected, advanced (compatible with FIGO stage III/IV) ovarian, primary peritoneal or fallopian tube cancer who fulfil other entry criteria, with clinical and/or imagin... | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2009-017600-89 | Sponsor Protocol Number: FC/hulp003 | Start Date*: 2010-06-24 |
| Sponsor Name:Asociación para la investigación de Nefrología Infantil | ||
| Full Title: Ensayo intrapaciente de biodisponibilidad relativa de dos formulaciones de tacrolimus: Prograf (comprimidos de liberación normal) y Advagraf (comprimidos de liberación sostenida) en niños trasplant... | ||
| Medical condition: Transplante renal | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-017620-11 | Sponsor Protocol Number: KINURA-2 | Start Date*: 2011-06-14 | |||||||||||
| Sponsor Name:Scheper Ziekenhuis | |||||||||||||
| Full Title: Onderzoek naar de farmacokinetiek van uracil na orale toediening bij patiënten met colorectaal carcinoom. | |||||||||||||
| Medical condition: Colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017658-11 | Sponsor Protocol Number: FER-ASAP-2009-01 | Start Date*: 2010-05-03 | |||||||||||
| Sponsor Name:Vifor Pharma | |||||||||||||
| Full Title: An open-label, multicentre, randomised, 2-arm study to investigate the comparative efficacy and safety of intravenous ferric carboxymaltose versus oral iron for the treatment of iron deficiency ana... | |||||||||||||
| Medical condition: Iron deficiency anaemia in pregnant woman | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-017675-16 | Sponsor Protocol Number: OFT113725 | Start Date*: 2010-11-30 | ||||||||||||||||
| Sponsor Name:Plymouth Hospitals NHS Trust | ||||||||||||||||||
| Full Title: Phase II Trial of Single Agent Ofatumumab in Relapsed / Refractory Mantle Cell Lymphoma | ||||||||||||||||||
| Medical condition: Relapsed or refractory Mantle Cell Lymphoma | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2009-015681-55 | Sponsor Protocol Number: C-09-023 | Start Date*: 2010-03-18 | ||||||||||||||||
| Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
| Full Title: A Dose-Escalation Study of AL-39324 Suspension versus Lucentis™ for the Treatment of Exudative Age-Related Macular Degeneration | ||||||||||||||||||
| Medical condition: Exudative Age-related macular degeneration | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2007-001287-75 | Sponsor Protocol Number: CPP-340 | Start Date*: 2007-06-11 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:CENTRE PAUL PAPIN - IRCAM | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: Proteomic and genetic analysis of neurotoxicity predicting markers in oxaliplatine treated patients with colorectal carcinoma. | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Colorectal cancer patients undergoing treatment with oxaliplatine every 15 days, 5 fluoro uracile and calcium levofolinate, for adjuvant or metastatic setting will be recruited in this study. T... | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2007-001292-11 | Sponsor Protocol Number: NMSG 17/07 | Start Date*: 2007-08-05 | |||||||||||
| Sponsor Name:Nordic Myeloma Study Group | |||||||||||||
| Full Title: Talidomid vs Velcade vid melfalanrefraktärt myelom | |||||||||||||
| Medical condition: Multiple myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-001633-34 | Sponsor Protocol Number: FLT3503 | Start Date*: 2008-06-17 | |||||||||||
| Sponsor Name:Mundipharma Research Ltd | |||||||||||||
| Full Title: A double blind, double dummy, randomised, multicentre, four arm parallel group study to assess the efficacy and safety of FlutiForm™ pMDI 250/10 µg (2 puffs bid) vs Fluticasone pMDI 250 µg (2 puffs... | |||||||||||||
| Medical condition: Asthma bronchial | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) LV (Completed) BG (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013259-31 | Sponsor Protocol Number: 6232 | Start Date*: 2009-12-29 | ||||||||||||||||
| Sponsor Name:UMC Utrecht | ||||||||||||||||||
| Full Title: A multicenter double blind placebo-controlled randomised trial for benign esophageal anastomotic strictures: Savary dilation vs savary dilation with Triamcinolon | ||||||||||||||||||
| Medical condition: Patients with first time dysphagia (grade 2-4) due to a benign anastomotic esophageal stricture | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2006-001661-41 | Sponsor Protocol Number: Ser01 | Start Date*: 2006-06-08 |
| Sponsor Name:Karolinska University Hospital | ||
| Full Title: Body Composition and Metabolic Changes During Antipsychotic Treatment. A Randomized Trial Comparing Sertindole and Olanzapine. | ||
| Medical condition: Patients with schizophrenia diagnosis (DSM-IV) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-009372-13 | Sponsor Protocol Number: 2009-01b | Start Date*: 2009-11-03 |
| Sponsor Name:Institut de Cancérologie de la Loire | ||
| Full Title: A phase II, multi-center, open-label, repeat-dose study of Lenalidomide (Revlimid ®) plus low-dose Dexamethasone in patients with refractory B-cell lineage acute lymphoblastic leukemia or in relaps... | ||
| Medical condition: Treatment for B-cell Acute lymphoblastic leukemia in relapse. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-009421-29 | Sponsor Protocol Number: AAA1 | Start Date*: 2009-05-14 | |||||||||||
| Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: Non - invasive assessment of inflammatory burden in small abdominal aortic aneurysms: A USPIO - enhanced Magnetic Resonance Imaging (MRI) study | |||||||||||||
| Medical condition: The thrust of this pilot study is to investigate the utility of USPIO - enhanced MR to image abdominal aortic aneurysms with the aim of highlighting focal areas of inflammation and macrophage infil... | |||||||||||||
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| Population Age: | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-009428-36 | Sponsor Protocol Number: CHUBX2008/34 | Start Date*: 2009-03-17 | |||||||||||
| Sponsor Name:CHU de Bordeaux | |||||||||||||
| Full Title: Imagerie moléculaire in vivo des transmissions cholinergique et dopaminergique dans les démences à corps de Lewy par tomographie d’émission monophotonique : Applications au diagnostic et à l’identi... | |||||||||||||
| Medical condition: Démences à corps de Lewy | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-005096-93 | Sponsor Protocol Number: 070864 | Start Date*: 2009-09-03 |
| Sponsor Name:Jordi Carratalá | ||
| Full Title: SIMVASTATINA EN LA NEUMONIA ADQUIRIDA EN LA COMUNIDAD QUE REQUIERE HOSPITALIZACION. ESTUDIO ALEATORIZADO, DOBLE-CIEGO, CONTROLADO CON PLACEBO (SIMVASTATIN IN COMMUNITY-ACQUIRED PNEUMONIA REQUIRIN... | ||
| Medical condition: NEUMONIA ADQUIRIDA EN LA COMUNIDAD QUE REQUIERE HOSPITALIZACION (COMMUNITY-ACQUIRED PNEUMONIA REQUIRING HOSPITALIZATION) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
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