- 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 451 of 2,219.
| EudraCT Number: 2009-015993-37 | Sponsor Protocol Number: SAN-FORST-001 | Start Date*: 2009-11-06 | |||||||||||
| Sponsor Name:Institut für Klinische Forschung und Entwicklung (ikfe) GmbH | |||||||||||||
| Full Title: Beta Cell Relieving and Cardiovascular Protective Effects of LANTUS Treatment in Type 2 Diabetes Patients – Investigation on Postprandial Excursions of Proinsulin and PAI-1 Levels | |||||||||||||
| Medical condition: Type 2 Diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003851-20 | Sponsor Protocol Number: C-10-151 | Start Date*: 2012-01-11 | |||||||||||
| Sponsor Name:Alcon Research, Ltd. | |||||||||||||
| Full Title: A Multicente, Observer-Masked Study of the Safety and Efficacy of MDPF Travoprost, 0.004% Compared to TRAVATAN in Patients with Open-Angle Glaucoma or Ocular Hypertension | |||||||||||||
| Medical condition: Open-Angle Glaucoma or Ocular Hypertension | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003866-34 | Sponsor Protocol Number: 2553 | Start Date*: 2012-09-24 | |||||||||||
| Sponsor Name:North Bristol NHS Trust (NBT) | |||||||||||||
| Full Title: A Placebo-Controlled, Randomised, Double-Blind Trial to Assess the Safety and Efficacy of Intermittent Bilateral Intraputamenal Glial Cell Line-Derived Neurotrophic Factor (GDNF) Infusions Administ... | |||||||||||||
| Medical condition: Parkinson's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-022240-21 | Sponsor Protocol Number: ISIS183750-CS4 | Start Date*: 2011-04-29 | |||||||||||
| Sponsor Name:Isis Pharmaceuticals Inc. | |||||||||||||
| Full Title: A Phase 1b/2 Study of Carboplatin-Paclitaxel, with or without ISIS 183750 (an eIF4E Inhibitor), in Patients with Stage IV Non-Small Cell Lung Cancer | |||||||||||||
| Medical condition: Stage IV Non-Small Cell Lung Cancer (NSCLC; including patients with pleural effusion who were previously classified as Stage IIIB) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) | |||||||||||||
| 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: 2010-019837-85 | Sponsor Protocol Number: CUTACETUX | Start Date*: 2010-05-12 | |||||||||||
| Sponsor Name:CHU de Poitiers | |||||||||||||
| Full Title: Étude de la toxicité cutanée du cétuximab (anti-Epidermal Growth Factor Receptor): recherche d’un lien entre la réponse inflammatoire cutanée et la réponse radiologique. | |||||||||||||
| Medical condition: METASTATIC COLORECTAL CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-002986-39 | Sponsor Protocol Number: DXM/AMT | Start Date*: 2011-09-12 | |||||||||||
| Sponsor Name:Profil Institut für Stoffwechselforschung GmbH | |||||||||||||
| Full Title: A Phase IIa, Double-Blind, Placebo-Controlled, Randomised, Fourfold Cross-Over Study to Investigate the Glucose Lowering Effects of Dextromethorphan and Amantadine in Subjects with Type 2 Diabetes ... | |||||||||||||
| Medical condition: Type 2 diabetes mellitus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001121-24 | Sponsor Protocol Number: P00804 | Start Date*: 2011-04-21 |
| Sponsor Name:Papworth Hospital NHS Trust | ||
| Full Title: Prospective randomised controlled trial of video assisted thorascopic (VATS) cytoreductive pleurectomy compared to talc pleurodesis in patients with suspected or proven malignant mesothelioma | ||
| Medical condition: Mesothelioma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-005529-74 | Sponsor Protocol Number: ML19982 | Start Date*: 2006-03-16 | |||||||||||
| Sponsor Name:Roche (Hungary) Ltd. | |||||||||||||
| Full Title: A randomised, open-label, multi-national, multi-center study to investigate the impact of bone-marker feedback (at 3 months) on adherence to once monthly ibandronate treatment of patients with post... | |||||||||||||
| Medical condition: osteoporosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: SI (Completed) SK (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000388-28 | Sponsor Protocol Number: 00658;MK-0683-201 | Start Date*: 2011-06-30 | |||||||||||
| Sponsor Name:University Medical Center Freiburg | |||||||||||||
| Full Title: Safety of Vorinostat in combination with Bortezomib, Doxorubicin and Dexamethasone (VBDD) in patients with refractory or relapsed multiple myeloma | |||||||||||||
| Medical condition: Relapsed or refractory multiple myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-004050-29 | Sponsor Protocol Number: PHI116581 | Start Date*: 2013-01-07 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A four-week Phase IIa, randomized, double-blind, placebocontrolled, parallel-group, multi-center study to evaluate the safety, efficacy and pharmacokinetics of GSK1278863 in subjects with anemia as... | |||||||||||||
| Medical condition: Anemia associated with chronic kidney disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019767-11 | Sponsor Protocol Number: Ö-PKU1 | Start Date*: 2010-09-08 |
| Sponsor Name:Graz Medical University | ||
| Full Title: Ö-PKU 1 – Evaluation of a Test for the identication of BH4 responsive PKU patients | ||
| Medical condition: Hyperphenylalaninaemia (HPA) in adult and paediatric patients of 4 years of age and over with phenylketonuria (PKU). | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-019777-15 | Sponsor Protocol Number: GLP114130 | Start Date*: 2010-09-10 | |||||||||||
| Sponsor Name:GlaxoSmithKline LLC | |||||||||||||
| Full Title: A Randomized, Double-Blind, Active-Controlled, Parallel-Group, Multicenter Study to Determine the Efficacy and Safety of Albiglutide as Compared With Sitagliptin in Subjects With Type 2 Diabetes Me... | |||||||||||||
| Medical condition: Type 2 Diabetes Mellitus With Renal Impairment | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) ES (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019778-34 | Sponsor Protocol Number: D1050292 | Start Date*: 2011-03-14 | |||||||||||
| Sponsor Name:Sunovion, Inc. | |||||||||||||
| Full Title: A RANDOMIZED, 6-WEEK, DOUBLE-BLIND, PLACEBO-CONTROLLED, FLEXIBLE-DOSE, PARALLEL-GROUP STUDY OF LURASIDONE ADJUNCTIVE TO LITHIUM OR DIVALPROEX FOR THE TREATMENT OF BIPOLAR I DEPRESSION IN SUBJECTS ... | |||||||||||||
| Medical condition: Bipolar disorder | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SK (Completed) LT (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005111-91 | Sponsor Protocol Number: RBHP2011LUSSON | Start Date*: 2012-01-19 | |||||||||||
| Sponsor Name:CHU de Clermont-Ferrand | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-023776-52 | Sponsor Protocol Number: Lisette-1 | Start Date*: 2011-01-19 | |||||||||||
| Sponsor Name: | |||||||||||||
| Full Title: Optimizing tamoxifen therapy through the induction of CYP3A4, CYP2C and CYP2D6 mediated metabolism | |||||||||||||
| Medical condition: Breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-023789-33 | Sponsor Protocol Number: 300904BS | Start Date*: 2011-02-17 | |||||||||||
| Sponsor Name:Valderm ApS | |||||||||||||
| Full Title: A phase IIa, multicenter, randomized, two-arm, observer-blind, vehicle and reference controlled proof of concept trial to investigate intra-individually (left/ right) the antipsoriatic efficacy and... | |||||||||||||
| Medical condition: Male or female subjects with stable plaque psoriasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003206-25 | Sponsor Protocol Number: NRL001-01/2011(SEFI) | Start Date*: 2012-01-25 | |||||||||||
| Sponsor Name:Norgine Ltd | |||||||||||||
| Full Title: A multi-centre, phase II, double-blind, randomised, placebo-controlled, parallel group, dose-ranging study in patients with faecal incontinence; to evaluate the efficacy, safety and tolerability of... | |||||||||||||
| Medical condition: Faecal incontinence | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) CZ (Completed) DE (Completed) ES (Completed) GB (Completed) IT (Completed) HU (Completed) | |||||||||||||
| Trial results: Removed from public view | |||||||||||||
| EudraCT Number: 2011-003208-19 | Sponsor Protocol Number: GWID10160 | Start Date*: 2011-11-16 | |||||||||||
| Sponsor Name:GW Pharma Ltd. | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled parallel group, pilot study of GWP42003 in the symptomatic treatment of ulcerative colitis. | |||||||||||||
| Medical condition: Symptoms of diarrhoea, rectal bleeding, stool frequency and inflammation in subjects with ulcerative colitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) CZ (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024657-36 | Sponsor Protocol Number: DSR-01 | Start Date*: 2011-05-17 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Statens Serum Institut | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: Metronidazol for the treatment of dientamoebiasis in children in Denmark – A randomized, placebo-controlled, double-blinded clinical trial. | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Presumed symptomatic gastrointestinal infection with the protozoan Dientamoeba fragilis. | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||
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