- Trials with a EudraCT protocol (44,341)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,341 result(s) found.
Displaying page 739 of 2,218.
EudraCT Number: 2008-003993-16 | Sponsor Protocol Number: IM-T-hPAM4-02 | Start Date*: 2009-04-03 | ||||||||||||||||
Sponsor Name:Immunomedics, Inc. | ||||||||||||||||||
Full Title: A Phase Ib/II Study of Fractionated 90-Y-hPAM4 Plus Gemcitabine in Patients with Previously Untreated Advanced Pancreatic Cancer | ||||||||||||||||||
Medical condition: This is a phase Ib, open-label, dose exploration study of 90-Y-hPAM4 administered as one or more treatment cycles of fractionated radioimmunotherapy in combination with radiosensitizing gemcitabine... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000878-42 | Sponsor Protocol Number: DANC-05 | Start Date*: 2005-06-20 |
Sponsor Name:Consorci Sanitari Terrassa | ||
Full Title: Ensayo clínico de la eficacia de dos estrategias terapéuticas en el tratamiento de la diverticulitis aguda no complicada | ||
Medical condition: Diverticulitis aguda no complicada | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004923-48 | Sponsor Protocol Number: 58408356 | Start Date*: 2008-09-16 | ||||||||||||||||
Sponsor Name:Vejle Sygehus | ||||||||||||||||||
Full Title: En fase II undersøgelse af Irinotecan og Panitumumab som 3. linje behandling til patienter med metastaserende colorectal cancer uden KRAS mutationer. | ||||||||||||||||||
Medical condition: Metastaserende colorectal cancer uden KRAS mutation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004152-71 | Sponsor Protocol Number: ICA 17043-17 | Start Date*: 2008-09-05 | |||||||||||
Sponsor Name:Icagen, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo Controlled, Parallel-Group, Multicenter Study to Assess the Safety and Efficacy of TWO Weeks of Oral Senicapoc Administration on Allergen challenge in ... | |||||||||||||
Medical condition: Asthma. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000790-38 | Sponsor Protocol Number: CRSV 604A 2203 | Start Date*: 2008-07-01 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A randomized, double-blind, placebo-controlled study to assess the safety, tolerability, and efficacy of oral RSV604 in healthy adults experimentally infected with respiratory syncytial virus | ||
Medical condition: infection with respiratory syncytial virus | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-003139-19 | Sponsor Protocol Number: CLCI699A2201 | Start Date*: 2008-09-12 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo and active controlled, parallel group, dose finding study to evaluate the efficacy and safety of LCI699 compared to placebo after 8 weeks treatment... | |||||||||||||
Medical condition: Essential Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SE (Completed) NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006696-36 | Sponsor Protocol Number: E2090-E044-318 | Start Date*: 2008-09-05 | |||||||||||
Sponsor Name:Eisai Limited | |||||||||||||
Full Title: Open label Extension Study Following Double-blind, Randomized, Placebo-controlled, Multicentre Study to Assess Efficacy and Safety of Adjunctive Zonisamide in Myoclonic Seizures associated with Idi... | |||||||||||||
Medical condition: myoclonic seizures in idiopathic generalised epilepsy (IGE). | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001605-42 | Sponsor Protocol Number: 20060317 | Start Date*: 2008-07-14 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Multicenter, Double-Blind, 3-Arm, Phase 1b/2 Study in Subjects with Unresectable Locally Advanced or Metastatic Gastric or Esophagogastric Junction Adenocarcinoma to Evaluate the Safety and Effi... | |||||||||||||
Medical condition: Unrespectable locally advanced or metastatic gastric or esophagogastric unction adenocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) IT (Prematurely Ended) GR (Completed) BE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005171-95 | Sponsor Protocol Number: MESOT-TREM-2008 | Start Date*: 2008-09-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
Full Title: A SECOND-LINE, SINGLE ARM, PHASE II CLINICAL STUDY WITH TREMELIMUMAB, A FULLY HUMANIZED ANTI-CTLA-4 MONOCLONAL ANTIBODY, AS MONOTHERAPY IN PATIENTS WITH UNRESECTABLE MALIGNANT MESOTHELIOMA | |||||||||||||
Medical condition: PATIENTS WITH UNRESECTABLE MALIGNANT MESOTHELIOMA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003059-56 | Sponsor Protocol Number: ICAND | Start Date*: 2008-07-29 | |||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO "CARLO BESTA" | |||||||||||||
Full Title: Phase II trial to assess safety and efficacy of Iron chelating agent Deferiprone in patients with Pantothenate Kinase-Associated Neurodegeneration ICAND Trial | |||||||||||||
Medical condition: PKAN | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002841-21 | Sponsor Protocol Number: H6D-MC-LVHJ(a) | Start Date*: 2008-10-28 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Parallel-Design, Multinational Study to Evaluate the Efficacy and Safety of Daily Tadalafil for 12 Weeks in Men With Signs and Symptoms of B... | |||||||||||||
Medical condition: Benign Prostatic Hyperplasia (BPH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000306-36 | Sponsor Protocol Number: 2008-000306-36 | Start Date*: 2009-04-16 | ||||||||||||||||||||||||||
Sponsor Name:Region Skåne | ||||||||||||||||||||||||||||
Full Title: Nexavar in Relapsed Peripheral T-cell Non-Hodgkins Lymphoma | ||||||||||||||||||||||||||||
Medical condition: Patients >18 years with relapsed or resitant peripheral T-cell lymphoma, defined as having progressed on 1st or 2nd line therapy. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004223-27 | Sponsor Protocol Number: GEMCAD-0802 | Start Date*: 2008-10-29 | |||||||||||
Sponsor Name:GEMCAD | |||||||||||||
Full Title: Estudio fase II, de la combinación de Oxaliplatino y Sorafenib en pacientes con Adenocarcinoma gástrico o de la unión gastroesofágica localmente avanzado o metastásico, en progresión tras un esque... | |||||||||||||
Medical condition: CANCER GASTRICO | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002315-92 | Sponsor Protocol Number: 12013A | Start Date*: 2008-11-12 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: A 52-week, randomised, double-blind, placebo-controlled, parallel-group, safety, tolerability and efficacy study of nalmefene, as needed use, in patients with alcohol dependence | |||||||||||||
Medical condition: Alcohol dependence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SK (Completed) EE (Completed) GB (Completed) LV (Completed) HU (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004626-17 | Sponsor Protocol Number: 1101/08 | Start Date*: 2009-03-23 | ||||||||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | ||||||||||||||||||
Full Title: Anti-inflammatory and Anti-platelet effect of Clopidogrel and Aspirin vs Aspirin alone in Symptomatic Polyvascular disease and in patients with multiple recurrent cardiovascular events. | ||||||||||||||||||
Medical condition: Polyvascular disease and in patients with multiple recurrent cardiovascular events. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005660-13 | Sponsor Protocol Number: He-08-01 | Start Date*: 2008-12-11 | |||||||||||
Sponsor Name:BOC Ltd. | |||||||||||||
Full Title: COPD exacerbation - Heliox Therapy - Assessment Heliox vs. Medical Air in Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Pilot Randomised Controlled Trial | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002447-16 | Sponsor Protocol Number: 111482 | Start Date*: 2008-11-10 | |||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled Phase III study to assess the efficacy of recMAGE-A3 + AS15 ASCI as adjuvant therapy in patients with MAGE-A3 positive resected stage III melanoma | |||||||||||||
Medical condition: Patients with histologically proven stage IIIB or IIIC cutaneous melanoma with macroscopic lymph node involvement suitable for surgical resection. Macroscopic lymph node involvement is defined as c... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) DE (Prematurely Ended) BE (Completed) CZ (Prematurely Ended) FR (Completed) NL (Prematurely Ended) IT (Prematurely Ended) SE (Prematurely Ended) EE (Prematurely Ended) ES (Completed) AT (Prematurely Ended) GR (Prematurely Ended) BG (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006435-13 | Sponsor Protocol Number: 5065 | Start Date*: 2008-10-15 | ||||||||||||||||
Sponsor Name:University of Southampton | ||||||||||||||||||
Full Title: GRACE (Genomics to combat Resistance against Antibiotics in Community-acquired LRTI in Europe).Workpackage 10: Antibiotic Trial One | ||||||||||||||||||
Medical condition: Lower Respiratory Tract Infection | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012035-15 | Sponsor Protocol Number: CL2-38093-009 | Start Date*: 2009-10-07 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Safety and efficacy of S 38093 and donepezil, during 4 weeks, in patients with mild to moderate Alzheimer's Disease. An international, multi-centre, randomised, double-blind, placebo controlled, ph... | |||||||||||||
Medical condition: Alzheimer's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002160-34 | Sponsor Protocol Number: ELP1020 | Start Date*: 2008-10-24 | |||||||||||
Sponsor Name:EleosInc Limited | |||||||||||||
Full Title: Aezea™ (cenersen) in combination with chemotherapy for the treatment of refractory acute myelogenous leukemia subjects ≥ 55 years of age with inadequate response to a single frontline induction cou... | |||||||||||||
Medical condition: Refractory acute myeloid leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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