Derniers essais


EudraCT Number: 2004-004148-34 Sponsor Protocol Number: B9E-XM-O435 Start Date: 2005-02-25
Sponsor Name: Dr. José Ignacio Chacón López-Muñiz
Full Title: ENSAYO EN FASE I/II DE LA COMBINACIÓN DE GEMCITABINA EN INFUSIÓN PROLONGADA Y PACLITAXEL ADMINISTRADOS DE FORMA QUINCENAL EN EL TRATAMIENTO DE PRIMERA LÍNEA DE PACIENTES CON CÁNCER DE MAMA AVANZADO
Medical condition: Cancer de mama avanzado
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Female
Trial protocol: ES (Ongoing)
Trial results: (No results available)

EudraCT Number: 2004-001060-50 Sponsor Protocol Number: CSPP100A2303 Start Date: 2005-02-25
Sponsor Name: Novartis Pharma Services AG
Full Title: An eight-week, randomized, double-blind, multi-center, active-controlled, parallel group study to evaluate the safety and efficacy of an aliskiren based regimen compared to a lisinopril based regim...
Medical condition: Hypertension
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: HU (Completed) ES (Completed)
Trial results: View results
EudraCT Number: 2005-000693-45 Sponsor Protocol Number: RCOMP05 Start Date: 2005-02-24
Sponsor Name: G.I.S.L. - GRUPPO ITALIANO STUDIO LINFOMI
Full Title: A phase II study for the treatment of patients with splenic marginal lymphoma with the combination of Cyclophosfamide, Vincristine, Liposomal Doxorubicin, Predinisone and Rituximab
Medical condition: Treatment of patients with newly diagnosed splenic marginal non Hodgkin lymphoma
Disease: Version SOC Term Classification Code Term Level
9.1 10062113 Splenic marginal zone lymphoma LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: IT (Completed)
Trial results: (No results available)

EudraCT Number: 2004-005101-29 Sponsor Protocol Number: KCH-MDS-04-1.0 Start Date: 2005-02-24
Sponsor Name: King's College Hospital NHS Foundation Trust [...] 1. King's College Hospital NHS Foundation Trust 2. King's College London
Full Title: THE EFFICACY AND SAFETY OF LENALIDOMIDE (Revlimid®) MONOTHERAPY IN RED BLOOD CELL TRANSFUSION DEPENDENT SUBJECTS WITH MYELODYSPLASTIC SYNDROME ASSOCIATED WITH A DEL (5q) CYTOGENETIC ABNORMALITY
Medical condition: Myelodysplastic Syndrome (MDS) associated with a Del (5q) cytogenetic abnormality
Disease: Version SOC Term Classification Code Term Level
16.0 100000004864 10067097 5q minus MDS LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: GB (Completed)
Trial results: View results
EudraCT Number: 2004-003866-13 Sponsor Protocol Number: CCR102881 Start Date: 2005-02-24
Sponsor Name: GlaxoSmithKline Research & Development Limited
Full Title: A phase IIb, 96 week, randomised, partially,double-blinded,multicentre,parallel group, repeat dose study to evaluate the safety, tolerability, pharmacokinetics and antiviral effect of GW873140 in c...
Medical condition: Treatment of HIV-1 infections
Disease: Version SOC Term Classification Code Term Level
Population Age: Adolescents, Adults Gender: Male, Female
Trial protocol: DE (Completed) IT (Prematurely Ended) GB (Prematurely Ended) BE (Completed) ES (Completed)
Trial results: View results

EudraCT Number: 2004-004160-67 Sponsor Protocol Number: Protocol F1J-MC-SBCT (a) Start Date: 2005-02-24
Sponsor Name: Eli Lilly and Company Limited
Full Title: Effect of Duloxetine on Valsalva Leak Point Pressure and Quantitative Rhabdosphincter Electromyography Measures in Women with Stress Urinary Incontinence
Medical condition: stress urinary incontinence
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Female
Trial protocol: GB (Completed) DK (Completed)
Trial results: View results
EudraCT Number: 2004-005074-24 Sponsor Protocol Number: Feb-02 Start Date: 2005-02-23
Sponsor Name: Febena Pharma GmbH
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF AN OINTMENT FORMULATION CONTAINING DEXAMETHASONE IN PATIENTS WITH RHINOSINUSITIS A CLINICAL PHASE IV ...
Medical condition: Patients with allergy-induced, non-infectious diseases of the nasal mucosa (e. g. hay fever) and the sinuses.
Disease: Version SOC Term Classification Code Term Level
12.1 10052106 Rhinosinusitis LLT
Population Age: Adults Gender: Male, Female
Trial protocol: DE (Ongoing)
Trial results: (No results available)

EudraCT Number: 2004-002020-17 Sponsor Protocol Number: 10908458 Start Date: 2005-02-23
Sponsor Name: Catalan Society of Family Medicine, represented by Dr Mariano de la Figuera Von Wichman and Gabriel
Full Title: ESTRATEGIAS PARA EL TRATAMIENTO DE LA HIPERTENSIÓN ARTERIAL. EVALUACIÓN DE UNA TERAPIA COMBINADA A DOSIS FIJAS (LOSARTÁN/HIDROCLOROTIAZIDA) vs MONOTERAPIA (ESTRATAAR). (STRATEGIES FOR THE TREATMENT...
Medical condition: Stage II arterial Hypertension
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: ES (Ongoing)
Trial results: (No results available)
EudraCT Number: 2004-004899-36 Sponsor Protocol Number: Mekos 05 P379/1 Start Date: 2005-02-23
Sponsor Name: Mekos Laboratories
Full Title: Clinical evaluation of the 3 allergens: Methyldibromoglutharonitrile, Parthenolide and Goldsodiumthiosulphate for "TRUE Test Panel 3" - a phase II, dose-response study.
Medical condition: Diagnosis of Allergic Contact Dermatitis.
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: SE (Ongoing) DK (Completed)
Trial results: (No results available)

EudraCT Number: 2004-000903-17 Sponsor Protocol Number: CN138-166 Start Date: 2005-02-23
Sponsor Name: Bristol-Myers Squibb International Corporation
Full Title: A Prospective, Multicenter, Open-Label Study to Evaluate the Effectiveness and the Effect on Cognitive Functioning of a Treatment with Aripiprazole in a Broad Range of Schizophrenic Patients
Medical condition: Schizophrenia
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: BE (Completed)
Trial results: View results
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