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EudraCT Number: 2004-002694-22 Sponsor Protocol Number: R092670PSY3002 Start Date: 2005-02-07
Sponsor Name: Janssen-Cilag International N.V
Full Title: A Randomized, Double-Blind, Parallel Group Non-inferiority Study of Flexibly Dosed Paliperidone Palmitate(25, 50, 75, 100 mg eq) Administered Every 4 weeks and Flexibly Dosed Risperdal Consta (25, ...
Medical condition: schizophrenia
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: HU (Completed) AT (Completed) SE (Completed) CZ (Completed) DK (Completed) EE (Completed) ES (Completed) LT (Completed)
Trial results: View results

EudraCT Number: 2004-003745-40 Sponsor Protocol Number: GS-IT-131-0151 Start Date: 2005-02-07
Sponsor Name: GILEAD SCIENCES S.R.L.
Full Title: Phase II pilot study on safety of administration of 3mg/kg/day three times a week until day 22 (21 days after transplantation day) and 7 mg/kg weekly from day 29 to the end of treatment ( day 50-8t...
Medical condition: Fungal Infection High risk patients undergoing allogeneic stem-cell transplantation.
Disease: Version SOC Term Classification Code Term Level
14.1 10021881 - Infections and infestations 10017528 Fungal infectious disorders HLGT
Population Age: Adults Gender: Male, Female
Trial protocol: IT (Completed)
Trial results: View results
EudraCT Number: 2004-000730-37 Sponsor Protocol Number: 42603ATT3002 Start Date: 2005-02-07
Sponsor Name: Janssen-Cilag Medical Affairs EMEA
Full Title: A multicentre, randomised, double-blind, placebo-controlled, parallel group, dose-response phase III A study to evaluate safety and efficacy of Prolonged Release (PR) OROS methylphenidate (18, 36 a...
Medical condition: Attention Deficit Hyperactivity Disorder (ADHD)
Disease: Version SOC Term Classification Code Term Level
10003731
Population Age: Adults Gender: Male, Female
Trial protocol: SE (Completed) DK (Completed) CZ (Completed) FI (Completed)
Trial results: View results

EudraCT Number: 2004-005138-38 Sponsor Protocol Number: 2602-415 Start Date: 2005-02-07
Sponsor Name: Hvidovre Hospital
Full Title: Antibiotikaprofylakse ved vaginalplastik
Medical condition: Uterine prolapse grade I-II, cystocele and/or rectocele and/or enterocele grade I - IV and/or defects of the perineal body where there is medical indication for vaginal repair, but no indication fo...
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Female
Trial protocol: DK (Prematurely Ended)
Trial results: (No results available)
EudraCT Number: 2004-004090-29 Sponsor Protocol Number: AVD100521 Start Date: 2005-02-07
Sponsor Name: GlaxoSmithKline Research & Development Ltd [...] 1. GlaxoSmithKline Research & Development Ltd 2. GlaxoSmithKline R&D
Full Title: A Phase III, 18 Month, Multicenter, Randomized, Double-Blind, Active-Controlled Clinical Trial to Compare Rosiglitazone versus Glipizide on the Progression of Atherosclerosis in Subjects with Type ...
Medical condition: atherosclerosis in Type 2 Diabetes Mellitus patients with cardiovascular disease
Disease: Version SOC Term Classification Code Term Level
7.1 10003601 LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: SE (Completed) DE (Completed) LV (Completed) IT (Completed) CZ (Completed) GR (Completed) ES (Completed)
Trial results: View results

EudraCT Number: 2004-003839-31 Sponsor Protocol Number: ELN100226-CD354 Start Date: 2005-02-05
Sponsor Name: Elan Pharma Ltd.
Full Title: A Phase III, Multicenter, Open-Label, Long-Term Study of the Tolerability of Intravenous Natalizumab in Crohn's Disease Subjects Who Have Previously Participated in Natalizumab Crohn's Disease Stud...
Medical condition: Crohn's Disease (CD)
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DK (Completed)
Trial results: (No results available)
EudraCT Number: 2004-003215-22 Sponsor Protocol Number: vit-001 Start Date: 2005-02-04
Sponsor Name: Antonio Noda Cabrera
Full Title: Ensayo clínico piloto, unicéntrico, aleatorizado, doble ciego, con dos grupos paralelos sobre el efecto del Tacalcitol en pacientes afectos de vitíligo.
Medical condition: vitiligo vulgaris
Disease: Version SOC Term Classification Code Term Level
5.0 10040829 NEC
Population Age: Adults Gender: Male, Female
Trial protocol: ES (Ongoing)
Trial results: (No results available)

EudraCT Number: 2004-001664-50 Sponsor Protocol Number: DS/04/FTMS/01 Start Date: 2005-02-04
Sponsor Name: ITALFARMACO
Full Title: An open label, phase II multicentre evaluation of the activity and safety of fotemustine administered to patients with recurrent or progressive glioblastoma multiforme.
Medical condition: Recurrent or progressive glioblastoma multiforme after radiotherapy and adjuvant chemiotherapy.
Disease: Version SOC Term Classification Code Term Level
10018337 PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: IT (Completed)
Trial results: (No results available)
EudraCT Number: 2004-004893-96 Sponsor Protocol Number: cat 2; version1.2; Start Date: 2005-02-04
Sponsor Name: Hammersmith Hospitals NHS trust
Full Title: Randomised double-blind trial of combination antibiotic therapy in rheumatoid arthritis
Medical condition: Patients with medical diagnosis of Rheumatoid Arthritis
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: GB (Completed)
Trial results: View results

EudraCT Number: 2004-004077-29 Sponsor Protocol Number: 2004112 Start Date: 2005-02-04
Sponsor Name: Procter & Gamble Pharmaceuticals
Full Title: A Double-blind, Randomized, Multicenter, Active-control, 56-day Study with a 28-day Follow-up to Assess the Efficacy and Safety of RDP58 200 mg/day plus Mesalazine 2.4 g/day and RDP58 600 mg/day pl...
Medical condition: Ulcerative colitis is characterized by acute and chronic inflammatory changes to the mucosa and submucosa of the colon and rectum. Clinical presentations include increased stool frequency, bloody d...
Disease: Version SOC Term Classification Code Term Level
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed) LT (Completed) SK (Completed) CZ (Completed) GB (Completed)
Trial results: (No results available)
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