- ICH GCP
- EU Clinical Trials Registry
Latest Trials
EudraCT Number: 2005-001614-41 | Sponsor Protocol Number: CSTI571BIT06 | Start Date: 2005-05-19 | |||||||||||
Sponsor Name: NOVARTIS FARMA | |||||||||||||
Full Title: OPEN-LABEL TRIAL OF GLIVEC IMATINIB MESYLATE IN PATIENTS WITH REFRACTORY DESMOPLASTIC SMALL ROUND CELL TUMORS DSRCT EXPRESSING A MOLECULAR TARGET OF GLIVEC PDGF-R AND/OR C-KIT | |||||||||||||
Medical condition: TREATMENT OF PATIENTS WITH REFRACTORY DESMOPLASTIC SMALL ROUND CELL TUMORS DSRCT . | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004042-41 | Sponsor Protocol Number: D5890C00003 | Start Date: 2005-05-18 | |||||||||||
Sponsor Name: AstraZeneca AB | |||||||||||||
Full Title: A comparison of the inflammatory control of asthma provided by one inhalation of Symbicort® Turbuhaler® 160/4.5 µg/inhalation b.i.d. plus as-needed versus one inhalation of Symbicort® Turbuhaler® 3... | |||||||||||||
Medical condition: This is a Phase IIIB trial to be conducted in adult asthmatic patients. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) GB (Completed) ES (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000897-38 | Sponsor Protocol Number: DAM/001/05 | Start Date: 2005-05-18 | |||||||||||
Sponsor Name: FARMACEUTICI DAMOR | |||||||||||||
Full Title: Open-label, controlled, randomised, multicentre, parallel group clinical trial of efficacy and tolerability of Fitostimoline soaked gauzes, Fitostimoline cream and Citrizan gel in the topical... | |||||||||||||
Medical condition: Topical treatment of second-degree superficial cutaneous burns | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003975-35 | Sponsor Protocol Number: 750201.01.014 | Start Date: 2005-05-18 | ||||||
Sponsor Name: Dr. Willmar Schwabe GmbH & Co. KG | ||||||||
Full Title: Multi-center, double-blind, placebo-controlled, randomized phase III study to prove the efficacy, safety and tolerability of Lavender oil WS 1265 (Lavandula angustifolia) in patients with restlessn... | ||||||||
Medical condition: restlessness and sleep disturbances MedDRA Code for RESTLESSNESS: 10038743 MedDRA Code für SLEEP DISTURBANCES: 10040997 | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2005-001371-35 | Sponsor Protocol Number: S241-GB-03 | Start Date: 2005-05-18 | |||||||||||
Sponsor Name: Stiefel Laboratories Maidenhead Ltd (commonly known as Stiefel Laboratories International Division) | |||||||||||||
Full Title: A Double-Blind, Placebo Controlled, Half-Head Design, CPO Solution Dose Ranging-Finding Study in Patients with Seborrhoeic Dermatitis of the Scalp | |||||||||||||
Medical condition: Seborrhoeic dermatitis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000192-17 | Sponsor Protocol Number: GO-80, V1 18 Mar 05 | Start Date: 2005-05-18 | ||||||
Sponsor Name: Barts & The London NHS Trust | ||||||||
Full Title: Gemcitabine and Oxaliplatin in the treatment of locally advanced or metastatic transitional cell carcinoma of the urinary tract in patients with impaired renal function and patients who have progr... | ||||||||
Medical condition: Locally advanced or metastatic transitional cell carcinoma of the urinary tract | ||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||
Trial protocol: GB (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2005-000685-39 | Sponsor Protocol Number: 2005-1 | Start Date: 2005-05-18 | ||||||
Sponsor Name: Universitetssjukhuset Örebro | ||||||||
Full Title: Postoperativ smärtlindring och mobilisering efter per- och postoperativ injektion av ropivakin, ketorolak och adrenalin givet i operationsområdet, infiltrativt och i knäleden, vid enkammarknäplasti... | ||||||||
Medical condition: Post-operativ smärta efter enkammarknäplastikoperation, s k miniknä | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-005122-45 | Sponsor Protocol Number: D1441L00032 | Start Date: 2005-05-18 | ||||||
Sponsor Name: AstraZeneca GmbH | ||||||||
Full Title: RACE : Rapid Dose Escalation of Quetiapine versus Conventional Escalation in the Treatment of Patients with Acute Schizophrenia – a Multicentre, Double-blind, Parallel group, Randomized Study | ||||||||
Medical condition: Patients hospitalised with a DSM-IV diagnosis of schizophrenia showing acute agitation and psychosis | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2005-000535-18 | Sponsor Protocol Number: ML17632 | Start Date: 2005-05-18 | ||||||
Sponsor Name: Roche Pharma (Schweiz) AG | ||||||||
Full Title: Prospective, multicenter study to evaluate the renal safety of 6 mg ibandronic acid infusions over 15 min or 60 min in patients with metastatic bone disease due to breast cancer. | ||||||||
Medical condition: The target population for this trial are female patients with primary breast cancer with metastatic bone disease. | ||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000959-15 | Sponsor Protocol Number: HOE901/4057 | Start Date: 2005-05-17 | ||||||
Sponsor Name: sanofi-aventis | ||||||||
Full Title: A multicenter clinical trial to evaluate quality of life in patients with Type 2 diabetes before and after changing therapy to a combination of insulin glargine and oral antidiabetic drugs in a rea... | ||||||||
Medical condition: Patients with Type 2 diabetes inadequately controlled on a combination of highest tolerable dose of oral antidiabetic drugs (OAD) + neutral protamine hagedorn (NPH) insulin for more than 3 months | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Completed) | ||||||||
Trial results: View results |