- ICH GCP
- EU 임상 시험 레지스트리
최신 시험
EudraCT Number: 2004-004933-32 | Sponsor Protocol Number: km 55/2004 – LORISTAH/CZ | Start Date: 2005-03-04 | ||||||
Sponsor Name: KRKA, d. d., Novo mesto | ||||||||
Full Title: Efficacy and safety of Lorista and Lorista H in the treatment of mild to moderate arterial hypertension | ||||||||
Medical condition: mild to moderate hypertension | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: CZ (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003734-34 | Sponsor Protocol Number: BT0800BEL001 | Start Date: 2005-03-03 | ||||||
Sponsor Name: Barrier Therapeutics nv | ||||||||
Full Title: A one-weel, randomized, double-blind, placebo-controlled pilot trial to evaluate oral R129160 (60 mg b.i.d.) on the alleviation of itch in atopic dermatitis patients | ||||||||
Medical condition: Atopic Dermatitis | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: BE (Ongoing) CZ (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-005012-80 | Sponsor Protocol Number: S245.4007 | Start Date: 2005-03-03 | ||||||
Sponsor Name: Solvay Pharmaceuticals GmbH | ||||||||
Full Title: Double-blind, multicenter, randomized, placebo-controlled, parallel-group study to investigate the effect of Creon 25 000 Minimicrospheres on body mass index (BMI) in patients after gastrectomy. | ||||||||
Medical condition: Patients atleast 18 years old with total or subtotal gastrektomy. | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: FI (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002344-99 | Sponsor Protocol Number: SKY0402-C-203 | Start Date: 2005-03-03 | |||||||||||
Sponsor Name: SkyePharma, Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Dose-Escalating/De-Escalating Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Sustained-Release Encapsulated Bupivacaine (SKY0402) ... | |||||||||||||
Medical condition: Pain following bunionectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004823-36 | Sponsor Protocol Number: AZ1-2004 | Start Date: 2005-03-03 | ||||||
Sponsor Name: daacro - diagnostic assessment and clinical research organization | ||||||||
Full Title: Effects of Alprazolam and Flupentixol on endocrine, autonomic and psychological parameters in the Trier Social Stress Test (TSST) | ||||||||
Medical condition: 69 healthy male subjects, age 18-45 undergo a laboratory stress test (TSST) | ||||||||
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Population Age: Adults | Gender: Male | |||||||
Trial protocol: DE (Completed) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004392-11 | Sponsor Protocol Number: ULg_GBM_04/1 | Start Date: 2005-03-03 | ||||||
Sponsor Name: Centre Hospitalier Universitaire de Liege | ||||||||
Full Title: Human phase 1/2 clinical study of the safety and efficacy of sulfasalazine as a therapy for recurrent or progressing high grade gliomas. | ||||||||
Medical condition: Recurrent or progressive high grade glioma, including gliobastoma, anaplastic astrocytoma and oligo-astrocytoma. | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: BE (Ongoing) | ||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004928-12 | Sponsor Protocol Number: VICER1 | Start Date: 2005-03-03 | ||||||
Sponsor Name: INO Therapeutics AB | ||||||||
Full Title: A pilot, unicenter, prospective, aleatorized, with parallel groups, controlled and open to evaluate the efficacy of the Nitric Oxide for Inhalation in the prevention of reperfusion in pulmonary donor | ||||||||
Medical condition: pulmonary graft dysfunction | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: ES (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2004-001332-23 | Sponsor Protocol Number: EORTC Study 08013 | Start Date: 2005-03-03 | |||||||||||
Sponsor Name: European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Phase II Study with Gefitinib (sequentially) following Gemcitabine/Cisplatin as induction regimen for patients with stage IIIA N2 NSCLC. | |||||||||||||
Medical condition: Advanced Non Small-Cell Lung Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000167-95 | Sponsor Protocol Number: Protocol F1J-MC-HMDI | Start Date: 2005-03-03 | ||||||
Sponsor Name: Eli Lilly and Company Limited | ||||||||
Full Title: Duloxetine Versus Placebo in the Prevention of Recurrence of Major Depressive Disorder | ||||||||
Medical condition: Major Depressive Disorder | ||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||
Trial protocol: SE (Completed) IT (Completed) DE (Completed) | ||||||||
Trial results: View results |
EudraCT Number: 2005-000127-42 | Sponsor Protocol Number: NRSily1 | Start Date: 2005-03-03 | ||||||
Sponsor Name: Medical University of Vienna | ||||||||
Full Title: Non Responder- STUDY: MULTICENTER STUDY TO EVALUATE THE EFFICACY OF SILYMARIN IN ADDITION TO COMBINATION-THERAPY WITH PEGYLATED INTERFERON ALFA 2A (PEG-IFN ALFA 2A) AND RIBAVIRIN IN PATIENTS WI... | ||||||||
Medical condition: HCV-patients, who have not responded to a previous therapy with INF or PEG-INF +/- Ribavirin. | ||||||||
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Population Age: Adults | Gender: Male, Female | |||||||
Trial protocol: AT (Completed) | ||||||||
Trial results: (No results available) |