Últimos testes


EudraCT Number: 2006-004632-69 Sponsor Protocol Number: P060309 Start Date: 2006-12-04
Sponsor Name: ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)
Full Title: Polymorphismes du gène codant pour le cytochrome 2C19 et réponse au clopidogrel chez le sujet sain
Medical condition: volontaire sain
Disease: Version SOC Term Classification Code Term Level
8.1 10043414 Therapeutic response decreased PT
Population Age: Adults Gender: Male
Trial protocol: FR (Ongoing)
Trial results: (No results available)

EudraCT Number: 2006-002060-26 Sponsor Protocol Number: 1401201 Start Date: 2006-12-04
Sponsor Name: Intendis GmbH
Full Title: A double-blind, randomized, vehicle-controlled, 6-week exploratory multicenter pilot study of the efficacy and safety of Azelaic Acid (AzA) 15% gel in the topical treatment of mild to moderate seb...
Medical condition: Patients with mild to moderate seborrheic dermatitis of the facial area and meeting the specific eligibility criteria
Disease: Version SOC Term Classification Code Term Level
8.1 10012488 Dermatitis seborrheic LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Completed)
Trial results: View results
EudraCT Number: 2006-004465-33 Sponsor Protocol Number: Cox052006 Start Date: 2006-12-04
Sponsor Name: Eero Kaasinen
Full Title: Oral Celecoxib combined with BCG instillation therapy in treatment of carcinoma in situ (CIS), TaG3 and T1 disease of urinary bladder
Medical condition: invasive bladder cancer
Disease: Version SOC Term Classification Code Term Level
8.1 10005014 Bladder carcinoma LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: FI (Ongoing)
Trial results: (No results available)

EudraCT Number: 2006-003577-27 Sponsor Protocol Number: A6631007 Start Date: 2006-12-01
Sponsor Name: Pfizer Luxembourg SARL Branch Office Estonia
Full Title: A 12-WEEK, PHASE 2A, RANDOMIZED, DOUBLE-BLIND, PLACEBOCONTROLLED STUDY TO INVESTIGATE THE SAFETY, PHARMACOKINETICS, AND EFFICACY OF PH-797804, ADMINISTERED ORALLY ONCE DAILY IN SUBJECTS WITH ACTIVE...
Medical condition: Treatment of rheumatoid arthritis (RA)
Disease: Version SOC Term Classification Code Term Level
8.1 10039073 Rheumatoid arthritis LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: EE (Completed) CZ (Completed) ES (Completed)
Trial results: View results
EudraCT Number: 2006-002361-39 Sponsor Protocol Number: BAY 79-4998 / 12331 Start Date: 2006-12-01
Sponsor Name: Bayer Vital GmbH
Full Title: A 4-week, open-label, multicenter, urodynamic pilot study to explore the efficacy, tolerability and safety of darifenacin (7.5 mg with up-titration to 15 mg) in patients with multiple sclerosis and...
Medical condition: Neurogenic overactive bladder disaese in patients with multiple sclerosis
Disease: Version SOC Term Classification Code Term Level
8.1 10059617 Overactive bladder LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: DE (Prematurely Ended)
Trial results: View results

EudraCT Number: 2006-003121-82 Sponsor Protocol Number: 4351 Start Date: 2006-12-01
Sponsor Name: University Hospital Southampton NHS Foundation Trust
Full Title: A prospective randomised open label trial of oxaliplatin / irinotecan plus fluorouracil versus oxaliplatin / irinotecan plus fluorouracil and cetuximab pre and post operatively in patients with res...
Medical condition: Colorectal Cancer Liver Metastasis
Disease: Version SOC Term Classification Code Term Level
14.1 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) 10052358 Colorectal cancer metastatic PT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: GB (Completed)
Trial results: (No results available)
EudraCT Number: 2005-001446-16 Sponsor Protocol Number: F05-TdI-301 Start Date: 2006-12-01
Sponsor Name: Sanofi Pasteur MSD
Full Title: Comparison of the immunogenicity and safety of a combined adsorbed low dose diphtheria, tetanus and inactivated poliomyelitis vaccine (REVAXIS®) with a combined diphtheria, tetanus and inactivated ...
Medical condition: Not applicable - Healthy volunteers - 6 year-old child
Disease: Version SOC Term Classification Code Term Level
Population Age: Children, Under 18 Gender: Male, Female
Trial protocol: FR (Completed)
Trial results: View results

EudraCT Number: 2006-001608-35 Sponsor Protocol Number: HUM-04-80 Start Date: 2006-12-01
Sponsor Name: Dr. Valérie gangji
Full Title: TREATMENT OF SCIATICA BY ADALIMUMAB INJECTION : A RANDOMIZED, DOUBLE BLIND CONTROLLED TRIAL.
Medical condition: To determine the efficacy of adalimumab in disc herniation-induced sciatica in a controlled randomised double blind pilot study.
Disease: Version SOC Term Classification Code Term Level
8.1 10039674 Sciatica LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: BE (Completed)
Trial results: (No results available)
EudraCT Number: 2006-002245-36 Sponsor Protocol Number: MKC-TI-103 Start Date: 2006-12-01
Sponsor Name: MannKind Corporation
Full Title: A Phase 3, 24-Week, Multi-Center, Open-Label, Randomized, Controlled Trial Comparing the Efficacy and Safety of Prandial Inhalation of Technosphere®/Insulin in Combination with Metformin or Technos...
Medical condition: Diabetes mellitus type II
Disease: Version SOC Term Classification Code Term Level
8.1 10012601 Diabetes mellitus LLT
Population Age: Adults, Elderly Gender: Male, Female
Trial protocol: CZ (Completed) ES (Ongoing)
Trial results: (No results available)

EudraCT Number: 2006-004510-41 Sponsor Protocol Number: GEICAM/2006-03 Start Date: 2006-12-01
Sponsor Name: GEICAM (GRUPO ESPAÑOL DE INVESTIGACION EN CANCER DE MAMA)
Full Title: ESTUDIO MULTICÉNTRICO FASE II DE DISTRIBUCIÓN ALEATORIA, PARA EVALUAR LA EFICACIA DE TRATAMIENTO NEOADYUVANTE SELECTIVO SEGÚN SUBTIPO INMUNOHISTOQUÍMICO EN CÁNCER DE MAMA HER2 NEGATIVO
Medical condition: Pacientes con cáncer de mama primario operable o localmente avanzado que presenten tumores mayores o iguales a 2 cm de diámetro o menores de 2 cm y afectación axilar.
Disease: Version SOC Term Classification Code Term Level
9.1 10057654 Breast cancer female PT
Population Age: Adults, Elderly Gender: Female
Trial protocol: ES (Ongoing)
Trial results: (No results available)
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