WHO ICTRP trial

Estudio internacional, multicéntrico, aleatorizado, doble ciego, con grupos…

EUCTR2010-022596-64-ES · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2010-022596-64-ES
Public title Estudio internacional, multicéntrico, aleatorizado, doble ciego, con grupos paralelos y controlado con placebo del efecto sobre la función cognitiva, la seguridad y la tolerabilidad de SAR110894D, administrado en dosis de 0,5 mg, 2 mg y 5 mg/día durante 24 semanas a pacientes con enfermedad de Alzheimer leve o moderada que reciben tratamiento estable con donepezilo__________________A multinational, multicenter, randomized, double-blind, parallel-group, placebo-controlled study of the effect on cognitive performance, safety, and tolerability of SAR110894D at the doses of 0.5 mg, 2 mg, and 5 mg/day for 24 weeks in patients with mild to moderate Alzheimer's Disease on stable donepezil therapy
Scientific title Estudio internacional, multicéntrico, aleatorizado, doble ciego, con grupos paralelos y controlado con placebo del efecto sobre la función cognitiva, la seguridad y la tolerabilidad de SAR110894D, administrado en dosis de 0,5 mg, 2 mg y 5 mg/día durante 24 semanas a pacientes con enfermedad de…
Primary sponsor sanofi-aventis recherche & développement
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Countries Portugal;Spain;Germany;Italy
Conditions Demencia tipo enfermedad de Alzheimer_______________ Dementia Alzheimer's type MedDRA version: 12.1 Level: LLT Classification code 10012271 Term: Dementia Alzheimer's type
Interventions Product Code: SAR110894D Pharmaceutical Form: Capsule, hard Current Sponsor code: SAR110894D Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 0.5- Pharmaceutical form of the placebo: Capsule, hard Route of…
Registration date Nov 17, 2010
Target size 520
Secondary IDs DRI10734
Registry page clinicaltrialsregister.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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