TerminatedPhase 2NCT00602680
Effect on Cognitive Performance and Safety/Tolerability of SSR180711C in Mild Alzheimer's Disease
Studying Early-onset autosomal dominant Alzheimer disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Sanofi
- Principal Investigator
- Bruno DUBOIS, MDScientific Advisory Committee
- Intervention
- SSR180711C(drug)
- Enrollment
- 1 target
- Eligibility
- 55-90 years · All sexes
- Timeline
- 2008 – 2008
Study locations (1)
- Sanofi-Aventis Administrative Office, Paris, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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