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Sunday, January 01, 2017 3:13:31 PM
not all 25 Patients have reached 15 months yet
Results
Safety: ANAVEX2-73 demonstrated a favorable safety profile in AD patients. The most common AEs were grade 1. Positive unexpected therapeutic response events, such as improved mood, improved social engagement and increased independent activities were recorded.
Exploratory Efficacy: 15-months data demonstrate that ANAVEX2-73 preserves average MMSE and ADCS-ADL scores and shows benefits over baseline for Cogstate and QEEG/ERP.
Conclusion
The safety of ANAVEX2-73 was assessed and MTD was determined. Despite not optimal dosing, both cognitive and functional performance is sustained over at least 12 months, suggesting that the effect of the compound does not seem to worsen AD symptoms with repeated dosing. In a progressive degenerative disease this is considered a positive outcome. The data support further clinical development of ANAVEX2-73 and preparation for a larger confirmatory study is underway.
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