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Data from EMERGE demonstrated a statistically significant change across all four primary and secondary clinical endpoints. ENGAGE did not meet its primary or secondary endpoints. A dose- and time-dependent reduction in pathophysiological markers of Alzheimer's disease was observed in both trials.
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Samantha Budd Haeberlein
Biogen (United States)
Paul Aisen
University College Dublin
Frederik Barkhof
University of Siena
The Journal of Prevention of Alzheimer s Disease
University College London
Inserm
University of Southern California
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Haeberlein et al. (Tue,) studied this question.
synapsesocial.com/papers/69d74ebff07a12db70b8a95f — DOI: https://doi.org/10.14283/jpad.2022.30
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