To evaluate the efficacy of CAD106 and CNP520 in participants at risk for the onset of Alzheimer’s disease

Mise à jour : Il y a 4 ans
Référence : EUCTR2015-002715-15

Femme et Homme

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Extrait

- To assess the effects of CAD106 and CNP520, respectively, vs. placebo on Time-to-event, with event defined as a diagnosis of MCI due to AD or dementia due to AD, whichever occurs first during the course of the study. - To assess the effects of CAD106 and CNP520, respectively, vs. placebo on cognition as measured by the change from Baseline to Month 60 in the APCC test score.


Critère d'inclusion

  • Alzheimer's disease