Official Title: A Phase 1b2 Multicenter Adaptive Double-blind Randomized Placebo-controlled Study to Assess the Safety Tolerability Immunogenicity and Pharmacodynamic Effects of ACI-24060 in Subjects With Prodromal Alzheimers Disease and in Adults With Down Syndrome ABATE
Status: RECRUITING
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to assess the safety tolerability immunogenicity and pharmacodynamic effects of ACI-24060 in subjects with prodromal Alzheimers disease and in non-demented adults with Down syndrome
Detailed Description: This phase 1b2 study will be in 2 parts Study Part 1 will involve subjects with prodromal Alzheimers disease Study Part 2 will involve subjects with Down syndrome
Study Oversight
Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID
Type
Domain
Link
2021-006195-17
EUDRACT_NUMBER
None
None
2022-500069-29-00
OTHER
European Union Drug Regulatory Authorities Clinical Trial System