At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Randomized, Placebo-Controlled, Double-Blind Study of XPro1595 in Patients With Early Alzheimer's Disease With Biomarkers of Inflammation
In Brief
A Phase 2 clinical trial evaluating XPro1595 and Placebo for Alzheimer Disease and 9 related conditions. Completed, enrolled 207 participants across 41 sites in 8 countries.
Signals
Detailed Summary
The goal of this Phase 2 Alzheimer's study is to determine whether 1.0 mg/kg XPro1595 confers a benefit on cognition, function, and biomarkers of white matter and to further evaluate safety and tolerability. The objectives of this study are to determine the safety, tolerability, and efficacy of XPro1595 in patients with early ADi.
Study Details
Timeline
Arms & Interventions
1.0 mg/kg of XPro1595 will be administered via subcutaneous injection once a week for 23 weeks.
1.0 mg/kg of Placebo will be administered via subcutaneous injection once a week for 23 weeks.
Interventions
XPro1595 will be delivered by subcutaneous injection once a week
Placebo will be delivered by subcutaneous injection once a week