A Phase 1, First-in-human, Randomized, Double-blind, Placebo-controlled, Single and Multiple Ascending Dose Study in Healthy Adults and Open-label Single Dose Study in Patients with Alzheimer's Disease to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of VG-3927.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
115
K2 Medical Research
Maitland, Florida, United States
Clinical Pharmacology of Miami
Miami, Florida, United States
Nucleus Network
Melbourne, Australia
Adverse Events
To evaluate the safety and tolerability of VG-3927
Time frame: 28 days post last dose
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