The purpose of the study is to examine the safety, tolerability, immunogenicity and pharmacokinetics of TTP4000 in subjects with Alzheimer's disease with mild cognitive impairment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Enrollment
8
Unnamed facility
Miami, Florida, United States
Unnamed facility
Durham, North Carolina, United States
Unnamed facility
High Point, North Carolina, United States
Number of participant with adverse events
Time frame: Day 0 to Day 84
Evaluation of participant plasma TTP4000 concentrations
Time frame: Day 0 to Day 84
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