This study will evaluate the safety, tolerability, and pharmacokinetics (PK) of ascending doses of GAP 134 administered as 6-day continuous IV infusions to healthy subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
25
Unnamed facility
Philadelphia, Pennsylvania, United States
Safety as determined by reported adverse events, laboratory test results, and ECGs
Time frame: 3 weeks
Pharmacokinetic parameters
Time frame: 9 days
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