The APD791-002 study is designed primarily to evaluate the safety, tolerability, and pharmacokinetics of APD791 when administered for 7 days to healthy adult subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
50
APD791 or matching placebo in escalating doses
MDS Pharma Services
Lincoln, Nebraska, United States
Safety measures to include adverse events, vital signs, 12-lead ECGs, physical examinations, and clinical lab parameters
Time frame: Throughout study duration
Pharmacokinetic assessments
Time frame: Throughout study duration
Pharmacodynamic assessments (e.g., platelet function)
Time frame: Throughout study duration
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