This is a Phase 2, multicenter, open-label, single-arm, sequential cohort study to be conducted in up to 30 subjects. The study will evaluate subjects undergoing primary, elective, off-pump CABG surgery with median sternotomy.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Masking
NONE
Enrollment
30
NU172 administered IV bolus followed by continuous infusion during CABG surgery
Safety and efficacy of NU172 in patients undergoing off-pump CABG surgery
Time frame: 30 day follow-up visit
Evaluate the pharmacokinetic (PK)profile of NU172 in patients undergoing off-pump CABG surgery
Time frame: 24 hours
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