This study aims to assess the safety, tolerability, and pharmacokinetics (PK) of oral doses of surotomycin (CB-183,315) administered for 14 consecutive days in healthy males and females.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
30
Two oral doses of surotomycin in hard gelatin capsules totaling either 0.5, 1 or 2 g per day, for 14 days
Two oral doses of placebo for surotomycin in hard gelatin capsules per day, for 14 days
Number of participants with an Adverse Event (AE)
Time frame: Up to Day 21
Number of participants who discontinued study treatment due to an AE
Time frame: Up to Day 14
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