This study aims to assess the safety, tolerability, and pharmacokinetics (PK) of a single oral dose of surotomycin (CB-183,315) at ascending dose levels when given to healthy males and females.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
40
A single oral dose of either 0.5, 1, 2 or 4 g surotomycin in hard gelatin capsules
A single oral dose of placebo for surotomycin in hard gelatin capsules
Number of participants with an Adverse Event (AE)
Time frame: Up to Day 9
Number of participants who discontinued study due to an AE
Time frame: Up to Day 9
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