The purpose of this study is to determine the toxicity, tolerability and safety of single ascending doses of AX-024.HCl in healthy male subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Enrollment
18
Simbec Research Ltd
Merthyr Tydfil, Cardiff Road, United Kingdom
Number of Participants with Serious and Non-Serious Adverse Events
Time frame: Over a 72 hours period and 7 days after last dose
Area Under the Concentration-Time Curve
Time frame: Over a 72 hours period post dose
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