The purpose of this study is to see how ALS-008176 is taken up, broken down, and removed from the body.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
12
Quotient Clinical
Nottingham, United Kingdom
Absolute Bioavailability
Determination of the absolute bioavailability of ALS-008112
Time frame: Days 1-8
Mass Balance
Mass balance recovery of total radioactivity in urine, faeces, and urine and faeces combined: amount excreted (Ae) and Ae as a percentage of the administered dose (%Ae)
Time frame: Days 1 - 14
Safety
Safety will be evaluated by recording adverse events, clinical laboratory results, vital signs, 12-lead ECGs, physical exams, etc.
Time frame: Days 1-14
To investigate the metabolic profile of [14C] - ALS-008176
To investigate the metabolic profile of \[14C\] - ALS-008176 in plasma, urine and faeces following oral administration in healthy male subjects (Part 2 only)
Time frame: Days 1-14
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