The purpose of this study is to determine the pharmacokinetics (PK) and to assess safety and tolerability of a single dose of ASP3291 in subjects with ulcerative colitis.
After an 11-day screening period, subjects check into a clinic, are dosed on Day 1 and stay in the clinic for 4 days to monitor pharmacokinetic and safety parameters.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
QUADRUPLE
Enrollment
16
Advanced Clinical Research Institute
Anaheim, California, United States
SNBL Clinical Pharmacology Center
Baltimore, Maryland, United States
Clinical Trials of Texas, Inc.
San Antonio, Texas, United States
Pharmacokinetic assessment through analysis of blood, fecal and urine samples
Time frame: Up to Day 4
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