FRTX-02 is an orally-available, potent and selective DYRK1A inhibitor.
This is a randomized, placebo controlled, double blind study in healthy subjects and subjects with atopic dermatitis that is designed to assess the safety and tolerability of FRTX-02 capsules at single and multiple ascending doses. Safety will be assessed through vital signs, ECG, adverse events and safety laboratory tests. Pharmacokinetic and pharmacodynamic information will also be collected.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
89
DYRK-1A Inhibitor
Matching Placebo
Syneos Health Quebec
Montreal, Quebec, Canada
The number of participants with treatment-emergent adverse events.
Number of participants with adverse events, abnormal vital signs, abnormal ECG readings and abnormal laboratory test results.
Time frame: Up to Day 8 (Part A: SAD); up to Day 21 (Part B MAD); up to Day 43 (Part 2)
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