A Study to Investigate the Safety, Tolerability and Pharmacokinetics of Multiple Doses of MT-8554 in Female Subjects Experiencing Vasomotor Symptoms
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Enrollment
24
Investigational center
City Name, Germany
Safety and Tolerability as measured by vital signs
Time frame: Up to Day 21
Safety and Tolerability as measured by number of participants with adverse events
Time frame: Up to Day 21
Plasma concentration of MT-8554 after dosing
Time frame: Up to Day 15
Change from baseline in core body temperature
Time frame: Up to Day 14
Frequency of Vasomotor Symptoms
Time frame: Up to Day 15
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