To investigate the safety and overall tolerability of co-administration two PDE5 inhibitors UK369,003 and sildenafil
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Enrollment
22
oral tablet, once a day
single oral dose on day 14 or day 17
single oral dose on day 14 or day 17
Pfizer Investigational Site
Singapore, Singapore
Safety and toleration assessed by non-leading questioning, incidence of adverse events and laboratory testing.
Time frame: hours
Incidence of postural hypotension.
Time frame: hours
Standing and supine pulse rate (PR) at each postdose time.
Time frame: hours
Standing systolic and diastolic blood pressure (BP) and supine systolic and diastolic BP at each postdose time.
Time frame: hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.