The purpose of this study is to compare the efficacy and assess the safety of CD07805/47 gel 0.5% applied topically once daily for 29 days versus vehicle control, in subjects with moderate to severe chronic persistent vascular facial erythema
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Composite success on both CEA (Clinician Erythema Assessment ) and PSA (Patient Self Assessment)
2-grade improvement on both CEA and PSA at Hours 3, and 6 after Pre-dose (T0)on Day 29
Time frame: Day 29
Composite improvement on both CEA (Clinician Erythema Assessment ) and PSA (Patient Self Assessment)
1-grade improvement on both CEA and PSA at 30 minutes after pre-dose (T0) on Day 1
Time frame: Day 1
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