This is a randomized, double-blind, vehicle-controlled, parallel-group comparison study to evaluate the safety and efficacy of Q301 Cream vs. vehicle in adult subjects with moderate to severe AD. Study drug (Q301 Cream or vehicle) will be administered topically twice a day for 8 consecutive weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
57
Unnamed facility
Denver, Colorado, United States
Unnamed facility
Berlin, New Jersey, United States
Unnamed facility
East Windsor, New Jersey, United States
Unnamed facility
Buffalo, New York, United States
Percentage of patients who have the IGA score of 0 or 1
Time frame: Week 8
Percent change from baseline on the VAS for pruritus
Time frame: Week 8
Percent change from baseline on the EASI
Time frame: Week 8
Percent change from baseline on the SCORAD
Time frame: Week 8
Percent change from baseline on the DLQI
Time frame: Week 8
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Unnamed facility
Winston-Salem, North Carolina, United States
Unnamed facility
Austin, Texas, United States
Unnamed facility
College Station, Texas, United States