Clinical Trial to Evaluate the Efficacy and Safety of CKD-342
A Randomized, Double-blind, Active-controlled, Multicenter phase 3 Clinical trial to evaluate the Efficacy and Safety of Concomitant Mometasone furoate and Levocabastine HCl in Perennial Allergic Rhinitis patients
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
459
treatment for 4 weeks after randomization
treatment for 4 weeks after randomization
treatment for 4 weeks after randomization
Samsung Medical Center
Irwon-dong, Gangnam-gu, Seoul, South Korea
change in rTNSS from baseline
Time frame: up to week 4
change in rTNSS from baseline
Time frame: up to week 2
change in AM rTNSS and PM rTNSS from baseline
Time frame: 2 weeks and 4 weeks after the baseline assessment
Physician assessed overall nasal symptom from baseline
Time frame: 2 weeks and 4 weeks after the basline assessment
change from baseline in RQLQ
Time frame: 2 weeks and 4 weeks after the baseline assessment
Changing in 4 nasal symptom score (sneezing, runny nose, nasal congestion, itchy nose) from baseline
Time frame: 2 weeks and 4 weeks after the basline assessment
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