Efficacy and safety of HCP1102 capsule : A randomized, double-blind, active-controlled, multicenter phase 3 clinical trial.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
228
Coadministration of HCP1102 with HGP0711 Placebo for 4-week
Coadministration of HCP1102 Placebo with HGP0711 for 4-week
Soon Chun Hyang University Hospital Bucheon
Bucheon-si, Gyunggi -do, South Korea
Change of Mean Daytime Nasal Symptom Score
Time frame: base line, 3-4week(2weeks)
Change of Mean Daytime Nasal Symptom Score
Time frame: base line, 1-2week(2weeks), 3-4week(2weeks)
Change of Runny nose (Mean Daytime Nasal Symptom Score)
Time frame: base line, 1-2week(2weeks), 3-4week(2weeks)
Change of Mean Nighttime Nasal Symptom Score
Time frame: base line, 1-2week(2weeks), 3-4week(2weeks)
Change of Mean Composite Symptom Score
Time frame: base line, 1-2week(2weeks), 3-4week(2weeks)
Change of sneezing (Mean Daytime Nasal Symptom Score)
Time frame: base line, 1-2week(2weeks), 3-4week(2weeks)
Change of pruritus (Mean Daytime Nasal Symptom Score)
Time frame: base line, 1-2week(2weeks), 3-4week(2weeks)
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.