Status and phase
Conditions
Treatments
About
This study is a multicenter, randomized, double blind, Restasis-controlled non-inferiority, Phase III Study to evaluate the efficacy and safety of HU007 eye drops in patients With dry eye syndrome
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Male and Female who over 19 years old
Those who meet below criteria at least one of two eyes
Woman with no possibility of pregnancy or negative pregnancy test results at a screening visit, Women or men who have agreed to maintain at least one contraceptive method during study period
Those who could understand this study and agree to informed consent voluntarily
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
216 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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