Clinical Trial to Evaluate the Efficacy and Safety of D064 and D701 Combination Therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
108
Experimental Group Subjects assigned to this group are treated with D064, D701, placebo of D012
Comparator Group Subjects assigned to this group are treated with D012, placebo of D064, placebo of D701
Samsung Medical Center
Seoul, South Korea
RECRUITINGChange from baseline in MSSBP
Compare experimental group with comparator group
Time frame: 8 weeks after drug administrations
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