Asset profile
CKD-506
Unknown / undisclosed
Evidence outlook · lead readout
NCT04204603 · Rheumatoid Arthritis
The completed lead evidence is positive, with design limits that temper confidence — see the rationale below for exactly which.
NCT04204603: The study was randomized, double-blind, and placebo-controlled, with 122 participants assigned to placebo or one of three CKD-506 doses. Its primary clinical endpoint was change in DAS28(CRP) at week 12, but no results or statistical comparison were posted, so whether the endpoint was met is unknown.
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