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Clinical Trials associated with HK-660SA randomized, double-blind, placebo-controlled, parallel group, 12 weeks, therapeutic exploratory phase 2 clinical study to evaluate the safety and efficacy of HK-660S in patients with Primary Sclerosing Cholangitis(PSC)
A Randomized, Double-blind, Placebo-controlled, Parallel Group, 12 Weeks, Therapeutic Exploratory Phase 2 Clinical Study to Evaluate the Safety and Efficacy of HK-660S in Patients With Primary Sclerosing Cholangitis (PSC)
The objective of this study is to evaluate the improvement of bile duct strictures following the administration of HK-660S in patients with Primary Sclerosing Cholangitis(PSC). Percentage of subjects who show improvement of severity of PSC as assessed by Magnetic Resonance Cholangiopancreatography(MRCP) at Week 12 from baseline, with improvement defined as a decrease of -1 or more in the MRCP and change of alkaline phosphatase(ALP) level will be assessed at Week 12 from baseline.
100 Clinical Results associated with HK-660S
100 Translational Medicine associated with HK-660S
100 Patents (Medical) associated with HK-660S
100 Deals associated with HK-660S