Efficacy and Safety of HK-660S in the Treatment of Primary Sclerosing Cholangitis

PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

105

Participants

Timeline

Start Date

August 18, 2025

Primary Completion Date

August 30, 2028

Study Completion Date

August 30, 2028

Conditions
Primary Sclerosing Cholangitis (PSC)
Interventions
DRUG

HK-660S 100mg

Administered orally

DRUG

HK-660S 200mg

Administered orally

DRUG

Placebo

Administered orally

Sponsors

Lead Sponsor

All Listed Sponsors
lead

CuromeBiosciences

INDUSTRY

NCT06975150 - Efficacy and Safety of HK-660S in the Treatment of Primary Sclerosing Cholangitis | Biotech Hunter | Biotech Hunter