CompletedPhase 1NCT06525311
A Study to Evaluate the Pharmacokinetics and Safety of K-808 (Pemafibrate) in Subjects With Primary Biliary Cholangitis With Compensated Cirrhosis and Without Cirrhosis.
Studying Primary biliary cholangitis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Kowa Research Institute, Inc.
- Principal Investigator
- Sara Neville, MDKowa Research Institute, Inc.
- Intervention
- K-808(drug)
- Enrollment
- 17 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2025
Study locations (10)
- Arizona Liver Health, Chandler, Arizona, United States
- Southern California Research Center, Inc, Coronado, California, United States
- Indiana University School of Medicine - Indianapolis, Indianapolis, Indiana, United States
- Houston Research Institute, Houston, Texas, United States
- Texas Liver Institute, San Antonio, Texas, United States
- Pinnacle Clinical Research, San Antonio, Texas, United States
- 303, Fukuoka, Japan
- 302, Kita-gun, Japan
- 304, Shinjuku-ku, Japan
- 301, Yufu, Japan
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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