A Follow-up Evaluation Study of PRI-724-1101
NCT02828254 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 8
Last updated 2022-07-07
Summary
The purpose of this study To evaluate the safety and efficacy of PRI-724 administration in patients with cirrhosis due to hepatitis C by 12-month follow-up.
Conditions
- Hepatitis C Virus-infected Cirrhosis
Interventions
- DRUG
-
PRI-724
Sponsors & Collaborators
-
Prism Pharma Co., Ltd.
collaborator INDUSTRY -
Japan Agency for Medical Research and Development
collaborator OTHER_GOV -
Komagome Hospital
lead OTHER
Principal Investigators
-
Kiminori Kimura, MD · Komagome Metropolitan Hospital
Eligibility
- Min Age
- 20 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-12-18
- Primary Completion
- 2017-03-27
- Completion
- 2018-01-31
Countries
- Japan
Study Locations
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