A Follow-up Evaluation Study of PRI-724-1101

NCT02828254 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 8

Last updated 2022-07-07

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02828254 on ClinicalTrials.gov