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Ongoing Chronic Hepatitis (HCV) Test and Treat Utilizing Simplified HCV Patient Education

Clinical Trial Details

This is a research study for men and women who are 18 years of age or older with ongoing chronic hepatitis (HCV) and are enrolled in a drug treatment program.
   
The purpose of this research study is to test and treat strategy with simplified video-based patient education versus standard of care referral with Health Care Provider (HCP) delivered patient education. This research study will also assess point of care Cepheid Viremia (RNA) test as compared to standardized laboratory HCV assessments.
   
This research study will use drug called glecaprevir/pibrentasvir (G/P). It contains two drugs for treating HCV in one pill. G/P belongs to a group of drugs called direct-acting antiviral agents (DAAs). G/P prevent HCV from multiplying and spreading in the human body. 
 
G/P is approved by the United States of America Food and Drug Administration (USA FDA) for the treatment of chronic hepatitis without or with cirrhosis (scarring of the liver).

Participation in this study will last approximately 24 weeks.

Key Eligibility: 
  1. Men and women who are 18 years and older. Women of child-bearing potential must not be pregnant or breastfeeding in order to participate.
  2. Have been diagnosed with ongoing chronic hepatitis (HCV).
  3. Enrolled in a drug treatment program.

Detailed eligibility reviewed when you contact the study team.

Study contact by location

Upper East Side - Manhattan

Contact(s)

GI/ Hepatology
(646) 962-4040
GIHepResearch@med.cornell.edu

Primary Investigator(s)

Protocol ID(s)

Weill Cornell Medicine IRB #:

2106023705

ClinicalTrials.gov:

NCT05582681

Sponsor:

AbbVie B20-236

Status

Open to Enrollment

Age Group

Adult

Sponsor