Viewing Study NCT02881762



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Last Modification Date: 2024-10-26 @ 12:08 PM
Study NCT ID: NCT02881762
Status: COMPLETED
Last Update Posted: 2024-05-01
First Post: 2016-08-10

Brief Title: Maraviroc Efficacy for Hepatitis C
Sponsor: University of Maryland Baltimore
Organization: University of Maryland Baltimore

Study Overview

Official Title: A Pilot Study to Evaluate Anti-Hepatitis C Virus Effect of Maraviroc in Patients Co-infected With Human Immunodeficiency Virus HIV and Hepatitis C
Status: COMPLETED
Status Verified Date: 2023-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: MAVERIC
Brief Summary: This is a single-site longitudinal open-label interventional study for evaluating the effect of maraviroc on hepatitis C viral levels in patients infected with both hepatitis C and human immunodeficiency virus HIV and taking antiretroviral therapy for HIV
Detailed Description: Recently in-vitro studies experiments performed in a laboratory not on a person have demonstrated that maraviroc a medication that is used in human immunodeficiency HIV therapy appears to have significant hepatitis C antiviral effect comparable to sofosbuvir-a potent anti-hepatitis C medication In this study the investigators will evaluate the antiviral effect of maraviroc on hepatitis C virus in people infected with both hepatitis C and HIV and whom have never been treated for hepatitis with direct antiviral agents Participants will take maraviroc for 4 weeks in addition to their regular HIV antiretrovirals ART The investigators will measure the hepatitis C viral load before during and after the 4-week maraviroc time

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: None