Antiviral Pharmacology and Adherence in Drug Users

HEPATITIS C Clinical Trial

Official title:

Antiviral Pharmacology and Adherence in Drug Users

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02573376
• Other study ID #: 15-0809
• Secondary ID: 1R01DA040499-01
• Status: Completed
• Phase: N/A
• Start date: November 2015
• Est. completion date: June 2021

Study information

• Verified date: March 2022
• Source: University of Colorado, Denver
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Approximately one half of all Americans living with Hepatitis C virus (HCV) are drug users, yet they are the least likely to receive HCV treatment. Drug users are presumed non-adherent and therefore denied potentially life-saving therapy. This assumption can only be confirmed or dispelled through prospective pharmacologic and adherence studies in this population. Such studies would be greatly enhanced by an objective, quantitative measure of adherence which does not currently exist in the HCV field. Through the work proposed in this application, sixty HIV/HCV co-infected drug users will be treated with direct acting antiviral agents (DAA) and randomized to receive directly observed DAA therapy (DOT) vs. no directly observed therapy (no-DOT). Patients randomized to no-DOT will have wirelessly observed therapy (WOT) which involves use of a portable medication dispenser that sends a signal to a server with the date and time when the dispenser is opened. In Aim 1, DAA concentrations will be compared in those randomized to DOT vs. no-DOT. DAA pharmacokinetics will also be defined accounting for clinical factors like degree of hepatic impairment and use of concomitant recreational and antiretroviral drugs. The goal is to quantify adherence in this population and the effect of variable adherence on drug concentrations. In Aim 2, DAA concentrations (plasma, cellular, hair) will be linked with adherence patterns identified using WOT and DOT. The goal is to identify a drug concentration biomarker that predicts adherence in this population. In Aim 3, the relationship between DAA adherence (as measured by WOT and DOT and drug concentrations) and rate of cure will be established. The goal is to define the degree of adherence needed for HCV cure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 73
• Est. completion date: June 2021
• Est. primary completion date: March 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Ability to give informed consent
• HIV-infected men and women
• Chronic HCV infection as documented by quantifiable HCV RNA
• HCV genotype 1, 4, 5, 6
• 18-70 years of age
• Willingness and ability to comply with study procedures, including DOT, WOT, and biweekly clinic visits
• Considered an active drug user by HCV provider and self-reported drug use within the past month

Exclusion Criteria:

• Glomerular filtration rate < 30 mL/min/1.73 m2
• Receipt of prior HCV treatment and radiographic, histologic, or clinical evidence of cirrhosis
• Decompensated liver disease (i.e., ascites, history of esophageal variceal bleeding, hepatic encephalopathy)
• Medications not recommended per the SOF/LDV prescribing information (e.g., tipranavir and other P-gp inducers, tenofovir disoproxil fumarate plus cobicistat, rosuvastatin, amiodarone)
• Any medical condition that in the opinion of the investigators will make it challenging to adhere to the study protocol, such as unstable heart disease or cancer
• Chronic Hepatitis B virus Infection
• For females, active pregnancy or any intent to become pregnant
• For both sexes, an unwillingness to use contraception during the study period
• On parole or impending sentencing

Related Conditions & MeSH terms

• Acquired Immunodeficiency Syndrome
• Hepatitis
• Hepatitis C
• HIV Infections
• Virus, Human Immunodeficiency

Intervention

Behavioral:
• Directly Observed Therapy

• Wirelessly Observed Therapy

Locations

Country	Name	City	State
United States	University of Colorado Anschutz Medical Campus	Aurora	Colorado

Sponsors (4)

Lead Sponsor	Collaborator
University of Colorado, Denver	Denver Health and Hospital Authority, Gilead Sciences, National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Compare each individual's modeled estimate of ledipasvir and metabolites of sofosbuvir (GS-331007 and GS-331007-TP) steady state concentrations (Css) from non-linear mixed effects modeling to Css in subjects receiving DOT vs. WOT.		12 weeks
Primary	Quantify GS-331007-TP concentrations in dried blood spots as a function of adherence (doses taken/doses prescribed).		12 weeks
Primary	Estimate the probability of HCV cure as a function of adherence using logistic regression.		24 weeks