Preferences and feasibility of long‐acting technologies for treatment of hepatitis C virus in low‐ and middle‐income countries: A survey of providers and policymakers

Author:

Gupta Neil1ORCID,Swindells Susan2,Scarsi Kimberly K.3,Furl Renae2,Thomas David L.4,Weld Ethel D.45,Ofimboudem Joelle Dountio6,Desalegn Hailemichael7,Hamid Saeed8,Rosas Alethse de la Torre9,Miranda Angelica E.10,Owen Andrew11,Rannard Steve12,Hiebert Lindsey1,Sun Katherine1,Ward John W.1

Affiliation:

1. Coalition for Global Hepatitis Elimination The Task Force for Global Health Decatur Georgia USA

2. Section of Infectious Diseases, Department of Internal Medicine The University of Nebraska Medical Center Omaha Nebraska USA

3. Department of Pharmacy Practice and Science, College of Pharmacy The University of Nebraska Medical Center Omaha Nebraska USA

4. Division of Infectious Diseases, Department of Medicine The Johns Hopkins University School of Medicine Baltimore Maryland USA

5. Division of Clinical Pharmacology, Department of Medicine The Johns Hopkins University School of Medicine Baltimore Maryland USA

6. Treatment Action Group New York New York USA

7. Medical Department St. Paul's Hospital Millennium Medical College Addis Ababa Ethiopia

8. Section of Gastroenterology, Department of Medicine Aga Khan University Karachi Pakistan

9. Centro Nacional para la Prevención y el Control del VIH y el SIDA Mexico City Mexico

10. Post‐Graduation Program in Infectious Diseases Federal University of Espirito Santo Vitória Brazil

11. Department of Pharmacology and Therapeutics, Centre of Excellence in Long acting Therapeutics (CELT) University of Liverpool Liverpool UK

12. Department of Chemistry, Centre of Excellence in Long acting Therapeutics (CELT) University of Liverpool Liverpool UK

Abstract

AbstractLong‐acting technologies (LATs) for hepatitis C virus (HCV) are under development as a strategy to improve linkage to care, treatment adherence and outcomes. We conducted a survey of HCV treatment prescribers and HCV policymakers in low‐ and middle‐income countries (LMICs) regarding acceptability and feasibility of HCV LATs. We included one‐time intramuscular injection, subdermal implant and transdermal patch as potential LAT options. We surveyed participants regarding optimal health system and patient characteristics, concerns, potential barriers, overall feasibility and preferences for HCV LAT as compared to daily oral medication. Overall, 122 providers and 50 policymakers from 42 LMICs completed the survey. Among providers, 93% (113/122) expressed willingness to prescribe LAT and 72% (88/120) of providers preferred LAT if provided at comparable efficacy, safety and cost as current oral treatments. Of providers preferring HCV LAT to daily oral medication, 67% (59/88) preferred injection, 24% (21/88) preferred patch and 9% (8/88) preferred implant. Only 20% (24/122) would prescribe LAT if it were more costly than oral treatment. In regression analysis, no provider characteristics were associated with preference for LAT over oral treatment. Policymakers reported high likelihood that LAT would be included in treatment guidelines (42/50; 84%) and national drug formularies (39/50; 78%) if efficacy, safety and cost were similar to oral treatment. HCV LATs could advance progress to HCV elimination in LMICs by diversifying treatment options to improve treatment coverage and outcomes. Provider preferences from LMICs are a critical consideration in the development of HCV LATs to ensure its early and equitable availability in LMICs.

Publisher

Wiley

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