drugset / Trial / NCT02786537

Study of Oral Treatments for Hepatitis C

NCT02786537

RandomizedParallel-groupOpen-labelTreatment

Summary

Phase 1 of this study compared the effectiveness of 3 approved DAA (direct-acting antiviral) HCV treatment regimens to learn whether they worked equally well under real-world conditions. Phase 2 of this study began early 2017 with removal of 1 DAA regimen, limiting randomization to just 2 FDA approved DAA regimens. Patients receiving HCV therapy in community and academic clinics were offered the opportunity to consent to be randomly assigned to one of three (phase 1) or one of two (phase 2) regimens and observed for outcomes. Once randomized, all medical care, laboratory testing, and any disease or side effect management were assumed by usual care conditions, and patient-reported outcomes were collected outside clinic in keeping with pragmatic design principles.

Timeline

Start
2016-06
Primary completion
2019-06-13
Completion
2020-09-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ribavirin Small molecule 200 mg
Comparator Ritonavir Other / unclassified 50 mg Oral
Comparator SOF/LDV Unknown 90 mg Oral
Comparator SOF/LDV Unknown 400 mg Oral
Comparator dasabuvir Small molecule 250 mg Oral
Comparator elbasvir/grazoprevir Unknown 50 mg
Comparator elbasvir/grazoprevir Unknown 100 mg
Comparator ombitasvir Small molecule 12.5 mg Oral
Comparator paritaprevir Small molecule 75 mg Oral