drugset / Trial / NCT02956850

A Study in Healthy Volunteers and in Participants With Chronic Hepatitis B to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Multiple Doses of RO7020531

NCT02956850

Phase 1 Completed 160 enrolled Hoffmann-La Roche
RandomizedParallel-groupDouble-blindTreatment

Summary

This sponsor-open, investigator- and participant-blinded, multi-center study will assess the safety, tolerability, pharmacokinetics and pharmacodynamics of RO7020531 in healthy participants and in participants with chronic hepatitis B. Part I will be conducted in two portions: Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) which will include only healthy volunteers. Part II will commence after completion of the MAD portion of Part I and will include only Chronic Hepatitis B (CHB) participants.

Timeline

Start
2016-12-12
Primary completion
2021-06-15
Completion
2021-06-15

Drugs

EvaluationDrugModalityDoseRoute
Subject RUZOTOLIMOD Small molecule 3 mg Oral
Subject RUZOTOLIMOD Small molecule 10 mg Oral
Subject RUZOTOLIMOD Small molecule 20 mg Oral
Subject RUZOTOLIMOD Small molecule 40 mg Oral
Subject RUZOTOLIMOD Small molecule 60 mg Oral
Subject RUZOTOLIMOD Small molecule 100 mg Oral
Subject RUZOTOLIMOD Small molecule 140 mg Oral
Subject RUZOTOLIMOD Small molecule 150 mg Oral
Subject RUZOTOLIMOD Small molecule 170 mg Oral