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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |