drugset / Trial / NCT04202354
Study of ARO-HSD in Healthy Volunteers and Patients With Non-Alcoholic Steatohepatitis (NASH) or Suspected NASH
RandomizedSequentialQuadruple-blindTreatment
Summary
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics of single and multiple doses of ARO-HSD in healthy adult volunteers and in patients with NASH or suspected NASH.
Timeline
- Start
- 2020-03-03
- Primary completion
- 2021-09-03
- Completion
- 2021-09-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ARO-HSD | Small interfering RNA (siRNA) | 25 mg | Subcutaneous |
| Subject | ARO-HSD | Small interfering RNA (siRNA) | 50 mg | Subcutaneous |
| Subject | ARO-HSD | Small interfering RNA (siRNA) | 100 mg | Subcutaneous |
| Subject | ARO-HSD | Small interfering RNA (siRNA) | 200 mg | Subcutaneous |