drugset / Trial / NCT04202354

Study of ARO-HSD in Healthy Volunteers and Patients With Non-Alcoholic Steatohepatitis (NASH) or Suspected NASH

NCT04202354 ↗

Phase 1/2 Completed 50 enrolled Arrowhead Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
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