drugset / Trial / NCT04375514
Study of ARO-ENaC in Healthy Volunteers and in Patients With Cystic Fibrosis
RandomizedSequentialQuadruple-blindTreatment
Summary
The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics (PK) of single doses of ARO-ENaC in healthy adult volunteers; and to evaluate the safety, tolerability, PK and efficacy of multiple doses of ARO-ENaC in patients with pulmonary cystic fibrosis.
Timeline
- Start
- 2020-07-30
- Primary completion
- 2021-05-09
- Completion
- 2022-05-13
Outcome
Outcome not reported
Stopped (Business): “Business decision”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ARO-ENaC | Unknown | 20 mg | Inhaled |
| Subject | ARO-ENaC | Unknown | 40 mg | Inhaled |
| Subject | ARO-ENaC | Unknown | 65 mg | Inhaled |
| Subject | ARO-ENaC | Unknown | 180 mg | Inhaled |