drugset / Trial / NCT03427710
A First In Human Study to Assess CiVi007 in Subjects With an Elevated LDL-Cholesterol Level
RandomizedParallel-groupDouble-blindTreatment
Summary
The primary objective of the study is to assess pharmacokinetics, dynamics, safety and tolerability of CiVi007 following single and multiple subcutaneous doses in subjects, including those on statin therapy
Timeline
- Start
- 2018-02-07
- Primary completion
- 2020-02-14
- Completion
- 2020-08-18
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CEPADACURSEN SODIUM | Unknown | — | Subcutaneous |