drugset / Trial / NCT06573528
Study to Evaluate Safety, Tolerability and Pharmacokinetics of CS060380 in Healthy and Elevated LDL-C Subjects
RandomizedParallel-groupDouble-blindTreatment
Summary
Study to Evaluate Safety, Tolerability and Pharmacokinetics of CS060380 in Healthy and Elevated LDL-C Subjects.
Timeline
- Start
- 2024-09-03
- Primary completion
- 2025-05-09
- Completion
- 2025-05-21
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CS060380 | Unknown | 0.1 mg | Oral |
| Subject | CS060380 | Unknown | 0.15 mg | Oral |
| Subject | CS060380 | Unknown | 0.2 mg | Oral |
| Subject | CS060380 | Unknown | 0.25 mg | Oral |
| Subject | CS060380 | Unknown | 0.5 mg | Oral |
| Subject | CS060380 | Unknown | 0.75 mg | Oral |
| Subject | CS060380 | Unknown | 1 mg | Oral |
| Subject | CS060380 | Unknown | 2 mg | Oral |
| Subject | CS060380 | Unknown | 5 mg | Oral |
| Subject | CS060380 | Unknown | 10 mg | Oral |
Indications
No indication recorded.