drugset / Trial / NCT06485245
Study to Evaluate Safety, Tolerability and Pharmacokinetics of CS060304 in Healthy and Elevated LDL-C Subjects
RandomizedParallel-groupDouble-blindTreatment
Summary
Study to Evaluate Safety, Tolerability and Pharmacokinetics of CS060304 in Healthy and Elevated LDL-C Subjects.
Timeline
- Start
- 2025-04-22
- Primary completion
- 2025-11-20
- Completion
- 2026-06-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CS060304 | Unknown | 0.2 mg | Oral |
| Subject | CS060304 | Unknown | 1 mg | Oral |
| Subject | CS060304 | Unknown | 2 mg | Oral |
| Subject | CS060304 | Unknown | 4 mg | Oral |
| Subject | CS060304 | Unknown | 5 mg | Oral |
| Subject | CS060304 | Unknown | 10 mg | Oral |
| Subject | CS060304 | Unknown | 20 mg | Oral |
| Subject | CS060304 | Unknown | 40 mg | Oral |
Indications
No indication recorded.