A Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SYH2053

PHASE1CompletedINTERVENTIONAL
Enrollment

39

Participants

Timeline

Start Date

January 8, 2024

Primary Completion Date

December 23, 2024

Study Completion Date

March 25, 2025

Conditions
Hyperlipemia
Interventions
DRUG

SYH2053

subcutaneous injection

DRUG

Placebo

subcutaneous injection

Trial Locations (1)

Unknown

10 Chedaogou Rd.,Haidian District, Beijing, China, Beijing

All Listed Sponsors
lead

CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.

INDUSTRY

NCT06229548 - A Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SYH2053 | Biotech Hunter | Biotech Hunter