Pharmacokinetics, Pharmacodynamics Profile and Tolerance of HRS-9231 in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

June 5, 2024

Primary Completion Date

October 6, 2024

Study Completion Date

October 6, 2024

Conditions
Healthy Volunteers
Interventions
DRUG

HRS-9231

HRS-9231 was administered intravenously;

DRUG

Placebo

Placebo was administered intravenously.

Trial Locations (1)

215006

The First Affiliated Hospital of Soochow University, Suzhou

All Listed Sponsors
lead

Shanghai Shengdi Pharmaceutical Co., Ltd

INDUSTRY

NCT07123376 - Pharmacokinetics, Pharmacodynamics Profile and Tolerance of HRS-9231 in Healthy Subjects | Biotech Hunter | Biotech Hunter