Overview

The Safety, Tolerability, and Pharmacokinetics of of SYH9017 in Chinese Participants With Overweight and Obesity

Status:
RECRUITING
Trial end date:
2026-10-01
Target enrollment:
Participant gender:
Summary
This is a randomized, double-blind, single-center, dose-escalation, single ascending dose and multiple ascending dose study of SYH9017 in Chinese participants with overweight and obesity.
Phase:
PHASE1
Details
Lead Sponsor:
CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.
Treatments:
semaglutide