drugset / Trial / NCT06830343

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

NCT06830343

Phase 1 Recruiting 66 enrolled CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2025-02-27
Primary completion
2026-08-01
Completion
2026-10-01

Drugs

EvaluationDrugModalityDoseRoute
Subject SYH9017 Unknown Subcutaneous
Comparator Semaglutide Peptide

Indications