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Clinical Trial Summary

The primary objective of this trial is to evaluate the efficacy of different doses and frequencies of administration of TG103 injection in the treatment of type 2 diabetes.


Clinical Trial Description

This trial is a randomized, double-blind, placebo-parallel, Dulaglutide-controlled,multicenter phase Ⅱ clinical trial. The whole trial consists of two parts, Part A and Part B, and 240 subjects are planned to be enrolled. Part A will be divided into three groups: TG103 15 mg group, TG103 22.5 mg group and placebo group, given once every two weeks (Q2W); Part B will be divided into four groups: TG103 7.5mg dose group, TG103 15 mg dose group ,placebo group and Dulaglutide group, once a week (QW). After Part A enrollment is completed, Part B will continue to be enrolled. The trial will include a screening period of up to 2 weeks, an initiation period of 2 weeks, a double-blind treatment period of 16 weeks, and a safety follow-up period of 3 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05348122
Study type Interventional
Source CSPC Baike (Shandong) Biopharmaceutical Co., Ltd.
Contact Huanhuan Gao
Phone +86-8031190343
Email lcgaohuanhuan@mail.ecspc.com
Status Not yet recruiting
Phase Phase 2
Start date June 15, 2022
Completion date November 1, 2023

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