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Clinical Trial Summary

The objective of this study is to evaluate the clinical equivalence of the test formulation of Linaclotide compared to the marketed formulation LINZESS® in patients with Chronic Idiopathic Constipation, and to evaluate the efficacy and safety of the test formulation of Linaclotide in the treatment of Chronic Idiopathic Constipation.


Clinical Trial Description

This is a randomized, double-blinded, placebo-controlled, multicenter study to evaluate the clinical equivalence of the test formulation of Linaclotide (manufactured by Jiangsu Hansoh Pharmaceutical Co., Ltd.) compared to the marketed formulation LINZESS® in patients with Chronic Idiopathic Constipation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04804267
Study type Interventional
Source Jiangsu Hansoh Pharmaceutical Co., Ltd.
Contact Jingyuan Fang, MD
Phone 86-021-53882001
Email fangjingyuan_new@163.com
Status Recruiting
Phase Phase 3
Start date March 5, 2021
Completion date August 31, 2022

See also
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