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Clinical Trial Summary

The main goal of this phase llb study is to compare the efficacy and safety of two doses of HEC585 tablets with placebo which is a look-alike substance that contains no active drug in patients with progressive fibrosing interstitial lung diseases. This study is divided into two stages, i.e. main study stage with 24 weeks treatment duration followed by up to 96 weeks treatment extended study stage.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05139719
Study type Interventional
Source Sunshine Lake Pharma Co., Ltd.
Contact HuaPing Dai, Ph.D
Phone 010-84206271
Email daihuaping@ccmu.edu.cn
Status Recruiting
Phase Phase 2
Start date February 15, 2023
Completion date December 2026