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Tolerability, Pharmacokinetics and Efficacy of ZSP1603 in Patients With Idiopathic Pulmonary Fibrosis （IPF）

Idiopathic Pulmonary Fibrosis (IPF) Clinical Trial

Official title:
A Multi-center, Phase Ib/IIa Clinical Trial to Evaluate the Tolerability, PK and Efficacy of ZSP1603 in Patients With Idiopathic Pulmonary Fibrosis

Clinical Trial Summary

This study was divided into two parts. The first part was a dose escalation study: a open label dose escalation design was used to evaluate the safety, tolerance and pharmacokinetic characteristics of ZSP1603 in IPF patients. The second part was a randomized double-blind placebo-controlled design was used to preliminatively investigate the efficacy and safety of ZSP1603 in the treatment of IPF at the target dose.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05119972
Study type Interventional
Source Guangdong Raynovent Biotech Co., Ltd
Contact Huiping Li, Professor
Phone 021-65115006
Email liw2013@126.com
Status Recruiting
Phase Phase 1/Phase 2
Start date October 21, 2021
Completion date December 21, 2023
View Details
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