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A Study to Assess the Efficacy and Tolerance of HRS-2261 in Subjects With Refractory Chronic Cough

Refractory Chronic Cough Clinical Trial

Official title:
A Multicenter, Randomized, Double-blind, Parallel, Placebo-controlled Phase II Study of Efficacy and Safety of HRS-2261 in Refractory Chronic Cough

Clinical Trial Summary

This is a phase II study that will investigate the efficacy, safety and tolerability of HRS-2261 in subjects with refractory chronic cough using a double blind, placebo controlled, randomized study design.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05733533
Study type Interventional
Source Guangdong Hengrui Pharmaceutical Co., Ltd
Contact
Status Enrolling by invitation
Phase Phase 2
Start date March 9, 2023
Completion date March 30, 2024
View Details
See also
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