drugset / Trial / NCT05733533

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

NCT05733533 ↗

Phase 2 Completed 97 enrolled Guangdong Hengrui Pharmaceutical Co., Ltd
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2023-03-09
Primary completion
2024-03-05
Completion
2024-03-05

Drugs

EvaluationDrugModalityDoseRoute
Subject HRS-2261 Unknown — Oral