Clinical Trials Directory

Trials / Terminated

TerminatedNCT05607446

To Evaluate the Efficacy and Safety of TQC3564 Tablets in the Treatment of Persistent Allergic Rhinitis

A Single-center, Randomized, Double-blind, Two-cycle, Two-way Crossover Phase Ib Study to Evaluate the Efficacy and Safety of TQC3564 Tablets in the Treatment of Persistent Allergic Rhinitis

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
12 (actual)
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd. · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

A clinical study to evaluate the efficacy and safety of tqc3564 tablets in the treatment of persistent allergic rhinitis. A total of 24 patients will be enrolled.

Conditions

Interventions

TypeNameDescription
DRUGTQC3564 tabletsTQC3564 tablets are CRTH2 antagonists.
DRUGPlacebo tabletsThe intervention drug is placebo.
DRUGTQC3564 tablets, montelukast sodium tabletsThe intervention drugs are TQC3564 tablets combined with montelukast sodium tablets. TQC3564 is a CRTH2 antagonist, montelukast sodium is Leukotriene receptor antagonist.
DRUGPlacebo tablets, montelukast sodium tabletsThe intervention drugs are placebo combined with montelukast sodium tablets. Montelukast sodium is Leukotriene receptor antagonist.

Timeline

Start date
2022-09-14
Primary completion
2023-05-09
Completion
2023-12-14
First posted
2022-11-07
Last updated
2024-11-26

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05607446. Inclusion in this directory is not an endorsement.