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
| Type | Name | Description |
|---|---|---|
| DRUG | TQC3564 tablets | TQC3564 tablets are CRTH2 antagonists. |
| DRUG | Placebo tablets | The intervention drug is placebo. |
| DRUG | TQC3564 tablets, montelukast sodium tablets | The intervention drugs are TQC3564 tablets combined with montelukast sodium tablets. TQC3564 is a CRTH2 antagonist, montelukast sodium is Leukotriene receptor antagonist. |
| DRUG | Placebo tablets, montelukast sodium tablets | The 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.