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Active Not RecruitingNCT07252908

A Phase II Clinical Trial on the Efficacy and Safety of TQC3721 Inhalation Powder

A Multicenter, Randomized, Double-blind, Placebo-controlled Phase II Clinical Trial to Evaluate the Efficacy and Safety of TQC3721 Inhalation Powder in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
195 (estimated)
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd. · Industry
Sex
All
Age
40 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To evaluate the efficacy and safety of TQC3721 inhalation powder in patients with moderate to severe Chronic obstructive pulmonary disease (COPD).

Conditions

Interventions

TypeNameDescription
DRUGTQC3721 inhalation powderTQC3721 inhalation powder is target inhibitor.
DRUGPlacebo for TQC3721 inhalation powderPlacebo for TQC3721 inhalation powder.

Timeline

Start date
2025-12-22
Primary completion
2026-05-01
Completion
2026-06-01
First posted
2025-11-28
Last updated
2026-04-06

Locations

29 sites across 1 country: China

Source: ClinicalTrials.gov record NCT07252908. Inclusion in this directory is not an endorsement.