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RecruitingNCT06411925

The Efficacy and Safety of Atock Dry Syrup With Acute Bronchitis Patients

A Multi-center, Randomized, Double-blinded, Active-controlled, Non-inferiority, Phase 4 Trial to Evaluate the Efficacy and Safety of Atock Dry Syrup Sama With Acute Bronchitis Patients

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
296 (estimated)
Sponsor
SamA Pharmaceutical Co., Ltd · Industry
Sex
All
Age
6 Months – 11 Years
Healthy volunteers
Not accepted

Summary

Clinical Study to Evaluate the Efficacy and Safety of Atock Dry Syrup with Acute bronchial Patients

Conditions

Interventions

TypeNameDescription
DRUGAtock Dry Syrup with placebo patchAtock Dry syrup (TID) with placebo patch (QD)
DRUGTulobuterol patch with placebo dry syrupTulobuterol patch (QD) with placebo dry syrup (TID)

Timeline

Start date
2023-11-10
Primary completion
2027-07-01
Completion
2027-09-01
First posted
2024-05-13
Last updated
2025-09-23

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06411925. Inclusion in this directory is not an endorsement.

The Efficacy and Safety of Atock Dry Syrup With Acute Bronchitis Patients (NCT06411925) · Clinical Trials Directory