Trials / Recruiting
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
| Type | Name | Description |
|---|---|---|
| DRUG | Atock Dry Syrup with placebo patch | Atock Dry syrup (TID) with placebo patch (QD) |
| DRUG | Tulobuterol patch with placebo dry syrup | Tulobuterol 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.