A Study to Evaluate the Efficacy and Safety of DW5121 Compared to DW51211 and DW51212

Not Applicable

Completed

• Conditions: Acute Bronchitis
• Interventions: Drug: DW5121; Drug: DW51211; Drug: DW51212

• Registration Number: NCT07093697
• Lead Sponsor: Daewon Pharmaceutical Co., Ltd.

Brief Summary

This is a Phase 3, randomized, double-blind, active-controlled, parallel-group, multi-center clinical trial to evaluate the efficacy and safety of DW5121 compared to DW51211 and DW51212 in patients with acute bronchitis. The primary objective is to demonstrate the superiority of DW5121 over DW51211 and DW51212 by comparing the change in total Bronchitis Severity Score (BSS) at Day 4 after administration. Approximately equal numbers of patients were randomized in a 1:1:1 ratio to receive DW5121, DW51211, or DW51212 for 7 days. Efficacy and safety assessments were conducted at Day 4 and Day 7, with a follow-up contact approximately 5 days after the end of treatment to monitor adverse events.

Detailed Description

Acute bronchitis is a common respiratory condition characterized by inflammation of the bronchial tubes, leading to symptoms such as coughing, sputum production, and discomfort. Effective treatment options with improved symptom control and safety profiles are needed.

This Phase 3, randomized, double-blind, parallel-group, multi-center, active-controlled, superiority trial aims to evaluate the efficacy and safety of DW5121 compared to DW51211 and DW51212 in patients with acute bronchitis. Eligible participants were randomized in a 1:1:1 ratio to receive either DW5121, DW51211, or DW51212 for 7 days.

The primary objective is to assess the change in total Bronchitis Severity Score (BSS) at Day 4 (±1 day) after drug administration, and to demonstrate the superiority of DW5121 compared to both comparators.

The secondary objectives include:

1. Comparison of BSS score changes at Day 4 between DW5121 and each comparator, including statistical significance.

2. Evaluation of overall efficacy and safety of DW5121 relative to DW51211 and DW51212.

Participants visited the study site at baseline, Day 4 (Visit 3), and Day 7 (Visit 4). A follow-up safety check (Visit 5) was conducted approximately 5 days after the last visit. Additional site visits or assessments were performed as necessary based on investigator's discretion to monitor adverse events.

This study provides important data on the potential benefits of DW5121 in managing symptoms of acute bronchitis, with an emphasis on both clinical efficacy and patient safety.

Study Timeline

• Study Start: 2024-03-28
• Primary Completion: 2025-05-27
• Study Completion: 2025-05-27
• Status Verified: 2025-06
• Study First Submitted: 2025-06-23
• Study First Submitted QC: 2025-07-22
• Last Update Submitted: 2025-07-22
• Study First Posted: 2025-07-30
• Last Update Posted: 2025-07-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 273

Inclusion Criteria

Subjects must meet all of the following criteria to be eligible for the study:

1. Male or female aged ≥19 years and <80 years at the time of informed consent.
2. Patients diagnosed with acute bronchitis with productive cough symptoms within 48 hours prior to randomization (diagnosis based on clinical symptoms and chest X-ray; additional bacterial or viral testing may be performed if necessary).
3. Subjects with a total Bronchitis Severity Score (BSS) of ≥5 and a sputum score of at least 1 at the randomization visit.
4. Subjects who voluntarily provided written informed consent to participate in this clinical trial.

Exclusion Criteria

Subjects who meet any of the following conditions will not be eligible to participate in this clinical trial:

1. History of hypersensitivity to any component of the investigational product or to drugs of a similar class.

2. Presence of any of the following medical histories or past surgical/interventional histories:

3. Active infections requiring systemic antibiotic therapy

4. Severe pulmonary diseases as determined by the investigator (e.g., bronchiectasis, bronchogenic carcinoma, interstitial lung disease, pneumonia, active tuberculosis, cystic fibrosis, chronic obstructive pulmonary disease, asthma, chronic bronchitis, emphysema, etc.) or clinically significant abnormal findings on chest X-ray

5. Obstructive sleep apnea syndrome

6. Glaucoma or elevated intraocular pressure

7. Lower urinary tract obstruction (e.g., benign prostatic hyperplasia) or voiding dysfunction

8. Hemorrhagic diathesis or bleeding tendency

9. Hepatic dysfunction (ALT or AST > 3 × upper limit of normal)

10. Renal impairment (glomerular filtration rate < 30 mL/min)

    *eGFR (mL/min/1.73m²) = 175 × (serum creatinine)^(-1.154) × (age)^(-0.203) × 0.742 (if female)

11. Uncontrolled thyroid dysfunction (TSH ≥ 1.5 × ULN)

12. Uncontrolled diabetes mellitus (HbA1c > 9.0%)

13. Uncontrolled hypertension (systolic or diastolic blood pressure ≥ 160/100 mmHg)

14. Significant cardiovascular diseases as determined by the investigator (e.g., heart failure of NYHA class III/IV, atherosclerosis, pulmonary hypertension, peripheral artery disease) or QTc interval > 450 msec or other clinically significant ECG abnormalities

15. Active peptic ulcer, gastrointestinal bleeding, or pyloroduodenal obstruction

16. Central nervous system diseases such as epilepsy

17. Subjects with rare hereditary problems of galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption

18. History of malignancy except in the following cases:

(1) Disease-free for at least 5 years following completion of cancer treatment

(2) Subjects who have completed curative resection of basal cell carcinoma or squamous cell carcinoma of the skin, curative surgery for papillary thyroid carcinoma, or successful treatment of cervical carcinoma in situ at least 3 years prior to screening

3. Subjects expected to require any of the following medications during the clinical trial:

4. Antibiotics, antivirals, systemic/inhaled glucocorticosteroids

5. ACE inhibitors or ARBs (Note: Subjects on long-term stable doses of ACEIs or ARBs may be included)

6. Mucolytics, expectorants, antitussives, herbal medicines with antitussive/expectorant effects

7. Leukotriene receptor antagonists, antihistamines, β2 agonists, anticholinergic bronchodilators, CNS stimulants

8. Coumarin-type anticoagulants (e.g., warfarin)

9. Symptomatic treatments for acute bronchitis, analgesics (Note: Acetaminophen up to 1.5 g/day taken ≥24 hours before efficacy assessments is permitted)

10. Sedatives

11. Central nervous system depressants

12. Phenytoin

13. Monoamine oxidase (MAO) inhibitors administered within 2 weeks prior to the investigational product or expected to be used during the trial (e.g., antidepressants, antipsychotics, mood stabilizers, anti-Parkinson drugs)

14. Heavy smokers (≥15 cigarettes/day)

• For e-cigarettes, 10 puffs are considered equivalent to one conventional cigarette.

  5. Pregnant or lactating women, or women who are unwilling to use appropriate contraception* or who are planning to become pregnant during the study period.

• Acceptable contraceptive methods include hormonal contraception, intrauterine devices, sterilization of the partner (vasectomy or tubal ligation), or double-barrier methods (e.g., male condom with female diaphragm, sponge, or cervical cap).

  6. Participation in another clinical trial and administration of an investigational drug or device within 4 weeks prior to screening

  7. Any other condition that, in the investigator's judgment, would make the subject unsuitable for participation in this clinical trial

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
DW5121 Group	DW5121	Participants receive DW5121, 2 tablets orally, DW51211 Placebo, 2 tablets orally, DW51212 Placebo, 1 tablets orally, 3 times a day after meals for 7 days
DW51211 Control Group	DW51211	Participants receive DW5121 placebo, 2 tablets orally, DW51211, 2 tablets orally, DW51212 Placebo, 1 tablets orally, 3 times a day after meals for 7 days
DW51212 Control Group	DW51212	Participants receive DW5121 placebo, 2 tablets orally, DW51211 placebo, 2 tablets orally, DW51212 , 1 tablets orally, 3 times a day after meals for 7 days

Primary Outcome Measures

Name	Time	Method
Change from baseline in Bronchitis Severity Score (BSS) total score at Day 4 after dosing	Day 4 after first dose	The primary efficacy endpoint is the change from baseline in total BSS score at Day 4 after administration of DW5121 compared to DW51211 and DW51212. The BSS is a clinician-rated scale assessing five symptoms of bronchitis (cough, sputum, rales/rhonchi, chest pain during coughing, and dyspnea), each scored from 0 (absent) to 4 (very severe), resulting in a total score ranging from 0(no symptoms) to 20(most severe symptoms) where higher scores indicate a worse outcome (more severe bronchitis symptoms).

Secondary Outcome Measures

Name	Time	Method
Treatment efficacy rate based on improvement at Days 4 and 7 after dosing	Days 4 and 7 after first dose	Treatment efficacy defined as "cure" or "significant improvement" based on investigator and patient assessment of overall improvement at Days 4 and 7 after dosing.
Patient satisfaction with treatment using a 5-point scale at Days 4 and 7 after dosing	Days 4 and 7 after first dose	Patient satisfaction with treatment will be assessed by the patient at Days 4 and 7 after dosing using a protocol-defined 5-point categorical scale. The scale consists of the following categories: 4 (very satisfied), 3 (satisfied), 2 (neutral), 1 (dissatisfied), 0 (very dissatisfied). Higher scores indicate better improvement.
Change from baseline in Bronchitis Severity Score (BSS) total score at Day 7 after dosing	Day 7 after first dose	Change from baseline in total BSS score at Day 7 after administration of DW5121 compared to DW51211 and DW51212. The BSS is a clinician-rated scale assessing five symptoms of bronchitis (cough, sputum, rales/rhonchi, chest pain during coughing, and dyspnea), each scored from 0 (absent) to 4 (very severe), resulting in a total score ranging from 0(no symptoms) to 20(most severe symptoms), where higher scores indicate a worse outcome (more severe bronchitis symptoms).
Change from baseline in Bronchitis Severity Score (BSS) symptom scores at Days 4 and 7 after dosing	Days 4 and 7 after first dose	Changes from baseline in individual BSS symptom scores at Days 4 and 7 after administration of DW5121 compared to DW51211 and DW51212. The BSS is a clinician-rated scale assessing five symptoms of bronchitis (cough, sputum, rales/rhonchi, chest pain during coughing, and dyspnea), each scored from 0 (absent) to 4 (very severe), resulting in a total score ranging from 0(no symptoms) to 20(most severe symptoms), where higher scores indicate a worse outcome (more severe bronchitis symptoms).
Response rate at Days 4 and 7 after dosing	Days 4 and 7 after first dose	Response defined as total BSS score ≤3 or a decrease of ≥7 points from baseline at Days 4 and 7 after dosing.
Comparison of Bronchitis Severity Score (BSS) total score changes at Days 4 and 7 after dosing(DW51211 vs DW51212)	Days 4 and 7 after first dose	Comparison of change from baseline in total BSS score at Days 4 and 7 after administration of DW51211 and DW51212. The BSS is a clinician-rated scale assessing five symptoms of bronchitis (cough, sputum, rales/rhonchi, chest pain during coughing, and dyspnea), each scored from 0 (absent) to 4 (very severe), resulting in a total score ranging from 0(no symptoms) to 20(most severe symptoms), where higher scores indicate a worse outcome (more severe bronchitis symptoms).
Investigator and patient assessment of overall improvement using a 5-point scale at Days 4 and 7 after dosing	Days 4 and 7 after first dose	Overall improvement will be assessed separately by the investigator and the patient at Days 4 and 7 after dosing using a protocol-defined 5-point categorical scale. The scale consists of the following categories: 4 (cure), 3 (significant improvement), 2 (improvement), 1 (some improvement), 0 (non-improvement or worsening of symptoms). Higher scores indicate better improvement.

Trial Locations

Locations (8)

Soonchunhyang University Bucheon Hospital; 🇰🇷 Bucheon, Korea, Republic of

Hallym University Chuncheon Sacred Heart Hospital; 🇰🇷 Chuncheon, Korea, Republic of

Yeungnam University Medical Center; 🇰🇷 Daegu, Korea, Republic of

Wonkwang University Hospital; 🇰🇷 Iksan, Korea, Republic of

Kangbuk Samsung Hospital; 🇰🇷 Seoul, Korea, Republic of

Konkuk University Medical Center; 🇰🇷 Seoul, Korea, Republic of

Hallym University Kangdong Sacred Heart Hospital; 🇰🇷 Seoul, Korea, Republic of

Korea University Guro Hospital; 🇰🇷 Seoul, Korea, Republic of