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

NCT ID: NCT07093697

Last Updated: 2025-07-30

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 273 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-03-28
• Study Completion Date: 2025-05-27

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.

Conditions

Acute Bronchitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

DW5121 Group

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

Group Type: EXPERIMENTAL

DW5121

Intervention Type: DRUG

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

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

Group Type: ACTIVE_COMPARATOR

DW51211

Intervention Type: DRUG

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

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

Group Type: ACTIVE_COMPARATOR

DW51212

Intervention Type: DRUG

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

Interventions

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

Intervention Type: DRUG

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

Intervention Type: DRUG

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

Intervention Type: DRUG

Eligibility Criteria

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:

1. Active infections requiring systemic antibiotic therapy

2. 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

3. Obstructive sleep apnea syndrome

4. Glaucoma or elevated intraocular pressure

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

6. Hemorrhagic diathesis or bleeding tendency

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

8. 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)

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

10. Uncontrolled diabetes mellitus (HbA1c > 9.0%)

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

12. 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

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

14. Central nervous system diseases such as epilepsy

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

16. 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:

1. Antibiotics, antivirals, systemic/inhaled glucocorticosteroids

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

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

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

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

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

7. Sedatives

8. Central nervous system depressants

9. Phenytoin

10. 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)

4. 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

• Minimum Eligible Age: 19 Years
• Maximum Eligible Age: 79 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Daewon Pharmaceutical Co., Ltd.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jaejeong Shim, Principal Investigator

Role: PRINCIPAL_INVESTIGATOR

Korea University Guro Hospital

Locations

Soonchunhyang University Bucheon Hospital

Bucheon-si, , South Korea

Hallym University Chuncheon Sacred Heart Hospital

Chuncheon, , South Korea

Yeungnam University Medical Center

Daegu, , South Korea

Wonkwang University Hospital

Iksan, , South Korea

Kangbuk Samsung Hospital

Seoul, , South Korea

Konkuk University Medical Center

Seoul, , South Korea

Hallym University Kangdong Sacred Heart Hospital

Seoul, , South Korea

Korea University Guro Hospital

Seoul, , South Korea

Countries

South Korea

Other Identifiers

DW5121-302

Identifier Type: -

Identifier Source: org_study_id