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NCT Number: NCT03851991

The Efficacy and Safety of Arbidol in Reducing the Frequency of AECOPD.

Chronic Obstructive Pulmonary Disease (COPD) is currently the fourth leading cause of death in the world. Acute exacerbations of COPD (AECOPD) are the most important events in the course of the disease because they negatively impact health status, life quality, disease progression, patients survival and economic and social burden. Reducing frequency of AECOPD is the key goal of management for COPD. Since respiratory viral infections are the mainly trigger of AECOPD, anti-viral therapy would be the affective method to prevent the exacerbation or reduce the attack severity. However, there are no positive study results of treating or preventing AECOPD used by current anti-viral drugs approved by FDA so far.

Arbidol is a non-nucleoside antiviral drug. It inhibits viral DNA and RNA synthesis by inhibiting fusion of viral lipid vesicle membrane with host cell membranes. Arbidol has broad-spectrum antiviral activity. In addition to inhibition of influenza virus, it against a variety of viruses including respiratory syncytial disease (RSV), parainfluenza virus, human rhinovirus, coxsackie virus (CV), adenovirus (ADV) and so on. In recent years, some fundamental and clinical researches have shown that arbidol has a significant role in prevention and treatment of influenza virus and other acute respiratory viral infections. Therefore, the investigators speculate that Arbidol will effectively control COPD combined with upper respiratory virus infection, thereby reducing acute exacerbations of COPD.

This is a prospective, multicenter, randomized, double-blind, placebo-controlled, 52-week study. The purpose of this study is to evaluate the efficacy and safety of arbidol in improving the frequency and extent of moderate or severe acute exacerbations in patients with COPD. Eligible subjects will be randomly assigned to treatment group or placebo group at a 2:1 ratio. Subjects of treatment group receive an on-demand arbidol 200 mg three times per day while placebo group receives matched placebo. When the subject has a new respiratory infection, original respiratory symptoms worsen, or fever (the lower body temperature is greater than 37.3℃), oral medication is given immediately. The subjects are required to receive the first dose of drug within 8 hours after the symptoms of upper respiratory tract infection.

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Key information

Conditions

COPD Patients

Age range

40 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Shenjing Hospital

Shenyang, Liaoning, 110004, China

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients from Outpatient clinic.
  • Informed consent and assent must be obtained before any study assessment is performed.
  • Aged ≥40 years.
  • Continuous respiratory symptoms, such as chronic cough, sputum or shortness of breath etc.
  • Exposure to risk factors: Host factors, Tobacco, Occupation, Indoor/outdoor pollution
  • FEV1/FVC less than 0.70 after withholding bronchodilator.
  • 2 or more acute exacerbations of COPD within the 12 months prior to visit 0. Or more than 1 hospitalizations due to AECOPD within the 12 months prior to visit 0.
  • Good compliance.

Exclusion criteria

  • Patients with any chronic diseases except COPD which in the opinion of the investigator may interfere with study evaluation or optimal participation in the study.
  • Patients with a history of chronic lung disease other than COPD, including (but not limited to) active tuberculosis, lung cancer, clinically significant bronchiectasis, primary pulmonary hypertension, sarcoidosis, interstitial lung disease, asthma (other than asthma COPD overlap), severe cor pulmonale.
  • Patients with acute coronary syndrome(ACS) or acute left heart failure within the 6 months prior to visit 0. Patients accepted Coronary interventional therapy or coronary artery bypass grafting due to ACS within the 3 months prior to visit 0.
  • Patients with uncontrolled hypertension.
  • Patients who started oral >10mg prednisolone or Equivalent systemic corticosteroids within 4 weeks prior to Visit 1. Or patients who received antibiotics within 4 weeks prior to Visit 1. Or patients who received standard treatment for COPD within 4 weeks prior to Visit 1. Or use of other investigational drugs within 5 half-lives of enrollment, or within 30 days, whichever is longer.
  • Patients who received influenza vaccine or other viral vaccine within the 12 months prior to visit 0.
  • The end of AECOPD therapy was within the 4 weeks prior to visit 0. Or Occurrence of AECOPD within the 6 weeks prior to visit 0.
  • History of arbidol sensitivity.
  • No person directly associated with the administration of the study is allowed to participate as a study subject.
  • Use of other investigational intervention within within 30 days.
  • Patients with obviously abnormal liver function, AST or ALT>2 times the upper limit of normal value or total bilirubin>1.3 times the upper limit of normal value.

Treatment and study plan

Arbidol

Drug

oral

Placebos

Drug

controle

Primary outcomes

  1. Frequency of moderate or severe acute exacerbation in patients with chronic obstructive pulmonary disease

    Time frame: 52 weeks

    Frequency of moderate or severe acute exacerbation in patients with chronic obstructive pulmonary disease

Secondary outcomes

  1. The frequency of Acute exacerbation of patients leads to hospitalization

    Time frame: 52 weeks

    The frequency of Acute exacerbation of patients leads to hospitalization

  2. The intervals to the next acute exacerbation after the first use of the study drug

    Time frame: 52 weeks

    The intervals to the next acute exacerbation after the first use of the study drug

  3. To assess the change of FEV1 from baseline

    Time frame: 52 weeks

    To assess the change of FEV1 from baseline

  4. Mean duration of moderate or severe acute exacerbation in chronic obstructive pulmonary disease

    Time frame: 52 weeks

    Mean duration of moderate or severe acute exacerbation in chronic obstructive

  5. Throat swab and virus separation experiment to detect the composition of respiratory viruses in patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD) requiring hospitalization

    Time frame: 52 weeks

    Throat swab and virus separation experiment to detect the composition of respiratory viruses in patients with acute exacerbation of chronic obstructive pulmonary disease (AECOPD) requiring hospitalization

  6. Number of unscheduled visits to a clinic for COPD exacerbation

    Time frame: 52 weeks

    Number of unscheduled visits to a clinic for COPD exacerbation

  7. Number of emergency room visits for AECOPD

    Time frame: 52 weeks

    Number of emergency room visits for AECOPD

  8. Number of hospitalizations due to AECOPD

    Time frame: 52 weeks

    Number of hospitalizations due to AECOPD

Sponsors and collaborators

Lead sponsor

Shengjing Hospital

Other

Registry information

Official study title

A 52-week Multicenter, Randomized, Double-blind, Placebo-controlled, Prospective Study to Evaluate the Efficacy and Safety of Arbidol in Reducing the Frequency of AECOPD.

Important dates

Study start
2019
Primary completion
2023
Study completion
2024
First posted
Feb 22, 2019
Registry last updated
Jul 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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