| Eligibility |
Inclusion Criteria:
- Patients who have signed informed consent form before initiation of any study related
procedure.
- Male or non-pregnant female patients between 40 to 75 years of age at Screening Visit.
- General good health (except the COPD diagnosis) and free of any concomitant conditions
or treatment that could interfere with study conduct.
- An established physician diagnosis of COPD (GOLD 2022).
- Post-bronchodilator FEV1=80% and =40% of predicted normal values (GLI-2012), and
post-bronchodilator FEV1/FVC ratio =0.70.
- Predose FEV1 values at Visits 4 and 5 within ± 20% of the Visit 3 FEV1.
- Able to replace their current short-acting bronchodilators with study-provided
albuterol/salbutamol inhalation aerosol provided at the Screening Visit (Visit 1) for
use as needed for the duration of the study.
- Patients must be able to discontinue their COPD maintenance medications during the
run-in and treatment periods.
- Patients must be able to withhold their short-acting ß2-agonists for at least 6 hours
prior to spirometry on each clinic visit at the discretion of the investigator.
- Current or ex-smokers with =10 pack-year smoking history (Note: Pack-Year= (cigarettes
smoked per day x years smoked)/20)).
- Not pregnant , breastfeeding, not a woman of childbearing potential (WOCBP) or WOCBP
using an acceptable contraceptive
- No occurrence of an upper or lower respiratory tract infection during the run-in
period.
- No COPD exacerbation, defined as any worsening of COPD requiring an emergency
department visit or hospitalization, or requiring excessive use of the
albuterol/salbutamol rescue medication during the run-in and/or treatment period at
the discretion of the Investigator, or the use of antibiotics and/or corticosteroids
during the run-in period and/or treatment period.
Exclusion Criteria:
- Treatment for COPD exacerbation within 12 weeks prior to the Screening Visit or 2 or
more exacerbations in the last year.
- Hospitalization for COPD or pneumonia within 12 weeks prior to the Screening Visit.
- History of a life-threatening COPD episode that required intubation and/or was
associated with hypercapnia, respiratory arrest, hypoxic seizures, or mMRC (Modified
Medical Research Council) dyspnea Grade 4.
- Acute upper or lower respiratory tract infection, sinusitis, rhinitis, pharyngitis,
urinary tract infection or illness within 8 weeks prior to the Screening Visit.
- Use of immediate-release (Oral or IV) corticosteroids within the last 30 days and/or
extended-release corticosteroids (Depot or Local) within the last 12 weeks prior to
the Screening Visit
- Patients with a history of asthma or a clinical diagnosis of asthma, allergic
rhinitis, or atopy; a total blood eosinophil count above 600/mm3.
- Patients with an abnormal/clinically significant 12-lead electrocardiogram (ECG) prior
to and during screening visit, during the run-in and treatment periods.
- Patients with myocardial infarction or unstable angina in the last 12 months; unstable
or life-threatening cardiac arrhythmia requiring intervention in the last 12 months;
or New York Heart Association Class II-IV heart failure.
- Patients with documented pulmonary hypertension or clinical signs of right heart
failure (indicated by an increase in jugular venous pressure with or without
peripheral edema) or patients who require chronic oxygen use for >12 hours per day.
- Presence of glaucoma or a history/family history of glaucoma.
- History of paradoxical bronchospasm, narrow-angle glaucoma, prostatic hyperplasia,
bladder-neck obstruction, or any other condition, which, in the opinion of the
Investigator, would contraindicate the use of an anticholinergic agent.
- Presence or history of urinary retention.
- Historical or current evidence of a clinically significant disease (Note: Significant
is defined as any disease that, in the opinion of the Investigator, would put the
safety of the patient at risk through participation, or which could affect the
efficacy or safety analysis if the disease/condition exacerbated during the study)
including, but not limited to:
- Cardiovascular (e.g., congestive heart failure, uncontrolled hypertension,
uncontrolled coronary artery disease, stroke, or non-controlled arrhythmias),
- Hepatic, renal, hematological, neuropsychological, endocrine (e.g., uncontrolled
diabetes mellitus, uncontrolled thyroid disorder, Addison's disease, and Cushing's
syndrome),
- Gastrointestinal (e.g., poorly-controlled peptic ulcer disease),
- Pulmonary disease other than COPD (e.g., alpha-1 antitrypsin deficiency, active
bronchiectasis, cystic fibrosis, broncho-pulmonary dysplasia, sarcoidosis, lung
fibrosis, pulmonary edema, interstitial lung disease, lung or mediastinum
proliferative process including malignancies).
- Patients who have undergone thoracotomy with pulmonary resection, have plans to
undergo lung transplantation or lung volume reduction therapy, or have had lung volume
reduction surgery within 12 months prior to the Screening Visit.
- Have any of the following conditions that, in the judgment of the Investigator, might
cause participation in this study to be detrimental to the patient, including but not
limited to:
- Current malignancy excluding basal cell carcinoma. (Note: History of malignancy is
acceptable only if the patient has been in remission for one year prior to the
Screening Visit. Remission is defined as no current evidence of malignancy and no
treatment for the malignancy in the 5 years prior to the Screening Visit.
- Current or untreated tuberculosis (Note: History of tuberculosis is acceptable only if
a patient has received an approved prophylactic treatment regimen or an approved
active treatment regimen and has had no evidence of active disease for a minimum of 2
years).
- Uncontrolled hypertension (systolic blood pressure [BP] =160 or diastolic BP >100).
- Stroke within 12 months prior to the Screening Visit
- Immunocompromised
- History of allergy or hypersensitivity to anticholinergic/muscarinic receptor
antagonist agents, beta-2 adrenergic agonists, lactose/milk proteins, or specific
intolerance to aerosolized tiotropium-containing products or its derivatives (e.g.,
ipratropium, oxitropium), or known hypersensitivity to any of the proposed ingredients
or components of the delivery system.
- History of alcohol or drug abuse within 2 years prior to the Screening Visit (Visit
1).
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