Depemokimab as an Extended treatmeNt Duration Biologic in Adults With Chronic Obstructive Pulmonary Disease (COPD) and Type 2 Inflammation (ENDURA -1)

Eligibility Criteria

• * Participants must be greater than or equal to (\>=) 40 to less than or equal to (\<=) 80 years of age, at the time of signing the informed consent.
• * Elevated blood eosinophil count (BEC).
• * Moderate to severe COPD with frequent exacerbations, defined as:
• * A clinically documented history of COPD as defined by the American Thoracic Society/European Respiratory Society for at least 1 year
• * A post-bronchodilator forced expiratory volume in one second (FEV1)/forced vital capacity (FVC) ratio of less than (\<) 0.70 and a post- bronchodilator FEV1 \>30 percent (%) and \<= 80% predicted normal values
• * A well-documented history of at least 2 moderate or 1 severe exacerbation in the 12 months prior to screening
• * COPD assessment test (CAT) score \>=10 at Visit 1.
• * Smoking status: Current or former cigarette smokers with a history of cigarette smoking of \>=10 pack-years.
• * Participants should be on optimized inhaler therapy, defined as inhaled corticosteroid (ICS) plus Long-acting muscarinic receptor antagonist (LAMA) plus Long-acting beta2-adrenergic receptor agonist (LABA) either as multiple inhalers or a single combination inhaler for at least 6 months prior to Screening Visit 1.
• * Body mass index (BMI) \>=16 kilogram per square meter (kg/m\^2).
• * Male or eligible female participants.
• * Participants with a current or prior physician diagnosis of asthma.
• * Other clinically significant lung disease: The Investigator must judge that COPD is the primary diagnosis accounting for the clinical manifestations of the lung disease.
• * Participants with pneumonia, COPD exacerbation, or lower respiratory tract infection within the 4 weeks prior to Screening Visit 1.
• * Lung resection: Participants with a history of, or plan for lung volume reduction surgery / endobronchial valve procedure.
• * Pulmonary rehabilitation: Participants in the acute phase of a pulmonary rehabilitation program within 4 weeks prior to Screening Visit 1.
• * Continuous oxygen: Participants requiring oxygen supplementation for more than 12 hours per day.
• * Cor pulmonale - resulting in right heart failure, severe pulmonary hypertension
• * Chronic hypercapnia requiring Non-invasive positive pressure ventilation (NIPPV) use (including Bi-Level Positive Airway Pressure \[BiPAP\] or Continuous Positive Airway Pressure \[CPAP\]).
• * Unstable cardiovascular disease or arrhythmia.
• * Parasitic Infection: Participants with a known, pre-existing parasitic infection within 6 months of Screening (Visit 1).