About this trial
This is a multicenter, parallel-group, double-blind, randomized phase 4 study designed to identify the optimal dose of CE1226 (2 active doses) to slow disease progression as assessed by reduced rates of annual lung density decline in alpha-1 antitrypsin (AAT) deficient participants over 3 years as compared with the marketed dose 60 milligrams per kilogram (mg/kg).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
• Age greater than or equal to (>=) 18 and less than or equal to (<=) 65 years at the time of providing written informed consent.
• Confirmed diagnosis of emphysema related to AATD with either the PiZZ, PiZ(null), or Pi(null/null) genotype with documented serum AAT levels less than (<) 11 micrometer (μM) (or < 50 mg/dL [milligram/deciliter]) at any time before the first administration of CE1226 on Day 1 (Baseline).
Disqualifiers
• Participants should not have acute illness or pulmonary exacerbation within 6 weeks before the first administration of CE1226 on Day 1 (Baseline).
• Participants should not have previously received gene therapy for AATD at any point.
• Participants with liver disease secondary to AATD.
Trial design
Parallel
Treatments tested in this trial
CE1226
Biological/VaccineCE1226 will be administered via intravenous (IV) infusion weekly over 3 years.
Treatment groups
Trial outcomes
Primary outcomes
Annual rate of change in adjusted lung density
The annual rate of change (expressed as gram per liter per year \[g/L/year\]) in adjusted lung density (15th percentile lung density \[PD15\]) will be calculated on CT scan assessments of whole lung at total lung capacity (TLC).
Secondary outcomes
Annual rate of change in forced expiratory volume in 1 second percent predicted (FEV1%)
The annual rate of change in FEV1% will be assessed by spirometry.
Annual rate of change in diffusion capacity of carbon monoxide (DLco)
The annual rate of change in DLco will be assessed by gas transfer using site machinery.
Number of severe pulmonary exacerbations
Pulmonary excerbations will be assessed by the investigator using Rodriguez-Roisin criteria, where an exacerbation is defined as: a sustained worsening of the patient's condition, from a stable state and beyond normal day-to-day variations, necessitating a change in regular medication in a patient with underlying chronic obstructive pulmonary disease (COPD). A severe exacerbation is defined as an event requiring the introduction of corticosteroids and / or antibiotics which results in hospitalization or death.
Duration of severe pulmonary exacerbations
Pulmonary excerbations will be assessed by the investigator using Rodriguez-Roisin criteria, where an exacerbation is defined as: a sustained worsening of the patient's condition, from a stable state and beyond normal day-to-day variations, necessitating a change in regular medication in a patient with underlying COPD. A severe exacerbation is defined as an event requiring the introduction of corticosteroids and / or antibiotics which results in hospitalization or death.
Locations
Sponsors and contacts
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