Phase 4, Double-blind Study Evaluating the Response on Computed Tomography (CT) Lung Density Decline Rates of Respreeza / Zemaira Weekly for 3 Years in Adults With alpha1 Antitrypsin Deficiency (AATD)

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-65
SponsorCSL Behring

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 volunteers

Qualifiers

• 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

Design model

Parallel

Treatments tested in this trial

  • CE1226

    Biological/Vaccine

    CE1226 will be administered via intravenous (IV) infusion weekly over 3 years.

Treatment groups

270 Participants
are divided into 3 treatment groups
Group A: CE1226 low doseActive comparator 1 intervention
Group B: CE1226 medium doseExperimental treatment 1 intervention
Group C: CE1226 high doseExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

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).

Time frame
From Baseline to Month 36

Secondary outcomes

1

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.

Time frame
From Baseline to Month 36
2

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.

Time frame
From Baseline to Month 36
3

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.

Time frame
From screening up to Month 36
4

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.

Time frame
From screening up to Month 36

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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