This is a Phase 1/2, multicenter, open-label, dose-exploration (Phase 1) and dose-expansion (Phase 2) study to evaluate the safety, tolerability, PK/PD, and efficacy of BEAM-302 in adult patients with AATD-associated lung disease and/or liver disease and to determine the optimal biological dose (OBD).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
106
BEAM-302 is a lipid nanoparticle (LNP)-based therapy for the treatment of patients with AATD
Clinical Study Center
Birmingham, Alabama, United States
RECRUITINGClinical Study Center
Boston, Massachusetts, United States
RECRUITINGPhase 1 Dose Exploration: Rates of treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs)
Numbers and percentages of patients reporting a given AE
Time frame: 2 years
Phase 2 Dose Expansion: Absolute blood levels of total AAT
Absolute Levels of AAT over time
Time frame: 2 Years
Phase 1 Dose Exploration: Absolute blood levels of total AAT
Absolute Levels of AAT over time
Time frame: 2 Years
Phase 2 Dose Expansion: Rates of TEAEs and SAEs
Numbers and percentages of patients reporting a given AE
Time frame: 2 Years
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Clinical Study Center
Charleston, South Carolina, United States
Clinical Study Center
Adelaide, Australia
RECRUITINGClinical Study Center
Fitzroy, Australia
RECRUITINGClinical Study Center
Dublin, Ireland
RECRUITINGClinical Study Center
Leiden, Netherlands
RECRUITINGClinical Study Center
Auckland, New Zealand
RECRUITINGClinical Study Center
Hamilton, New Zealand
RECRUITINGClinical Study Center
London, United Kingdom
RECRUITING...and 1 more locations