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
Adelaide, Australia
RECRUITINGClinical Study Center
Fitzroy, Australia
RECRUITINGClinical Study Center
Leiden, Netherlands
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
Auckland, New Zealand
RECRUITINGClinical Study Center
Hamilton, New Zealand
RECRUITINGClinical Study Center
London, United Kingdom
RECRUITING