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A Study to Evaluate the Safety and Efficacy of BEAM-302 in Adult Patients With Alpha-1 Antitrypsin Deficiency (AATD)
NCT06389877 · View on ClinicalTrials.gov ↗
Study Summary
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).
Conditions Studied
Interventions
- DRUG BEAM-302
Study Locations (11)
Other
- Clinical Study Center — Adelaide
- Clinical Study Center — Fitzroy
- Clinical Study Center — Dublin
- Clinical Study Center — Leiden
- Clinical Study Center — Auckland
- Clinical Study Center — Hamilton
- Clinical Study Center — London
- Clinical Study Center — Southampton
Alabama
- Clinical Study Center — Birmingham
Massachusetts
- Clinical Study Center — Boston
South Carolina
- Clinical Study Center — Charleston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 106 participants |
| Start Date | 2024-06-19 |
| Est. Completion | 2030-05 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06389877
The ClinicalTrials.gov registry entry for NCT06389877 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 106 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Beam Therapeutics, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Alpha 1-Antitrypsin Deficiency appearing as the primary indexed condition, and to 1 intervention — of which BEAM-302 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06389877 reports 11 study locations spanning 4 distinct geographic areas — top geographies include Other, Alabama, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06389877 about?
NCT06389877 is a clinical study titled "A Study to Evaluate the Safety and Efficacy of BEAM-302 in Adult Patients With Alpha-1 Antitrypsin Deficiency (AATD)". 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...
What is the current status of trial NCT06389877?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 106 participants. The study started on 2024-06-19. Estimated completion is 2030-05.
What conditions does trial NCT06389877 study?
This clinical trial studies the following conditions: Alpha 1-Antitrypsin Deficiency. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06389877?
The interventions under investigation include: BEAM-302 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06389877?
This trial is sponsored by Beam Therapeutics, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06389877 being conducted?
This trial has 11 study locations across Alabama, Massachusetts, South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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