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RECRUITING

A Long-term Follow-up Study in Patients Who Received BEAM-101

NCT07373639 · View on ClinicalTrials.gov ↗

Study Summary

This is a Long-term Follow-up (LTFU) study in patients who received BEAM-101 in the parent study (Study BTX-AUT-001). Eligible patients who received BEAM-101 will be asked to participate in this LTFU study prior to completing Study BTX-AUT-001. Patients who enter into this study will be followed for 13 years (a total of 15 years after receiving BEAM-101).

Interventions

  • DRUG Long-Term Follow-up Study of patients who received BEAM-101

Study Locations (17)

Ohio

  • University Hospitals Clevland Medical Center — Cleveland
  • The Clevland Clinic Foundation — Cleveland

Tennessee

  • St. Jude Children's Research Hospital — Memphis
  • The Children's Hospital at TriStar Centennial — Nashville

Alabama

  • University of Alabama at Birmingham — Birmingham

Arizona

  • Phoenix Children's Hospital — Phoenix

Florida

  • Mayo Clinic Florida — Jacksonville

Georgia

  • Children's Healthcare of Atlanta - Aflac Cancer and Blood Disorders Center- Egleston — Atlanta

Massachusetts

  • Boston Children's Hospital — Boston

Michigan

  • Henry Ford Cancer Center — Detroit

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2025-12-15
Est. Completion 2043-02-12

Sponsor

Beam Therapeutics

5 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07373639

The ClinicalTrials.gov registry entry for NCT07373639 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 50 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 2 conditions, with Sickle Cell Disease appearing as the primary indexed condition, and to 1 intervention — of which Long-Term Follow-up Study of patients who received BEAM-101 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: NCT07373639 reports 17 study locations spanning 15 distinct geographic areas — top geographies include Ohio, Tennessee, Alabama. 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 NCT07373639 about?

NCT07373639 is a clinical study titled "A Long-term Follow-up Study in Patients Who Received BEAM-101". This is a Long-term Follow-up (LTFU) study in patients who received BEAM-101 in the parent study (Study BTX-AUT-001). Eligible patients who received BEAM-101 will be asked to participate in this LTFU study prior to completing Study BTX-AUT-001. Patients who enter into this study will be followed for...

What is the current status of trial NCT07373639?

This trial is currently recruiting. The enrollment target is 50 participants. The study started on 2025-12-15. Estimated completion is 2043-02-12.

What conditions does trial NCT07373639 study?

This clinical trial studies the following conditions: Sickle Cell Disease, Hemoglobinopathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07373639?

The interventions under investigation include: Long-Term Follow-up Study of patients who received BEAM-101 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07373639?

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 NCT07373639 being conducted?

This trial has 17 study locations across Alabama, Arizona, Florida, Georgia, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial