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RECRUITING Phase 1

CRISPR-Edited Allogeneic Anti-CD19 CAR-T Cell Therapy for Relapsed/Refractory B Cell Non-Hodgkin Lymphoma (ANTLER)

NCT04637763 · View on ClinicalTrials.gov ↗

Study Summary

CB010A is a study evaluating safety, emerging efficacy, pharmacokinetics and immunogenicity of CB-010 in adults with relapsed/refractory B cell non-Hodgkin lymphoma after lymphodepletion consisting of cyclophosphamide and fludarabine.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Fludarabine
  • GENETIC CB-010

Study Locations (20)

Arizona

  • Banner MD Anderson Cancer Center — Gilbert
  • HonorHealth — Scottsdale
  • University of Arizona Cancer Center — Tucson

California

  • University of California San Diego Moores Cancer Center — La Jolla
  • University of Southern California, Norris Comprehensive Cancer Center — Los Angeles
  • Chao Family Comprehensive Cancer Center/University of California Irvine — Orange

Georgia

  • Bone and Marrow Transplant Group of Georgia — Atlanta
  • Georgia Cancer Center at Augusta University — Augusta

Kentucky

  • University of Kentucky Markey Cancer — Lexington
  • Norton Cancer Institute — Louisville

New Jersey

  • Hackensack Medical Center — Hackensack
  • Atlantic Health System — Morristown

New York

  • Nyu Langone Health — New York
  • Montefiore Medical Center — The Bronx

Alabama

  • University of Alabama at Birmingham — Birmingham

Arkansas

  • University of Arkansas — Little Rock

Trial Details

FieldValue
Enrollment Target 72 participants
Start Date 2021-05-26
Est. Completion 2025-09
Phase Phase 1

Sponsor

Caribou Biosciences

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04637763

The ClinicalTrials.gov registry entry for NCT04637763 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 72 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Caribou Biosciences, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 7 conditions, with Lymphoma appearing as the primary indexed condition, and to 3 interventions — of which Cyclophosphamide 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: NCT04637763 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Arizona, California, Georgia. 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 NCT04637763 about?

NCT04637763 is a clinical study titled "CRISPR-Edited Allogeneic Anti-CD19 CAR-T Cell Therapy for Relapsed/Refractory B Cell Non-Hodgkin Lymphoma (ANTLER)". CB010A is a study evaluating safety, emerging efficacy, pharmacokinetics and immunogenicity of CB-010 in adults with relapsed/refractory B cell non-Hodgkin lymphoma after lymphodepletion consisting of cyclophosphamide and fludarabine.

What is the current status of trial NCT04637763?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 72 participants. The study started on 2021-05-26. Estimated completion is 2025-09.

What conditions does trial NCT04637763 study?

This clinical trial studies the following conditions: Lymphoma, Lymphoma, Non-Hodgkin, Non Hodgkin Lymphoma, Refractory B-Cell Non-Hodgkin Lymphoma, B Cell Lymphoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04637763?

The interventions under investigation include: Cyclophosphamide (DRUG), Fludarabine (DRUG), CB-010 (GENETIC). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04637763?

This trial is sponsored by Caribou Biosciences, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04637763 being conducted?

This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Florida. 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