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Search / Trial NCT04637763

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

Launched by CARIBOU BIOSCIENCES, INC. · Nov 16, 2020

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

The ANTLER clinical trial is studying a new treatment called CB010A for adults with a type of blood cancer known as relapsed or refractory B-cell non-Hodgkin lymphoma. This means the lymphoma has either come back after treatment or has not responded well to previous therapies. The trial aims to find out how safe this new treatment is, how well it works, and how the body processes it after receiving it. Participants will first undergo a procedure to prepare their bodies for the treatment, which includes using other medications to help improve the effectiveness of the new therapy.

To be eligible for this trial, participants must be at least 18 years old and have a documented diagnosis of relapsed or refractory non-Hodgkin lymphoma after standard treatments. They should also be in relatively good health, meaning they should be able to perform daily activities without much difficulty. However, there are some conditions that would exclude someone from participating, such as having had certain previous treatments or other serious health issues. If chosen for the trial, participants can expect to be closely monitored for their health and wellbeing throughout the study. This trial is currently recruiting, and all genders are welcome to apply.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age greater than or equal to 18 at the time of enrollment
  • Documented diagnosis of relapsed or refractory non-Hodgkin lymphoma after prior standard of care
  • Eastern Cooperative Oncology Group performance status 0 or 1
  • Adequate hematologic, renal, liver, cardiac and pulmonary organ function
  • Exclusion Criteria:
  • Prior therapy with an anti-CD19 targeting agent
  • Active or chronic graft versus host disease requiring therapy
  • Prior allogeneic stem cell transplantation
  • Central nervous system (CNS) lymphoma, prior CNS malignancy
  • Prior seizure disorder, cerebrovascular ischemia, dementia, cerebellar disease or autoimmune disease with CNS involvement.
  • Primary immunodeficiency
  • Current or expected need for systemic corticosteroid therapy
  • Current thyroid disorder. Hypothyroidism controlled with stable hormone replacement is permitted
  • Other malignancy within 2 years of study entry, except curatively treated malignancies or malignancies with low risk of recurrence
  • Unwillingness to follow extended safety monitoring

About Caribou Biosciences, Inc.

Caribou Biosciences, Inc. is a leading biotechnology company focused on harnessing the power of CRISPR gene-editing technology to advance innovative therapeutics for a range of diseases. With a commitment to transforming the landscape of genetic medicine, Caribou is dedicated to developing next-generation cell therapies and genomic medicines that address unmet medical needs. The company's robust pipeline includes programs targeting cancer and other serious conditions, leveraging its proprietary CRISPR platform to create precise, effective, and safe treatment options. Through rigorous scientific research and collaboration, Caribou Biosciences aims to drive breakthroughs that improve patient outcomes and enhance the quality of life for individuals affected by complex diseases.

Locations

Philadelphia, Pennsylvania, United States

Milwaukee, Wisconsin, United States

Seattle, Washington, United States

Westmead, New South Wales, Australia

Perth, Western Australia, Australia

Birmingham, Alabama, United States

Boston, Massachusetts, United States

Bronx, New York, United States

Little Rock, Arkansas, United States

Hackensack, New Jersey, United States

Portland, Oregon, United States

Norfolk, Virginia, United States

Houston, Texas, United States

Tucson, Arizona, United States

Cincinnati, Ohio, United States

Louisville, Kentucky, United States

Jerusalem, , Israel

Salt Lake City, Utah, United States

Nashville, Tennessee, United States

Richmond, Victoria, Australia

Morristown, New Jersey, United States

Scottsdale, Arizona, United States

Gilbert, Arizona, United States

Dallas, Texas, United States

New York, New York, United States

Iowa City, Iowa, United States

Jerusalem, , Israel

Louisville, Kentucky, United States

Los Angeles, California, United States

Orlando, Florida, United States

Petah Tikva, , Israel

Augusta, Georgia, United States

Tel Aviv, , Israel

Houston, Texas, United States

Richmond, Virginia, United States

Columbus, Ohio, United States

La Jolla, California, United States

Orange, California, United States

Atlanta, Georgia, United States

Lexington, Kentucky, United States

Tel Hashomer, , Israel

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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