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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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