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Terminated Phase 1Phase 2 Interventional Results available

A Safety and Efficacy Study Evaluating CTX110 in Subjects With Relapsed or Refractory B-Cell Malignancies (CARBON)

ClinicalTrials.gov ID: NCT04035434

Public ClinicalTrials.gov record NCT04035434. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 16, 2026, 4:09 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/2 Dose Escalation and Cohort Expansion Study of the Safety and Efficacy of Allogeneic CRISPR-Cas9-Engineered T Cells (CTX110) in Subjects With Relapsed or Refractory B-Cell Malignancies (CARBON)

Study identification

NCT ID
NCT04035434
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
CRISPR Therapeutics AG
Industry
Enrollment
93 participants

Conditions and interventions

Interventions

  • CTX110 Biological

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 21, 2019
Primary completion
Oct 3, 2024
Completion
Oct 3, 2024
Last update posted
Oct 23, 2025

2019 – 2024

United States locations

U.S. sites
21
U.S. states
18
U.S. cities
21
Facility City State ZIP Site status
Cedars Sinai Los Angeles California 90048
UCSF Medical Center San Francisco California 94143
Mayo Clinic Jacksonville Florida 32224
Emory University Winship Cancer Institute Atlanta Georgia 30322
University of Chicago Chicago Illinois 60637
University of Kansas Westwood Kansas 66205
Markey Cancer Center, University of Kentucky Lexington Kentucky 40536
University of Maryland Baltimore Maryland 21201
Beth Israel Deaconess Medical Center Boston Massachusetts 02215
University of Minnesota Minneapolis Minnesota 55455
Washington University St Louis Missouri 63130
Roswell Park Cancer Insitute Buffalo New York 14203
Weill Cornell Medical College / New York Presbyterian Hospital New York New York 10021
Duke University Durham North Carolina 27710
Oregon Health and Science University Portland Oregon 97239
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
Sarah Cannon Research Institute Nashville Tennessee 37203
Harold C. Simmons Comprehensive Cancer Center, UT Southwestern Medical Center Dallas Texas 75390
Texas Transplant Institute San Antonio Texas 78229
Virginia Commonwealth University Massey Cancer Center Richmond Virginia 23298
Swedish Cancer Institute Seattle Washington 98104

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04035434, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 23, 2025 · Synced May 16, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04035434 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →