Lentiviral Gene Therapy (Zamtocabtagene Autoleucel) LTFU

Description

This is an observational long-term follow-up (LTFU) study for subjects who previously received zamtocabtagene autoleucel, known as MB-CART2019.1.

Conditions

Non Hodgkin Lymphoma

Study Overview

Study Details

Study overview

This is an observational long-term follow-up (LTFU) study for subjects who previously received zamtocabtagene autoleucel, known as MB-CART2019.1.

A Prospective, Observational, Long-term Follow-up Study for Subjects Who Previously Received Zamtocabtagene Autoleucel in a United States Miltenyi Biomedicine-Sponsored Clinical Study

Lentiviral Gene Therapy (Zamtocabtagene Autoleucel) LTFU

Condition
Non Hodgkin Lymphoma
Intervention / Treatment

-

Contacts and Locations

Stanford

Stanford University, Stanford, California, United States, 94305

New Haven

Yale University, New Haven, Connecticut, United States, 06520

Baltimore

University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore, Maryland, United States, 21201

Boston

Dana Farber Cancer Institute, Boston, Massachusetts, United States, 02215

Milwaukee

Froedtert Hospital and the Medical College of Wisconsin, Milwaukee, Wisconsin, United States, 53226

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Received zamtocabtagene autoleucel in a Miltenyi Biomedicine-sponsored clinical study and have either completed the study or have discontinued early from the study.
  • * Provided written informed consent to participate in this study.
  • * None

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Miltenyi Biomedicine GmbH,

Remi Kaleta, MD, STUDY_DIRECTOR, Miltenyi Biomedicine GmbH

Study Record Dates

2039-12-01