A Long-term Study for Participants Previously Treated With Ciltacabtagene Autoleucel

Description

The purpose of this study is to collect long-term follow-up data on delayed adverse events after administration of ciltacabtagene autoleucel (cilta-cel), and to characterize and understand the long-term safety profile of cilta-cel.

Conditions

Multiple Myeloma

Study Overview

Study Details

Study overview

The purpose of this study is to collect long-term follow-up data on delayed adverse events after administration of ciltacabtagene autoleucel (cilta-cel), and to characterize and understand the long-term safety profile of cilta-cel.

Long-term Follow-up Study for Participants Previously Treated With Ciltacabtagene Autoleucel

A Long-term Study for Participants Previously Treated With Ciltacabtagene Autoleucel

Condition
Multiple Myeloma
Intervention / Treatment

-

Contacts and Locations

Phoenix

Mayo Clinic Cancer Center-Scottsdale, Phoenix, Arizona, United States, 85054

Duarte

City of Hope, Duarte, California, United States, 91010

San Francisco

University of California San Francisco, San Francisco, California, United States, 94143

Stanford

Stanford University Medical Center, Stanford, California, United States, 94305-5623

Atlanta

Emory University, Atlanta, Georgia, United States, 30322

Chicago

Northwestern University, Chicago, Illinois, United States, 60611

Chicago

University of Chicago, Chicago, Illinois, United States, 60637

Indianapolis

Indiana University, Indianapolis, Indiana, United States, 46202

Westwood

Kansas University Medical Center, Westwood, Kansas, United States, 66205

Boston

Dana Farber Cancer Institute, Boston, Massachusetts, United States, 02115

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

  • * Participants who have received at least one dose of cilta-cel in a Company-sponsored clinical study
  • * Participants who have provided informed consent for this study

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Janssen Research & Development, LLC,

Janssen Research & Development, LLC Clinical Trial, STUDY_DIRECTOR, Janssen Research & Development, LLC

Study Record Dates

2037-07-29