RecruitingNCT05768269

A Study for Participants Previously Treated With Century Therapeutics Cellular Therapy Product

A Long-Term Follow-up Study for Subjects Previously Treated With A Century Therapeutics Cellular Therapy Product


Sponsor

Century Therapeutics, Inc.

Enrollment

375 participants

Start Date

Apr 29, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

This study is designed to collect long-term safety and survival data from participants previously treated in an eligible Century-sponsored index trial. This is an observational study, and the elements of the study design allow for important follow-up for safety, survival, and the continued evaluation of any late adverse events (AEs) that may appear after treatment with such cellular products. Additionally, collection of persistence data from participants will support the identification of any long-term risks or late AEs that may be causally related to treatment with such cellular products.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Participant has provided written informed consent prior to any long-term follow-up (LTFU) study-specific procedures.
  • Participants received at least one treatment with a cellular therapy product in an eligible index trial.
  • Participant was withdrawn, early discontinued or completed an eligible index trial.
  • Participant is willing and able to comply with scheduled visits, study plan, and other study procedures.

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Interventions

OTHERNo Intervention

As this is a non-interventional rollover, long-term safety follow-up study, no intervention will be administered.


Locations(7)

Banner MD Anderson Cancer Center

Gilbert, Arizona, United States

University of Southern California - Norris Comprehensive Cancer Center

Los Angeles, California, United States

University of Maryland Medical Center

Baltimore, Maryland, United States

Corewell Health

Grand Rapids, Michigan, United States

Levine Cancer Institute

Charlotte, North Carolina, United States

University of Cincinnati Medical Center

Cincinnati, Ohio, United States

Swedish Cancer Institute

Seattle, Washington, United States

View Full Details on ClinicalTrials.gov

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NCT05768269


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