For Healthcare Professionals

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

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About the study

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.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:

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 Participant was withdrawn, early discontinued or completed an eligible index trial.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

EXCLUSION CRITERIA

Exclusion Criteria:

-This study has no exclusion criteria.

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 888-688-0644Email iconEmail Study Center

Study Details


Contition

Hematological Malignancy,Solid Tumor Malignancy

Age

18+

Participants Needed

375

Est. Completion Date

Mar 31, 2040

Treatment Type

OBSERVATIONAL


Sponsor

Century Therapeutics, Inc.

ClinicalTrials.gov NCT Identifier

NCT05768269

Study Number

CNTY-LTFU-01

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