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Long-term Follow-up Study of Lentiviral-based Gene-edited Immune Cell Therapy

Sponsor: Pell Bio-Med Technology Co., Ltd. · NCT05377307 on ClinicalTrials.gov ↗

Conditions studied

Diffuse Large B Cell LymphomaLarge B-cell LymphomaPrimary Mediastinal Large B Cell LymphomaFollicular Lymphoma Grade 3AFollicular Lymphoma Grade 3B

What it tests

  • Pell's lentiviral-based gene-edited immune cell therapygenetic

Where it's running5 sites

5 international sites
  • Kaohsiung Medical University Chung-Ho Memorial Hospital

    Kaohsiung, Taiwan, Taiwan 807377

    Recruiting now
    • Yi-Chang Liu(principal investigator)
  • National Taiwan University Hospital

    Taipei, Taiwan, Taiwan 10025

    Recruiting now
    • Shang-Ju Wu(principal investigator)
  • Taipei Veterans General Hospital

    Taipei, Taiwan, Taiwan 112201

    Recruiting now
    • Jyh-Pyng Gau(principal investigator)
  • Chi Mei Medical Center

    Tainan, Taiwan 710

    Recruiting now
    • Hung-Chang Wu(principal investigator)
  • Taipei Medical University - Taipei Medical University Hospital

    Taipei, Taiwan 11031

    Recruiting now
    • Chao-Hua Chiu(contact)
See the official eligibility language

Shown exactly as written on ClinicalTrials.gov. Your oncologist is the right person to judge whether it fits your situation.

Inclusion Criteria:

1. Patients must have ever received Pell's lentiviral-based gene-edited immune cell as monotherapy or as combination therapy in clinical trials.
2. The last lentiviral-based gene-edited immune cell infusion within 15 years.
3. Patient/patient's parent/legal guardian is capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.

Exclusion Criteria:

There are no specific exclusion criteria for this study.

Updated 2025-05-13 on ClinicalTrials.gov. Always confirm current details with the study team or your oncologist.