Phase 2 Lymphoma Trial, Recruiting NCT06479356 Sponsor: Shanghai Ming Ju Biotechnology Co., Ltd. Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06479356
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are 18 years of age or older
  • People who are willing and able to sign a consent form for the study
  • People who have been diagnosed with Large B-cell Lymphoma confirmed by a tissue sample test
  • People whose lymphoma has come back, stopped responding, or gotten worse after receiving at least two rounds of treatment, including a specific type of chemotherapy (anthracyclines), an anti-cancer antibody targeting CD20 (such as rituximab), and a stem cell transplant using their own cells
  • People whose lymphoma can be detected and measured using PET and CT scans, according to standard lymphoma assessment guidelines
  • People who are in generally good physical condition, able to carry out normal daily activities with little or no limitation (rated 0 or 1 on a standard health scale used in clinical trials)
  • People whose heart, liver, kidneys, and other organs are functioning well enough to meet the trial's requirements
  • People who have suitable veins or blood vessel access to allow a blood cell collection procedure called leukapheresis
  • People who have previously received a treatment targeting CD19, where it has been confirmed that their lymphoma cells still carry the CD19 marker
  • Women who could become pregnant must agree to use highly effective contraception for one year after the last dose of the study treatment (Relma-cel)
  • Men whose partners could become pregnant must agree to use effective barrier contraception for one year after the last dose of the study treatment (Relma-cel)

Who may not be able to join:

  • People whose lymphoma started in the brain or spinal cord (primary CNS lymphoma)
  • People who have had another separate cancer that has not been in remission for at least two years
  • People who have an active infection with hepatitis B, hepatitis C, HIV, or syphilis at the time of screening
  • People who have an active blood clot in a vein or in the lungs, or who have needed blood-thinning medication for a clot within the three months before signing the consent form
  • People who have an infection (fungal, bacterial, viral, or other) that is not under control
  • People who have a condition called graft-versus-host disease (GVHD), either current or ongoing, which can occur after certain types of transplants
  • People with a history of serious heart disease or significant brain or nervous system conditions
  • People who are pregnant or currently breastfeeding
  • People who have recently received certain other treatments for lymphoma — including chemotherapy, steroids, experimental drugs, radiation, or a donor stem cell transplant — and have not waited long enough since their last dose (confirm with trial site for specific timeframes)
  • People who are unable or unwilling to follow the procedures and requirements set out in the study plan
  • People who have previously received CAR T-cell therapy or any other type of genetically modified T-cell therapy

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 9 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Huilai Zhang, Tianjin Cancer Hospital

Phone: +86 21 50464201

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Shanghai Ming Ju Biotechnology Co., Ltd.
Registry
ClinicalTrials.gov
Start date
15 August 2024
Est. completion
30 April 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Objective response rate (ORR) in LBCL subjects

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 9 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov