Phase 2 Lymphoma Trial, Recruiting NCT05842707 Sponsor: Aibin Liang,MD,Ph.D. Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT05842707
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 willing to take part voluntarily and sign a consent form
  • Adults aged 18 to 75, of any gender
  • People who have been diagnosed (confirmed by tissue testing) with certain types of B-cell lymphoma, including diffuse large B-cell lymphoma (DLBCL), transformed follicular lymphoma, primary mediastinal B-cell lymphoma, mantle cell lymphoma, or related types — and whose cancer has come back or stopped responding to previous treatments (specific treatment history requirements vary by lymphoma type — confirm with trial site)
  • People who have at least one measurable area of disease that is 1.5 cm or larger
  • People whose life expectancy, apart from their lymphoma, is estimated to be more than 12 weeks
  • People whose lymphoma has previously tested positive for CD19 or CD70 markers
  • People with a general health and activity level score (called ECOG status) of 0 to 3, meaning they range from fully active to limited in self-care (confirm with trial site)
  • People whose liver, kidney, heart, and blood counts meet specific minimum levels of function as determined by blood tests and heart scans
  • People who have previously had one autologous stem cell transplant (a procedure using their own stem cells)
  • People who have waited the required time since their last treatment before receiving the study cell infusion (at least 3 weeks after chemotherapy or immunotherapy, or at least 2 weeks after targeted drug therapy alone)
  • People whose previous CAR-T therapy has failed or whose disease came back at the 3-month assessment point
  • People of childbearing or child-fathering potential who are willing to use birth control throughout the study, and women who can become pregnant must have a negative pregnancy test
  • People who have tested negative for COVID-19 on two separate PCR or nucleic acid tests

Who may not be able to join:

  • People who are allergic to any ingredient in the study cell product
  • People who have had, or currently have, another type of cancer
  • People who developed moderate to severe graft-versus-host disease (a complication from transplant) after a previous stem cell transplant, or who are still receiving treatment for it
  • People who have had systemic gene therapy within the past 3 months
  • People with an active, serious infection involving fungal, viral, or bacterial causes (though preventive infection treatments are permitted)
  • People with a known history of hepatitis B (with certain virus levels), hepatitis C, syphilis, HIV, or other immune deficiency conditions
  • People with severe heart failure classified as Class III or IV by standard medical criteria
  • People still experiencing significant side effects (above a minor level) from previous treatments, with the exception of hair loss, tiredness, or reduced appetite
  • People with a known history of active seizures, ongoing seizure activity, or other diseases affecting the brain or nervous system
  • People whose scans (CT or MRI) show lymphoma affecting the brain or spinal fluid
  • People who are currently breastfeeding
  • People who, in the opinion of the trial doctor, have any other circumstances that could increase risk or affect the reliability of the study results

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 21 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: aibin Liang, Shanghai Tongji Hospital, Tongji University School of Medicine

Phone: 18601670600

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
Aibin Liang,MD,Ph.D.
Registry
ClinicalTrials.gov
Start date
18 January 2023
Est. completion
18 January 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

incidence of dose limiting toxicity(DLTs)

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: 21 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