Phase 1 Lymphoma Trial, Recruiting NCT06464861 Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT06464861
Recruiting Phase 1

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 aged 18 to 75 years old, 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 (MCL), or other similar types that have converted from a slower-growing form
  • People whose lymphoma has come back or stopped responding to treatment — the specific requirements depend on the type of lymphoma (confirm with trial site for your specific situation)
  • People whose previous treatment included a type of drug called a CD20 antibody (unless their cancer cells do not carry the CD20 marker) and a type of chemotherapy called anthracyclines
  • People who have at least one area of disease that can be measured on a scan, with the largest spot being at least 1.5 cm across
  • People with an expected survival of at least 12 weeks
  • People whose tumour tissue tests positive for a marker called CD19
  • People with a general health/activity score of 0–2 on a standard medical scale (meaning able to carry out daily activities, with at most some limitations)
  • People whose liver, kidney, and heart are functioning well enough to meet specific laboratory test thresholds (confirm details with trial site)
  • People whose resting blood oxygen level is above 92% in normal indoor air
  • People who have previously had a stem cell transplant
  • People who have finished other anti-lymphoma treatments (such as chemotherapy, radiotherapy, or immunotherapy) at least 3 weeks before starting this trial
  • People who previously received CAR-T cell therapy but whose treatment failed or whose disease came back at least 3 months after that therapy was assessed
  • Women of childbearing age who have a negative pregnancy test and agree to use effective contraception during the trial
  • People who have tested negative for COVID-19 and swine flu on two separate tests

Who may not be able to join:

  • People who are allergic to any ingredient in the cell therapy product used in this trial
  • People who have a history of any other cancer
  • People who have had, or are currently being treated for, a serious immune reaction called graft-versus-host disease (GvHD) — specifically moderate to severe forms (Grade II–IV)
  • People who received gene therapy within the past 3 months
  • People who have an active infection currently requiring treatment (minor infections like simple urinary tract infections or bacterial throat infections may be acceptable — confirm with trial site)
  • People who are infected with hepatitis B, hepatitis C, syphilis, HIV, or other conditions that weaken the immune system (some hepatitis B cases may still be considered — confirm with trial site)
  • People with serious heart problems classified as Grade III or IV by a standard medical heart-function scale
  • People who still have significant side effects from previous cancer treatment that have not recovered to a mild level (with the exception of tiredness, loss of appetite, or hair loss)
  • People with a history of epilepsy or other conditions affecting the brain or nervous system
  • People whose brain scans show signs that the lymphoma has spread to the central nervous system
  • Women who are currently breastfeeding and unwilling to stop
  • People who have any other condition or factor that the trial doctor believes could increase risk or affect the trial 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 12 July 2026
Phase 1: approximately ~10% 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: Wenbin Wenbin, Professor, Zhejiang University

Phone: +8613605801032

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 1
Registry
ClinicalTrials.gov
Start date
20 June 2024
Est. completion
30 June 2026

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: 12 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