Phase 1 Lymphoma Trial, Recruiting NCT06707259 Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University Condition: Lymphoma
Back to Lymphoma

Phase 1 Lymphoma Trial, Recruiting

NCT06707259
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 who have volunteered to take part and have signed a consent form
  • 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 related types, where the disease has come back or stopped responding to previous treatments under specific conditions (confirm with trial site for full details)
  • People who have at least one measurable area of disease that is 1.5 cm or larger in its longest measurement
  • People whose expected survival is at least 12 weeks
  • People whose tumour tissue has tested positive for a protein called CD19
  • People with a general health and activity level rated 0 to 2 on a standard scale (confirm with trial site)
  • People whose liver, kidney, and heart are functioning well enough to meet specific test result thresholds (confirm with trial site for exact values)
  • People who have previously had a stem cell transplant
  • People who have finished their most recent cancer treatment (such as chemotherapy, radiotherapy, or immunotherapy) at least 3 weeks before starting this trial
  • People who have previously received CAR-T cell therapy but whose disease came back or did not respond, assessed at least 3 months after that therapy
  • 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 on two separate tests

Who may not be able to join:

  • People who have had an allergic reaction to any ingredient in the type of cell product used in this trial
  • People who have a history of any other type of cancer
  • People who have previously experienced moderate to severe graft-versus-host disease (a complication sometimes seen after certain transplants), or who are currently receiving treatment for it
  • People who have received gene therapy within the past 3 months
  • People who have an active infection currently requiring treatment (other than simple urinary tract infections or bacterial throat infections)
  • People with hepatitis B (with certain test result exceptions — confirm with trial site), hepatitis C, syphilis, HIV, or other conditions affecting the immune system
  • People whose heart function is rated as Grade III or IV under a standard medical classification system
  • People who still have significant side effects from previous cancer treatments that have not yet recovered to an acceptable level (with some exceptions such as tiredness, loss of appetite, or hair loss)
  • People with a history of epilepsy or other conditions affecting the brain or central nervous system
  • People whose brain scan shows signs that lymphoma has spread to the central nervous system
  • People who have previously received or are currently receiving another treatment that targets CD19
  • Women who are breastfeeding and are not willing to stop
  • People whom the trial doctors consider may face increased risk or whose participation may affect the reliability of 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 7 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

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
1 December 2024
Est. completion
1 December 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: 7 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