Lymphoma Trial, Recruiting NCT06850285 Sponsor: Shanxi Bethune Hospital Condition: Lymphoma
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Lymphoma Trial, Recruiting

NCT06850285
Recruiting Not Applicable

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 15 to 80 years old, of any gender
  • People diagnosed with a type of blood cancer (lymphoma) where cancer cells test positive for a protein called CD30
  • People whose cancer cells show CD30 on more than 10% of cells, confirmed by a laboratory tissue test
  • People who have at least one tumour or affected area that can be measured using standard imaging methods
  • People who are not suitable for a stem cell transplant using their own cells, or whose cancer came back after having that type of transplant
  • People who are not suitable for a treatment called BV (brentuximab vedotin), or whose cancer came back after BV treatment, with CD30 confirmed by a tissue test
  • People whose doctors estimate they are likely to survive for at least 3 months
  • People who are generally well enough to carry out light activities, based on standard medical fitness scales (ECOG 0–2, KPS above 60%)
  • People whose liver, kidney, and heart are functioning well enough to meet specific laboratory and test thresholds (confirm exact values with trial site)
  • People with enough healthy blood cells and suitable vein access to allow a blood collection procedure called apheresis
  • People whose brain and spinal cord scans (MRI) show the lymphoma has not spread to the central nervous system
  • People who are able to have children and are willing to use reliable contraception during the trial
  • People (or their legal guardian) who are able to understand and sign a consent form agreeing to take part

Who may not be able to join:

  • People who have a serious complication of lymphoma called haemophagocytic syndrome
  • People who are pregnant, breastfeeding, or planning to become pregnant within six months
  • People who test positive for Hepatitis B (unless the virus is confirmed inactive by DNA testing), Hepatitis C, HIV, or syphilis
  • People who have had another type of cancer, unless it was a certain type of skin cancer or early-stage cervical cancer that has been fully treated
  • People who received a CD30-targeted antibody treatment within 4 weeks before joining the trial
  • People who still have unresolved side effects rated above Grade 1 from any previous cancer treatment
  • People with active uncontrolled bleeding or a known condition that causes abnormal bleeding
  • People who had a stem cell transplant using their own cells within the past 6 weeks
  • People with an active bacterial or fungal infection that is not under control
  • People with a known allergy to the study drug or any of its ingredients
  • People with an active autoimmune disease that currently requires ongoing medical treatment
  • People with a mental health condition that would make it difficult to cooperate with treatment or assessments
  • People who have taken part in another clinical trial within 1 month before this study
  • People who have previously had a stem cell transplant using cells from another person (allogeneic transplant)
  • People with any other condition that the treating doctor feels could interfere with the trial or put the participant at risk

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 19 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: jia wei, Shanxi Bethune Hospital

Phone: 13986102084

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
Not Applicable
Sponsor
Shanxi Bethune Hospital
Registry
ClinicalTrials.gov
Start date
5 September 2025
Est. completion
1 June 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall response rate; To evaluate safety and dose limiting toxicities (DLT) of autologous CD30 CAR-T and establish the recommended Phase dose

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: 19 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