Phase 2 Lymphoma Trial, Recruiting NCT06996132 Sponsor: Institute of Hematology & Blood Diseases Hospital, China Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06996132
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 diagnosed with a relapsed or refractory aggressive B-cell lymphoma, specifically diffuse large B-cell lymphoma (DLBCL), high-grade B-cell lymphoma, or a large B-cell lymphoma that developed from another condition.
  • People whose lymphoma has come back or stopped responding to treatment, fitting into one of two groups:
    • Group 1: People who have had 2 or more prior treatment courses (including both a targeted antibody therapy and a chemotherapy type called anthracycline) and whose disease has progressed after the last treatment — OR people whose lymphoma came back or did not respond well enough to their first course of treatment.
    • Group 2: People whose PET-CT scan still shows active disease after 2 cycles of initial treatment, or whose remaining disease has been confirmed by biopsy after initial therapy.
  • People aged 18 to 65 years old.
  • People who are generally able to care for themselves and carry out daily activities, with only limited restrictions (confirm with trial site for the specific activity level required).
  • People whose blood cell counts meet minimum levels at screening — unless low counts are caused by lymphoma in the bone marrow (confirm exact values with trial site).
  • People whose liver and kidney function results fall within the levels required at screening (confirm exact values with trial site).
  • People whose heart pumping function is within the normal range, as measured by an ultrasound of the heart.
  • People whose blood oxygen level is above 92% while breathing normal air.
  • People whose doctor estimates they have a life expectancy of at least 3 months.

Who may not be able to join:

  • People with lymphoma that started in the brain or spinal cord (primary central nervous system lymphoma).
  • People who have previously had a stem cell transplant, either using their own cells or donated cells.
  • People with an active hepatitis B or hepatitis C infection detected in their blood.
  • People with serious ongoing conditions that are not well controlled, such as active infections, heart or blood vessel problems, blood clotting disorders, or connective tissue diseases.
  • People with a history of epilepsy or other conditions affecting the brain or nervous system.
  • People who are pregnant or currently breastfeeding.
  • People with an HIV infection.
  • People who have had another type of cancer, unless they have been free of that cancer for 5 or more years — or unless the previous cancer was a non-melanoma skin cancer, a localised skin cancer, or cervical carcinoma in situ that has been treated and cured.
  • People whom the trial investigators determine are not suitable for other reasons (confirm with trial site).

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 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: Dehui Zou, Institute of Hematology & Blood Diseases Hospital, China

Phone: 86-022-23608461

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
Institute of Hematology & Blood Diseases Hospital, China
Registry
ClinicalTrials.gov
Start date
9 May 2025
Est. completion
30 May 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

complete response rate after CAR-T±ASCT

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