Phase 2 Lymphoma Trial, Recruiting NCT05257018 Sponsor: Fudan University Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT05257018
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 aged between 18 and 75 years
  • People whose general health and ability to carry out daily activities falls within an acceptable range for this trial (rated on a standard scale as 0, 1, or 2) (confirm with trial site)
  • People who have been diagnosed with diffuse large B-cell lymphoma (a type of blood cancer) confirmed by a tissue test, have not yet received treatment for it, and are considered at high risk of the cancer spreading to the brain and spinal cord based on specific scoring criteria or the location of the lymphoma in the body (confirm with trial site)
  • People who have at least one tumour that can be measured on a scan, meeting minimum size requirements
  • People whose blood counts are within an acceptable range, showing the bone marrow is functioning adequately (the trial site may still consider people whose blood counts are affected by the lymphoma itself)
  • People whose liver function test results are within an acceptable range
  • People whose kidney function is within an acceptable range
  • People whose heart pumping function, as measured by a scan or test, is at an acceptable level
  • People of reproductive age who agree to use appropriate contraception during the trial; women of reproductive age must have a negative pregnancy blood test within 2 weeks before joining
  • People who agree to provide a tissue sample from their diagnosis (either a wax-embedded tissue block from within the past six months, or 20 prepared tissue slides)
  • People whose life expectancy is at least 3 months
  • People who have signed a consent form agreeing to take part

Who may not be able to join:

  • People with a known history of severe allergic reactions to certain types of antibody-based medicines, or who have a medical reason preventing them from receiving the treatment combinations used in this trial
  • People who already have signs, symptoms, or test results showing the lymphoma has spread to the brain or spinal cord
  • People with certain specific subtypes of diffuse large B-cell lymphoma that are not appropriate for the treatment approach used in this trial (confirm with trial site)
  • People with serious heart conditions, including severe heart failure, unstable chest pain, a heart attack within the past 6 months, congestive heart failure, or a specific abnormality on a heart tracing test
  • People who had a significant surgical procedure within three weeks before starting treatment
  • People currently being treated for another cancer, or diagnosed with another cancer within the past 5 years — though some exceptions may apply, such as certain fully treated skin cancers or cervical changes with no signs of disease remaining
  • People with significant problems with blood clotting
  • People who have previously received any treatment aimed at their lymphoma, other than a short course of steroid medication (up to 10 days)
  • People with a severe active infection
  • People with other serious, uncontrolled health conditions that could affect participation, such as uncontrolled diabetes, certain lung conditions, uncontrolled high blood pressure, or other significant conditions
  • People with active hepatitis B or hepatitis C infections at certain levels, or with HIV, or other immune deficiency conditions
  • People who are pregnant or breastfeeding

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 20 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: Dongmei Ji, doctor, Fudan University

Phone: 13564183928

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
Registry
ClinicalTrials.gov
Start date
26 February 2022
Est. completion
30 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

2-year central nervous system relapse rate; Concentration of doxorubicin in cerebrospinal fluid after using doxorubicin hydrochloride liposome injection

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: 20 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