Phase 2 Lymphoma Trial, Recruiting NCT05931328 Sponsor: The First Affiliated Hospital with Nanjing Medical University Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT05931328
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 who have been diagnosed with primary central nervous system lymphoma (a type of lymphoma affecting the brain or spinal cord), confirmed by a pathology test using 2016 WHO standards, and who have already received at least one round of chemotherapy but whose disease has come back or continued to grow.
  • People aged 18 to 75 years old.
  • People whose general physical condition falls within an accepted range on a standard medical scoring scale (ECOG performance score of 0 to 4) (confirm with trial site).
  • People whose doctors expect them to live for more than 3 months.
  • People who have had a full-body PET/CT scan and a head MRI within 28 days before joining the trial, showing at least one measurable area of disease, OR who have abnormal results from a spinal fluid test, OR who have confirmed disease in the retina or the gel-like fluid inside the eye.
  • People whose liver, kidney, heart, blood clotting, and thyroid function all meet certain minimum health thresholds as measured by blood tests (confirm with trial site for specific values).
  • Women who could become pregnant must use contraception or have a negative pregnancy test before joining, and must continue using contraception during the trial and for 90 days after the last dose.
  • Men must use contraception during the trial and for 90 days after the last dose, or must have had a surgical sterilisation procedure.
  • People who are willing to take part, sign a consent form, follow the study requirements, and attend follow-up appointments.

Who may not be able to join:

  • Women who are pregnant or breastfeeding.
  • People whose lymphoma has spread to parts of the body outside the central nervous system (brain and spinal cord).
  • People with poor bone marrow function, specifically those with very low levels of certain blood cells (neutrophils, platelets, or haemoglobin) below set thresholds (confirm with trial site for exact values).
  • People who have been diagnosed with another cancer (other than lymphoma), unless they were successfully treated more than 5 years ago with no known active disease, or unless they had certain skin conditions (basal cell carcinoma or cervical pre-cancer) that were fully treated with no remaining signs of disease.
  • People who have a known allergy to any ingredient in the study drug.
  • People who have previously received an organ transplant or stem cell transplant from another person.
  • People who may need to receive other cancer treatments during the study period.
  • People who have HIV, active hepatitis, or other serious infections that are not under control.
  • People with a known history of significant neurological or psychiatric conditions.
  • People whose drug use, or medical, psychological, or social circumstances might interfere with the study or make it difficult to assess the results.
  • People considered unsuitable for the trial by the medical team running the study.

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 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

Phone: 13951699449

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
15 October 2022
Est. completion
1 October 2024

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall Response Rate (ORR); Adverse event rate

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