Phase 2 Lymphoma Trial, Recruiting NCT05641428 Sponsor: University Medical Center Groningen Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT05641428
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 certain types of large B-cell lymphoma (confirmed by tissue testing), including specific subtypes defined by a standard medical classification system, whose cancer has come back or stopped responding to at least 2 previous rounds of treatment
  • People aged 18 or older
  • People whose general physical wellbeing falls within a certain range on a standard health scale (meaning they are able to carry out daily activities, with at most limited restrictions)
  • People whose lymphoma has spread to the brain or spinal cord may still be eligible, provided they have no symptoms from that spread that would make it difficult for doctors to properly monitor for a specific type of side effect affecting the nervous system
  • People whose life expectancy (from causes other than the lymphoma itself) is estimated to be more than 3 months
  • People who are able to have children and are willing to use birth control from the time of joining the trial and for four months after receiving the pre-treatment regimen
  • People who have read, understood, and signed a consent form before any trial-related procedures begin
  • People who are able to give informed consent on their own behalf

Who may not be able to join:

  • People whose blood test results show that certain white blood cell counts, platelet counts, or lymphocyte (immune cell) counts are below specific thresholds
  • People whose lymphoma started in the brain or spinal cord (primary CNS lymphoma)
  • People with a known history of hepatitis B or C infection, unless they have been treated and confirmed by a specific type of blood test to have no detectable virus
  • People with an active HIV infection where the virus is still detectable in the blood, or where a specific immune cell count has fallen below a certain level
  • People with a known history of seizures, or who have been taking anti-seizure medication at any point in the past 12 months
  • People who have had a stroke in the past 12 months
  • People with unstable neurological problems (issues affecting the brain or nervous system that are not stable)
  • People with a known history or current diagnosis of an autoimmune disease affecting the brain or nervous system, such as multiple sclerosis or optic neuritis
  • People with an active autoimmune disease that currently requires medication to suppress the immune system
  • People with a brain or nervous system condition that, in the treating doctor's judgement, would make it difficult to properly monitor for neurological side effects, or a level of memory or thinking impairment that would interfere with treatment or monitoring (assessed using a standard test at the start of the trial)
  • People with an active fungal, viral, or bacterial infection
  • People with significant heart failure or a heart pumping function below a certain level on testing
  • People whose blood oxygen level at rest, while breathing normal air, falls below 92%
  • People with significant liver problems, as shown by certain blood test results being more than 5 times above the normal range — unless the liver results are directly caused by the lymphoma or by a specific inherited condition called Gilbert's disease
  • People whose kidneys are not filtering blood efficiently enough, based on a standard calculation
  • People who are pregnant or breastfeeding
  • People who are currently being treated for another active cancer
  • People who require long-term use of medications that suppress the immune system, with the exception of a low dose of a specific steroid (prednisolone at less than 10 mg per day)
  • People who have had a severe allergic reaction to any drug or its ingredients that is planned to be used during the trial (confirm with trial site)
  • People whose personal, family, social, or geographic circumstances may make it difficult to follow the trial schedule and requirements

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 26 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: T. (Tom) van Meerten, UMCG / HOVON

Phone: +31 (0)10 7041560

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
18 October 2022
Est. completion
1 December 2025

Where this trial is recruiting

🇳🇱 Netherlands

Primary endpoints

Progression-free survival (PFS) from date of IMP infusion (if applicable)

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: 26 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