Phase 2 Lymphoma Trial, Recruiting NCT05245656 Sponsor: Kim, Seok Jin Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT05245656
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 newly diagnosed with mantle cell lymphoma (a type of blood cancer) that has not yet been treated, and whose diagnosis has been confirmed by a tissue sample showing a specific marker called CD20+
  • People aged 70 or older, or people aged 60–69 if a doctor has determined they are not suitable for high-intensity treatment involving stem cell transplantation
  • People whose general health and ability to carry out daily activities meets a certain minimum level, as assessed by a standard medical scoring tool (confirm with trial site)
  • People whose heart is functioning well enough, as measured by a specific heart scan showing the heart pumping at least 50% efficiency
  • People whose kidneys are functioning well enough, based on blood or urine test results falling within acceptable ranges
  • People whose liver is functioning well enough, based on blood test results falling within acceptable ranges
  • People whose blood cell counts are at acceptable levels (with some flexibility if low counts are caused by the lymphoma affecting the bone marrow)
  • People who are able to give written consent to take part in the trial

Who may not be able to join:

  • People whose mantle cell lymphoma is classified as "in-situ" (a very early, localised form)
  • People whose lymphoma is classified as Stage 1 (the earliest and most localised stage)
  • People who have received treatment for any form of lymphoma (Hodgkin or non-Hodgkin) within the past 5 years
  • People who have had another active cancer within the past 3 years, unless it was a limited skin cancer (non-melanoma), papillary thyroid cancer, cervical cancer in situ, breast cancer in situ, or a localised prostate cancer that has been fully treated
  • People whose lymphoma has spread to the central nervous system (the brain or spinal cord)
  • People who test positive for certain markers of hepatitis B infection, unless a doctor has already started them on appropriate antiviral medication to manage this
  • People with a history of hepatitis C infection, unless testing shows the virus is no longer active in their blood
  • People with a known history of HIV infection
  • People with certain serious or unstable health conditions, including:
    • Severe heart failure
    • A heart attack, unstable chest pain, or serious heart rhythm problems within the past 6 months
    • A significant history of neurological or psychological conditions, including dementia or seizure disorders
    • Severe chronic lung disease causing low oxygen levels
    • A stroke or mini-stroke (TIA) within the past 6 months
    • Wounds, ulcers, or bone fractures that are not healing
    • An active, uncontrolled infection (bacterial, viral, or fungal) requiring ongoing treatment
  • People who are currently taking part in another experimental drug trial
  • People with a known serious allergic reaction to any of the study drugs: bendamustine, rituximab, cytarabine, or mannitol
  • People who have had a major surgery or serious physical injury within 28 days before the trial starts, or a tissue biopsy (open) within 7 days before the trial starts
  • Men who have not had a vasectomy and whose partner could become pregnant, unless they agree to use medically recommended contraception during the trial

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 23 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: 82-10-9933-1766

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
Kim, Seok Jin
Registry
ClinicalTrials.gov
Start date
18 October 2022
Est. completion
31 December 2029

Where this trial is recruiting

🇰🇷 South Korea

Primary endpoints

Progression-freesurvival

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: 23 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