Phase 2 Lymphoma Trial, Recruiting NCT06736613 Sponsor: Memorial Sloan Kettering Cancer Center Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06736613
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 signed an informed consent form and are willing and able to follow the study requirements.
  • People who are 18 years of age or older.
  • People diagnosed with certain types of aggressive B-cell lymphoma that carry a high risk of the cancer spreading to the brain, including: Diffuse Large B-cell Lymphoma (DLBCL) with a high CNS risk score (4 or above); advanced-stage High Grade B-cell Lymphoma with certain gene changes (MYC, BCL2, and/or BCL6); DLBCL that started in the breast, testicle, skin of the leg, or blood vessels; advanced-stage DLBCL in people living with HIV; or DLBCL involving certain organs (such as the kidney, adrenal gland, bone marrow, spine area, nose/sinuses, uterus, testicle, or skull) combined with a high CNS risk score.
  • People whose DLBCL developed from a previously slower-growing (indolent) B-cell lymphoma, as long as the cancer has never previously spread to the brain or spinal fluid.
  • People who are planned to receive standard chemotherapy combined with immunotherapy as their treatment.
  • People who are able to safely undergo a lumbar puncture (a procedure to collect fluid from around the spine), with no conditions that would make this unsafe.
  • People who have not yet received any systemic (whole-body) treatment for an aggressive B-cell lymphoma before joining the study — prior treatment for a slower-growing lymphoma is permitted, and limited short-term steroid use may also be permitted (confirm with trial site).
  • People with a general health and activity level rated 0 to 2 on the ECOG scale, meaning they are fully active to capable of basic self-care (confirm with trial site for exact definition).

Who may not be able to join:

  • People who have received active systemic treatment for another cancer (other than a slow-growing B-cell lymphoma) within the past 2 years — note that local treatments like surgery or targeted radiation given with the aim of curing another cancer within 2 years may still be permitted (confirm with trial site).
  • People who currently have another active cancer, with the exception of certain low-risk or localised cancers such as basal cell skin cancer, localised squamous cell skin cancer, localised prostate cancer, or early-stage cancers in the cervix, breast, or bladder.
  • People with an uncontrolled medical condition that, in the doctor's judgement, would make it unsafe to receive intensive chemotherapy — for example, serious active infections, uncontrolled high blood pressure, chest pain, heart rhythm problems, lung disease, or autoimmune conditions.
  • People with a known active infection (bacterial, viral, fungal, or other) at the time of joining the study, or who have needed intravenous antibiotics or a hospital stay for an infection within the 2 weeks before starting treatment.
  • People with a psychiatric illness or personal circumstances that would significantly affect their ability to safely participate in or follow the study 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 27 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: Jennifer Lue, MD, Memorial Sloan Kettering Cancer Center

Phone: 646-608-4160

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
11 December 2024
Est. completion
11 December 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Incidence of positive cerebral spinal fluid/CSF ctDNA

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: 27 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