Phase 2 Lymphoma Trial, Recruiting
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:
- You are between 65 and 79 years old and have been assessed as "unfit" or "frail" based on a standard health and fitness assessment, OR you are 80 years old or older (any fitness level)
- You have been diagnosed with a specific type of aggressive lymphoma (DLBCL, high-grade B-cell lymphoma, or a lymphoma that has transformed), confirmed by a tissue sample (biopsy)
- You have not previously received any systemic (whole-body) treatment for your lymphoma — a short course of low-dose steroids (prednisone up to 100 mg/day for up to 7 days) is allowed
- Your lymphoma is at an advanced or bulky stage (Stage 2 bulky, Stage 3, or Stage 4)
- Your heart is pumping well enough to receive a specific type of chemotherapy — confirmed by a heart scan showing at least 45% pumping function
- You have at least one measurable area of lymphoma visible on a CT or MRI scan
- You are well enough to carry out basic daily activities (as assessed by your doctor using a standard scale)
- Your blood counts, kidney function, and liver function meet minimum required levels (your doctor will check these with blood tests)
- You have tested negative for HIV, OR if HIV-positive, you are stable on treatment, your immune cell count is adequate, and the virus is undetectable in your blood
- You are willing and able to follow all study procedures, in your doctor's opinion
- Female patients must be past menopause or have had surgery that means they cannot become pregnant; male patients must agree to use reliable contraception or remain abstinent during treatment and for a specified period afterwards, and must not donate sperm during this time
Who may not be able to join:
- You have previously received systemic (whole-body) treatment for lymphoma (localised radiotherapy, steroids, and antibiotics are still allowed)
- You have previously had a solid organ transplant (such as a kidney, liver, or heart transplant)
- You have previously had a bone marrow or stem cell transplant from a donor
- Your lymphoma has spread to your brain or spinal cord (central nervous system)
- You have uncontrolled HIV, or an active hepatitis B or C infection (confirm with trial site if you have a history of hepatitis B or C)
- You have an active serious infection that is not under control
- You have had major surgery within the last 4 weeks before starting the trial (exceptions may be possible — confirm with trial site)
- You have significant heart disease, such as a heart attack in the last 3 months, severe heart failure, unstable heart rhythm, or unstable chest pain
- You have an autoimmune condition that is not well controlled
- You have a history of a serious brain condition called progressive multifocal leukoencephalopathy (PML)
- You have another serious illness or condition that your doctor believes could put you at risk or affect the study results
- You are unable to follow the study procedures, in your doctor's opinion
- You have a known allergy or serious reaction to any of the study drugs, or to similar types of antibody-based medicines
- You have received certain immune-based cancer treatments (including monoclonal antibodies for cancer) within the past 3 months
- You have taken part in another experimental cancer treatment trial within the last 28 days
- You have previously had radiotherapy to the chest area around your heart
- You are currently taking high-dose steroids (more than 50 mg/day of prednisone or equivalent) for reasons unrelated to your lymphoma symptoms (some lower-dose or inhaled steroid use may be permitted — confirm with trial site)
- You have or have had another cancer that could interfere with the trial, unless it was successfully treated and has been in remission without treatment for at least 2 years, or meets other specific exceptions (confirm with trial site)
- You have received a live vaccine (such as a live flu vaccine) within the 4 weeks before starting treatment, or expect to need one during 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.
Contact this trial
Principal Investigator: Pallawi Torka, MD, Memorial Sloan Kettering Cancer Center
Phone: 201-775-7808
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
Where this trial is recruiting
Primary endpoints
evaluate the complete response rate (CRR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.