Phase 3 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:
- People who have been confirmed through a tissue biopsy to have a type of blood cancer called diffuse large B-cell lymphoma (DLBCL), diagnosed according to standard medical guidelines
- People whose cancer shows up as active on a PET scan (a type of imaging test), scoring 4 or 5 on a standard 5-point scale
- People who have not yet received any treatment for their DLBCL
- People who are generally able to carry out daily activities, as measured by a standard medical scoring system (rated 0 to 2 out of 5), assessed within 7 days before joining the trial
- People whose heart is pumping at 45% efficiency or above, as measured by a heart ultrasound or a specific heart scan
- People living with HIV, provided their HIV is well managed with medication
- People who have hepatitis B, provided they are on antiviral treatment and the virus is undetectable in their blood before joining the trial
- People with a history of hepatitis C, provided the virus is undetectable in their blood at the time of screening
Who may not be able to join:
- People whose DLBCL developed from a slower-growing (indolent) lymphoma that transformed into this more aggressive type
- People diagnosed with a related but different type of lymphoma called primary mediastinal B-cell lymphoma or Grey zone lymphoma
- People whose DLBCL is classified as Stage I (the earliest, most localised stage) according to a standard staging system
- People with serious heart or blood vessel conditions, including a stroke or heart attack within the past 6 months, unstable chest pain, significant heart failure, or a serious irregular heartbeat requiring medication
- People with significant fluid buildup around the heart or lungs
- People experiencing ongoing nerve problems (such as tingling, numbness, or weakness) that are moderate or worse in severity
- People who have a specific inherited nerve condition called Charcot-Marie-Tooth disease (the demyelinating form)
- People living with HIV who have also had Kaposi's sarcoma or a condition called Multicentric Castleman's Disease
- People currently taking corticosteroid medications (such as prednisone)
- People who have received a live vaccine within 30 days before starting the trial (non-live/killed vaccines are permitted)
- People who have or have had another cancer that is still active or has required treatment within the past 2 years
- People with lymphoma that has spread to the brain or spinal cord (central nervous system)
- People with an autoimmune disease that has required whole-body treatment within the past 2 years
- People with an active infection that requires medication to treat
- People who have both active hepatitis B and active hepatitis C at the same time
- People who have previously received an organ or tissue transplant from another person
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: Medical Director, Merck Sharp & Dohme LLC
Phone: 1-888-577-8839
Australian sites
+61744333549
0870745898
+61353204000
+61384058000
+61864775013
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
5 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Progression-free survival (PFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.