NCT06504394
Who may be able to join
Who might be able to join this trial:
- You have been diagnosed with classical Hodgkin lymphoma (a type of blood cancer) or primary mediastinal B-cell lymphoma (a type of lymphoma in the chest), confirmed by a tissue biopsy
- Your cancer can be measured on a scan, as assessed by the study doctor using standard guidelines
- You are expected to live for more than 3 months
- If you have HIV, it must be well controlled with HIV medication
- If you have hepatitis B, you must have been on hepatitis B treatment for at least 4 weeks and have no detectable virus in your blood before joining
- If you have had hepatitis C in the past, you must have completed a full course of hepatitis C treatment at least 4 weeks before joining, with no detectable virus in your blood
- You are generally well enough to carry out light daily activities (you will be assessed on a standard health scale within 7 days before starting treatment)
Who may not be able to join:
- You have serious, active heart or blood vessel disease
- You have fluid around your heart or a significant amount of fluid around your lungs
- You have another cancer that is growing or has needed active treatment in the past 2 years
- You have a condition that weakens your immune system, or have taken steroid or immune-suppressing medication within 7 days before starting the trial
- You have received a type of cancer treatment called a monoclonal antibody within the past 4 weeks, or have not recovered from side effects of earlier treatments
- You have previously been treated with certain immunotherapy drugs that target specific proteins on immune cells (called PD-1, PD-L1, or PD-L2 inhibitors) (confirm with trial site)
- You have received any cancer treatment, including experimental treatments, within 4 weeks before starting the trial
- You have had radiotherapy within 2 weeks before starting the trial, or still have side effects from radiation that need steroid treatment
- You have received a live vaccine within 30 days before starting the trial
- You are currently receiving cancer treatment not included in this trial's plan
- You have active cancer that has spread to your brain or the lining around your brain and spinal cord
- You have an autoimmune disease (where your immune system attacks your own body) that has needed treatment in the past 2 years
- You have a history of, or currently have, lung inflammation that required steroid treatment
- You have an active infection that requires treatment with medicines given throughout your body (with some exceptions — confirm with trial site)
- You currently have both hepatitis B and hepatitis C infections at the same time
- You have had a solid organ transplant at any point, or a bone marrow/stem cell transplant from a donor within the last 5 years
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.
Trial details
Where this trial is recruiting
1 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Objective Response Rate (ORR) per Lugano Classification Criteria as Assessed by Investigator; Maximum Concentration (Cmax) of Pembrolizumab After Administration of SC Pembrolizumab Coformulated with Hyaluronidase; Lowest Plasma Concentration (Ctrough) of Pembrolizumab After Administration of SC Pembrolizumab Coformulated with Hyaluronidase; Area Under the Concentration-Time Curve of Pembrolizumab After Administration of SC Pembrolizumab Coformulated with Hyaluronidase from Week 0-Week 6 (AUC0-6weeks)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 30 June 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.