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 have been diagnosed with Hodgkin Lymphoma (HL) or Acute Myeloid Leukemia (AML) that has come back or gotten worse after previous treatment (previous immunotherapy treatments are allowed)
- If you have HL that has spread beyond the lymph nodes to other parts of the body
- If you have HL and your doctors do not consider you a candidate for high-dose standard chemotherapy
- You are at least 1 year old (there is no upper age limit; the trial includes children, teenagers, and adults treated at the pediatric/adolescent center)
- You are well enough to carry out some daily activities, as measured by standard medical scoring tools (confirm with trial site)
- Your kidneys are working well enough, unless any problems are caused by your illness
- Your liver is working well enough, with certain blood test results within acceptable ranges, unless affected by your illness
- You are able and willing to sign a consent form agreeing to take part in the study
- If you are a woman who could become pregnant, you must have a negative pregnancy test within 72 hours before starting treatment and before each new dose
- Women who could become pregnant must agree to use reliable contraception during the study and for 4 months after the last treatment
- Men must agree to use reliable contraception during the study and for 1 month after the last treatment, not donate sperm during the study or for 30 days after the last treatment, and use a condom during this time; they must also tell their doctor right away if their partner becomes or suspects she may be pregnant
Who may not be able to join:
- You have a known allergy to azacitidine, pembrolizumab, or any of their ingredients
- You have serious, uncontrolled health conditions, such as an active uncontrolled infection, uncontrolled high blood pressure, severe heart failure, or a significant irregular heartbeat
- You are known to have HIV, or currently have active Hepatitis B or C
- You have any other medical, mental health, or personal situation that the study doctor believes could interfere with your safe participation in the trial
- You are currently pregnant or breastfeeding
- You have received a live vaccine (such as certain flu or travel vaccines) within 30 days before starting the study
- You have taken medications that suppress the immune system within 14 days before starting treatment (with some exceptions, such as low-dose steroids, steroid nasal sprays, inhalers, skin creams, or steroid injections into a joint — confirm with trial site)
- You have been diagnosed with certain autoimmune diseases (such as inflammatory bowel disease, celiac disease, or Wegener syndrome) that were active within the past 2 years (note: some milder conditions like asthma, vitiligo, or psoriasis not needing systemic treatment may not disqualify you — confirm with trial site)
- You have known active cancer spread to the brain or the fluid surrounding the brain and spinal cord
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: David McCall, MD, M.D. Anderson Cancer Center
Phone: (713) 792-6604
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
To assess the overall response rate (ORR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.