Phase 2 Lymphoma Trial, Recruiting NCT05355051 Sponsor: M.D. Anderson Cancer Center Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT05355051
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:

  • 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.

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 19 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: 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

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
5 October 2022
Est. completion
31 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

To assess the overall response rate (ORR)

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: 19 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