RecruitingPhase 2NCT05355051
A Phase II Study of the Combination of Azacitidine and Pembrolizumab for Patients Relapsed/Refractory Hodgkin's Lymphoma
Sponsor
M.D. Anderson Cancer Center
Enrollment
24 participants
Start Date
Oct 5, 2022
Study Type
INTERVENTIONAL
Conditions
Summary
This study is a Phase II single-center clinical trial designed to assess the efficacy, safety, and tolerability of pembrolizumab in combination with the 7-day regimen of azacitidine for the treatment of relapsed/refractory HL.
Eligibility
Min Age: 1 Year
Plain Language Summary
Simplified for easier understanding
This study is testing a combination of two drugs — azacitidine (a chemotherapy that reactivates silenced genes) and pembrolizumab (an immune checkpoint inhibitor that helps the immune system attack cancer) — for people with Hodgkin's lymphoma that has returned or stopped responding to previous treatments.
**You may be eligible if...**
- You have relapsed or progressive Hodgkin's lymphoma and are not a candidate for high-dose chemotherapy
- You are at least 1 year old (this study includes both pediatric and adult patients)
- Your organ function and performance status are adequate (ECOG ≤3 or Lansky ≥50 for pediatric)
- You have received prior treatments and are willing to use contraception if applicable
**You may NOT be eligible if...**
- You are allergic to azacitidine or pembrolizumab
- You have uncontrolled infection, hypertension, or heart failure
- You have HIV or active Hepatitis B or C
- You have an active autoimmune disease (e.g., inflammatory bowel disease, Wegener's syndrome)
- You have recently received a live vaccine (within 30 days)
- You are pregnant or breastfeeding
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
DRUGAzacytidine
Given by Vein (IV)
DRUGPembrolizumab
Given by Vein (IV)
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT05355051
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