Actively Recruiting
Feasibility and Clinical Utility of Cell-free DNA (cfDNA) in Identifying Actionable Alterations and Minimal Residual Disease for Lymphoma Patients Across Community Centers in Texas
Led by M.D. Anderson Cancer Center · Updated on 2025-10-31
517
Participants Needed
2
Research Sites
183 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To test the feasibility of collecting cell-free DNA (cfDNA) samples from DLBCL patients before and after treatment. cfDNA is DNA traveling in your blood outside of a cell and is easily collected from blood samples drawn using the vein puncture method.
CONDITIONS
Official Title
Feasibility and Clinical Utility of Cell-free DNA (cfDNA) in Identifying Actionable Alterations and Minimal Residual Disease for Lymphoma Patients Across Community Centers in Texas
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female patients who are at least 18 years old on the day of informed consent signing
- Histologically confirmed diffuse large B-cell lymphoma requiring therapy
- Ability to provide written informed consent for the study
- Pregnant women are not included
- Cognitively impaired adults are not included
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
MD Anderson Cancer Center
Houston, Texas, United States, 77030
Actively Recruiting
2
Cancer Therapy and Research Center at The UT Health Science Center at San Antonio
San Antonio, Texas, United States, 78229
Actively Recruiting
Research Team
C
Chijioke Nze, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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