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Clinical Trial

Defining ctDNA Metrics in Posttransplant Lymphoproliferative Disorder (PTLD)

NCT: NCT06954805 · RECRUITING

NCT IDNCT06954805
StatusRECRUITING
Start Date2025-04-14
Completion2028-04-14

Brief Summary

The purpose of this study is to find out if there is a benefit to giving rituximab with etoposide, prednisone, vincristine, cyclophosphamide and doxorubicin (R-EPOCH) in participants who have high-risk B-cell PTLD in their 2nd phase of treatment (consolidation) while those with low-risk disease will be spared of chemotherapy and treated with rituximab consolidation alone. This study is also being done to find out about the usefulness of circulating tumor DNA (ctDNA), a novel blood test which, has been shown to help guide treatment decisions in other types of lymphoma. The goal is to answer the question if ctDNA is a viable and informative tool in treating PTLD with the hope that in the future it may be used to individualize study treatment for participants with PTLD in a way that limits study treatment toxicity without losing the effectiveness of the treatment plan.

Frequently Asked Questions

What is Defining ctDNA Metrics in Posttransplant Lymphoproliferative Disorder (PTLD)?

Defining ctDNA Metrics in Posttransplant Lymphoproliferative Disorder (PTLD) is a clinical trial registered under NCT06954805. Current status: RECRUITING.

What is the status of NCT06954805?

The current status of NCT06954805 (Defining ctDNA Metrics in Posttransplant Lymphoproliferative Disorder (PTLD)) is: RECRUITING.

When did Defining ctDNA Metrics in Posttransplant Lymphoproliferative Disorder (PTLD) start?

Defining ctDNA Metrics in Posttransplant Lymphoproliferative Disorder (PTLD) started on 2025-04-14.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.