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NCT05254821

Cell-free Tumor DNA as Minimal Residual Disease in Hodgkin Lymphoma Patients

Status unknown Last updated 14 November 2022
What this trial tests

trial in Hodgkin Lymphoma in 130 participants. Status unknown.

Timeline
10 January 2022
Primary endpoint
3 February 2024
3 February 2026

Quick facts

Lead sponsorFederico II University
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment130
Start date10 January 2022
Primary completion3 February 2024
Estimated completion3 February 2026
Sites1 location across Italy

Conditions studied

Sponsor

Federico II University

Who can join

18 and older, any sex, with Hodgkin Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Molecular analysis identifies residual disease by overcoming the sensitivity of imaging methods and therefore has the potential for integrating with therapy provided by FDG-PET alone. It is a well known fact that tumor DNA circulating in plasma (ctDNA) reflects the mutational profile of tumor cells and can be used to non-invasively detect specific mutations of Hodgkin's lymphoma without the need for microdissecting the histological sample.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Liquid Biopsy in B and T Cell Lymphomas: From Bench to Bedside.
    Almasri M, Maher N, Al Deeban B, Diop NM, et al · · 2025 · cited 9× · PMID 40430009 · DOI 10.3390/ijms26104869

Verify or expand the search:

Other recruiting trials for Hodgkin Lymphoma

Currently open trials in the same condition.

Other Federico II University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05254821.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing