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NCT04226937: DIRECT

DLBCL Interim Response Evaluation for Customised Therapy

Status unknown Last updated 5 August 2022
What this trial tests

trial testing Not Applicable as this is a translational, sample collection study. in High-grade B-cell Lymphoma in 150 participants. Status unknown.

Timeline
17 September 2020
Primary endpoint
1 September 2025
1 September 2025

Quick facts

Lead sponsorCambridge University Hospitals NHS Foundation Trust
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment150
Start date17 September 2020
Primary completion1 September 2025
Estimated completion1 September 2025
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Cambridge University Hospitals NHS Foundation Trust

Who can join

18 and older, any sex, with High-grade B-cell Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The aim of the DIRECT Study is to establish a robust pipeline to identify those patients with high-grade B cell lymphoma most suitable for novel agent clinical trials based upon genomic subtype and an integrated response evaluation determined early in first-line therapy.

Publications & conference data

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

  1. The DIRECT study: A roadmap for ctDNA-based risk prediction, molecular profiling and MRD detection in Diffuse Large B Cell Lymphoma
    Krupka JA, Moutsopoulos I, Cutmore NH, Trethewey CS, et al · · 2025 · DOI 10.1101/2025.04.14.25325806

Verify or expand the search:

Other recruiting trials for High-grade B-cell Lymphoma

Currently open trials in the same condition.

Other Cambridge University Hospitals NHS Foundation Trust 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/NCT04226937.

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