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NCT01381705

Biomarkers in Predicting Response to Rituximab Treatment in Samples From Patients With Indolent Follicular Lymphoma

Completed Last updated 17 May 2017
What this trial tests

trial testing rituximab in Lymphoma in 259 participants. Completed in 6 July 2012.

Timeline
6 February 2012
Primary endpoint
6 July 2012
6 July 2012

Quick facts

Lead sponsorECOG-ACRIN Cancer Research Group
StatusCompleted
Study typeOBSERVATIONAL
Enrollment259
Start date6 February 2012
Primary completion6 July 2012
Estimated completion6 July 2012

Drugs / interventions tested

Conditions studied

Sponsor

ECOG-ACRIN Cancer Research Group

Who can join

Adults 18 to 120, any sex, with Lymphoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

RATIONALE: Studying samples of blood and tumor tissue from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how well patients will respond to treatment. PURPOSE: This research study is studying biomarkers in predicting response to rituximab treatment in samples from patients with indolent follicular lymphoma.

Publications & conference data

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

  1. Clinical Potential of Copy Number Aberration as a Diagnostic and Prognostic Biomarker in Lymphoma.
    Zhang X, Yang Z, Yan S, Zhan M, et al · · 2025 · PMID 41071909 · DOI 10.1177/15330338251383634

Verify or expand the search:

Other trials of rituximab

Trials testing the same drug.

Other recruiting trials for Lymphoma

Currently open trials in the same condition.

Other ECOG-ACRIN Cancer Research Group 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/NCT01381705.

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