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NCT01123460

Biomarkers Predicting Response in Patients With Non-Small Cell Lung Cancer Previously Treated With Erlotinib Hydrochloride

Completed Last updated 17 May 2017
What this trial tests

trial testing enzyme-linked immunosorbent assay in Lung Cancer in 127 participants. Completed in 12 June 2010.

Timeline
12 April 2010
Primary endpoint
12 June 2010
12 June 2010

Quick facts

Lead sponsorECOG-ACRIN Cancer Research Group
StatusCompleted
Study typeOBSERVATIONAL
Enrollment127
Start date12 April 2010
Primary completion12 June 2010
Estimated completion12 June 2010

Drugs / interventions tested

Conditions studied

Sponsor

ECOG-ACRIN Cancer Research Group

Who can join

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

Sponsor's own description

RATIONALE: Studying samples of blood in the laboratory from patients receiving erlotinib hydrochloride may help doctors learn more about the effects of erlotinib hydrochloride on cells. It may also help doctors understand how well patients respond to treatment. PURPOSE: This research study is studying biomarkers predicting response in patients with non-small cell lung cancer previously treated with erlotinib hydrochloride.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of enzyme-linked immunosorbent assay

Trials testing the same drug.

Other recruiting trials for Lung Cancer

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/NCT01123460.

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