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NCT01255150 · ClinicalTrials.gov registry record

Frequency of EGFR Mutations in Latinos/Hispanics With Non-Small Cell Lung Cancer

A clinical trial, sponsored by National Cancer Institute (NCI).

Completed
Registry status
15
Enrollment target

NCT01255150: Completed study, sponsored by National Cancer Institute (NCI).

NCT01255150 is a clinical trial that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 15 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01255150 has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
15 participants
Enrollment target

Study Summary

Background: \- Research has shown that the Epidermal Growth Factor Receptor (EGFR) gene is an important target for personalized lung cancer treatment. Individuals who have mutations in the EGFR gene have better responses when treated with certain personalized or targeted therapies compared with conventional chemotherapy. These mutations are more frequent in females with lung cancer who have never smoked, and different ethnic groups have different levels of frequency of the mutations. Researchers are interested in collecting more information on EGFR genetic mutations in Hispanics/Latinos with lung cancer, comparing the frequency of these mutations in males and females and smokers and nonsmokers. This study may lead to better, more personalized care approaches for all individuals with lung cancer. Objectives: \- To study the frequency of Epidermal Growth Factor Receptor mutations in Hispanic/Latino individuals who have been diagnosed with non-small cell lung cancer. Eligibility: \- Hispanic or Latino individuals who have been diagnosed with non-small cell lung cancer and who have lung tissue from a previous biopsy or surgery available for research purposes. Design: * Participants will provide consent for researchers to examine lung tissue collected from a previous biopsy or surgery. * Treatment will not be provided as part of this protocol.

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2010-12-01
Est. Completion 2015-04-29

Sponsor

National Cancer Institute (NCI)

3,257 total trials

What the Registry Record Tells You About NCT01255150

The ClinicalTrials.gov registry entry for NCT01255150 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Cancer Institute (NCI), which has 3,257 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 0 interventions.

NCT01255150 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01255150 about?

NCT01255150 is a clinical study titled "Frequency of EGFR Mutations in Latinos/Hispanics With Non-Small Cell Lung Cancer". Background: \- Research has shown that the Epidermal Growth Factor Receptor (EGFR) gene is an important target for personalized lung cancer treatment. Individuals who have mutations in the EGFR gene have better responses when treated with certain personalized or targeted therapies compared with con...

What is the current status of trial NCT01255150?

This trial is currently completed. The enrollment target is 15 participants. The study started on 2010-12-01. Estimated completion is 2015-04-29.

Who is sponsoring clinical trial NCT01255150?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.