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NCT01754025 · ClinicalTrials.gov registry record

INHERIT EGFR - Studying Germline EGFR Mutations

A clinical trial of Lung Cancer, sponsored by Dana-Farber Cancer Institute.

Active
Registry status
121
Enrollment target
2
Study locations

NCT01754025: Active study of Lung Cancer, sponsored by Dana-Farber Cancer Institute.

NCT01754025 is a study of Lung Cancer that is active but no longer recruiting, run by Dana-Farber Cancer Institute. The registered enrollment target is 121 participants, below the 936-participant average among 409 other Lung Cancer trials with a reported enrollment target (87% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01754025, a study of Lung Cancer, is active but no longer recruiting, sponsored by Dana-Farber Cancer Institute.

ACTIVE NOT RECRUITING
Registry status
121 participants
Enrollment target
2
Study locations

Study Summary

Lung cancer is a common malignancy that is associated with cigarette smoking but can also affect individuals who never smoked. It is not well understood whether there are hereditary risk factors that influence the risk of lung cancer. It has been recently found that a small number of families have an inherited (passed from parent to child) change in one of their genes that may contribute to an increased tendency to develop lung cancers, even in never smokers. In some lung cancer patients this gene, called "EGFR", contains a DNA change known as an "inherited EGFR mutation". Early data indicate that these inherited EGFR mutations may be associated with an increased risk of lung cancer. So far, only a small number of families have been found to carry inherited EGFR mutations. For this reason the risk of lung cancer associated with inherited EGFR mutations is not well understood. Understanding the risk may help investigators find ways of detecting lung cancer sooner or reducing the risk of developing lung cancer. It was recently discovered that lung cancer patients who are found to carry one rare EGFR mutation in their cancer cells, called "T790M", have an increased risk of carrying an inherited EGFR mutation in their normal cells as well. This represents a new strategy for finding individuals and families carrying inherited EGFR mutations. This research study is designed to find cancer patients whose tumors have this EGFR mutation, T790M, to find out if they also have an inherited EGFR mutation. Subjects will not have to undergo a biopsy to participate in this research study. Investigators will collect a saliva specimen from patients with a T790M in their cancer to find out if they also have an inherited EGFR mutation. Study participants found or known to carry an inherited EGFR mutation will have the option of offering their close relative the opportunity to also participate in this study. Close relatives can consider testing to see if they also carry the inherit

Primary Outcome

To determine the prevalence of germline EGFR mutations in lung cancer patients with EGFR T790M mutations in their tumor and in relatives of carriers of germline EGFR mutations

Conditions Studied

Study Locations (2)

Massachusetts

  • Dana-Farber Cancer Institute - Boston

Tennessee

  • Vanderbilt-Ingram Cancer Center - Nashville

Trial Details

FieldValue
Enrollment Target 121 participants
Start Date 2012-12-28
Est. Completion 2029-12-31
Dana-Farber Cancer Institute

781 total trials

What the registry record for NCT01754025 still lists

NCT01754025 is an observational study that tracks outcomes without assigning an intervention. The registered 121 participants enrollment target is mid-sized for trials with a published cap, below the 936-participant average among 409 other Lung Cancer trials with a reported enrollment target (87% lower).

The record links to 1 condition, with Lung Cancer appearing as the primary indexed condition, and to 0 interventions.

NCT01754025 reports a single indexed study location in Massachusetts, Tennessee.

Frequently Asked Questions

What is clinical trial NCT01754025 about?

NCT01754025 is a clinical study titled "INHERIT EGFR - Studying Germline EGFR Mutations". Lung cancer is a common malignancy that is associated with cigarette smoking but can also affect individuals who never smoked. It is not well understood whether there are hereditary risk factors that influence the risk of lung cancer. It has been recently found that a small number of families have ...

What is the current status of trial NCT01754025?

This trial is currently active not recruiting. The enrollment target is 121 participants. The study started on 2012-12-28. Estimated completion is 2029-12-31.

What conditions does trial NCT01754025 study?

This clinical trial studies the following conditions: Lung Cancer.

Who is sponsoring clinical trial NCT01754025?

This trial is sponsored by Dana-Farber Cancer Institute, which has 781 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01754025 being conducted?

This trial has 2 study locations across Massachusetts, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Lung Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01754025's enrollment target sits among peer trials

121 168th of 409 higher than 241 of 409 other Lung Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Lung Cancer trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01754025, the US trial registry maintained by the National Library of Medicine. NCT01754025 (mid enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.