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NCT02610439 · ClinicalTrials.gov registry record

Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Peripheral Neuropathy Receiving Paclitaxel for Breast Cancer

A clinical trial of Breast Carcinoma and Neuropathy, sponsored by National Cancer Institute (NCI).

Recruiting
Registry status
575
Enrollment target
1
Study location

NCT02610439 is a study of Breast Carcinoma and Neuropathy that is actively recruiting participants, run by National Cancer Institute (NCI). The registered enrollment target is 575 participants, below the 765-participant average among 106 other Breast Carcinoma trials with a reported enrollment target (25% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02610439, a study of Breast Carcinoma and Neuropathy, is actively recruiting participants, sponsored by National Cancer Institute (NCI).

RECRUITING
Registry status
575 participants
Enrollment target
1
Study location

Study Summary

This research trial studies whole exome sequencing in finding causative variants in germline deoxyribonucleic acid (DNA) samples from patients with peripheral neuropathy receiving chemotherapy for breast cancer. Studying samples of germline DNA in the laboratory from patients with peripheral neuropathy receiving paclitaxel for breast cancer may help doctors learn more about changes that occur in DNA and identify biomarkers related to peripheral neuropathy.

Interventions

  • OTHER Laboratory Biomarker Analysis

Study Locations (1)

Massachusetts

  • Eastern Cooperative Oncology Group - Boston

Trial Details

FieldValue
Enrollment Target 575 participants
Start Date 2014-03-25
Est. Completion 2100-01-01

Sponsor

National Cancer Institute (NCI)

3,257 total trials

What the Registry Record Tells You About NCT02610439

The ClinicalTrials.gov registry entry for NCT02610439 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 575 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 765-participant average among 106 other Breast Carcinoma trials with a reported enrollment target (25% lower). The listed sponsor is National Cancer Institute (NCI), which has 3,257 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Breast Carcinoma appearing as the primary indexed condition, and to 1 intervention - of which Laboratory Biomarker Analysis is the first listed.

NCT02610439 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT02610439 about?

NCT02610439 is a clinical study titled "Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Peripheral Neuropathy Receiving Paclitaxel for Breast Cancer". This research trial studies whole exome sequencing in finding causative variants in germline deoxyribonucleic acid (DNA) samples from patients with peripheral neuropathy receiving chemotherapy for breast cancer. Studying samples of germline DNA in the laboratory from patients with peripheral neuropa...

What is the current status of trial NCT02610439?

This trial is currently recruiting. The enrollment target is 575 participants. The study started on 2014-03-25. Estimated completion is 2100-01-01.

What conditions does trial NCT02610439 study?

This clinical trial studies the following conditions: Breast Carcinoma, Neuropathy.

What interventions are being tested in trial NCT02610439?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER).

Who is sponsoring clinical trial NCT02610439?

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

Where is trial NCT02610439 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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