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NCT03749421 · ClinicalTrials.gov registry record

Prospective Study of the Prosigna Assay on Neoadjuvant Clinical Decision-making in Women With HR+/Her2- Breast Cancer

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

Active
Registry status
60
Enrollment target
1
Study location

NCT03749421 is a study of Breast Cancer that is active but no longer recruiting, run by Dana-Farber Cancer Institute. The registered enrollment target is 60 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03749421, a study of Breast Cancer, is active but no longer recruiting, sponsored by Dana-Farber Cancer Institute.

ACTIVE NOT RECRUITING
Registry status
60 participants
Enrollment target
1
Study location

Study Summary

This research study is evaluating a genomic analysis called Predictor Analysis of Microarray 50 (PAM50, by Prosigna®) as a tool to possibly guide the participant and the treating physician to choose the most personalized pre-operative treatment for breast cancer.

Conditions Studied

Interventions

  • OTHER Prosigna PAM-50 assay

Study Locations (1)

Massachusetts

  • Dana-Farber Cancer Institute - Boston

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2019-03-21
Est. Completion 2026-12-31

Sponsor

Dana-Farber Cancer Institute

781 total trials

What the Registry Record Tells You About NCT03749421

The ClinicalTrials.gov registry entry for NCT03749421 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (98% lower). The listed sponsor is Dana-Farber Cancer Institute, which has 781 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Breast Cancer appearing as the primary indexed condition, and to 1 intervention - of which Prosigna PAM-50 assay is the first listed.

NCT03749421 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT03749421 about?

NCT03749421 is a clinical study titled "Prospective Study of the Prosigna Assay on Neoadjuvant Clinical Decision-making in Women With HR+/Her2- Breast Cancer". This research study is evaluating a genomic analysis called Predictor Analysis of Microarray 50 (PAM50, by Prosigna®) as a tool to possibly guide the participant and the treating physician to choose the most personalized pre-operative treatment for breast cancer.

What is the current status of trial NCT03749421?

This trial is currently active not recruiting. The enrollment target is 60 participants. The study started on 2019-03-21. Estimated completion is 2026-12-31.

What conditions does trial NCT03749421 study?

This clinical trial studies the following conditions: Breast Cancer.

What interventions are being tested in trial NCT03749421?

The interventions under investigation include: Prosigna PAM-50 assay (OTHER).

Who is sponsoring clinical trial NCT03749421?

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

Where is trial NCT03749421 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

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, or report a data error.