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NCT06960707 · ClinicalTrials.gov registry record · Phase 3
Two Versus One Week Breast Radiotherapy (RT)
A Phase 3 study of Breast Cancer, sponsored by Weill Medical College of Cornell University.
- Recruiting
- Registry status
- Phase 3
- Development phase
- 400
- Enrollment target
- 3
- Study locations
NCT06960707 is a Phase 3 study of Breast Cancer that is actively recruiting participants, run by Weill Medical College of Cornell University. The registered enrollment target is 400 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (86% lower). The trial reports 3 study locations across 1 state.
The verdict
NCT06960707, a Phase 3 study of Breast Cancer, is actively recruiting participants, sponsored by Weill Medical College of Cornell University.
- RECRUITING
- Registry status
- Phase 3
- Development phase
- 400 participants
- Enrollment target
- 3
- Study locations
Study Summary
This study is comparing two different radiation therapy approaches for early breast cancer to see which one is better for patients. One group will receive radiation over one week (based on the FAST-FORWARD trial), and the other group will receive radiation over two weeks with an extra focused dose (called a "concomitant boost"). The study will look at how the treatments affect side effects, breast appearance, and cancer control in the breast. It also aims to find out if the two-week treatment does a better job at preventing cancer from coming back in the breast over the long term.
Conditions Studied
Interventions
- RADIATION Radiation therapy - 1 week
- RADIATION Radiation therapy - 2 weeks
Study Locations (3)
New York
- Brooklyn Methodist Hospital - New York
- New York Presbyterian Hospital - New York
- New York-Presbyterian Weill Cornell Medical College - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2025-04-29 |
| Est. Completion | 2040-12-31 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06960707
The ClinicalTrials.gov registry entry for NCT06960707 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 400 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 (86% lower). The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Breast Cancer appearing as the primary indexed condition, and to 2 interventions - of which Radiation therapy - 1 week is the first listed.
NCT06960707 reports 3 study locations spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT06960707 about?
NCT06960707 is a clinical study titled "Two Versus One Week Breast Radiotherapy (RT)". This study is comparing two different radiation therapy approaches for early breast cancer to see which one is better for patients. One group will receive radiation over one week (based on the FAST-FORWARD trial), and the other group will receive radiation over two weeks with an extra focused dose (...
What is the current status of trial NCT06960707?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 400 participants. The study started on 2025-04-29. Estimated completion is 2040-12-31.
What conditions does trial NCT06960707 study?
This clinical trial studies the following conditions: Breast Cancer.
What interventions are being tested in trial NCT06960707?
The interventions under investigation include: Radiation therapy - 1 week (RADIATION), Radiation therapy - 2 weeks (RADIATION).
Who is sponsoring clinical trial NCT06960707?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06960707 being conducted?
This trial has 3 study locations across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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