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Active, not recruiting Phase 2 Interventional

Testing the Addition of Radium Therapy (Radium-223 Dichloride) to the Usual Chemotherapy Treatment (Paclitaxel) for Advanced Breast Cancer That Has Spread to the Bones

ClinicalTrials.gov ID: NCT04090398

Public ClinicalTrials.gov record NCT04090398. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 12:08 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase II Trial of Radium-223 Dichloride in Combination With Paclitaxel in Patients With Bone Metastatic Breast Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This phase II trial studies how well radium-223 dichloride and paclitaxel work in treating patients with advanced breast cancer that has spread to the bones. Radium-223 dichloride is a radioactive drug that behaves in a similar way to calcium and collects in cancer that has spread to the bones (bone metastases). The radioactive particles in radium-223 dichloride act on bone metastases, killing the tumor cells and reducing the pain that they can cause. Drugs used in chemotherapy, such as paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving radium-223 dichloride and paclitaxel may work better in treating patients with metastatic breast cancer compared to paclitaxel alone.

Study identification

NCT ID
NCT04090398
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Enrollment
70 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 4, 2020 (Actual)
Primary completion
Jun 30, 2027 (Estimated)
Completion
Jun 30, 2027 (Estimated)
Last update posted
Sep 18, 2026

2020 – 2027

United States locations

U.S. sites
30
U.S. states
15
U.S. cities
29
Facility City State ZIP Site status
University of Alabama at Birmingham Cancer Center Birmingham Alabama 35233 —
City of Hope Comprehensive Cancer Center Duarte California 91010 —
UC Irvine Health/Chao Family Comprehensive Cancer Center Orange California 92868 —
University of California Davis Comprehensive Cancer Center Sacramento California 95817 —
UM Sylvester Comprehensive Cancer Center at Coral Gables Coral Gables Florida 33146 —
UM Sylvester Comprehensive Cancer Center at Deerfield Beach Deerfield Beach Florida 33442 —
University of Miami Miller School of Medicine-Sylvester Cancer Center Miami Florida 33136 —
UM Sylvester Comprehensive Cancer Center at Kendall Miami Florida 33176 —
UM Sylvester Comprehensive Cancer Center at Plantation Plantation Florida 33324 —
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637 —
UC Comprehensive Cancer Center at Silver Cross New Lenox Illinois 60451 —
University of Chicago Medicine-Orland Park Orland Park Illinois 60462 —
University of Kansas Clinical Research Center Fairway Kansas 66205 —
University of Kansas Cancer Center Kansas City Kansas 66160 —
University of Kansas Cancer Center-Overland Park Overland Park Kansas 66210 —
University of Kansas Health System Saint Francis Campus Topeka Kansas 66606 —
University of Kansas Hospital-Westwood Cancer Center Westwood Kansas 66205 —
University of Kentucky/Markey Cancer Center Lexington Kentucky 40536 —
Wayne State University/Karmanos Cancer Institute Detroit Michigan 48201 —
Weisberg Cancer Treatment Center Farmington Hills Michigan 48334 —
University of Kansas Cancer Center - North Kansas City Missouri 64154 —
University of Kansas Cancer Center - Lee's Summit Lee's Summit Missouri 64064 —
University of Kansas Cancer Center at North Kansas City Hospital North Kansas City Missouri 64116 —
Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center Lebanon New Hampshire 03756 —
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08903 —
Laura and Isaac Perlmutter Cancer Center at NYU Langone New York New York 10016 —
Wake Forest University Health Sciences Winston-Salem North Carolina 27157 —
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210 —
UPMC Hillman Cancer Center Pittsburgh Pennsylvania 15232 —
University of Virginia Cancer Center Charlottesville Virginia 22908 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04090398, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 18, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04090398 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →