Completed

ENRICHA Phase 3 Randomized, Open-label Comparative Study of Standard Whole Brain Radiation Therapy With Supplemental Oxygen, With or Without Concurrent RSR13 (Efaproxiral), in Women With Brain Metastases From Breast Cancer

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What is being tested

Efaproxiral

+ Whole Brain Radiation Therapy (WBRT)

+ Supplemental Oxygen

DrugRadiationOther
Who is being recruted

Brain Diseases+13

+ Brain Neoplasms

+ Breast Diseases

Over 18 Years
+3 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 3
Interventional
Study Start: February 2004
See protocol details

Summary

Principal SponsorSpectrum Pharmaceuticals, Inc
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 2004

Actual date on which the first participant was enrolled.

The screening process will include documentation of the cancer, which which will require a brain scan and may include a liver scan. Other screening measurements will include a Karnofsky Performance Status (KPS) assessment, measurement of the amount of oxygen in the blood, using a non-invasive device most often placed on the finger, lung function tests that will require blowing into a machine, and an electrocardiogram (ECG). About 2 teaspoons, or 10 mL, of blood will be taken for specific laboratory tests, and a pregnancy test will be done on the blood of women of childbearing potential. All study patients will receive supplemental oxygen and whole brain radiation therapy (WBRT) (30 Gy, 3 Gy fractions) every weekday for 2 weeks. Half of the patients will be randomized (assigned) to receive RSR13 prior to WBRT, and will need to have a central catheter placed for treatment unless one is already in place. Patients who receive RSR13 will also need to continue to receive oxygen in the clinic until the amount of oxygen in their blood is near normal. This level has returned to near normal in most patients within 1 to 2 hours. During treatment and follow-up visits, physical and neurological exam, KPS assessment, weight, height, and vital sign measurements, and about 2 teaspoons of blood may be required. Patients will need to return for follow-up visits 1 month after completion of treatment, 2 months later, and every 3 months thereafter until their doctor tells them otherwise.

Official TitleA Phase 3 Randomized, Open-label Comparative Study of Standard Whole Brain Radiation Therapy With Supplemental Oxygen, With or Without Concurrent RSR13 (Efaproxiral), in Women With Brain Metastases From Breast Cancer
Principal SponsorSpectrum Pharmaceuticals, Inc
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

368 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Brain DiseasesBrain NeoplasmsBreast DiseasesBreast NeoplasmsCentral Nervous System DiseasesNeoplasm MetastasisNeoplasmsNeoplasms by SiteNeoplastic ProcessesNervous System DiseasesNervous System NeoplasmsPathologic ProcessesSkin DiseasesPathological Conditions, Signs and SymptomsCentral Nervous System NeoplasmsSkin and Connective Tissue Diseases

Criteria

2 inclusion criteria required to participate
Adult women with brain metastases from breast cancer

Minimum KPS of 70

1 exclusion criteria prevent from participating
Previous treatment for brain metastases, including brain surgery and any form of radiation to the brain

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental

Group II

Active Comparator

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 94 locations

Suspended

Virginia G. Piper Cancer Center, Arizona Oncology Services

Phoenix, United StatesOpen Virginia G. Piper Cancer Center, Arizona Oncology Services in Google Maps
Suspended

Arizona Cancer Center, University of Arizona

Tucson, United States
Suspended

The University of Arkansas for Medical Sciences

Little Rock, United States
Suspended

Alta Bates Comprehensive Cancer Center

Berkeley, United States
Completed94 Study Centers