Patient Guide: A Pivotal Phase II Clinical Trial of Utidelone Injection Plus Capecitabine in HER2-negative Breast Cancer Patients With Brain Metastases

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 16 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06764940
Status: 🟢 Enrolling Now
Condition: HER2-negative Breast Cancer Patients With Brain Metastases
Phase: PHASE2

Where You Can Participate

This study is available at 16 locations across the country.

Top locations include:
  • • Duarte, California
  • • Los Alamitos, California
  • • Oxnard, California
  • • And 13 more locations

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A Pivotal Phase II Clinical Trial of Utidelone Injection Plus Capecitabine in HER2-negative Breast Cancer Patients With Brain Metastases - Join Clinical Trial NCTNCT06764940

How to Join This Clinical Trial - NCTNCT06764940

Learn how to participate in this PHASE2 trial studying an investigational therapy for HER2-negative Breast Cancer Patients With Brain Metastases. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with HER2-negative Breast Cancer Patients With Brain Metastases. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
HER2-negative Breast Cancer Patients With Brain Metastases
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06764940 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 16 locations. Find a study site near you:

Clinical Research Site

Duarte, California 91010 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Los Alamitos, California 90720 - United States

Status: RECRUITING

Clinical Research Site

Oxnard, California 93030 - United States

Status: RECRUITING

Clinical Research Site

San Diego, California 92121 - United States

Status: RECRUITING

Clinical Research Site

Aurora, Colorado 80045 - United States

Status: RECRUITING

Clinical Research Site

Hialeah, Florida 33013 - United States

Status: RECRUITING

Clinical Research Site

Margate, Florida 33063 - United States

Status: RECRUITING

Clinical Research Site

Augusta, Georgia 30912 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Chicago, Illinois 60611 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Farmington Hills, Michigan 48334 - United States

Status: RECRUITING

And 6 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for HER2-negative Breast Cancer Patients With Brain Metastases:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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