Patient Guide: A Study to Investigate Efficacy and Safety With Oral AZD9833 Compared With Intramuscular Fulvestrant in Post-menopausal Women at Least 18 Years of Age With Advanced ER-positive HER2 Negative Breast Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 91 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04214288
Status: ACTIVE_NOT_RECRUITING
Condition: Advanced ER-Positive HER2-Negative Breast Cancer
Phase: PHASE2

Where You Can Participate

This study is available at 91 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Long Beach, California
  • • Fort Myers, Florida
  • • And 88 more locations

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A Study to Investigate Efficacy and Safety With Oral AZD9833 Compared With Intramuscular Fulvestrant in Post-menopausal Women at Least 18 Years of Age With Advanced ER-positive HER2 Negative Breast Cancer - Join Clinical Trial NCTNCT04214288

How to Join This Clinical Trial - NCTNCT04214288

Learn how to participate in this PHASE2 trial studying an investigational therapy for Advanced ER-Positive HER2-Negative Breast Cancer. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Advanced ER-Positive HER2-Negative Breast Cancer. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Advanced ER-Positive HER2-Negative Breast Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04214288 - 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 91 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35205 - United States

Status: Contact for availability

Clinical Research Site

Long Beach, California 90806 - United States

Status: Contact for availability

Clinical Research Site

Fort Myers, Florida 33901 - United States

Status: Contact for availability

Clinical Research Site

Saint Petersburg, Florida 33705 - United States

Status: Contact for availability

Clinical Research Site

Lincoln, Nebraska 68506 - United States

Status: Contact for availability

Clinical Research Site

Canton, Ohio 44710 - United States

Status: Contact for availability

Clinical Research Site

Chattanooga, Tennessee 37404 - United States

Status: Contact for availability

Clinical Research Site

Nashville, Tennessee 37203 - United States

Status: Contact for availability

Clinical Research Site

Eagle River, Wisconsin 54521 - United States

Status: Contact for availability

Clinical Research Site

Brasschaat, 2930 - Belgium

Status: Contact for availability

And 81 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 Advanced ER-Positive HER2-Negative Breast Cancer:

  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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