Patient Guide: A Comparative Study of AZD9833 Plus Palbociclib Versus Anastrozole Plus Palbociclib in Patients With ER-Positive HER2 Negative Breast Cancer Who Have Not Received Any Systemic Treatment for Advanced Disease

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 263 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04711252
Status: ACTIVE_NOT_RECRUITING
Condition: Breast Neoplasms
Phase: PHASE3

Where You Can Participate

This study is available at 263 locations across the country.

Top locations include:
  • • Mobile, Alabama
  • • Springdale, Arkansas
  • • Harbor City, California
  • • And 260 more locations

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A Comparative Study of AZD9833 Plus Palbociclib Versus Anastrozole Plus Palbociclib in Patients With ER-Positive HER2 Negative Breast Cancer Who Have Not Received Any Systemic Treatment for Advanced Disease - Join Clinical Trial NCTNCT04711252

How to Join This Clinical Trial - NCTNCT04711252

Learn how to participate in this PHASE3 trial studying an investigational therapy for Breast Neoplasms. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Breast Neoplasms. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Breast Neoplasms
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04711252 - 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 263 locations. Find a study site near you:

Clinical Research Site

Mobile, Alabama 36604 - United States

Status: Contact for availability

Clinical Research Site

Springdale, Arkansas 72762 - United States

Status: Contact for availability

Clinical Research Site

Harbor City, California 90710 - United States

Status: Contact for availability

Clinical Research Site

Solvang, California 93463 - United States

Status: Contact for availability

Clinical Research Site

Lone Tree, Colorado 80124 - United States

Status: Contact for availability

Clinical Research Site

Fort Myers, Florida 33901-8101 - United States

Status: Contact for availability

Clinical Research Site

Jacksonville, Florida 32256 - United States

Status: Contact for availability

Clinical Research Site

West Palm Beach, Florida 33401 - United States

Status: Contact for availability

Clinical Research Site

Indianapolis, Indiana 46256 - United States

Status: Contact for availability

Clinical Research Site

Baton Rouge, Louisiana 70809 - United States

Status: Contact for availability

And 253 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Breast Neoplasms:

  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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