Patient Guide: Safety Extension Study for Subjects With HR+, HER2- Breast Cancer for Subjects Who Have Completed the OVELIA Study

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 35 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05645536
Status: ENROLLING_BY_INVITATION
Condition: Breast Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 35 locations across the country.

Top locations include:
  • • Greenbrae, California
  • • Fort Lauderdale, Florida
  • • Lexington, Kentucky
  • • And 32 more locations

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Safety Extension Study for Subjects With HR+, HER2- Breast Cancer for Subjects Who Have Completed the OVELIA Study - Join Clinical Trial NCTNCT05645536

How to Join This Clinical Trial - NCTNCT05645536

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

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with 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
Breast Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ENROLLING_BY_INVITATION
Study Identifier
NCTNCT05645536 - 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 35 locations. Find a study site near you:

Clinical Research Site

Greenbrae, California 94904 - United States

Status: Contact for availability

Clinical Research Site

Fort Lauderdale, Florida 33308 - United States

Status: Contact for availability

Clinical Research Site

Lexington, Kentucky 40503 - United States

Status: Contact for availability

Clinical Research Site

Louisville, Kentucky 40207 - United States

Status: Contact for availability

Clinical Research Site

Columbia, Maryland 21044 - United States

Status: Contact for availability

Clinical Research Site

East Syracuse, New York 13057 - United States

Status: Contact for availability

Clinical Research Site

Fayetteville, North Carolina 28304 - United States

Status: Contact for availability

Clinical Research Site

Wynnewood, Pennsylvania 19096 - 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

And 25 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 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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