Patient Guide: Study to Evaluate Efficacy & Safety of Afuresertib Plus Fulvestrant in Patients With Locally Advanced or Metastatic HR+/HER2- Breast Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 55 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04851613
Status: 🟢 Enrolling Now
Condition: Breast Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 55 locations across the country.

Top locations include:
  • • Santa Monica, California
  • • Atlanta, Georgia
  • • Iowa City, Iowa
  • • And 52 more locations

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Study to Evaluate Efficacy & Safety of Afuresertib Plus Fulvestrant in Patients With Locally Advanced or Metastatic HR+/HER2- Breast Cancer - Join Clinical Trial NCTNCT04851613

How to Join This Clinical Trial - NCTNCT04851613

Learn how to participate in this PHASE3 trial studying an investigational therapy for Breast Cancer. This study is currently enrolling participants.

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
Currently enrolling participants
Study Identifier
NCTNCT04851613 - 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 55 locations. Find a study site near you:

Clinical Research Site

Santa Monica, California 90404 - United States

Status: COMPLETED

Clinical Research Site

Atlanta, Georgia 30318 - United States

Status: COMPLETED

Clinical Research Site

Iowa City, Iowa 52242 - United States

Status: COMPLETED

Clinical Research Site

Jackson, Mississippi 39216 - United States

Status: COMPLETED

Clinical Research Site

Burlington, Vermont 05401 - United States

Status: COMPLETED

Clinical Research Site

Fairfax, Virginia 22031 - United States

Status: RECRUITING

Clinical Research Site

Bengbu, Anhui 233004 - China

Status: RECRUITING

Clinical Research Site

Hefei, Anhui 230031 - China

Status: RECRUITING

Clinical Research Site

Beijing, Beijing Municipality 100021 - China

Status: RECRUITING

Clinical Research Site

Beijing, Beijing Municipality 100142 - China

Status: RECRUITING

And 45 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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