Patient Guide: Fulvestrant and Ipatasertib for Advanced HER-2 Negative and Estrogen Receptor Positive (ER+) Breast Cancer Following Progression on First Line CDK 4/6 Inhibitor and Aromatase Inhibitor

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 39 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04650581
Status: ACTIVE_NOT_RECRUITING
Condition: Breast Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 39 locations across the country.

Top locations include:
  • • Bowral, New South Wales
  • • Gateshead, New South Wales
  • • Gosford, New South Wales
  • • And 36 more locations

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Fulvestrant and Ipatasertib for Advanced HER-2 Negative and Estrogen Receptor Positive (ER+) Breast Cancer Following Progression on First Line CDK 4/6 Inhibitor and Aromatase Inhibitor - Join Clinical Trial NCTNCT04650581

How to Join This Clinical Trial - NCTNCT04650581

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

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
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04650581 - 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 39 locations. Find a study site near you:

Clinical Research Site

Bowral, New South Wales 2576 - Australia

Status: Contact for availability

Clinical Research Site

Gateshead, New South Wales 2324 - Australia

Status: Contact for availability

Clinical Research Site

Gosford, New South Wales 2250 - Australia

Status: Contact for availability

Clinical Research Site

Macquarie University, New South Wales 2109 - Australia

Status: Contact for availability

Clinical Research Site

Nowra, New South Wales 2541 - Australia

Status: Contact for availability

Clinical Research Site

Birtinya, Queensland 4575 - Australia

Status: Contact for availability

Clinical Research Site

Toowoomba, Queensland 4350 - Australia

Status: Contact for availability

Clinical Research Site

East Melbourne, Victoria 3002 - Australia

Status: Contact for availability

Clinical Research Site

Epping, Victoria 3076 - Australia

Status: Contact for availability

Clinical Research Site

Frankston, Victoria 3199 - Australia

Status: Contact for availability

And 29 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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