Patient Guide: Elacestrant for Treating ER+/HER2- Breast Cancer Patients With ctDNA Relapse (TREAT ctDNA)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 94 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05512364
Status: 🟢 Enrolling Now
Condition: ER-positive Breast Cancer, HER2-negative Breast Cancer, Stage IIB Breast Cancer, Stage III Breast Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 94 locations across the country.

Top locations include:
  • • Anderlecht,
  • • Brasschaat,
  • • Brussels,
  • • And 91 more locations

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Elacestrant for Treating ER+/HER2- Breast Cancer Patients With ctDNA Relapse (TREAT ctDNA) - Join Clinical Trial NCTNCT05512364

How to Join This Clinical Trial - NCTNCT05512364

Learn how to participate in this PHASE3 trial studying an investigational therapy for ER-positive Breast Cancer, HER2-negative Breast Cancer, Stage IIB Breast Cancer, Stage III Breast Cancer. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with ER-positive Breast Cancer, HER2-negative Breast Cancer, Stage IIB Breast Cancer, Stage III 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
ER-positive Breast Cancer, HER2-negative Breast Cancer, Stage IIB Breast Cancer, Stage III Breast Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05512364 - 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 94 locations. Find a study site near you:

Clinical Research Site

Anderlecht, 1070 - Belgium

Status: RECRUITING

Clinical Research Site

Brasschaat, 2930 - Belgium

Status: RECRUITING

Clinical Research Site

Brussels, 1200 - Belgium

Status: RECRUITING

Clinical Research Site

Charleroi, 6000 - Belgium

Status: RECRUITING

Clinical Research Site

Haine-Saint-Paul, 7100 - Belgium

Status: RECRUITING

Clinical Research Site

Kortrijk, 8500 - Belgium

Status: RECRUITING

Clinical Research Site

Leuven, 3000 - Belgium

Status: RECRUITING

Clinical Research Site

Namur, 5000 - Belgium

Status: RECRUITING

Clinical Research Site

Roeselare, 8800 - Belgium

Status: RECRUITING

Clinical Research Site

Turnhout, 2300 - Belgium

Status: RECRUITING

And 84 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 ER-positive Breast Cancer, HER2-negative Breast Cancer, Stage IIB Breast Cancer, Stage III 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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