Patient Guide: TACTIVE-U: A Study to Learn About the Study Medicine (Vepdegestrant) When Given With Other Medicines in People With Advanced or Metastatic Breast Cancer. (Sub-Study C)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 21 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06125522
Status: ACTIVE_NOT_RECRUITING
Condition: Breast Neoplasms
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 21 locations across the country.

Top locations include:
  • • Fayetteville, Arkansas
  • • Rogers, Arkansas
  • • Springdale, Arkansas
  • • And 18 more locations

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TACTIVE-U: A Study to Learn About the Study Medicine (Vepdegestrant) When Given With Other Medicines in People With Advanced or Metastatic Breast Cancer. (Sub-Study C) - Join Clinical Trial NCTNCT06125522

How to Join This Clinical Trial - NCTNCT06125522

Learn how to participate in this PHASE1, PHASE2 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
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06125522 - 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 21 locations. Find a study site near you:

Clinical Research Site

Fayetteville, Arkansas 72703 - United States

Status: Contact for availability

Clinical Research Site

Rogers, Arkansas 72758 - United States

Status: Contact for availability

Clinical Research Site

Springdale, Arkansas 72762 - United States

Status: Contact for availability

Clinical Research Site

Palo Alto, California 94304 - United States

Status: Contact for availability

Clinical Research Site

Palo Alto, California 94304 - United States

Status: Contact for availability

Clinical Research Site

Fort Collins, Colorado 80524 - United States

Status: Contact for availability

Clinical Research Site

Fort Collins, Colorado 80528 - United States

Status: Contact for availability

Clinical Research Site

Greeley, Colorado 80634 - United States

Status: Contact for availability

Clinical Research Site

Loveland, Colorado 80538 - United States

Status: Contact for availability

Clinical Research Site

Shiloh, Illinois 62269 - United States

Status: Contact for availability

And 11 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1, PHASE2 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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