Patient Guide: A Study of Izalontamab Brengitecan Versus Chemotherapy in Participants With Previously Untreated, Locally Advanced, Recurrent Inoperable, or Metastatic Triple-negative Breast Cancer Ineligible for Anti-PD(L)1 Drugs (IZABRIGHT-Breast01)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 260 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06926868
Status: 🟢 Enrolling Now
Condition: Breast Neoplasms
Phase: PHASE2, PHASE3

Where You Can Participate

This study is available at 260 locations across the country.

Top locations include:
  • • Hot Springs, Arkansas
  • • Cerritos, California
  • • Cerritos, California
  • • And 257 more locations

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A Study of Izalontamab Brengitecan Versus Chemotherapy in Participants With Previously Untreated, Locally Advanced, Recurrent Inoperable, or Metastatic Triple-negative Breast Cancer Ineligible for Anti-PD(L)1 Drugs (IZABRIGHT-Breast01) - Join Clinical Trial NCTNCT06926868

How to Join This Clinical Trial - NCTNCT06926868

Learn how to participate in this PHASE2, PHASE3 trial studying an investigational therapy for Breast Neoplasms. This study is currently enrolling participants.

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
PHASE2, PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06926868 - 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 260 locations. Find a study site near you:

Clinical Research Site

Hot Springs, Arkansas 71913 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Cerritos, California 90703 - United States

Status: WITHDRAWN

Clinical Research Site

Cerritos, California 90703 - United States

Status: WITHDRAWN

Clinical Research Site

Cerritos, California 90703 - United States

Status: WITHDRAWN

Clinical Research Site

Long Beach, California 90805 - United States

Status: WITHDRAWN

Clinical Research Site

Los Angeles, California 90033 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Los Angeles, California 90067 - United States

Status: RECRUITING

Clinical Research Site

Newport Beach, California 92663 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Stanford, California 94305 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Whittier, California 90603 - United States

Status: NOT_YET_RECRUITING

And 250 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2, PHASE3 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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