Patient Guide: A Study of Atezolizumab Versus Placebo as Adjuvant Therapy in Patients With High-Risk Muscle-Invasive Bladder Cancer Who Are ctDNA Positive Following Cystectomy

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 161 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04660344
Status: ACTIVE_NOT_RECRUITING
Condition: Muscle-invasive Bladder Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 161 locations across the country.

Top locations include:
  • • Santa Monica, California
  • • Littleton, Colorado
  • • Rockledge, Florida
  • • And 158 more locations

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A Study of Atezolizumab Versus Placebo as Adjuvant Therapy in Patients With High-Risk Muscle-Invasive Bladder Cancer Who Are ctDNA Positive Following Cystectomy - Join Clinical Trial NCTNCT04660344

How to Join This Clinical Trial - NCTNCT04660344

Learn how to participate in this PHASE3 trial studying an investigational therapy for Muscle-invasive Bladder Cancer. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Muscle-invasive Bladder Cancer. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Muscle-invasive Bladder Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04660344 - 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 161 locations. Find a study site near you:

Clinical Research Site

Santa Monica, California 90404 - United States

Status: Contact for availability

Clinical Research Site

Littleton, Colorado 80120 - United States

Status: Contact for availability

Clinical Research Site

Rockledge, Florida 32955 - United States

Status: Contact for availability

Clinical Research Site

Las Vegas, Nevada 89102 - United States

Status: Contact for availability

Clinical Research Site

Winston-Salem, North Carolina 27157 - United States

Status: Contact for availability

Clinical Research Site

Cleveland, Ohio 44195 - United States

Status: Contact for availability

Clinical Research Site

Pittsburgh, Pennsylvania 15212 - United States

Status: Contact for availability

Clinical Research Site

Buenos Aires, 1019 - Argentina

Status: Contact for availability

Clinical Research Site

Buenos Aires, 1426 - Argentina

Status: Contact for availability

Clinical Research Site

Brasschaat, 2930 - Belgium

Status: Contact for availability

And 151 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 Muscle-invasive Bladder 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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