Patient Guide: Study of Nivolumab in Combination With Ipilimumab or Standard of Care Chemotherapy Compared to the Standard of Care Chemotherapy Alone in Treatment of Participants With Untreated Inoperable or Metastatic Urothelial Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 174 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT03036098
Status: ACTIVE_NOT_RECRUITING
Condition: Urothelial Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 174 locations across the country.

Top locations include:
  • • Anchorage, Alaska
  • • Fresno, California
  • • Santa Rosa, California
  • • And 171 more locations

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Study of Nivolumab in Combination With Ipilimumab or Standard of Care Chemotherapy Compared to the Standard of Care Chemotherapy Alone in Treatment of Participants With Untreated Inoperable or Metastatic Urothelial Cancer - Join Clinical Trial NCTNCT03036098

How to Join This Clinical Trial - NCTNCT03036098

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

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Urothelial Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT03036098 - 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 174 locations. Find a study site near you:

Clinical Research Site

Anchorage, Alaska 99503 - United States

Status: Contact for availability

Clinical Research Site

Fresno, California 93703 - United States

Status: Contact for availability

Clinical Research Site

Santa Rosa, California 95403 - United States

Status: Contact for availability

Clinical Research Site

Boca Raton, Florida 33486 - United States

Status: Contact for availability

Clinical Research Site

Fort Lauderdale, Florida 33308 - United States

Status: Contact for availability

Clinical Research Site

Jacksonville, Florida 32256 - United States

Status: Contact for availability

Clinical Research Site

Athens, Georgia 30607 - United States

Status: Contact for availability

Clinical Research Site

Thomasville, Georgia 31792 - United States

Status: Contact for availability

Clinical Research Site

Chicago, Illinois 60612 - United States

Status: Contact for availability

Clinical Research Site

New Orleans, Louisiana 70121 - United States

Status: Contact for availability

And 164 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 Urothelial 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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