Patient Guide: A Study of Subcutaneous Nivolumab Versus Intravenous Nivolumab in Participants With Previously Treated Clear Cell Renal Cell Carcinoma That is Advanced or Has Spread

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 89 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04810078
Status: ACTIVE_NOT_RECRUITING
Condition: Clear Cell Renal Cell Carcinoma
Phase: PHASE3

Where You Can Participate

This study is available at 89 locations across the country.

Top locations include:
  • • Chicago, Illinois
  • • Buffalo, New York
  • • West Reading, Pennsylvania
  • • And 86 more locations

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A Study of Subcutaneous Nivolumab Versus Intravenous Nivolumab in Participants With Previously Treated Clear Cell Renal Cell Carcinoma That is Advanced or Has Spread - Join Clinical Trial NCTNCT04810078

How to Join This Clinical Trial - NCTNCT04810078

Learn how to participate in this PHASE3 trial studying an investigational therapy for Clear Cell Renal Cell Carcinoma. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Clear Cell Renal Cell Carcinoma
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04810078 - 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 89 locations. Find a study site near you:

Clinical Research Site

Chicago, Illinois 60611 - United States

Status: Contact for availability

Clinical Research Site

Buffalo, New York 14263 - United States

Status: Contact for availability

Clinical Research Site

West Reading, Pennsylvania 19611 - United States

Status: Contact for availability

Clinical Research Site

Capital Federal, Buenos Aires C1419AHN - Argentina

Status: Contact for availability

Clinical Research Site

Mar del Plata, Buenos Aires 7600 - Argentina

Status: Contact for availability

Clinical Research Site

Pergamino, Buenos Aires B2700CPM - Argentina

Status: Contact for availability

Clinical Research Site

Parana, Córdoba Province 5000 - Argentina

Status: Contact for availability

Clinical Research Site

Río Cuarto, Córdoba Province 5800 - Argentina

Status: Contact for availability

Clinical Research Site

Viedma, Río Negro Province R8500ACE - Argentina

Status: Contact for availability

Clinical Research Site

Buenos Aires, C1426ANZ - Argentina

Status: Contact for availability

And 79 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 Clear Cell Renal Cell Carcinoma:

  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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