Patient Guide: Study of RP3 Monotherapy and RP3 in Combination With Nivolumab in Patients With Solid Tumours

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 13 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04735978
Status: ACTIVE_NOT_RECRUITING
Condition: Advanced Solid Tumor
Phase: PHASE1

Where You Can Participate

This study is available at 13 locations across the country.

Top locations include:
  • • Iowa City, Iowa
  • • Pittsburgh, Pennsylvania
  • • Houston, Texas
  • • And 10 more locations

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Study of RP3 Monotherapy and RP3 in Combination With Nivolumab in Patients With Solid Tumours - Join Clinical Trial NCTNCT04735978

How to Join This Clinical Trial - NCTNCT04735978

Learn how to participate in this PHASE1 trial studying an investigational therapy for Advanced Solid Tumor. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Advanced Solid Tumor
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04735978 - 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 13 locations. Find a study site near you:

Clinical Research Site

Iowa City, Iowa 52242 - United States

Status: Contact for availability

Clinical Research Site

Pittsburgh, Pennsylvania 15232 - United States

Status: Contact for availability

Clinical Research Site

Houston, Texas 77030 - United States

Status: Contact for availability

Clinical Research Site

Villejuif, 94805 - France

Status: Contact for availability

Clinical Research Site

Athens, 11527 - Greece

Status: Contact for availability

Clinical Research Site

Athens, 12462 - Greece

Status: Contact for availability

Clinical Research Site

Barcelona, 08035 - Spain

Status: Contact for availability

Clinical Research Site

Barcelona, 08036 - Spain

Status: Contact for availability

Clinical Research Site

Madrid, 28050 - Spain

Status: Contact for availability

Clinical Research Site

Valencia, 46010 - Spain

Status: Contact for availability

And 3 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 clinical trial for Advanced Solid Tumor:

  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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