Patient Guide: Rollover Study for Continued Safety and Tolerability in Subjects Treated With Spartalizumab Alone or in Combination With Other Study Treatments

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 48 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04058756
Status: ACTIVE_NOT_RECRUITING
Condition: Advanced Solid Tumors
Phase: PHASE1

Where You Can Participate

This study is available at 48 locations across the country.

Top locations include:
  • • New York, New York
  • • Portland, Oregon
  • • Houston, Texas
  • • And 45 more locations

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Rollover Study for Continued Safety and Tolerability in Subjects Treated With Spartalizumab Alone or in Combination With Other Study Treatments - Join Clinical Trial NCTNCT04058756

How to Join This Clinical Trial - NCTNCT04058756

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

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Advanced Solid Tumors. 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 Tumors
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04058756 - 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 48 locations. Find a study site near you:

Clinical Research Site

New York, New York 10032 - United States

Status: Contact for availability

Clinical Research Site

Portland, Oregon 97123 - United States

Status: Contact for availability

Clinical Research Site

Houston, Texas 77030 - United States

Status: Contact for availability

Clinical Research Site

Leuven, 3000 - Belgium

Status: Contact for availability

Clinical Research Site

Liege, 4000 - Belgium

Status: Contact for availability

Clinical Research Site

Toronto, Ontario M5G 2M9 - Canada

Status: Contact for availability

Clinical Research Site

Montreal, Quebec H3T 1E2 - Canada

Status: Contact for availability

Clinical Research Site

Guangzhou, Guangdong 510515 - China

Status: Contact for availability

Clinical Research Site

Guangzhou, 510060 - China

Status: Contact for availability

Clinical Research Site

Brno, Czech Republic 656 53 - Czechia

Status: Contact for availability

And 38 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 Tumors:

  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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