Patient Guide: Continued Access Study for Participants Deriving Benefit in Pfizer-Sponsored Avelumab Parent Studies That Are Closing

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 68 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05059522
Status: ACTIVE_NOT_RECRUITING
Condition: Advanced Malignancies, NSCLC, Ovarian Cancer, Urothelial Cancer, Solid Tumors
Phase: PHASE3

Where You Can Participate

This study is available at 68 locations across the country.

Top locations include:
  • • Fayetteville, Arkansas
  • • Rogers, Arkansas
  • • Springdale, Arkansas
  • • And 65 more locations

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Continued Access Study for Participants Deriving Benefit in Pfizer-Sponsored Avelumab Parent Studies That Are Closing - Join Clinical Trial NCTNCT05059522

How to Join This Clinical Trial - NCTNCT05059522

Learn how to participate in this PHASE3 trial studying an investigational therapy for Advanced Malignancies, NSCLC, Ovarian Cancer, Urothelial Cancer, Solid Tumors. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Advanced Malignancies, NSCLC, Ovarian Cancer, Urothelial Cancer, 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 Malignancies, NSCLC, Ovarian Cancer, Urothelial Cancer, Solid Tumors
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05059522 - 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 68 locations. Find a study site near you:

Clinical Research Site

Fayetteville, Arkansas 72703 - United States

Status: Contact for availability

Clinical Research Site

Rogers, Arkansas 72758 - United States

Status: Contact for availability

Clinical Research Site

Springdale, Arkansas 72762 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90095 - United States

Status: Contact for availability

Clinical Research Site

Tampa, Florida 33612 - United States

Status: Contact for availability

Clinical Research Site

Basking Ridge, New Jersey 07920 - United States

Status: Contact for availability

Clinical Research Site

Middletown, New Jersey 07748 - United States

Status: Contact for availability

Clinical Research Site

Montvale, New Jersey 07645 - United States

Status: Contact for availability

Clinical Research Site

Commack, New York 11725 - United States

Status: Contact for availability

Clinical Research Site

Harrison, New York 10604 - United States

Status: Contact for availability

And 58 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 Advanced Malignancies, NSCLC, Ovarian Cancer, Urothelial Cancer, 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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