Patient Guide: A Study of Belrestotug Plus Dostarlimab Compared With Placebo Plus Pembrolizumab in Previously Untreated Participants With Programmed Death Ligand 1 (PD-L1) High Non-small-cell Lung Cancer (NSCLC)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 178 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06472076
Status: ACTIVE_NOT_RECRUITING
Condition: Lung Neoplasms, Carcinoma, Non-Small-Cell Lung
Phase: PHASE3

Where You Can Participate

This study is available at 178 locations across the country.

Top locations include:
  • • Ocala, Florida
  • • Honolulu, Hawaii
  • • Edgewood, Kentucky
  • • And 175 more locations

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A Study of Belrestotug Plus Dostarlimab Compared With Placebo Plus Pembrolizumab in Previously Untreated Participants With Programmed Death Ligand 1 (PD-L1) High Non-small-cell Lung Cancer (NSCLC) - Join Clinical Trial NCTNCT06472076

How to Join This Clinical Trial - NCTNCT06472076

Learn how to participate in this PHASE3 trial studying an investigational therapy for Lung Neoplasms, Carcinoma, Non-Small-Cell Lung. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Lung Neoplasms, Carcinoma, Non-Small-Cell Lung
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06472076 - 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 178 locations. Find a study site near you:

Clinical Research Site

Ocala, Florida 34474 - United States

Status: Contact for availability

Clinical Research Site

Honolulu, Hawaii 96819 - United States

Status: Contact for availability

Clinical Research Site

Edgewood, Kentucky 41017 - United States

Status: Contact for availability

Clinical Research Site

Lexington, Kentucky 40503 - United States

Status: Contact for availability

Clinical Research Site

Lexington, Kentucky 40509 - United States

Status: Contact for availability

Clinical Research Site

Omaha, Nebraska 68114 - United States

Status: Contact for availability

Clinical Research Site

Chattanooga, Tennessee 37404 - United States

Status: Contact for availability

Clinical Research Site

Nashville, Tennessee 37203 - United States

Status: Contact for availability

Clinical Research Site

Fort Worth, Texas 76104 - United States

Status: Contact for availability

Clinical Research Site

Olympia, Washington 98506 - United States

Status: Contact for availability

And 168 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 Lung Neoplasms, Carcinoma, Non-Small-Cell Lung:

  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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