Patient Guide: A Trial to Learn How the Cancer Vaccine BNT116 in Combination With Cemiplimab Works and How Safe the Combination is in Adults With Advanced Non-small Cell Lung Cancer (EMPOWERVAX Lung 1)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 52 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05557591
Status: ACTIVE_NOT_RECRUITING
Condition: Advanced Non-Small Cell Lung Cancer
Phase: PHASE2

Where You Can Participate

This study is available at 52 locations across the country.

Top locations include:
  • • Los Angeles, California
  • • Santa Monica, California
  • • Louisville, Kentucky
  • • And 49 more locations

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A Trial to Learn How the Cancer Vaccine BNT116 in Combination With Cemiplimab Works and How Safe the Combination is in Adults With Advanced Non-small Cell Lung Cancer (EMPOWERVAX Lung 1) - Join Clinical Trial NCTNCT05557591

How to Join This Clinical Trial - NCTNCT05557591

Learn how to participate in this PHASE2 trial studying an investigational therapy for Advanced Non-Small Cell Lung Cancer. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Advanced Non-Small Cell Lung Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05557591 - 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 52 locations. Find a study site near you:

Clinical Research Site

Los Angeles, California 90033 - United States

Status: Contact for availability

Clinical Research Site

Santa Monica, California 90095 - United States

Status: Contact for availability

Clinical Research Site

Louisville, Kentucky 40202 - United States

Status: Contact for availability

Clinical Research Site

Farmington, New Mexico 87401 - United States

Status: Contact for availability

Clinical Research Site

New York, New York 10065 - United States

Status: Contact for availability

Clinical Research Site

Pinehurst, North Carolina 28374 - United States

Status: Contact for availability

Clinical Research Site

Houston, Texas 77090 - United States

Status: Contact for availability

Clinical Research Site

Fairfax, Virginia 22031 - United States

Status: Contact for availability

Clinical Research Site

Tacoma, Washington 98405 - United States

Status: Contact for availability

Clinical Research Site

Batumi, 6000 - Georgia

Status: Contact for availability

And 42 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Advanced Non-Small Cell Lung Cancer:

  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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