Patient Guide: A Study to Compare ABP 234 and Keytruda® (Pembrolizumab) in Participants With Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 204 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06311721
Status: 🟢 Enrolling Now
Condition: Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 204 locations across the country.

Top locations include:
  • • Beverly Hills, California
  • • Cerritos, California
  • • Los Alamitos, California
  • • And 201 more locations

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A Study to Compare ABP 234 and Keytruda® (Pembrolizumab) in Participants With Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer - Join Clinical Trial NCTNCT06311721

How to Join This Clinical Trial - NCTNCT06311721

Learn how to participate in this PHASE3 trial studying an investigational therapy for Advanced or Metastatic Non-squamous Non-Small Cell Lung Cancer. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Advanced or Metastatic Non-squamous 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 or Metastatic Non-squamous Non-Small Cell Lung Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06311721 - 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 204 locations. Find a study site near you:

Clinical Research Site

Beverly Hills, California 90212 - United States

Status: RECRUITING

Clinical Research Site

Cerritos, California 90703 - United States

Status: RECRUITING

Clinical Research Site

Los Alamitos, California 90720-3309 - United States

Status: RECRUITING

Clinical Research Site

Los Angeles, California 90067 - United States

Status: TERMINATED

Clinical Research Site

Whittier, California 90602 - United States

Status: RECRUITING

Clinical Research Site

Hollywood, Florida 33024 - United States

Status: RECRUITING

Clinical Research Site

Tamarac, Florida 33321 - United States

Status: RECRUITING

Clinical Research Site

Plainfield, Illinois 60585 - United States

Status: COMPLETED

Clinical Research Site

Ames, Iowa 50010 - United States

Status: RECRUITING

Clinical Research Site

Farmington Hills, Michigan 48334 - United States

Status: RECRUITING

And 194 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 or Metastatic Non-squamous 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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