Patient Guide: A Study of Adagrasib Plus Pembrolizumab Plus Chemotherapy vs. Placebo Plus Pembrolizumab Plus Chemotherapy in Participants With Previously Untreated Non-squamous Non-small Cell Lung Cancer With KRAS G12C Mutation (KRYSTAL-4)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 328 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06875310
Status: 🟢 Enrolling Now
Condition: Carcinoma, Non-Small-Cell Lung
Phase: PHASE3

Where You Can Participate

This study is available at 328 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Fullerton, California
  • • Long Beach, California
  • • And 325 more locations

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A Study of Adagrasib Plus Pembrolizumab Plus Chemotherapy vs. Placebo Plus Pembrolizumab Plus Chemotherapy in Participants With Previously Untreated Non-squamous Non-small Cell Lung Cancer With KRAS G12C Mutation (KRYSTAL-4) - Join Clinical Trial NCTNCT06875310

How to Join This Clinical Trial - NCTNCT06875310

Learn how to participate in this PHASE3 trial studying an investigational therapy for Carcinoma, Non-Small-Cell Lung. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with 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
Carcinoma, Non-Small-Cell Lung
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06875310 - 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 328 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35294-3300 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Fullerton, California 92835 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Long Beach, California 90805 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Newport Beach, California 92663 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Orange, California 92868 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Santa Barbara, California 93105 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Denver, Colorado 80206 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Gainesville, Florida 32610 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Palm Bay, Florida 32901 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Tamarac, Florida 33321 - United States

Status: NOT_YET_RECRUITING

And 318 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 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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