Patient Guide: A Study to Evaluate the Safety, Pharmacokinetics, and Activity of GDC-6036 Alone or in Combination in Participants With Advanced or Metastatic Solid Tumors With a KRAS G12C Mutation

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 74 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04449874
Status: 🟢 Enrolling Now
Condition: Non-Small Cell Lung Cancer, Colorectal Cancer, Advanced Solid Tumors
Phase: PHASE1

Where You Can Participate

This study is available at 74 locations across the country.

Top locations include:
  • • Duarte, California
  • • La Jolla, California
  • • Orange, California
  • • And 71 more locations

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A Study to Evaluate the Safety, Pharmacokinetics, and Activity of GDC-6036 Alone or in Combination in Participants With Advanced or Metastatic Solid Tumors With a KRAS G12C Mutation - Join Clinical Trial NCTNCT04449874

How to Join This Clinical Trial - NCTNCT04449874

Learn how to participate in this PHASE1 trial studying an investigational therapy for Non-Small Cell Lung Cancer, Colorectal Cancer, Advanced Solid Tumors. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Non-Small Cell Lung Cancer, Colorectal Cancer, Advanced 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
Non-Small Cell Lung Cancer, Colorectal Cancer, Advanced Solid Tumors
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT04449874 - 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 74 locations. Find a study site near you:

Clinical Research Site

Duarte, California 91010 - United States

Status: WITHDRAWN

Clinical Research Site

La Jolla, California 92093 - United States

Status: RECRUITING

Clinical Research Site

Orange, California 92868 - United States

Status: COMPLETED

Clinical Research Site

San Francisco, California 94158 - United States

Status: WITHDRAWN

Clinical Research Site

New Haven, Connecticut 06511 - United States

Status: RECRUITING

Clinical Research Site

Sarasota, Florida 34232 - United States

Status: COMPLETED

Clinical Research Site

Boston, Massachusetts 02215 - United States

Status: RECRUITING

Clinical Research Site

New York, New York 10021 - United States

Status: COMPLETED

Clinical Research Site

Oklahoma City, Oklahoma 73104 - United States

Status: RECRUITING

Clinical Research Site

Philadelphia, Pennsylvania 19104 - United States

Status: RECRUITING

And 64 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1 clinical trial for Non-Small Cell Lung Cancer, Colorectal Cancer, Advanced 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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