Patient Guide: A Phase II Clinical Trial Comparing the Efficacy of RO7198457 Versus Watchful Waiting in Patients With ctDNA-positive, Resected Stage II (High Risk) and Stage III Colorectal Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 118 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04486378
Status: 🟢 Enrolling Now
Condition: Colorectal Cancer Stage II, Colorectal Cancer Stage III
Phase: PHASE2

Where You Can Participate

This study is available at 118 locations across the country.

Top locations include:
  • • Scottsdale, Arizona
  • • Concord, California
  • • Glendale, California
  • • And 115 more locations

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A Phase II Clinical Trial Comparing the Efficacy of RO7198457 Versus Watchful Waiting in Patients With ctDNA-positive, Resected Stage II (High Risk) and Stage III Colorectal Cancer - Join Clinical Trial NCTNCT04486378

How to Join This Clinical Trial - NCTNCT04486378

Learn how to participate in this PHASE2 trial studying an investigational therapy for Colorectal Cancer Stage II, Colorectal Cancer Stage III. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Colorectal Cancer Stage II, Colorectal Cancer Stage III. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Colorectal Cancer Stage II, Colorectal Cancer Stage III
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT04486378 - 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 118 locations. Find a study site near you:

Clinical Research Site

Scottsdale, Arizona 85259 - United States

Status: RECRUITING

Clinical Research Site

Concord, California 94520 - United States

Status: RECRUITING

Clinical Research Site

Glendale, California 91204 - United States

Status: WITHDRAWN

Clinical Research Site

Greenbrae, California 94904 - United States

Status: RECRUITING

Clinical Research Site

Orange, California 92868 - United States

Status: RECRUITING

Clinical Research Site

Santa Barbara, California 93105 - United States

Status: RECRUITING

Clinical Research Site

Denver, Colorado 80218 - United States

Status: RECRUITING

Clinical Research Site

Boca Raton, Florida 33486 - United States

Status: RECRUITING

Clinical Research Site

Fort Myers, Florida 33916 - United States

Status: WITHDRAWN

Clinical Research Site

Jacksonville, Florida 32224 - United States

Status: RECRUITING

And 108 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 Colorectal Cancer Stage II, Colorectal Cancer Stage III:

  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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