Patient Guide: A Study to Assess Adverse Events and Change in Disease Activity in Adult Participants Receiving Intravenously Infused Telisotuzumab Adizutecan Alone or With Standard of Care in Participants With Post Adjuvant Circulating Tumor DNA Positive Colorectal Cancer and No Radiographic Evidence of Disease

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 17 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT07023289
Status: 🟢 Enrolling Now
Condition: Colorectal Cancer
Phase: PHASE2

Where You Can Participate

This study is available at 17 locations across the country.

Top locations include:
  • • Minneapolis, Minnesota
  • • Lake Success, New York
  • • Portland, Oregon
  • • And 14 more locations

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A Study to Assess Adverse Events and Change in Disease Activity in Adult Participants Receiving Intravenously Infused Telisotuzumab Adizutecan Alone or With Standard of Care in Participants With Post Adjuvant Circulating Tumor DNA Positive Colorectal Cancer and No Radiographic Evidence of Disease - Join Clinical Trial NCTNCT07023289

How to Join This Clinical Trial - NCTNCT07023289

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

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Colorectal Cancer. 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
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT07023289 - 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 17 locations. Find a study site near you:

Clinical Research Site

Minneapolis, Minnesota 55404 - United States

Status: RECRUITING

Clinical Research Site

Lake Success, New York 11042 - United States

Status: RECRUITING

Clinical Research Site

Portland, Oregon 97227-1800 - United States

Status: RECRUITING

Clinical Research Site

Nashville, Tennessee 37203 - United States

Status: RECRUITING

Clinical Research Site

Austin, Texas 78705 - United States

Status: RECRUITING

Clinical Research Site

Grapevine, Texas 76051 - United States

Status: RECRUITING

Clinical Research Site

Vejle, Region Syddanmark 7100 - Denmark

Status: RECRUITING

Clinical Research Site

Gifu, Gifu 501-1194 - Japan

Status: RECRUITING

Clinical Research Site

Yokohama, Kanagawa 232-0024 - Japan

Status: RECRUITING

Clinical Research Site

Osaka, Osaka 540-0006 - Japan

Status: RECRUITING

And 7 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:

  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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