Patient Guide: An Observational Study to Learn More About How Well a Treatment Works When Given After Treatment With Atezolizumab and Bevacizumab or Another Similar Combination of Drugs in Adults With Liver Cancer That Cannot be Treated With Surgery

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 20 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06117891
Status: 🟢 Enrolling Now
Condition: Unresectable Hepatocellular Carcinoma
Phase: Not Specified

Where You Can Participate

This study is available at 20 locations across the country.

Top locations include:
  • • Baltimore, Maryland
  • • Ann Arbor, Michigan
  • • Buffalo, New York
  • • And 17 more locations

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An Observational Study to Learn More About How Well a Treatment Works When Given After Treatment With Atezolizumab and Bevacizumab or Another Similar Combination of Drugs in Adults With Liver Cancer That Cannot be Treated With Surgery - Join Clinical Trial NCTNCT06117891

How to Join This Clinical Trial - NCTNCT06117891

Learn how to participate in this Not Specified trial studying an investigational therapy for Unresectable Hepatocellular Carcinoma. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Unresectable Hepatocellular Carcinoma. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Unresectable Hepatocellular Carcinoma
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06117891 - 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 20 locations. Find a study site near you:

Clinical Research Site

Baltimore, Maryland 21202 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Ann Arbor, Michigan 48109 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Buffalo, New York 14203 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Cincinnati, Ohio 45219 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Philadelphia, Pennsylvania 19104 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Philadelphia, Pennsylvania 19141 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Multiple Locations, - Argentina

Status: RECRUITING

Clinical Research Site

Multiple Locations, - Brazil

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Multiple Locations, - China

Status: RECRUITING

Clinical Research Site

Multiple Locations, - Colombia

Status: RECRUITING

And 10 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Unresectable Hepatocellular Carcinoma:

  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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