Patient Guide: A Study Evaluating The Efficacy and Safety of Neoadjuvant Immunotherapy Combinations in Patients With Surgically Resectable Hepatocellular Carcinoma

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 33 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05908786
Status: ACTIVE_NOT_RECRUITING
Condition: Carcinoma, Hepatocellular
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 33 locations across the country.

Top locations include:
  • • Los Angeles, California
  • • Santa Monica, California
  • • Washington, District of Columbia
  • • And 30 more locations

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A Study Evaluating The Efficacy and Safety of Neoadjuvant Immunotherapy Combinations in Patients With Surgically Resectable Hepatocellular Carcinoma - Join Clinical Trial NCTNCT05908786

How to Join This Clinical Trial - NCTNCT05908786

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Carcinoma, Hepatocellular. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Carcinoma, Hepatocellular
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05908786 - 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 33 locations. Find a study site near you:

Clinical Research Site

Los Angeles, California 90033 - United States

Status: Contact for availability

Clinical Research Site

Santa Monica, California 90404-2023 - United States

Status: Contact for availability

Clinical Research Site

Washington, District of Columbia 20007 - United States

Status: Contact for availability

Clinical Research Site

Detroit, Michigan 48201-2013 - United States

Status: Contact for availability

Clinical Research Site

New York, New York 10032 - United States

Status: Contact for availability

Clinical Research Site

Dallas, Texas 75390-8813 - United States

Status: Contact for availability

Clinical Research Site

Seattle, Washington 98109-4433 - United States

Status: Contact for availability

Clinical Research Site

Klagenfurt am Worthersee, 9020 - Austria

Status: Contact for availability

Clinical Research Site

Vienna, 1100 - Austria

Status: Contact for availability

Clinical Research Site

Vienna, 1180 - Austria

Status: Contact for availability

And 23 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, PHASE2 clinical trial for Carcinoma, Hepatocellular:

  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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