Patient Guide: ALTUS: Performance of a Multi- Target Hepatocellular Carcinoma (HCC) Test in Subjects With Increased Risk

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 72 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05064553
Status: 🟢 Enrolling Now
Condition: Hepatocellular Carcinoma, Hepatocellular Cancer, Hepatitis B, Cirrhosis, Liver Cancer
Phase: Research Study

Where You Can Participate

This study is available at 72 locations across the country.

Top locations include:
  • • Chandler, Arizona
  • • Sun City, Arizona
  • • Bakersfield, California
  • • And 69 more locations

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ALTUS: Performance of a Multi- Target Hepatocellular Carcinoma (HCC) Test in Subjects With Increased Risk - Join Clinical Trial NCTNCT05064553

How to Join This Clinical Trial - NCTNCT05064553

Learn how to participate in this clinical trial studying an investigational therapy for Hepatocellular Carcinoma, Hepatocellular Cancer, Hepatitis B, Cirrhosis, Liver Cancer. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Hepatocellular Carcinoma, Hepatocellular Cancer, Hepatitis B, Cirrhosis, Liver Cancer
Treatment Being Tested
Investigational treatment
Study Phase
Clinical trial phase - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05064553 - 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 72 locations. Find a study site near you:

Clinical Research Site

Chandler, Arizona 85225 - United States

Status: COMPLETED

Clinical Research Site

Sun City, Arizona 85251 - United States

Status: RECRUITING

Clinical Research Site

Bakersfield, California 93301 - United States

Status: RECRUITING

Clinical Research Site

Escondido, California 92025 - United States

Status: RECRUITING

Clinical Research Site

Los Angeles, California 90048 - United States

Status: RECRUITING

Clinical Research Site

Mission Hills, California 91345 - United States

Status: RECRUITING

Clinical Research Site

Murrieta, California 92563 - United States

Status: COMPLETED

Clinical Research Site

Palo Alto, California 94303 - United States

Status: RECRUITING

Clinical Research Site

Palo Alto, California 94304 - United States

Status: RECRUITING

Clinical Research Site

Pasadena, California 91107 - United States

Status: COMPLETED

And 62 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this clinical trial for Hepatocellular Carcinoma, Hepatocellular Cancer, Hepatitis B, Cirrhosis, Liver 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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