Patient Guide: A Study of Sequential Therapy With Daplusiran/Tomligisiran (DAP/TOM) Followed by Bepirovirsen in Participants Living With Chronic Hepatitis B (CHB)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 81 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06537414
Status: ACTIVE_NOT_RECRUITING
Condition: Chronic Hepatitis B Virus Infection, Hepatitis B
Phase: PHASE2

Where You Can Participate

This study is available at 81 locations across the country.

Top locations include:
  • • San Francisco, California
  • • San Jose, California
  • • Minneapolis, Minnesota
  • • And 78 more locations

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A Study of Sequential Therapy With Daplusiran/Tomligisiran (DAP/TOM) Followed by Bepirovirsen in Participants Living With Chronic Hepatitis B (CHB) - Join Clinical Trial NCTNCT06537414

How to Join This Clinical Trial - NCTNCT06537414

Learn how to participate in this PHASE2 trial studying an investigational therapy for Chronic Hepatitis B Virus Infection, Hepatitis B. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Chronic Hepatitis B Virus Infection, Hepatitis B
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06537414 - 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 81 locations. Find a study site near you:

Clinical Research Site

San Francisco, California 94115 - United States

Status: Contact for availability

Clinical Research Site

San Jose, California 95128 - United States

Status: Contact for availability

Clinical Research Site

Minneapolis, Minnesota 55415 - United States

Status: Contact for availability

Clinical Research Site

New York, New York 10029 - United States

Status: Contact for availability

Clinical Research Site

Philadelphia, Pennsylvania 19104 - United States

Status: Contact for availability

Clinical Research Site

Westmead, New South Wales 2145 - Australia

Status: Contact for availability

Clinical Research Site

Fitzroy, Victoria 3065 - Australia

Status: Contact for availability

Clinical Research Site

Bruxelles, 1000 - Belgium

Status: Contact for availability

Clinical Research Site

Edegem, 2650 - Belgium

Status: Contact for availability

Clinical Research Site

Gent, 9000 - Belgium

Status: Contact for availability

And 71 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 Chronic Hepatitis B Virus Infection, Hepatitis B:

  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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