Clinical Trial for Hepatocellular Carcinoma

A US Study to Evaluate Transarterial Radioembolization (TARE) in Combination With Durvalumab and Bevacizumab Therapy in People With Unresectable Hepatocellular Carcinoma Amenable to TARE (EMERALD-Y90)

A Phase II single-arm study conducted in participants with unresectable Hepatocellular carcinoma (HCC) eligible for embolization and not eligible for or who have declined treatment with resection and/or ablation or liver transplant.

Eligibility Requirements:

  • 18 and older
  • Participants with confirmed unresectable HCC
  • Participants with no evidence of extrahepatic disease on any available imaging

Exclusion Criteria:

  • Disease amenable to curative surgery or transplantation or curative ablation.
  • Participants co-infected with HBV and HDV
  • Any history of nephrotic or nephritic syndrome.
  • Clinically significant (e.g., active) cardiovascular disease
  • Participants with uncontrolled hypertension
  • History of hepatic encephalopathy

All study participants will receive the assigned study treatment, study-related medical exams, and study-related laboratory tests at no cost. Travel assistance may be available. Further details about study support can be discussed with the study team. Learn more about this study.

Emerald-Y90 Participation Information Brochure
Emerald-Y90 Participant Study Guide

Study Contact
1-877-240-9479
information.center@astrazeneca.com

The American Liver Foundation receives contributions and funding from clinical trial and study sponsors but does not evaluate or endorse any clinical trials or studies and is not affiliated with any of the sponsors.