Georgia's Online Cancer Information Center

Find A Clinical Trial

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

Status
Active
Cancer Type
Liver Cancer / Hepatoblastoma
Trial Phase
Phase II
Eligibility
18 - 130 Years, Male and Female
Study Type
Treatment
NCT ID
NCT06040099
Protocol IDs
D933GC00002 (primary)
NCI-2023-10167
Study Sponsor
AstraZeneca Pharmaceuticals LP

Summary

The purpose of this study is to measure the efficacy and safety of durvalumab intravenous
(IV) solution plus bevacizumab IV solution after transarterial radioembolization (Yttrium
90 glass microspheres TARE) in participants with unresectable hepatocellular carcinoma
(HCC) amenable to embolization.

Objectives

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.

Participants with previous Transarterial Chemoembolization (TACE) or TARE associated with
the curative setting are permitted with a 6-month washout.

Approximately 125 participants with unresectable but amenable to locoregional therapy HCC
eligible for embolization will be enrolled in the study at approximately 20 sites in the
US to treat approximately 100 participants.

Eligibility

  1. Participants with confirmed unresectable HCC
  2. Participants with Lung dose threshold for Yttrium 90 glass microspheres of 30 Gy (equal or less than 30 Gy per treatment for glass) and an estimated Future liver remnant volume (FLRV) = 30% of whole liver volume
  3. Participants with no evidence of extrahepatic disease on any available imaging
  4. Participants with one or more measurable lesions, unilobar disease for participants with segmental or right anterior/posterior portal vein invasion (Vp1/Vp2) and eligible for Yttrium 90 glass microspheres TARE.
  5. Participants having Child-Pugh score class A.
  6. Participants having ECOG performance status of 0 or 1 at enrollment
  7. Adequate organ and marrow function

Treatment Sites in Georgia

Northside Hospital Cancer Institute


1000 Johnson Ferry Road NE
Atlanta, GA 30342
404-303-3355
www.northside.com

Winship Cancer Institute of Emory University


1365 Clifton Road NE
Building C
Atlanta, GA 30322
winshipcancer.emory.edu

**Clinical trials are research studies that involve people. These studies test new ways to prevent, detect, diagnose, or treat diseases. People who take part in cancer clinical trials have an opportunity to contribute to scientists’ knowledge about cancer and to help in the development of improved cancer treatments. They also receive state-of-the-art care from cancer experts... Click here to learn more about clinical trials.