Study identifier:D933GC00002
ClinicalTrials.gov identifier:NCT06040099
EudraCT identifier:N/A
CTIS identifier:N/A
Phase II Single-Arm Study of Durvalumab and Bevacizumab Following Transarterial Radioembolization Using Yttrium-90 Glass Microspheres (TheraSphere™) in Unresectable Hepatocellular Carcinoma Amenable to Locoregional Therapy
Hepatocellular Carcinoma (HCC)
Phase 2
No
Durvalumab, Bevacizumab
All
100
Interventional
18 Years - 130 Years
Allocation: N/A
Endpoint Classification: -
Intervention Model: Single Group Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Oct 2024 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Yttrium 90 glass microspheres TARE in combination with Durvalumab and Bevacizumab Participants will undergo Yttrium 90 glass microspheres TARE according to the dosimetry recommendation. | - |