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Study identifier: NCT05377034 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Multinational Phase II Trial to Compare Safety and Efficacy of SIRT (Y-90 Resin Microspheres) Followed by Atezolizumab Plus Bevacizumab, vs SIRT (SIRT-Y90) Followed by Placebo in Locally Advanced HCC Patients

Condition: Locally Advanced Hepatocellular Carcinoma  ·  Sponsor: National Cancer Centre, Singapore

PhasePhase 2
Planned participants100
Who can joinAll sexes, 21 Years to 99 Years
Healthy volunteersNo

About this study

This is a multi-national, phase II, parallel-arm, double-blind, placebo-controlled, two-arm study designed to assess the efficacy and safety of SIRT-Y90 followed by atezolizumab plus bevacizumab \[study arm\], versus SIRT-Y90 followed by placebo \[control arm\] in patients with locally advanced Hepatocellular Carcinoma (HCC).

This description comes directly from the study's public registry record.

Talk to the study team

Professor Pierce CHOW, MD, PhD  ·  +65 6436 8000  ·  pierce.chow.k.h@singhealth.com.sg

Vennese LOW  ·  +65 6306 5456  ·  low.minxiu.vennese@nccs.com.sg

Always discuss trial participation with your own doctor first.

Locations (14)

Beijing Tsinghua Changgung HospitalBeijing, ChinaRecruiting
People's Liberation Army General Hospital (1st and 6th Medical Centre)Beijing, ChinaNot Yet Recruiting
West China Hospital, Sichuan UniversityChengdu, ChinaRecruiting
Shandong Cancer HospitalJinan, ChinaNot Yet Recruiting
National University HospitalSingapore, SingaporeRecruiting
National Cancer Centre SingaporeSingapore, SingaporeRecruiting
Samsung Medical CenterSeoul, South KoreaRecruiting
Seoul National University HospitalSeoul, South KoreaRecruiting
Severance Hospital Yonsei University Health SystemSeoul, South KoreaRecruiting
Kaohsiung Chang Gung Memorial HospitalKaohsiung City, TaiwanRecruiting
Taichung Veterans General HospitalTaichung, TaiwanRecruiting
National Taiwan University Cancer CenterTaipei, TaiwanRecruiting

+ 2 more locations — full list on the registry record.

Follow this study

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Source record: clinicaltrials.gov/study/NCT05377034