About this trial

This Phase 1/ 2a study is a multicenter study to evaluate the safety, tolerability and efficacy of SCG101 in subjects with hepatitis B virus-related hepatocellular carcinoma

Eligibility criteria

Qualifiers

Histologically or cytologically confirmed Hepatocellular carcinoma (HCC)

Subjects with HCC who have received at least 2 standard systemic therapies

HLA-A *02

BCLC stage B or C

Disqualifiers

Subjects with history of another primary cancer

Untreated or active central nervous system (CNS) or leptomeningeal metastasis, or history of hepatic encephalopathy, or other clinically significant CNS diseases

Autoimmune diseases requiring immunosuppressive therapy (except topical medication) or subjects with significant persistent immune rejection

Known history of neurological or mental disorder, including epilepsy or dementia

Trial design

Treatments tested in this trial

  • SCG101

Treatment groups

46 Participants
are divided into 1 treatment group

Locations

6
Hong Kong
Hong Kong is. Hong Kong Hong Kong
Hong Kong NT Hong Kong Hong Kong
Singapore
Singapore169610, Singapore Singapore
Singapore228510, Singapore Singapore

Sponsors and collaborators

SCG Cell Therapy Pte. Ltd.

Lead sponsor