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Study on the clinical efficacy of Ye Xiazhu Anti-Cheng Zu Tang combined with western medical therapies on HBV-associated middle and late-stage hepatocellular carcinoma

Study on the clinical efficacy of Ye Xiazhu Anti-Cheng Zu Tang combined with western medical therapies on HBV-associated middle and late-stage hepatocellular carcinoma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000802
Enrollment
Unknown
Registered
2026-03-30
Start date
2022-12-14
Completion date
Unknown
Last updated
2026-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HCC

Interventions

A Group:Western medicine treatment: Lenvatinib 8 mg once daily (for body weight <60 kg) or 12 mg once daily (for body weight =60 kg), Tislelizumab 200 mg every 3 weeks, local treatment (TACE or HAIC).
C Group:atilizumab in combination with bevacizumab anti (T+A) therapy, localized therapy (TACE or HAIC). Traditional Chinese medicine treatment: Ye Xiazhu Wuzhong Tang plus subtraction
B Group:Western medicine treatment: Lenvatinib 8mg qd (body weight less than 60kg) or 12mg qd (body weight greater than or equal to 60mg), Tirilizumab 200mg Q3W, localized therapy (TACE or HAIC). (TAC
D Group:atilizumab in combination with bevacizumab anti (T+A) therapy, localized therapy (TACE or HAIC). Herbal therapy: no

Sponsors

Shenzhen Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Hepatocellular carcinoma associated with HBV infection confirmed clinically and pathologically; 2) CNLC staging: Stage IIb Stage IIIa Stage IIIb and clinically proven to be not directly resectable by surgery; 3) Child-pugh: Grade A; 4) Not receiving systemic treatment; 5) Male or female aged greater than or equal to18 years and less than or equal to 65 years who have signed an informed consent form; 6) ECOG score of 0 or 1 and expected survival of more than 3 months.

Exclusion criteria

Exclusion criteria: 1 Combined with other hepatophilic viruses and HIV infection; 2 Persons with severe cardiac renal pulmonary hematologic metabolic and gastrointestinal disorders; 3 Pregnant or lactating women. 4 Allergic or allergic to multiple drugs.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;

Secondary

MeasureTime frame
Disease control rate;Overall survival;Progression-free survival;Time to disease progression;Success rate of conversion surgery;Quality of life;Safety and tolerability;

Countries

China

Contacts

Public Contactliujiulin

Shenzhen Hospital of Traditional Chinese Medicine

szliujialin@126.com13714754393

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026