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Preceding local therapy to STRIDE for pretreated patients

Phase II study of preceding local therapy to Single Tremelimumab Regular Interval Durvalumab for patients with hepatocellular carcinoma treated with systemic chemotherapy

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1041230013
Enrollment
36
Registered
2023-04-22
Start date
2023-05-15
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Hepatocellular carcinoma Hepatocellular carcinoma

Interventions

After local therapy (radiofrequency ablation, radiation therapy, hepatic arterial chemoembolization, or hepatic arterial chemotherapy), a single dose of 1500 mg durvalumab and 300 mg tremelimumab is a
Local therapy, STRIDE, Durvalmab, Tremelimumab

Sponsors

Yamashita Taro
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) clinically diagnosed as hepatocellular carcinoma 2) unsuitable for radical local therapy due to biloblar multiple nodules, ductal invasion, metastatic lesions, or other factors 3) previously treated by one or more systemic therapy 4) target lesion for paliative local therapy 5) preserved liver function 6) 18 years or older 7) ECOG Performance status <=2 8) preservation of major organ function 9) written informed consent

Exclusion criteria

Exclusion criteria: 1) refractory ascites or pleural effusion 2) unsuitable for paliative local therapy 3) risky varices without prophylactic procedures 4) double cancer 5) metastases to central nervous system 6) severe complication 7) active infectious disease 8) pregnant or lactating women, or women of childbearing potential 9) mental disorder 10) patients who investigator regards as inappropriate for candidate

Design outcomes

Primary

MeasureTime frame
Progression-free survival

Secondary

MeasureTime frame
Immunological response, Objective response rate, Tumor control rate, Overall survival, Subsequent therapy, Adverse events

Contacts

Public ContactTakeshi Terashima

Kanazawa University Hospital

tera@m-kanazawa.jp+81-76-265-2235

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026