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Preceding RFA to STRIDE trial

Phase II study of preceding radiofrequency ablation to Durvalumab plus Tremelimumab for hepatocellular carcinoma patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs041240049
Enrollment
36
Registered
2024-06-18
Start date
2024-06-24
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Hepatocellular carcinoma RFA

Interventions

Radiofrequency ablation, Durvalumab plus Tremelimumab

Sponsors

Yamashita Taro
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: clinically diagnosed as hepatocellular carcinoma; unsuitable for local therapy; previously treated by systemic therapy; Preserved liver function; 18 years or older; ECOG Performance status <=2; preservation of major organ function; written informed consent

Exclusion criteria

Exclusion criteria: 1) Active double cancer 2) Receiving any combination of chemotherapy, investigational drugs, and biologic or hormonal therapy for the treatment of cancer 3) With previous radiotherapy 4) Active infection 5) Fever of 38 degrees Celsius or higher 6) Active autoimmune or inflammatory disease or a confirmed history of such disease 7) Taking antiplatelet or anticoagulant medication 8) Complicated by one or more of interstitial pneumonia, pulmonary fibrosis, or severe emphysema 9) Unhealed fistulas, ulcerative lesions, and active bleeding 10) Metastases to central nervous system 11) Moderate or severe ascites and/or pleural effusion 12) Severe complication 13) Poorly controlled diabetes 14) Pregnant or lactating women 15) Mental disorder 16) Patients who investigator regards as inappropriate for candidate

Design outcomes

Primary

MeasureTime frame
Progression-free survival

Secondary

MeasureTime frame
Overall survival, Objective response rate, Tumor control rate, Subsequent therpay, Severe adverse events

Contacts

Public ContactTakeshi Terashima

Kanazawa Medical University Hospital

tera@kanazawa-med.ac.jp+81-76-286-2211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026