Clinical trial · Interventional
Study of PolyIC and PD-1 mAb in Subjects With Unresectable Hepatocellular Carcinoma
A Phase II Study on the Safety and Therapeutic Effect of Combination of PolyIC and PD-1 mAb in Subjects With Unresectable Hepatocellular Carcinoma
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
When multi-kinase inhibitors based therapies (sorafenib and regorafenib) are limited in late-stage liver cancer patients, there is no alternative options. PD-1 blockade has became a promising immunotherapeutic strategy in many cancers. While it showed limited efficacy in liver cancer. Polyinosinic-polycytidylic acid (PolyIC) has been widely studied as a new anti-tumor drug and recent study showed that polyIC and PD-L1 mAb has a quite synergetic effect on the hepatocellular carcinoma (HCC). This study is aimed to evaluate the safety and efficacy of the combination of PolyIC and PD-1 mAb in unresectable late-stage HCC patients.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Carcinoma, Hepatocellular | Hepatocellular Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| PD-1 mAb | Drug | — | UNRESOLVED |
| PolyIC | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- 'PolyIC plus PD-1 mAb' and 'PD-1 mAb'
- description
- 'PolyIC plus PD-1 mAb' group: PolyIC, 2mg, i.m., every other day, for three weeks. PD-1 mAb, 200mg, i.v., every three weeks. 'PD-1 mAb' group: PD-1 mAb, 200mg, i.v., every three weeks.
- interventionNames
- Drug: PD-1 mAb
- Drug: PolyIC
Primary outcomes (1)
- measure
- Objective response rate (ORR)
- timeFrame
- Up to approximately 5 years
- description
- Percentage of patients whose cancer shrinks or disappears after treatment
Secondary outcomes (6)
- measure
- Disease control rate (DCR)
- timeFrame
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Hepatocellular carcinoma with imaging diagnosis, in barcelona stage C, or stage B but resistant/recurrent to prior local treatment (e.g., TACE). 2. Eastern cooperative oncology group physical fitness score: 0-2. 3. Predicted survival time≥3 months. 4. Liver function of Child-Pugh A-B, no hepatic encephalopathy or physical examined ascites. 5. Routine blood tests were in accordance with the following criteria: White blood cell (WBC)≥2.0x10\^9/L, Neutrophil≥1.0x10\^9/L, platelet (PLT)≥50x10\^9/L, hemoglobin (HB)≥80 g/dL, creatinine≤1.5xULN (upper limit of normal value), Alanine transaminase (ALT) and aspartate aminotransferase (AST)≤5xULN, total bilirubin (TB)≤51.3umol/L, international normalized ratio (INR) or prothrombin time (PT)≤1.7xULN, activated partial thromboplastin time (APTT)≤1.5xULN, serum albumin≥28g/L 6. Patients will be informed consent, and understand and are willing to cooperate with the trial and sign related documents. Exclusion Criteria: 1. Has a history of malignant tumor in last 2 years, except basal and skin squamous cell carcinoma, cervical carcinoma in situ, papillary thyroid carcinoma, superficial bladder cancer and carcinoma in situ of breast. 2. Received the treatment of polyIC or immune checkpoint inhibitors (e.g., PD-1/PD-L1 mAb or CTLA-4 mAb) in last 2 years. 3. Received the therapies of multi-kinase inhibitors (e.g., sorafenib, regorafenib), systemic chemotherapy, local therapy (e.g., TACE, radiotherapy), vaccination, immunomodulating therapy (e.g., interleukins, thymosin) or any other clinical trial in last 4 weeks. 4. Received any corticosterone or immunosuppressive drug in last 2 weeks. 5. Toxicity induced by previous anti-tumor therapies has not returned to the status of baseline or stability. 6. HIV positive (including previous anti-retroviral therapy), active HCV infection or active syphilis. 7. Any severe liver disease (e.g., severe liver cirrhosis, severe liver adenoma) 8. Any active or recurrent autoimmune disease. 9. Any interstitial pneumonia, non-infectious pneumonia, or uncontrolled systemic disease (e.g., uncontrolled hypertension or diabetes). 10. Severe cardiovascular risk factors. 11. Has a history of allogeneic stem cell transplantation or organ transplantation. 12. Imaging confirmed brain or meninges metastases. 13. Has the plan of pregnancy, or lactation. 14. Any kind of psychiatric disease or laboratory test abnormality that may result in the subject's failure to fully comply with the laboratory protocol.
References
Publications (0)
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