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An open-label, single-arm, Ib study of the efficacy and safety of IBI310 combined with sintilimab in patients with advanced hepatocellular carcinoma
In this study, approximately 18 to 47 patients who have previously received sorafenib, lenvatinib, or oxaliplatin-containing chemotherapy . After determining the dose of IBI310, the study will enter the expansion phase
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| IBI310 | Experimental | An open-label, single-arm, Ib study of the efficacy and safety of IBI310 combined with sintilimab in patients with advanced hepatocellular carcinoma |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| IBI308 200mg | Drug | Received IBI310 combined with sintilizumab 200mg |
|
| Measure | Description | Time Frame |
|---|---|---|
| adverse event | 21-42days | |
| Evaluation of the objective response rate of IBI310 combined with 308 in the second-line treatment of advanced hepatocellular carcinoma | 21-42days |
| Measure | Description | Time Frame |
|---|---|---|
| Evaluate the ORR of IBI310 combined with 308 in the second-line treatment of advanced hepatocellular carcinoma (researched by the investigator according to RECIST V1.1). | 1years |
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inclusion criteria:
exclusion criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Zhongshan Hospital Affiliated to Fudan University | Shanghai | China |
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| ID | Term |
|---|---|
| C000632826 | sintilimab |
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