drugset / Trial / NCT05162352

Donafenib Plus Sintilimab for Advanced HCC

NCT05162352 ↗

NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the efficacy and safety of donafenib combined with sintilimab in patients with advanced hepatocellullar carcinoma (HCC).

Timeline

Start
2021-12-04
Primary completion
2022-10-28
Completion
2023-08-31

Outcome

Met primary endpoint

paper The primary endpoint was met with a median PFS of 6.2 (95% confidence interval [CI], 4.4-8.0) months per mRECIST PMID 39910472 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Donafenib Small molecule 200 mg Oral
Subject Sintilimab Monoclonal antibody 200 mg Intravenous