BENITIONSClinical Trial Intelligence

Study of Durvalumab and Tremelimumab as First-line Treatment in Patients With Advanced Hepatocellular Carcinoma

3期 进行中(已停止招募) NCT03298451

适应症Hepatocellular Carcinoma
分期3期
申办方AstraZeneca
状态进行中(已停止招募)
受试者人数1,324 人
干预(药物)Durvalumab, Tremelimumab (Regimen 1), Tremelimumab (Regimen 2), Sorafenib, Durvalumab (Regimen 1)
开始日期2017年10月11日
完成日期2021年8月27日
结果公布日2023年6月18日

摘要

This is a randomized, open-label, multi-center, global, Phase III study to assess the efficacy and safety of durvalumab plus tremelimumab combination therapy and durvalumab monotherapy versus sorafenib in the treatment of patients with no prior systemic therapy for unresectable HCC. The patients cannot be eligible for locoregional therapy

Overall Survival (OS) - Treme 300 mg x1 Dose + Durva 1500 mg vs Sora 400 mg

From the date of randomization until death due to any cause, assessed up to the data cut-off date (27Aug2021, to a maximum of approximately 46 months). · months

Durva 1500 mg16.56 months
Treme 300 mg x1 Dose + Durva 1500 mg16.43 months
Treme 75 mg x4 Doses + Durva 1500 mg16.36 months
Sora 400 mg13.77 months
p-value0.0035

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

同一适应症的其他试验

全部试验

本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。