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 |
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| 分期 | 3期 |
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| 申办方 | AstraZeneca |
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| 状态 | 进行中(已停止招募) |
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| 受试者人数 | 1,324 人 |
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| 干预(药物) | Durvalumab, Tremelimumab (Regimen 1), Tremelimumab (Regimen 2), Sorafenib, Durvalumab (Regimen 1) |
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| 开始日期 | 2017年10月11日 |
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| 完成日期 | 2021年8月27日 |
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| 结果公布日 | 2023年6月18日 |
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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 mg | 16.56 months |
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| Treme 300 mg x1 Dose + Durva 1500 mg | 16.43 months |
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| Treme 75 mg x4 Doses + Durva 1500 mg | 16.36 months |
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| Sora 400 mg | 13.77 months |
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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。