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Liangzhi Xie

Beijing Engineering Research Center of Protein and Antibody
H指数:20
被引数:1,666

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Phase Ib Trial of Finotonlimab Combined With SCT200 in Patients With Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

奋尼妥利单抗联合SCT200治疗复发或转移性头颈部鳞状细胞癌的Ib期临床试验

2026-09-300
OAAI
Finotonlimab (PD-1 inhibitor) plus bevacizumab (bevacizumab biosimilar) as first-tier therapy for late-stage hepatocellular carcinoma: a randomized phase 2/3 trial

Finotonlimab (PD-1抑制剂) 联合贝伐单抗 (贝伐单抗生物仿制药) 作为晚期肝细胞癌的一线治疗: 一项随机2/3期试验

2025-08-060
OAAI
Efficacy and safety of finotonlimab plus docetaxel vs. docetaxel in previously treated advanced squamous cell non-small-cell lung cancer: a randomized, double-blinded, phase III trial

finotonlimab联合多西他赛对比多西他赛治疗既往经治的晚期鳞状细胞非小细胞肺癌的疗效与安全性:一项随机、双盲、III期临床试验

2025-04-010
OA
Sustained immunogenicity of bivalent protein COVID-19 vaccine SCTV01C against antigen matched and mismatched variants

双价蛋白COVID-19疫苗SCTV01C对抗原匹配和不匹配变体的持续免疫原性

2025-01-270
OA
Safety and Immunogenicity of the Tetravalent Recombinant COVID-19 Protein Vaccine SCTV01E in Children and Adolescents Aged 3 to 17 Years: A Randomized, Double-Blind, Placebo-Controlled Phase 2 Clinical Trial

四价重组新型冠状病毒肺炎蛋白疫苗SCTV01E在3至17岁儿童和青少年中的安全性和免疫原性: 一项随机,双盲,安慰剂对照的2期临床试验

2025-01-070
OAAI
Intermediate-dose immune tolerance induction outperforms with faster success, less bleeding, and no added cost in comparison with low dose: a multicenter randomized clinical trial

中剂量免疫耐受诱导方案相较于低剂量方案,具有更快的达标速度、更少的出血事件且不增加医疗成本:一项多中心随机对照临床试验

2025-01-010
OAAI
Efficacy and Safety of Biosimilar SCT510 Compared with Bevacizumab for the First-Line Treatment of Advanced Non-Squamous Non-Small Cell Lung Cancer: A Randomized, Double-Blind, Phase III Study
2024-09-040
PRE
Efficacy of the tetravalent protein COVID-19 vaccine, SCTV01E: a phase 3 double-blind, randomized, placebo-controlled trial
2024-07-240
OAAI
Finotonlimab with chemotherapy in recurrent or metastatic head and neck cancer: a randomized phase 3 trial

Finotonlimab联合化疗治疗复发或转移性头颈癌: 一项随机3期试验

2024-06-280
PRE