Novavax已在英国开始COVID-19候选疫苗NVX-CoV2373的III期临床试验

2020-09-28 Allan MedSci原创

Novavax近日表示,已经启动了其第一项III期临床试验,以评估其COVID-19疫苗候选NVX-CoV2373的功效、安全性和免疫原性。

Novavax近日表示,已经启动了其第一项III期临床试验,以评估其COVID-19疫苗候选NVX-CoV2373的功效、安全性和免疫原性。该试验正在英国进行,预计将在接下来的四到六周内招募10,000名年龄在18至84岁之间的参与者。

Novavax的研发负责人Gregory Glenn评论说:“在英国观察到高水平的SARS-CoV-2传播并将继续这种趋势,我们对这一关键的III期临床试验持乐观态度”。后期研究的数据将支持欧盟和其他国家/地区的监管许可申请。

50%的试验参与者将接受两次疫苗注射,其中包括5 mcg的蛋白质抗原和50 mcg的Matrix-M佐剂,间隔21天给药;另一半将被给予安慰剂。据Novavax称,该试验旨在招募至少25%的65岁以上的参与者,并优先考虑受COVID-19影响最大的群体。此外,作为这项研究的一部分,多达400人还将接种季节性流感疫苗,以评估共同给药的潜在益处。

 

原始出处:

https://www.firstwordpharma.com/node/1760367?tsid=4

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这篇研究的目的是为了评估中国湖北省新冠疫情封闭结束后1个月牙髓治疗的恢复情况。

Obstet Gynecol:COVID-19孕妇吸入高浓度一氧化氮疗效分析

目前,临床缺乏用于治疗或预防2019冠状病毒病(COVID-19)孕妇缺氧性呼吸衰竭进展的治疗手段。

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J Clin Med:COVID-19住院患者血栓形成和出血风险评分与死亡率密切相关

本研究提示COVID-19血栓形成和出血风险评分高的患者死亡率更高。

Front Med:COVID-19住院患者Casirivimab/imdevimab失败预测评分的开发和验证

Casirivimab和imdevimab是两种非竞争性、高亲和力的人IgG1抗COVID-19单克隆抗体,它们特异性结合COVID-19病毒刺突糖蛋白的受体结合域,从而阻断病毒进入宿主细胞。

Biomedicines:2型糖尿病住院患者COVID-19的长期预后

在T2D合并COVID-19患者中,随访观察到住院死亡率、卒中和心血管住院率增加。

Cureus:2型糖尿病状态、糖尿病并发症严重程度指数评分及其与COVID-19严重程度的关系

与非糖尿病患者相比,我们样本中的糖尿病患者发生COVID-19不良临床结果和住院死亡率的几率更高。

Lancet Infect Dis:口服VV116用于治疗轻中度COVID-19成人患者的有效性和安全性评价

目前,治疗COVID-19的医疗需求仍未得到满足,新型抗病毒药物-VV116可用于治疗轻中度COVID-19成人患者,能够显著缩短临床症状持续时间,与其他药物较少发生药物间相互作用,且安全性良好。

论文解读|Yihua Wang教授团队新研究揭示了揭示COVID-19对肺癌治疗和研究的深远影响

该文章揭示了此次大流行对肺癌治疗、临床试验、研究活动的影响。