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,williamhill asia 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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  8. 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  9. 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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。

9月21日全球新冠肺炎(COVID-19)疫情简报,确诊超3121万,第二波疫情明显到来

Worldometers世界实时统计数据显示,截至北京时间9月21日5时38分,全球新冠肺炎(COVID-19)累计确诊病例突破3121万例,达到31,216,782例,累计死亡病例超过96.4万例,

J Endod:中国COVID-19爆发严重地区牙髓治疗的恢复情况:一项网络调查

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。

拓展阅读

JAMA Intern Med:奈玛特韦-利托那韦与成人感染SARS-CoV-2急性期后遗症

目前新冠急性期后遗症(PASC)已经对全球人类的生活质量和身体状态产生了严重影响。本研究结果显示疗程15天的奈玛特韦-利托那韦用于伴有PASC的患者是安全的,但并未明显改善PASC症状的严重程度。

Haematologica:地塞米松治疗COVID-19增加血液恶性肿瘤患者死亡率

该研究旨在分析不同治疗策略对血液肿瘤患者生存率的影响,研究发现,血液恶性肿瘤患者使用地塞米松治疗COVID-19与更高的90天死亡率相关,特别是在未同时应用抗病毒治疗的情况下。

Genes&Diseases:Guixue Wang教授等合作团队:COVID-19对人类生殖影响的文献计量学研究

研究阐明了该领域的研究框架、核心主题和研究趋势,并对当前研究中存在的限制和争议进行了总结和讨论。

JAMA Netw Open:COVID-19大流行后儿童呼吸道合胞病毒住院率变化

2021年和2022年的RSV和支气管炎住院均显示出非典型的季节性,RSV的医院就诊总体上有所增加。

JAMA Netw Open:COVID-19大流行后儿童和青少年精神药物处方变化

这些发现提示,迫切需要对推动这一趋势的潜在因素进行更深入的研究。

J Clin Med:重症COVID-19肺炎患者急性肾损伤和慢性肾病及其对预后的影响

COVID-19患者AKI与ICU转院次数多、发病率高、重症标志物高相关。