Safety profile of self-amplifying mRNA SARS-CoV-2 vaccine ARCT-154 in adults: a pooled phase 1/2/3 randomized clinical study.

IF 5.5 3区 医学 Q1 IMMUNOLOGY
Nhan Thi Ho, Igor Smolenov, Ly Thi Le Tran, Van Thu Nguyen, Van Thanh Ta, Thuong Vu Nguyen, Hung Ngoc Pham, Anh Thi Van Pham, Quang Chan Luong, Men Van Chu, Mai Thi Ngoc Dang, Toan Trong Nguyen, Vy Thi Tuong Le, Quang Vinh Trinh, Thang Van Nguyen, Anh Ngoc Nguyen, Ha Thai Pham, Giang Duc Dao, Carmen Baccarini, Ekpeno Nnah, Alia Hawkes, Suezanne Parker, Carole Verhoeven, Judd L Walson, Xuan-Hung Nguyen
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Abstract

Background: Public health concerns due to ongoing emergence of SARS-CoV-2 variants necessitates further development of improved COVID-19 vaccines. One major innovation are self-amplifying mRNA vaccines such as ARCT-154 (Arcturus Therapeutics Inc.) which induces superior immunogenicity compared with conventional mRNA in terms of magnitude, breadth and persistence of neutralizing antibodies.

Research design and methods: In a pivotal placebo-controlled trial in Vietnam combining phase 1, 2 and 3 cohorts, over 17,000 adults received at least one dose of ARCT-154. Here we report the safety and reactogenicity observations made.

Results: ARCT-154 elicited more local reactions than the saline placebo, most reports of injection site pain were mild/moderate with only a few reporting severe pain. Most frequent solicited adverse events were fatigue, myalgia, headache, arthralgia and chills. Solicited local and systemic reactogenicity resolved within 7 days. Long-term follow-up has not revealed any safety concerns, with no reports of myocarditis or pericarditis. Acceptable tolerability of ARCT-154 was also observed in older participants and in those liable to severe consequences of COVID-19 due to underlying medical conditions. No serious consequences occurred in several pregnancies reported after vaccination, with normal outcomes when followed to term.

Conclusions: Data from this large trial suggest that ARCT-154 is safe and well tolerated.

自扩增mRNA SARS-CoV-2疫苗ARCT-154在成人中的安全性:一项合并1/2/3期随机临床研究
背景:持续出现的SARS-CoV-2变体引起的公共卫生问题要求进一步开发改进型COVID-19疫苗。一项重大创新是自扩增mRNA疫苗,如ARCT-154 (Arcturus Therapeutics Inc.),与传统mRNA相比,在中和抗体的大小、广度和持续时间方面,它具有更强的免疫原性。研究设计和方法:在越南的一项关键安慰剂对照试验中,超过17,000名成年人接受了至少一剂ARCT-154。在这里,我们报告安全性和反应原性观察。结果:与生理盐水安慰剂相比,ARCT-154引起了更多的局部反应,大多数报告的注射部位疼痛是轻度/中度的,只有少数报告严重的疼痛。最常见的不良事件是疲劳、肌痛、头痛、关节痛和寒战。征求局部和全身反应性在7天内解决。长期随访未发现任何安全性问题,没有心肌炎或心包炎的报告。在老年参与者和因潜在医疗条件易患COVID-19严重后果的参与者中,也观察到可接受的ARCT-154耐受性。接种疫苗后,几例妊娠未发生严重后果,随访至足月均正常。结论:这项大型试验的数据表明,ARCT-154是安全且耐受性良好的。
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来源期刊
Expert Review of Vaccines
Expert Review of Vaccines 医学-免疫学
CiteScore
9.10
自引率
3.20%
发文量
136
审稿时长
4-8 weeks
期刊介绍: Expert Review of Vaccines (ISSN 1476-0584) provides expert commentary on the development, application, and clinical effectiveness of new vaccines. Coverage includes vaccine technology, vaccine adjuvants, prophylactic vaccines, therapeutic vaccines, AIDS vaccines and vaccines for defence against bioterrorism. All articles are subject to rigorous peer-review. The vaccine field has been transformed by recent technological advances, but there remain many challenges in the delivery of cost-effective, safe vaccines. Expert Review of Vaccines facilitates decision making to drive forward this exciting field.
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