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莫努匹拉韦在日本新冠肺炎患者中的安全性和有效性:日本上市后监测的最终报告

Safety and Effectiveness of Molnupiravir in Japanese Patients with COVID-19: Final Report of Post-marketing Surveillance in Japan.

作者信息

Shinozaki Shohei, Watanabe Asuka, Kimata Masahiro, Miyazaki Makoto, Maekawa Shinichiroh

机构信息

Medical Affairs MSD K.K., Kitanomaru Square, 1-13-12 Kudan-Kita, Chiyoda-Ku, Tokyo, 102-8667, Japan.

Pharmacovigilance MSD K.K., Kitanomaru Square, 1-13-12 Kudan-Kita, Chiyoda-Ku, Tokyo, 102-8667, Japan.

出版信息

Infect Dis Ther. 2024 Jan;13(1):189-205. doi: 10.1007/s40121-023-00915-w. Epub 2024 Jan 17.

Abstract

INTRODUCTION

Molnupiravir is an orally available prodrug of N-hydroxycytidine that received special approval for emergency treatment of coronavirus disease 2019 (COVID-19) in Japan in December 2021 and full approval in April 2023. To assess the real-world safety and effectiveness of molnupiravir in Japanese patients with COVID-19, we conducted nationwide post-marketing surveillance to collect data at registered institutions in Japan.

METHODS

The surveillance data were collected from December 27, 2021, to May 2, 2023. All reported adverse events were collected for safety analysis. Adverse drug reactions (ADRs) were assessed by the treating physicians. Effectiveness was assessed by the composite of hospitalization or all-cause death in outpatients and the composite of oxygen/mechanical ventilation initiation or all-cause death in inpatients. The observation period was from molnupiravir initiation through day 29.

RESULTS

Of 3214 patients enrolled in the survey, 3179 were analyzed for safety. At baseline, 52.31% (1663/3179) of patients were male, the median (range) age was 69.0 (18-107) years, 82.38% (2619/3179) received COVID-19 vaccines, and 95.72% (3043/3179) had risk factors for severe COVID-19 illness. COVID-19 severity at baseline was mild in 86.44% (2748/3179) and moderate I in 10.22% (325/3179). A total of 205 ADRs occurred in 5.50% (175/3179) of patients; ADRs that occurred in > 0.5% of patients were diarrhea (1.86% [59/3179]) and rash (0.69% [22/3179]). Seven serious ADRs were reported in seven patients. In the effectiveness analysis population, the incidence of all-cause death through day 29 was 1.14% (34/2988), and the incidence of death through day 29 related to COVID-19 was 0.40% (12/2988). The cumulative incidence of the composite endpoint was 2.34% (47/2006) in outpatients and 4.60% (38/826) in inpatients.

CONCLUSIONS

This large-scale survey showed that molnupiravir was safe and effective in real-world settings in highly vaccinated Japanese patients with COVID-19, including older patients and those with comorbidities.

摘要

引言

莫努匹拉韦是N-羟基胞苷的口服前体药物,于2021年12月在日本获得用于2019冠状病毒病(COVID-19)紧急治疗的特别批准,并于2023年4月获得全面批准。为评估莫努匹拉韦在日本COVID-19患者中的真实世界安全性和有效性,我们在日本的注册机构开展了全国性上市后监测以收集数据。

方法

监测数据收集时间为2021年12月27日至2023年5月2日。收集所有报告的不良事件用于安全性分析。治疗医生对药物不良反应(ADR)进行评估。有效性通过门诊患者住院或全因死亡的综合指标以及住院患者启动氧疗/机械通气或全因死亡的综合指标进行评估。观察期为从开始使用莫努匹拉韦至第29天。

结果

在参与调查的3214例患者中,3179例进行了安全性分析。基线时,52.31%(1663/3179)的患者为男性,中位(范围)年龄为69.0(18 - 107)岁,82.38%(2619/3179)的患者接种了COVID-19疫苗,95.72%(3043/3179)的患者有重症COVID-19疾病的危险因素。基线时COVID-19严重程度为轻度的患者占86.44%(2748/3179),中度I级的患者占10.22%(325/3179)。共有205例ADR发生在5.50%(175/3179)的患者中;发生在超过0.5%患者中的ADR为腹泻(占1.86% [59/3179])和皮疹(占0.69% [22/3179])。7例患者报告了7例严重ADR。在有效性分析人群中,至第29天全因死亡的发生率为1.14%(34/2988),至第29天与COVID-19相关的死亡发生率为0.40%(12/2988)。门诊患者复合终点的累积发生率为2.34%(47/2006),住院患者为4.60%(38/826)。

结论

这项大规模调查表明,莫努匹拉韦在接种疫苗比例高的日本COVID-19患者的真实世界环境中是安全有效的这些患者包括老年患者和合并症患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/139d/10828263/e168769b2ed5/40121_2023_915_Fig1_HTML.jpg

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