A Phase III Randomized Controlled Trial of Plitidepsin, a Marine-Derived Compound, in Hospitalized Adults With Moderate COVID-19.

IF 8.2 1区 医学 Q1 IMMUNOLOGY
Pedro Landete, Olga-Adriana Caliman-Sturdza, Jose A Lopez-Martin, Liliana Preotescu, Mihaela-Catalina Luca, Anastasia Kotanidou, Paula Villares, Shirley-Patricia Iglesias, Pablo Guisado-Vasco, Elena-Maria Saiz-Lou, Maria Del Carmen Farinas-Alvarez, Esperanza Merino de Lucas, Eduardo Perez-Alba, Jose-Miguel Cisneros, Vicente Estrada, Carmen Hidalgo-Tenorio, Garyfallia Poulakou, Miguel Torralba, Jesus Fortun, Paula Garcia-Ocana, Adrien Lemaignen, Miguel Marcos-Martin, Maria Molina, Roger Paredes, Maria Teresa Perez-Rodriguez, Dimitar Raev, Pablo Ryan, Fernanda Meira, Javier Gomez, Nadia Torres, Diego Lopez-Mendoza, Jose Jimeno, Jose-Felipe Varona
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引用次数: 0

Abstract

Background: Plitidepsin has shown potent preclinical activity against severe acute respiratory syndrome coronavirus 2 and was generally well tolerated in a phase I trial of hospitalized patients with coronavirus disease 2019 (COVID-19). NEPTUNO, a phase III, multicenter, randomized, controlled trial, was designed to evaluate the efficacy and safety of plitidepsin in the management of moderate COVID-19 in hospitalized adult patients.

Methods: Included patients had documented severe acute respiratory syndrome coronavirus 2 infection, required oxygen therapy, and had adequate organ function. The planned sample size was 609 patients. Patients were randomized 1:1:1 to at least 3 days of dexamethasone plus either plitidepsin (1.5 mg/day or 2.5 mg/day, for 3 days) or standard of care (control). The primary endpoint was the time to sustained withdrawal of supplemental oxygen. Secondary endpoints included time to sustained hospital discharge, clinical status, duration of oxygen support, percentage of patients requiring admission to the intensive care unit, and safety.

Results: After randomizing 205 patients, NEPTUNO was discontinued due to a notable drop in COVID-19-related hospitalizations. Available data suggest a 2-day improvement in the median time to sustained oxygen therapy discontinuation (5 vs 7 days) favoring both plitidepsin arms (hazard ratio, 1.37; 95% confidence interval, .96-1.96; P = .08 for plitidepsin 1.5 mg vs control; hazard ratio, 1.06; 95% confidence interval, .73-1.53; P = .78 for plitidepsin 2.5 mg vs control). Plitidepsin was generally well tolerated.

Conclusions: Despite the trial limitations, these results suggest that plitidepsin may have a positive benefit-risk ratio in the management of patients requiring oxygen therapy. Further studies with plitidepsin, including those in immunosuppressed patients, are warranted.Results from this phase III trial suggest that plitidepsin, a first-in-class antiviral, may have a positive benefit-risk ratio in the management of hospitalized patients requiring oxygen therapy for moderate COVID-19.

在患有中度 COVID-19 的住院成人中开展的普利替普酶(一种海洋衍生化合物)III 期随机对照试验。
背景:普利替普酶对SARS-CoV-2具有很强的临床前活性,在一项针对COVID-19住院患者的I期试验中,普利替普酶的耐受性普遍良好。NEPTUNO 是一项 III 期多中心随机对照试验,旨在评估普利肝素治疗中度 COVID-19 住院成年患者的疗效和安全性:纳入的患者均有 SARS-CoV-2 感染记录,需要氧气治疗,且器官功能正常。计划样本量为 609 例患者。患者按1:1:1的比例随机接受至少3天的地塞米松加普利替平(1.5毫克/天或2.5毫克/天,共3天)或标准治疗(对照组)。主要终点是持续停止补充氧气的时间。次要终点包括持续出院时间、临床状态、氧气支持持续时间、需要入住重症监护室的患者比例以及安全性:在对205名患者进行随机分组后,由于与COVID-19相关的住院率显著下降,NEPTUNO被终止。现有数据显示,停用持续氧疗的中位时间(5天 vs 7天)缩短了2天,普利替平治疗组更有利(普利替平1.5毫克 vs 对照组的危险比[HR]为1.37,95%置信区间[CI]为0.96-1.96,P=0.08;普利替平2.5毫克 vs 对照组的危险比[HR]为1.06,95%置信区间[CI]为0.73-1.53,P=0.78)。普利替普酶的耐受性总体良好:尽管试验存在局限性,但这些结果表明,普利替普酶在治疗需要氧疗的患者方面可能具有积极的效益-风险比。有必要对普利替平进行进一步研究,包括对免疫抑制患者的研究:本试验由西班牙马德里 Pharmamar 公司资助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Infectious Diseases
Clinical Infectious Diseases 医学-传染病学
CiteScore
25.00
自引率
2.50%
发文量
900
审稿时长
3 months
期刊介绍: Clinical Infectious Diseases (CID) is dedicated to publishing original research, reviews, guidelines, and perspectives with the potential to reshape clinical practice, providing clinicians with valuable insights for patient care. CID comprehensively addresses the clinical presentation, diagnosis, treatment, and prevention of a wide spectrum of infectious diseases. The journal places a high priority on the assessment of current and innovative treatments, microbiology, immunology, and policies, ensuring relevance to patient care in its commitment to advancing the field of infectious diseases.
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