Ronald Reagan UCLA Medical Center, Los Angeles, California, USA.
Theravance Biopharma Inc, South San Francisco, California, USA.
BMJ Open Respir Res. 2023 Jul;10(1). doi: 10.1136/bmjresp-2023-001627.
The inhaled lung-selective pan-Janus kinase inhibitor nezulcitinib had favourable safety and potential efficacy signals in part 1 of a phase 2 trial in patients with severe COVID-19, supporting progression to part 2.
Part 2 was a randomised, double-blind phase 2 study (NCT04402866). Hospitalised patients aged 18-80 years with confirmed symptomatic COVID-19 requiring supplemental oxygen (excluding baseline invasive mechanical ventilation) were randomised 1:1 to nebulised nezulcitinib 3 mg or placebo for up to 7 days with background standard-of-care therapy (including corticosteroids). Efficacy endpoints included respiratory failure-free (RFF) days through day 28 as the primary endpoint. Secondary endpoints included safety and change from baseline oxygen saturation (SaO2)/fraction of inspired oxygen (FiO2) ratio on day 7, and 28-day mortality rate was a prespecified exploratory endpoint.
Between June 2020 and April 2021, 205 patients were treated (nezulcitinib, 103; placebo, 102). There was no statistically significant difference between nezulcitinib versus placebo in the primary endpoint (RFF days; median, 21.0 vs 21.0; p=0.6137) or secondary efficacy endpoints. Nezulcitinib was generally well tolerated with a favourable safety profile.
Although the prespecified primary, secondary and exploratory efficacy endpoints, including RFF through day 28, change from baseline SaO2/FiO2 ratio on day 7, and 28-day mortality rate, were not met, nezulcitinib was generally well tolerated and had a favourable safety profile. Further studies are required to determine if treatment with nezulcitinib confers clinical benefit in specific inflammatory biomarker-defined populations of patients with COVID-19.
吸入型肺部选择性泛 Janus 激酶抑制剂奈舒利替尼在重症 COVID-19 患者的 2 期临床试验的第 1 部分中表现出良好的安全性和潜在疗效信号,支持其进入第 2 部分。
第 2 部分是一项随机、双盲的 2 期研究(NCT04402866)。纳入年龄在 18 至 80 岁之间、有症状且需要补充氧气(不包括基线时的有创机械通气)的确诊 COVID-19 住院患者,按 1:1 比例随机分配接受雾化奈舒利替尼 3mg 或安慰剂治疗,疗程最长 7 天,同时给予背景标准治疗(包括皮质类固醇)。主要终点为第 28 天无呼吸衰竭(RFF)天数。次要终点包括第 7 天的血氧饱和度(SaO2)/吸氧分数(FiO2)比值与基线的变化,28 天死亡率是预先指定的探索性终点。
2020 年 6 月至 2021 年 4 月,共有 205 名患者接受治疗(奈舒利替尼 103 例,安慰剂 102 例)。在主要终点(RFF 天数;中位数,21.0 天比 21.0 天;p=0.6137)和次要疗效终点方面,奈舒利替尼与安慰剂之间无统计学差异。奈舒利替尼总体耐受性良好,安全性良好。
尽管主要、次要和探索性疗效终点(包括第 28 天的 RFF 天数、第 7 天 SaO2/FiO2 比值与基线的变化、28 天死亡率)均未达到,但奈舒利替尼总体耐受性良好,安全性良好。需要进一步研究以确定奈舒利替尼治疗是否能为 COVID-19 患者的特定炎症生物标志物定义人群带来临床获益。