ALN-RSV01 for prevention of bronchiolitis obliterans syndrome after respiratory syncytial virus infection in lung transplant recipients

医学 闭塞性细支气管炎 安慰剂 队列 内科学 利巴韦林 入射(几何) 毛细支气管炎 胃肠病学 随机对照试验 肺移植 呼吸系统 免疫学 病毒 病理 丙型肝炎病毒 物理 替代医学 光学
作者
Jens Gottlieb,Martin R. Zamora,Tony N. Hodges,A W Musk,Urte Sommerwerk,Daniel F. Dilling,Selim M. Arcasoy,John P. DeVincenzo,Verena Karsten,Shaily Shah,Brian R. Bettencourt,Jeffrey Cehelsky,Sara Nochur,Jared Gollob,Akshay Vaishnaw,Amy Simon,Allan R. Glanville
出处
期刊:Journal of Heart and Lung Transplantation [Elsevier BV]
卷期号:35 (2): 213-221 被引量:147
标识
DOI:10.1016/j.healun.2015.08.012
摘要

Respiratory syncytial virus (RSV) infection in lung transplant (LTx) patients is associated with an increased incidence of bronchiolitis obliterans syndrome (BOS). ALN-RSV01 is a small interfering RNA targeting RSV replication that was shown in an earlier Phase 2a trial to be safe and to reduce the incidence of BOS when compared with placebo.We performed a Phase 2b randomized, double-blind, placebo-controlled trial in RSV-infected LTx patients to examine the impact of ALN-RSV01 on the incidence of new or progressive BOS. Subjects were randomized (1:1) to receive aerosolized ALN-RSV01 or placebo daily for 5 days.Of 3,985 symptomatic patients screened, 218 were RSV-positive locally, of whom 87 were randomized to receive ALN-RSV01 or placebo (modified intention-to-treat [mITT] cohort). RSV infection was confirmed by central laboratory in 77 patients (ALN-RSV01, n = 44; placebo, n = 33), which comprised the primary analysis cohort (central mITT [mITTc]). ALN-RSV01 was found to be safe and well-tolerated. At Day 180, in ALN-RSV01-treated patients, compared with placebo, in the mITTc cohort there was a trend toward a decrease in new or progressive BOS (13.6% vs 30.3%, p = 0.058), which was significant in the per-protocol cohort (p = 0.025). Treatment effect was enhanced when ALN-RSV01 was started <5 days from symptom onset, and was observed even without ribavirin treatment. There was no significant impact on viral parameters or symptom scores.These results confirm findings of the earlier Phase 2a trial and provide further support that ALN-RSV01 reduces the risk of BOS after RSV in LTx recipients.
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