PATH, Seattle, Washington, United States of America.
Pharmaron, Baltimore, Maryland, United States of America.
PLoS Negl Trop Dis. 2021 Nov 18;15(11):e0009969. doi: 10.1371/journal.pntd.0009969. eCollection 2021 Nov.
Cholera remains a major cause of infectious diarrhea globally. Despite the increased availability of cholera vaccines, there is still an urgent need for other effective interventions to reduce morbidity and mortality. Furthermore, increased prevalence of antibiotic-resistant Vibrio cholerae threatens the use of many drugs commonly used to treat cholera. We developed iOWH032, a synthetic small molecule inhibitor of the cystic fibrosis transmembrane conductance regulator chloride channel, as an antisecretory, host-directed therapeutic for cholera. In the study reported here, we tested iOWH032 in a Phase 2a cholera controlled human infection model. Forty-seven subjects were experimentally infected with V. cholerae El Tor Inaba strain N16961 in an inpatient setting and randomized to receive 500 mg iOWH032 or placebo by mouth every 8 hours for 3 days to determine the safety and efficacy of the compound as a potential treatment for cholera. We found that iOWH032 was generally safe and achieved a mean (± standard deviation) plasma level of 4,270 ng/mL (±2,170) after 3 days of oral dosing. However, the median (95% confidence interval) diarrheal stool output rate for the iOWH032 group was 25.4 mL/hour (8.9, 58.3), compared to 32.6 mL/hour (15.8, 48.2) for the placebo group, a reduction of 23%, which was not statistically significant. There was also no significant decrease in diarrhea severity and number or frequency of stools associated with iOWH032 treatment. We conclude that iOWH032 does not merit future development for treatment of cholera and offer lessons learned for others developing antisecretory therapeutic candidates that seek to demonstrate proof of principle in a cholera controlled human infection model study. Trial registration: This study is registered with ClinicalTrials.gov as NCT04150250.
霍乱仍然是全球范围内主要的传染性腹泻病因。尽管霍乱疫苗的供应有所增加,但仍迫切需要其他有效的干预措施来降低发病率和死亡率。此外,抗生素耐药性霍乱弧菌的流行威胁到许多常用于治疗霍乱的药物的使用。我们开发了 iOWH032,一种囊性纤维化跨膜电导调节剂氯离子通道的合成小分子抑制剂,作为一种抗分泌、宿主定向的霍乱治疗药物。在本报告的研究中,我们在 2a 期霍乱对照人体感染模型中测试了 iOWH032。47 名受试者在住院环境中经实验感染 El Tor Inaba 血清型 N16961 的霍乱弧菌,并随机接受 500mg iOWH032 或安慰剂,每天口服 3 次,每 8 小时 1 次,以确定该化合物作为霍乱潜在治疗药物的安全性和疗效。我们发现 iOWH032 通常是安全的,在 3 天口服给药后平均(±标准差)血浆水平为 4270ng/mL(±2170)。然而,iOWH032 组的中位(95%置信区间)腹泻粪便排出率为 25.4 毫升/小时(8.9,58.3),而安慰剂组为 32.6 毫升/小时(15.8,48.2),减少了 23%,但无统计学意义。iOWH032 治疗也没有显著降低腹泻严重程度以及粪便的数量或频率。我们得出结论,iOWH032 不适宜进一步开发用于治疗霍乱,并为其他开发抗分泌治疗候选药物的人提供了在霍乱对照人体感染模型研究中证明原理的经验教训。
本研究在 ClinicalTrials.gov 注册为 NCT04150250。