4.3 Article

A randomized, placebo-controlled study to evaluate safety and pharmacokinetics of inhaled ribavirin

期刊

CTS-CLINICAL AND TRANSLATIONAL SCIENCE
卷 15, 期 9, 页码 2159-2171

出版社

WILEY
DOI: 10.1111/cts.13350

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资金

  1. Bausch Health Inc. Research and Development division
  2. Cliantha Research, Mississauga, Canada

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This study evaluated the safety and pharmacokinetics of four single-dose regimens of ribavirin aerosol in healthy volunteers. The results showed that ribavirin aerosol demonstrated systemic exposure with minimal systemic effects, supporting its continued clinical development as a treatment option for coronaviruses.
Ribavirin is an inosine monophosphate dehydrogenase inhibitor. Studies suggest ribavirin aerosol could be a safe and efficacious treatment option in the fight against coronaviruses. However, current treatment is long (12-18 h per day, 3-7 days), limiting clinical utility. A reduction in treatment time would reduce treatment burden. We aimed to evaluate safety and pharmacokinetics (PK) of four, single-dose regimens of ribavirin aerosol in healthy volunteers. Thirty-two subjects were randomized, to four cohorts of aerosolized ribavirin (active) or placebo. Cohort 1 received 50 mg/ml ribavirin/placebo (10 ml total volume); cohort 2, 50 mg/ml ribavirin/placebo (20 ml total volume); cohort 3, 100 mg/ml ribavirin/placebo (10 ml total volume); and cohort 4, 100 mg/ml ribavirin/placebo (20 ml total volume). Intense safety monitoring and PK sampling took place on days 1, 2, 3, and 40. Subjects were (mean +/- SD, active vs. placebo) aged 57 +/- 4.5 vs. 60 +/- 2.5 years; 83% vs. 88% were female; and 75% vs. 50% were Caucasian. Some 12.5% (3/24) and 25% (2/8) experienced at least one treatment-emergent adverse event (TEAE) (two moderate; five mild) in the active and placebo groups, respectively. No clinically significant safety concerns were reported. Mean maximum observed concentration (C-max) and area under the curve (AUC) values were higher in cohort 4, whereas cohorts 2 and 3 showed similar PK values. Ribavirin absorption reached C-max within 2 h across cohorts. Four single-dose regimens of ribavirin aerosol demonstrated systemic exposure with minimal systemic effects. Results support continued clinical development of ribavirin aerosol as a treatment option in patients with coronaviruses.

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