生物利用度
病毒
呼吸系统
病毒学
安慰剂
病毒载量
药理学
化学
抗病毒药物
肺
医学
内科学
病理
替代医学
作者
G. Stuart Cockerill,Richard Angell,Alexandre F. Bedernjak,Irina Chuckowree,Ian S. Fraser,Jose M. Gascon-Simorte,Morgan S. A. Gilman,James A. D. Good,Rachel Harland,Sara M. Johnson,John Ludes-Meyers,Edward Littler,James A. Lumley,Graham Lunn,Neil Mathews,Jason S. McLellan,Michael Paradowski,Mark E. Peeples,Claire Scott,Dereck Tait
标识
DOI:10.1021/acs.jmedchem.0c01882
摘要
RV521 is an orally bioavailable inhibitor of respiratory syncytial virus (RSV) fusion that was identified after a lead optimization process based upon hits that originated from a physical property directed hit profiling exercise at Reviral. This exercise encompassed collaborations with a number of contract organizations with collaborative medicinal chemistry and virology during the optimization phase in addition to those utilized as the compound proceeded through preclinical and clinical evaluation. RV521 exhibited a mean IC50 of 1.2 nM against a panel of RSV A and B laboratory strains and clinical isolates with antiviral efficacy in the Balb/C mouse model of RSV infection. Oral bioavailability in preclinical species ranged from 42 to >100% with evidence of highly efficient penetration into lung tissue. In healthy adult human volunteers experimentally infected with RSV, a potent antiviral effect was observed with a significant reduction in viral load and symptoms compared to placebo.
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