Suvorexant for the treatment of insomnia

被引:36
作者
Jacobson, Laura H. [1 ]
Callander, Gabrielle E. [1 ,2 ]
Hoyer, Daniel [1 ,2 ]
机构
[1] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville, Vic 3052, Australia
[2] Univ Melbourne, Fac Med, Fac Med Dent & Hlth Sci, Dept Pharmacol & Therapeut,Sch Med, Parkville, Vic 3010, Australia
关键词
almorexant; Belsorma; drug development; FDA; hypocretin; insomnia; NDA; orexin; orexin receptor antagonists; pharmacodynamics; pharmacokinetics; SB649868; sleep disorders; suvorexant; OREXIN RECEPTOR ANTAGONIST; POWER SPECTRAL PROFILE; REM-SLEEP; HYPOCRETIN OREXIN; PHARMACOLOGICAL CHARACTERIZATION; MESSENGER-RNA; DOUBLE-BLIND; NARCOLEPSY; NEURONS; CATAPLEXY;
D O I
10.1586/17512433.2014.966813
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Suvorexant (Belsorma (R)) is the first orexin receptor antagonist approved by the US FDA (August 2014) for insomnia treatment. Following comprehensive Phase II/III studies, with up to 12 months of treatment in adult and elderly patients, there is little doubt that suvorexant induces and maintains sleep. However, the FDA and sponsor disagreed about effective versus safe doses (November 2012). The FDA considered that 5-15 mg were efficient and probably safe, whereas the sponsors had proposed 15-40 mg. The final approved doses are 5, 10, 15 and 20 mg. The major issues are next-morning somnolence and safety as seen in driving tests, with possible signs of muscle weakness, weird dreams, sleep walking, other nighttime behaviors and suicidal ideation. Despite its limitations, suvorexant's market entry offers a truly novel treatment for insomnia, paving the way for follow-up compounds and opening therapeutic avenues in other disorders for orexin receptor modulating compounds.
引用
收藏
页码:711 / 730
页数:20
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