Long-acting Neuraminidase Inhibitor Laninamivir Octanoate as Post-exposure Prophylaxis for Influenza

نویسندگان

  • Seizaburo Kashiwagi
  • Akira Watanabe
  • Hideyuki Ikematsu
  • Mitsutoshi Uemori
  • Shinichiro Awamura
  • Seizaburo Kashiwagi
  • Akira Watanabe
  • Hideyuki Ikematsu
  • Katsuyasu Ishida
  • Shinichiro Awamura
  • Satoshi Nishioka
  • Koji Isobe
  • Tokuhito Sumitani
  • Toshiko Yamaguchi
  • Yutaka Igarashi
  • Hideki Sato
  • Kouta Saito
  • Tomoyuki Shibuya
  • Shinya Enomoto
  • Eiki Oshika
  • Yasuko Murakawa
  • Haruo Kuroki
  • Koji Maehara
  • Yuko Miyazono
  • Yoshihiro Umezawa
  • Ryuta Ono
  • Kenji Saito
  • Jiro Takei
  • Mikiko Takano
  • Hideki Amemiya
  • Kazuo Arakawa
  • Shigenori Matsubara
  • Kazumasa Sugimoto
  • Hiroshi Kikumori
  • Toshihiko Sunami
  • Ryota Yoshimura
  • Toshikazu Takahashi
  • Yutaka Nakamura
  • Keiichi Tsuboi
  • Hidehisa Shinohara
  • Shigeru Onari
  • Michiko Tanabe
  • Hiroshi Taniguchi
  • Mikio Kihara
  • Tatsuo Yoshimitsu
  • Takato Yokoyama
  • Yoshio Takasaki
  • Yuji Yamashita
  • Hiroshi Harada
  • Katsumaro Aida
  • Shizuo Shindo
  • Kunihisa Shimomura
  • Yumi Kiyomatsu
  • Toru Umezu
  • Motohisa Ikeda
  • Minako Iwaya
  • Masaki Higashikawa
  • Takeshi Inamitsu
  • Yasuyuki Tokunaga
  • Satoru Okazaki
  • Yoichi Tokunaga
  • Tetsunari Maeda
  • Hirofumi Tahara
چکیده

BACKGROUND A single administration of laninamivir octanoate, a long-acting neuraminidase inhibitor, has been proven to be effective in the treatment of influenza but not for post-exposure prophylaxis. METHODS We conducted a double-blind, multicenter, randomized, placebo-controlled study to determine if a single administration of laninamivir octanoate 40 mg was superior to placebo for post-exposure prophylaxis. Eligible participants who had cohabited with an influenza patient within 48 hours of symptom onset were randomly assigned (1:1:1) to 1 of 3 groups: 40 mg of laninamivir octanoate single administration (LO-40SD), 20 mg of laninamivir octanoate once daily for 2 days (LO-20TD), or placebo. The primary efficacy endpoint was the proportion of participants who developed clinical influenza (defined as influenza virus positive, an axillary temperature >37.5°C, and at least 2 symptoms) over a 10-day period. RESULTS A total of 803 participants were enrolled, with 801 included in the primary analysis. The proportions of participants with clinical influenza were 4.5% (12/267), 4.5% (13/269), and 12.1% (32/265) in the LO-40SD, LO-20TD, and placebo groups, respectively. A single administration of laninamivir octanoate 40 mg significantly reduced the development of influenza compared with placebo (P = .001). The relative risk reductions compared with the placebo group were 62.8% and 63.1% for the LO-40SD and LO-20TD groups, respectively. The incidence of adverse events in the LO-40SD group was similar to that of the LO-20TD and placebo groups. CONCLUSIONS A single administration of laninamivir octanoate was effective and well tolerated as post-exposure prophylaxis to prevent the development of influenza. CLINICAL TRIALS REGISTRATION JapicCTI-142679.

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Laninamivir octanoate for post-exposure prophylaxis of influenza in household contacts: a randomized double blind placebo controlled trial

Laninamivir octanoate, a long-acting neuraminidase inhibitor, is an effective treatment for influenza. However, its effectiveness for the prevention of influenza has not yet been demonstrated. We conducted a double-blind, multicenter, randomized, placebo-controlled trial to determine whether laninamivir octanoate was superior to a placebo for post-exposure prophylaxis of influenza in household ...

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عنوان ژورنال:

دوره 63  شماره 

صفحات  -

تاریخ انتشار 2016