TY - JOUR
T1 - Long-acting Neuraminidase Inhibitor Laninamivir Octanoate as Post-exposure Prophylaxis for Influenza
AU - Laninamivir Prophylaxis Study Group
AU - Kashiwagi, Seizaburo
AU - Watanabe, Akira
AU - Ikematsu, Hideyuki
AU - Uemori, Mitsutoshi
AU - Awamura, Shinichiro
AU - Ishida, Katsuyasu
AU - Nishioka, Satoshi
AU - Isobe, Koji
AU - Sumitani, Tokuhito
AU - Yamaguchi, Toshiko
AU - Igarashi, Yutaka
AU - Sato, Hideki
AU - Saito, Kouta
AU - Shibuya, Tomoyuki
AU - Enomoto, Shinya
AU - Oshika, Eiki
AU - Murakawa, Yasuko
AU - Kuroki, Haruo
AU - Maehara, Koji
AU - Miyazono, Yuko
AU - Umezawa, Yoshihiro
AU - Ono, Ryuta
AU - Saito, Kenji
AU - Takei, Jiro
AU - Takano, Mikiko
AU - Amemiya, Hideki
AU - Arakawa, Kazuo
AU - Matsubara, Shigenori
AU - Sugimoto, Kazumasa
AU - Kikumori, Hiroshi
AU - Sunami, Toshihiko
AU - Yoshimura, Ryota
AU - Takahashi, Toshikazu
AU - Nakamura, Yutaka
AU - Tsuboi, Keiichi
AU - Shinohara, Hidehisa
AU - Onari, Shigeru
AU - Tanabe, Michiko
AU - Taniguchi, Hiroshi
AU - Kihara, Mikio
AU - Yoshimitsu, Tatsuo
AU - Yokoyama, Takato
AU - Takasaki, Yoshio
AU - Yamashita, Yuji
AU - Harada, Hiroshi
AU - Aida, Katsumaro
AU - Shindo, Shizuo
AU - Shimomura, Kunihisa
AU - Kiyomatsu, Yumi
AU - Umezu, Toru
N1 - Publisher Copyright:
© 2016 The Author 2016. Published by Oxford University Press for the Infectious Diseases Society of America.
PY - 2016/8/1
Y1 - 2016/8/1
N2 - 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.
AB - 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.
KW - influenza
KW - laninamivir
KW - neuraminidase inhibitor
KW - post-exposure
KW - prophylaxis
UR - http://www.scopus.com/inward/record.url?scp=84981287575&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84981287575&partnerID=8YFLogxK
U2 - 10.1093/cid/ciw255
DO - 10.1093/cid/ciw255
M3 - Review article
C2 - 27118785
AN - SCOPUS:84981287575
SN - 1058-4838
VL - 63
SP - 330
EP - 337
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 3
ER -