A 12-Week, Open-Label, Multicenter Pilot Study to Evaluate the Efficacy and Safety of Lemborexant in Patients with Insomnia Comorbid with Depressive Episodes (SELENADE)
A 12-Week, Open-Label, Multicenter Pilot Study to Evaluate the Efficacy and Safety of Lemborexant in Patients with Insomnia Comorbid with Depressive Episodes (SELENADE)
Koichiro Watanabe, Hiroyuki Muraoka, Yoshiteru Takekita, Michinori Koebis et al.
Journal
CNS Drugs
Topics
Sleep and related disorders
article
A 12-Week, Open-Label, Multicenter Pilot Study to Evaluate the Efficacy and Safety of Lemborexant in Patients with Insomnia Comorbid with Depressive Episodes (SELENADE)
Kurume University (JP), Kansai Medical University (JP), Oita University (JP), Kyorin University (JP), Akita University (JP), Fukuoka University (JP), University of the Ryukyus (JP), Minamiaoyama Eye Clinic (JP), Eisai (Japan) (JP), Kitasato University (JP)
Funders
Eli Lilly and Company, Pfizer, EA Pharma Co., Ltd., Kowa Company, Boehringer Ingelheim Japan, Nipro, Eisai, Meiji Seika Pharma, Shionogi, Otsuka Pharmaceutical, Teijin Pharma, Mitsubishi Tanabe Pharma Corporation, Ono Pharmaceutical, H. Lundbeck A/S, Novartis Pharma, Pfizer Japan, Eli Lilly Japan, Japan Society for the Promotion of Science, Daiichi Sankyo Europe