The aim of this study is to assess the effectiveness in preventing exacerbation of 52 weeks lysozyme administration in patients with COPD.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
408
LYL 90mg capsule: Three times daily for 52 weeks.
Matching Placebo capsule: Three times daily for 52 weeks.
Unnamed facility
Nishio, Aichi-ken, Japan
Unnamed facility
Noda, Chiba, Japan
Unnamed facility
Acute exacerbation of COPD
Time frame: 52 weeks
Yearly reduction in FEV1 and QOL assessed by CAT
Time frame: 52 weeks
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Fukuoka, Fukuoka, Japan
Unnamed facility
Kasuga, Fukuoka, Japan
Unnamed facility
Kyoto-gun, Fukuoka, Japan
Unnamed facility
Yanagawa, Fukuoka, Japan
Unnamed facility
Mabashi, Gunma, Japan
Unnamed facility
Takasaki, Gunma, Japan
Unnamed facility
Kitahiroshima, Hokkaido, Japan
Unnamed facility
Sapporo, Hokkaido, Japan
...and 15 more locations