365
Participants
Start Date
September 30, 2022
Primary Completion Date
January 31, 2024
Study Completion Date
June 13, 2024
Fremanezumab
"Pharmaceutical form: solution for injection~Route of administration: subcutaneous injection"
Placebo
"Pharmaceutical form: solution for injection~Route of administration: subcutaneous injection"
Teva Investigational Site 88011, Shijiazhuang
Teva Investigational Site 88004, Beijing
Teva Investigational Site 88001, Beijing
Teva Investigational Site 88016, Shenyang
Teva Investigational Site 88008, Changchun
Teva Investigational Site 88009, Changchun
Teva Investigational Site 88026, Harbin
Teva Investigational Site 88021, Shanghaishi
Teva Investigational Site 88025, Shanghaishi
Teva Investigational Site 88015, Suzhou
Teva Investigational Site 88010, Lianyungang
Teva Investigational Site 88033, Rizhao
Teva Investigational Site 88024, Tianjin
Teva Investigational Site 88023, Tianjin
Teva Investigational Site 88017, Wenzhou
Teva Investigational Site 88019, Fuzhou
Teva Investigational Site 88029, Chongqing
Teva Investigational Site 88022, Changsha Shi
Teva Investigational Site 88030, Changsha Shi
Teva Investigational Site 88012, Wuhan
Teva Investigational Site 88006, Wuhan
Teva Investigational Site 88034, Zhengzhou
Teva Investigational Site 88020, Guangzhou
Teva Investigational Site 88031, Zhanjiang
Teva Investigational Site 88013, Guiyang
Teva Investigational Site 88003, Chengdu
Teva Investigational Site 88032, Xining
Teva Investigational Site 88005, Luoyang
Teva Investigational Site 88028, Baotou
Teva Branded Pharmaceutical Products R&D, Inc.
INDUSTRY