A Phase III Study to Evaluate the Efficacy and Safety of Recombinant Botulinum Toxin Type A for Injection in the Treatment of Moderate to Severe Glabellar Lines

PHASE3CompletedINTERVENTIONAL
Enrollment

529

Participants

Timeline

Start Date

December 28, 2023

Primary Completion Date

March 29, 2024

Study Completion Date

May 31, 2024

Conditions
Moderate to Severe Glabellar Lines
Interventions
BIOLOGICAL

Rcombinant botulinum neurotoxin type A for injection (YY001)

Single treatment,intramuscularly injected into five sites.The total injection volume is 0.25 ml,0.05 ml per site.

BIOLOGICAL

OnabotulinumtoxinA

Single treatment,intramuscularly injected into five sites.The total injection volume is 0.25 ml,0.05 ml per site.

BIOLOGICAL

Placebo

Single treatment,intramuscularly injected into five sites.The total injection volume is 0.25 ml,0.05 ml per site.

Trial Locations (16)

Unknown

Guangdong Second People's Hospital, Guangzhou

Nanfang Hospital, Southern Medical University, Guangzhou

The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan

The Second Affiliated Hospital Of Xi'an Jiaotong University, Xian

West China School of Medicine/West China Hospital of Sichuan University, Chengdu

Affiliated Hangzhou First People's Hospital, Westlake University, School of Medicine, Hangzhou

Zhejiang Provincial People's Hospital, Hangzhou

Beijing Tsinghua Changgung Hospital, Beijing

Peking Union Medical College Hospital , Chinese Academy of Medical Sciences, Beijing

Peking University First Hospital, Beijing

Peking University Third Hospital, Beijing

Plastic Surgery Hospital, Chinese Academy of Medical Science, Beijing

The First Affiliated Hospital of Chongqing Medical University, Chongqing

Tianjin Medical University General Hospital, Tianjin

Tan

The Third Xiangya Hospital of Central South University, Changsha

All Listed Sponsors
lead

Chongqing Claruvis Pharmaceutical Co., Ltd.

INDUSTRY

NCT06499688 - A Phase III Study to Evaluate the Efficacy and Safety of Recombinant Botulinum Toxin Type A for Injection in the Treatment of Moderate to Severe Glabellar Lines | Biotech Hunter | Biotech Hunter