A Study to Assess the Adverse Events and Effectiveness of BOTOX Injections for the Treatment of Moderate to Severe Forehead Lines in Chinese Adult Participants

AbbVie140 enrolled

Overview

Facial lines (such as glabellar lines \[GL\], lateral canthal lines \[LCL\], and forehead lines \[FHL\]) are perhaps the most visible signs of aging. Hyperfunctional facial lines that develop from repeated facial expression may be treated by selectively weakening specific muscles with small quantities of botulinum toxin. The purpose of this study is to assess adverse events and effectiveness of BOTOX in Chinese adults with moderate to severe FHL. Participants are placed in 1 of 2 groups, called treatment arms. Around 140 adult participants with moderate to severe FHL will be enrolled in the study. Participants in the treatment group will receive intramuscular injections on Day 1 and followed for up to 180 Days. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at the study site. The effect of the treatment will be checked by medical assessments, checking for side effects and completing questionnaires.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

140

Conditions

Forehead Lines

Interventions

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Sufficient visual acuity without the use of eyeglasses (contact lens use acceptable) to accurately assess their facial wrinkles. * Participant must have symmetrical FHL of moderate or severe rating at maximum contraction as assessed by both investigator and participant using the Facial Wrinkle Scale with Asian Photonumeric Guide (FWS-A) at Day 1 prior to study treatment. * Participant must have glabellar lines (GL) severity of moderate or severe rating at maximum contraction as assessed by investigator using the FWS-A at Day 1 prior to study treatment. Exclusion Criteria: * Participants with history of known immunization or hypersensitivity to any botulinum toxin serotype. * Participants with history of an allergic reaction or significant sensitivity to constituents of the study drug (and its excipients) and/or other products in the same class. * Presence of tattoos, jewelry, or clothing which obscures or interferes with the target area of interest and cannot be removed. * Participant with history of treatments to the mid- or upper face.

Locations (12)

Beijing Hospital /ID# 250059

Beijing, Beijing Municipality, China

Peking University First Hospital /ID# 249912

Xicheng District, Beijing Municipality, China

Guangdong Second Provincial General Hospital /ID# 250742

Guangzhou, Guangdong, China

The Third Affiliated Hospital, Sun Yat-Sen University /ID# 250148

Guangzhou, Guangdong, China

Peking university shenzhen hospital /ID# 249913

Shenzhen, Guangdong, China

Union Hospital Tongji Medical College Huazhong University of Science and Technol /ID# 250022

Wuhan, Hubei, China

Nanjing Drum Tower Hospital /ID# 250020

Nanjing, Jiangsu, China

Zhongda Hospital Southeast University /ID# 249970

Nanjing, Jiangsu, China

Huashan Hospital, Fudan University /ID# 249854

Shanghai, Shanghai Municipality, China

Tangdu Hospital of The Fourth Military Medical University, PLA /ID# 249856

Xi’an, Shanxi, China

...and 2 more locations

Outcomes

Primary Outcomes

Percentage of Participants who Achieved 'None' or 'Mild' on Facial Wrinkle Scale with Asian Photonumeric Guide (FWS-A) According to the Investigator Assessment of Forehead Lines (FHL) Severity

The investigator assesses FHL severity using the FWS-A 4-point scale ranging from 0=None to 3=Severe.

Time frame: Day 30

Percentage of Participants who Achieved 'None' or 'Mild' on FWS-A According to the Participant Assessment of FHL Severity

The participant assesses FHL severity using the FWS-A 4-point scale ranging from 0=None to 3=Severe.

Time frame: Day 30

Number of Participants with Adverse Events (AEs)

An adverse event (AE) is defined as any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product which does not necessarily have a causal relationship with the treatment. The investigator assesses the relationship of each event to the use of study drug.

Time frame: Day 180

Secondary Outcomes

Percentage of Participants who Achieved at least 1-Grade Improvement from Baseline on FWS-A According to the Investigator Assessment of FHL Severity

The investigator assesses FHL severity using the FWS-A 4-point scale ranging from 0=None to 3=Severe.

Time frame: Baseline to Day 30

Percentage of Participants with Responder Status of 'Very Satisfied' or 'Mostly Satisfied' on Satisfaction with Treatment on the Facial Line Satisfaction Questionnaire (FLSQ) follow up Item 5

The FLSQ consists of 13 questions that assess treatment satisfaction and psychosocial impact. Participants assessed their satisfaction with FHL using the FLSQ 5-point scale ranging from -2=Very dissatisfied to 2=Very satisfied.

Time frame: Day 60

Percentage of Participants with Responder Status of 'Very Satisfied' or 'Mostly Satisfied' on Satisfaction with Natural Look on the FLSQ follow up Item 4

Time frame: Day 30

Percentage of Participants who Achieved at Least a 20-Point Psychosocial Impact Improvement from Baseline on the FLSQ Impact Domain

Time frame: Baseline to Day 30

Percentage of Participants who Achieved at least 2-Grade Improvement from Baseline on FWS-A According to the Investigator Assessment of FHL Severity

The investigator assesses FHL severity using the FWS-A 4-point scale ranging from 0=None to 3=Severe.

Time frame: Baseline to Day 30

Percentage of Participants who Achieved at least 2-Grade Improvement from Baseline on FWS-A According to the Participant Assessment of FHL Severity

The participant assesses FHL severity using the FWS-A 4-point scale ranging from 0=None to 3=Severe.

Time frame: Baseline to Day 30