Clinical Trials Directory

Trials / Completed

CompletedNCT05152576

A Study To Assess the Adverse Effects and Change in Condition of OnabotulinumtoxinA X Injection in Adult Participants With Forehead Lines

A Phase 2, Multicenter, Randomized, Placebo-controlled Study to Evaluate the Safety and Efficacy of OnabotulinumtoxinA X for Forehead Lines

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
124 (actual)
Sponsor
Allergan · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Facial lines that develop from repeated facial expression, such as forehead lines (FHL), are typically treated by selectively weakening specific muscles with small quantities of botulinum toxin. OnabotulinumtoxinA X is being investigated as another form of treatment to treat FHL by inhibiting the release of the neurotransmitter that causes the overactivity of the muscles responsible for the severity of these facial lines. The purpose of this study is to evaluate the safety and change in condition of 3 doses of OnabotulinumtoxinA X for the treatment of moderate to severe forehead lines. Study doctors will determine if a subject is eligible for the study. If so, the subject will be randomized into 1 of the 4 groups, called treatment arms. There is a 1 in 4 chance that a participant will be assigned to placebo. Around 120 adult participants with FHL will be enrolled in the study in approximately 10 sites in the United States. Participants will receive either intramuscular injections of onabotulinumtoxinA X or placebo. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular monthly visits during the study at the study site.

Conditions

Interventions

TypeNameDescription
DRUGOnabotulinumtoxinA XIntramuscular Injection
DRUGPlaceboIntramuscular Injection

Timeline

Start date
2021-11-29
Primary completion
2022-09-06
Completion
2022-09-06
First posted
2021-12-10
Last updated
2025-07-16
Results posted
2025-07-16

Locations

8 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05152576. Inclusion in this directory is not an endorsement.