The objective of this study is to evaluate the safety and efficacy of AGN-151586 for the treatment of moderate to severe forehead lines (FHL) in adult participants.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
80
Injection
Eye Research Foundation /ID# 282193
Newport Beach, California, United States
RECRUITINGPrivate Practice - Dr. Steven G. Yoelin /ID# 282334
Newport Beach, California, United States
RECRUITINGLuxurgery /ID# 282336
New York, New York, United States
Number of Participants with Adverse Events (AEs)
An AE is defined as any untoward medical occurrence in a patient or clinical investigation in which a participant is administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment.
Time frame: Up to Approximately 42 Days
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Wilmington Dermatology Center /ID# 282192
Wilmington, North Carolina, United States
RECRUITINGAustin Institute for Clinical Research - Pflugerville /ID# 282195
Pflugerville, Texas, United States
RECRUITING