This is a safety and efficacy study of botulinum toxin type A in subjects with glabellar frown lines.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
268
Intramuscular injection (IM)
IM injection
IM injection
Unnamed facility
Vancouver, British Columbia, Canada
Proportion of subjects assessed as responders by investigator assessment of severity of glabellar lines at maximum frown
Time frame: Week 24
Duration of response assessed by investigator assessment of severity of glabellar lines at maximum frown from the date of injection to when subject reverts to baseline severity
Time frame: Up to Week 36
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