Proven Efficacy

Efficacy confirmed by primary statistical study endpoint*

  • 55% of BOTOX® patients achieved primary statistical study endpoint1

*Results from a 52-week, randomized, multicenter, double-blind, placebo-controlled study of 322 patients.

Patients who showed ≥2-grade HDSS improvement from baseline value 4 weeks after both of the first 2 treatment sessions or had a sustained response after treatment 1 and did not receive treatment 2 during the study1



Results from a 52-week, randomized, multicenter, double-blind, placebo-controlled study of 322 patients
§ Based on patients who received a second treatment session during the study

References

  1. BOTOX® Prescribing Information.
  2. Data on file, Allergan, Inc.; Pivotal clinical trial, Study 016.

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APC31BJ09