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Treatment of Moderate to Severe Lateral Canthal Lines

Treatment of Moderate to Severe Lateral Canthal Lines

Recruiting
18 years and older
All
Phase 3

Overview

The objective of the study is to evaluate the efficacy and safety of a single dose of QM1114-DP compared to placebo for the treatment of moderate to severe LCL.

Eligibility

Inclusion Criteria:

  1. Male or female 18 years of age or older.
  2. Moderate to severe LCL at maximum smile as assessed by the Investigator.
  3. Moderate to severe LCL at maximum smile as assessed by the subject.

Exclusion Criteria:

  1. Previous use of any Botulinum toxin treatment in facial areas within 9 months prior to study treatment.
  2. Female who is pregnant, breast feeding, or intends to conceive a child during the study.
  3. Known allergy or hypersensitivity to any component of the investigational product (QM1114-DP) or any botulinum toxin serotype.

Study details
    Lateral Canthal Lines

NCT04249687

Q-Med AB

16 February 2024

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