Treatment of Moderate to Severe Lateral Canthal Lines

  • STATUS
    Recruiting
  • participants needed
    300
  • sponsor
    Q-Med AB
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Updated on 19 February 2024
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Summary

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.

Details
Condition Lateral Canthal Lines
Age 18years - 100years
Treatment Placebo, botulinum toxin
Clinical Study IdentifierNCT04249687
SponsorQ-Med AB
Last Modified on19 February 2024

Eligibility

 Yes No Not Sure

Inclusion Criteria

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

Exclusion Criteria

Previous use of any Botulinum toxin treatment in facial areas within 9 months prior to study treatment
Female who is pregnant, breast feeding, or intends to conceive a child during the study
Known allergy or hypersensitivity to any component of the investigational product (QM1114-DP) or any botulinum toxin serotype
Clear my responses
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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