New injection shows promise for smoothing frown lines and Crow's feet
NCT ID NCT05148000
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a new injection called QM1114-DP in 25 adults with moderate to severe frown lines and crow's feet. Participants received one treatment and were asked to rate how much their appearance improved. The goal was to see if the treatment could make these wrinkles look better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- QM1114-DP (a botulinum toxin type A injection)
- What this could lead to
- If successful, this could provide a new option for temporarily reducing the appearance of frown lines and crow's feet.
- What could go wrong
- This is a small, completed Phase 3 study with only 25 participants. Results may not apply to everyone, and effects are temporary. Allergic reactions or bruising at injection site are possible.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
25 people
The number who actually took part.
- Started
-
Jan 2023
- Finished
-
Jun 2023
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or Female 18 years or older * Moderate to severe bilaterally symmetrical LCL as assessed by the investigator * Moderate to severe GL at maximum frown as assessed by the Investigator Exclusion Criteria: * Previous use of any botulinum toxin in facial areas within 9 months prior to study treatment * Female who was pregnant, breast feeding or intended to conceive a child during the study. * Known allergy to hypersensitivity or any component of the Investigational product
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Galderma Research Site
New York, New York, 10021, United States
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