Extension Study for 43USSA1705

Completed · Not applicable

Conditions studied: Nasolabial Folds

In brief

To evaluate the long-term safety of Sculptra Aesthetic as a single regimen for correction of Nasolabial Fold (NLF) contour deficiencies after changes in reconstitution and injection procedures compared to the approved label.

Key facts

Study ID

NCT04225273

Run by

Galderma R&D

People needed

38

Starts

2019-12-03

Expected to finish

2021-01-29

Last updated by the study team

2025-03-12

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Randomized to Sculptra Aesthetic 8ml reconstitution and successfully completed study 43USSA1705

You may not qualify if…

• Medical condition that in the opinion of the Investigator would make the subject unsuitable for inclusion
• Other condition preventing the subject from entering the study in the Investigator's opinion
• Participation in any interventional clinical study throughout the duration of the study

Where it is running

• Galderma Study Site — Scottsdale, Arizona, United States
• Galderma Study Site — Bradenton, Florida, United States
• Galderma Study Site — Austin, Texas, United States
• Galderma Study Site — Spring, Texas, United States

Full record on ClinicalTrials.gov

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