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Extension Study for 43USSA1705 | Clinical Trials | Clareo Health

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COMPLETEDNANCT04225273

Extension Study for 43USSA1705

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 compare...

Lead sponsor: Galderma R&D•4 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Galderma R&D

Age

22 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

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

Exclusion Criteria

•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

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: March 12, 2025Terms

Trial snapshot

StatusCOMPLETED

PhaseNA

Enrollment38

Start dateDec 2019

Last updatedMar 12, 2025

Condition

Nasolabial Folds

Locations shown

Galderma Study Site

Scottsdale, Arizona

Galderma Study Site

Bradenton, Florida

Galderma Study Site

Austin, Texas

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: March 12, 2025Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions