For Healthcare Professionals

Sculptra® is a poly-L-lactic acid (PLLA)–based treatment that works deep within the skin to help stimulate collagen production. Unlike hyaluronic acid fillers, Sculptra helps stimulates the skin’s own natural collagen production.1-3

Patients can achieve natural-looking results that can last up to 2 years.3*

*Clinical study ended at 96 weeks (2 years).

Actual patient. Individual results may vary.

Sculptra Clinical Study Results
Sustained improvements that last for up to 2 years3‡
graph of Sculptra patient results after two years

Patient = Clinical trial participant

§WAS=Wrinkle Assessment Scale. Data from left NLF only. Right NLF data was similar

8 mL SWFI + 1 mL 2% lidocaine immediate use Sculptra cohort (N=38) in a 96-week (2 years) extension clinical study

100%
of patients showed aesthetic improvement for up to 2 years.3‡§

Sculptra shows high satisfaction ratings4‡
94%
of patients agreed that the treatment results look natural at 2 years after last treatment
90%
of patients were satisfied with their appearance at 6 months, with sustained satisfaction of 82% at 1 year and 77% at 2 years after last treatment

Patient = Clinical trial participant

8 mL SWFI + 1 mL 2% lidocaine immediate use Sculptra cohort (N=38) in a 96-week (2 years) extension clinical study with additional assessments at 24 weeks (6 months) and 48 weeks (1 year) after last treatment

sculptra patient headshot
Gradual results that last longer are preferred
89%

At 2 years after last treatment, 89% of patients agreed that subtle results over time was worth it4‡


Patients = clinical trial participant

8 mL SWFI + 1 mL 2% lidocaine immediate use Sculptra cohort (N=38) in a 96-week (2 years) extension clinical study

Find a Specialist Feature

The Find a Specialist feature on Sculptra.com makes it easy for website visitors to locate and contact you regarding treatment with Sculptra.

All you have to do to remain listed on the Sculptra Find a Specialist feature is place an order for Sculptra a minimum of every six months.

Contact a sales representative at ContactUs@GaldermaSupport.com.

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Make every order count by joining ASPIRE Galderma Rewards, the program that offers physicians faster ways to earn instant savings, product discounts and quarterly rebates. The program is also designed to enhance your practice by enabling loyal patients to redeem their own ASPIRE Galderma Rewards points with you.

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Looking for information on injecting Sculptra?

Visit MYGAINTRAINING.com to learn more about injection techniques and training.

Have questions? Contact Galderma today.

If you would like to place an order or have any product questions, please call 1-844-GALDERM (1-844-425-3376) to speak with a sales rep or email customer service at ContactUs@GaldermaSupport.com.

For any medical inquiries, including reporting adverse medical reactions to a Galderma product, please call 1-866-735-4137 or email customer service at ContactUs@GaldermaSupport.com.


References:
  1. Stein P, Vitavska O, Kind P, Hoppe W, Wieczorek H, Schürer NY. The biological basis for poly-L-lactic acid-induced augmentation. J Dermatol Sci. 2015;78(1):26–33.
  2. Goldberg D, Guana A, Volk A, Daro-Kaftan E. Single-arm study for the characterization of human tissue response to injectable poly-L-lactic acid. Dermatol Surg. 2013;39(6):915–922.
  3. Sculptra injectable poly-L-lactic acid. Instructions for Use. Galderma Laboratories. 2021.
  4. Data on file. 43USSA1705ext clinical study report. Fort Worth, TX: Galderma Laboratories, L.P. 2021.

Patient Brochure

Click here for patient information about Sculptra® (PDF)

Important Safety Information

Indication: Sculptra® (injectable poly-L-lactic acid) is indicated for use in people with healthy immune systems for the correction of shallow to deep nasolabial fold contour deficiencies and other facial wrinkles.

Sculptra should not be used by people that are allergic to any ingredient of the product or have a history of keloid formation or hypertrophic scarring. Safety has not been established in patients who are pregnant, lactating, breastfeeding, or under 18 years of age.

Sculptra has unique injection requirements and should only be used by a trained healthcare practitioner. Contour deficiencies should not be overcorrected because they are expected to gradually improve after treatment.

Sculptra should not be injected into the blood vessels as it may cause vascular occlusion, infarction or embolic phenomena. Use at the site of skin sores, cysts, pimples, rashes, hives or infection should be postponed until healing is complete. Sculptra should not be injected into the red area (vermillion) of the lip or in the peri-orbital area.

The most common side effects after initial treatment include injection site swelling, tenderness, redness, pain, bruising, bleeding, itching and lumps. Other side effects may include small lumps under the skin that are sometimes noticeable when pressing on the treated area. Larger lumps, some with delayed onset with or without inflammation or skin discoloration, have also been reported.

Sculptra is available only through a licensed practitioner. View the complete Instructions for Use.

Important Safety Information | Instructions for Use

Indication: Sculptra® (injectable poly-L-lactic acid) is indicated for use in people with healthy immune systems for the correction of shallow to deep nasolabial fold contour deficiencies and other facial wrinkles.