Business Wire

Galderma to Present New Clinical Data and High Patient Satisfaction Across Their Portfolio of Dermal Fillers, Collagen Biostimulators and Liquid Neuromodulators at AMWC 2022


Galderma will present a range of new scientific data on its portfolio on their hyaluronic acid dermal filler range, their first liquid neuromodulator and their original collagen biostimulator at the Aesthetic & Anti-Aging Medicine World Congress (AMWC) taking place in Monaco and virtually from 31 March to 2 April 2022.

Dr Philippe Kestemont will present an overview of clinical data for Alluzience®, Galderma’s recently approved and Europe’s first ready-to-use liquid neuromodulator for the treatment of moderate to severe glabellar (frown) lines.1

Pooled data from two Phase III studies (NCT02353871 and NCT02493946) show that Alluzience® successfully improved glabellar lines regardless of severity with rapid onset and results lasting up to 6 months.2,3 Improvements in GL severity, satisfaction and psychological wellbeing were also consistent over several cycles of treatment with Alluzience®.2,3

The latest long-lasting efficacy and safety results will also be presented on the new formulation of Sculptra®, the original and only poly-L-lactic acid (PLLA) approved by the FDA. The new constitution means it can be reconstituted to 5ml or 8ml, used immediately and an optional 1mL of lidocaine can be added for patient comfort. The open-label extension study evaluating the new formulation of 8mL showed Sculptra® was well tolerated and had a long-lasting duration of effect, with subject satisfaction up to 96 weeks.4

“We are proud to sponsor the Aesthetics & Anti-Aging Medicine World Congress 2022 and we look forward to engaging with the aesthetics community, both in person in Monaco and virtually.

At Galderma, we believe in the benefits of delivering individualized aesthetics results. We are excited to host a symposium to bring this vision to the aesthetics community and share new data with a series of posters in our drive for innovation across our aesthetics portfolio.”

– Flemming Ørnskov, MD, MPH, Chief Executive Officer, Galderma

Galderma will also present data demonstrating the effectiveness and high patient satisfaction in patients treated with hyaluronic acid fillers. Results from Dr Andreas Nikolis’ CHEEKY post-market study evaluated treatment with Restylane® Lyft™ for those needing a projection effect and Restylane® Volyme™ for a contouring/volumizing effect.5

In addition, Dr Steven Dayan will detail positive results from a post-marketing study evaluating facial harmony and patient satisfaction after treatment with Restylane® Defyne™, a flexible hyaluronic acid filler, using a stepwise treatment approach.6

Finally, at AMWC, Galderma will be hosting a symposium that has been developed with some of the world’s most talented aesthetic physicians. Focusing on ‘A New Patient Centric Approach to turn your AART™ into a HIT™, the Galderma symposium will focus on how to use AART™ – Anatomy, Assessment, Regimen and Therapy – to deliver a Holistic Individualized Treatment (HIT) for each patient.

Moderated by Dr Andreas Nikolis (Canada), the symposium will feature interactive sessions with Sebastian Cotofana (US), Kay Durairaj (USA), Christoph Martschin (Sweden), Marcus Morais (Brazil) and Frank Rosengaus (Mexico), as well as live injections and a panel assessment.

The complete list of the new clinical data that Galderma and independent researchers will present is below:





Ready-to-use liquid abobotulinumtoxinA for treatment of glabellar lines: An overview of available clinical data



An open-label extension study to evaluate safety and effectiveness of a biostimulatory poly-L-lactic acid injectable implant after changes in reconstitution and injection procedure


Restylane® Lyft™ Restylane® Volyme™

The CHEEKY Study: effectiveness of cheek treatment with hyaluronic acid fillers HA-VOL and HA-LYF


Restylane® Defyne™

A randomized, post-marketing study to evaluate facial harmony and subject satisfaction after treatment with HA-DEF using a stepwise treatment approach


For more information, the AMWC 2022 program is available here.

About Galderma
Galderma is the world’s largest independent dermatology company, present in approximately 100 countries. Since our inception in 1981, we have been driven by a complete dedication to dermatology. We deliver an innovative, science-based portfolio of sophisticated brands and services across Aesthetics, Consumer Care and Prescription Medicine.

Focused on the needs of consumers and patients, we work in partnership with healthcare professionals to ensure superior outcomes. Because we understand that the skin we’re in shapes our life stories, we are advancing dermatology for every skin story. For more information:

About Alluzience® (liquid botulinum toxin type A)
Alluzience® (liquid botulinum toxin type A) is the first ready-to-use BoNT-A liquid neuromodulator formulation to be introduced in Europe. Alluzience® should only be administered by a physician with appropriate qualifications and expertise in this treatment using the required equipment.1 Dosing and treatment intervals depend on assessment of the individual patient’s response.1 The treatment interval should be no more frequent than every three months.1 For more information, please see the Summary of Product Characteristics.1

Alluzience® is a product under license from Ipsen. Alluzience® is a registered trademark of Ipsen. Galderma has an exclusive license from Ipsen to develop, promote and distribute Alluzience® in the approved indication in Europe (excluding Czech Republic, Slovakia, Greece, Lithuania, Estonia, Latvia, Hungary).

About Sculptra®:
SCULPTRA® works to stimulate the skin’s own collagen production7 and is suitable for increasing the volume of depressed areas, particularly to correct skin depressions such as skin creases, wrinkles, folds and scars, and for signs of skin aging.8 SCULPTRA is also suitable for large volume corrections of the signs of facial fat loss (lipoatrophy).8

SCULPTRA® is an injectable biostimulator containing microparticles of poly-L-lactic acid (PLLA) which gradually revitalizes the skin’s structural foundation, providing natural-looking, long-term results for up to 25 months.7,9 SCULPTRA was first approved in 1999 in Europe and it is currently available in more than 40 countries globally.

About Galderma’s Restylane portfolio
RESTYLANE is the original non-animal stabilized hyaluronic acid filler with over 25 years of achievement and over 50 million treatments worldwide.10 NASHA™ and OBT™ technologies make RESTYLANE the world’s most diverse range of fillers to deliver truly individualized results.11.12



  1. Summary of Product Characteristics, 10 June 2021.
  2. Ascher et al. Aesthet Surg J 2020;40:93-104.
  3. Kestemont et al. Aesthet Surg J 2021;Sep 2;sjab329.
  4. Prather et al. Poster #3802 to be presented at AMWC 2022.
  5. Nikolis A., Poster #3719 to be presented at AMWC 2022.
  6. Dayan S., Poster #3730 to be presented at AMWC 2022.
  7. Bohnert K et al. Plast Reconstr Surg 2019;127(4):1684–92.
  8. Sculptra IFU. 2018.
  9. Brown SA et al. Plast Reconstr Surg 2011;127(4):1684–92.
  10. Data on file (MA-39680).
  11. Data on file (MA-33939).
  12. Öhrlund A., Poster presented at AMWC 2019.

Prescribing information, trademarks and registration status may vary depending on local approval in each country. Always refer to local materials such as the prescribing information and/or the Summary of Product Characteristics (SPC)

To view this piece of content from, please give your consent at the top of this page.

Contact information


Rachel Mooney, Head of Franchise Communications at Galderma

Michelle Tombs, Senior Account Manager at Ashfield Health

About Business Wire

For more than 50 years, Business Wire has been the global leader in press release distribution and regulatory disclosure.

Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

US Streaming Technology Giant Conviva Launches Full-Scale Continuous Measurement Analytics in Japan18.5.2022 04:00:00 EEST | Press release

Conviva (Headquartered at Foster City, California, USA; Japan Office: Chiyoda-ku, Tokyo; hereinafter referred to as Conviva or the Company), which provides continuous measurement analytics through real-time, server side sessionization of video streaming data, today announced the opening of the Japan office, which will serve as a base for sales and customer support in the rapidly-growing Japanese market. The Company also released a current State of Streaming Report for Japan highlighting key streaming trends in the market. This press release features multimedia. View the full release here: Conviva State of Streaming Japan Report (Graphic: Business Wire) “Conviva invented continuous measurement analytics for streaming video and has been driving the development of the global market including Japan with over 58 technology patents over the past decade,” comments Conviva CEO Keith Zubchevich. “Today, we are pleased to announce the est

Starr Insurance Companies Expands in Thailand17.5.2022 23:33:00 EEST | Press release

Starr Insurance Companies (Starr) announced an agreement with FPG Insurance Holdings Limited (HK) (FPG) and local Thai shareholders to purchase FPG Insurance Public Company Limited (FPG Thailand), a Thai non-life insurance company, together with local Thai parties. Starr’s investment will be held by its Bermuda insurance company, Starr Insurance & Reinsurance Limited. The transaction is expected to close in the second quarter of 2022, subject to certain customary closing conditions, including any necessary regulatory approvals. “Thailand is an important, fast-growing insurance market — one of the cornerstones of the Southeast Asia economy,” said Maurice R. Greenberg, Starr’s Chairman & CEO. “Asia is both commercially and culturally important to Starr, as we trace our roots to an American-owned company founded in Shanghai more than 100 years ago. We look forward to serving the needs of local Thai companies and consumers through this new insurance capability.” David Zuellig, FPG regional

Emendo Biotherapeutics’ next generation CRISPR gene editing technologies achieve breakthrough results with allele-specific approach for ELANE-related Severe Congenital Neutropenia as presented at ASGCT Annual Meeting17.5.2022 23:15:00 EEST | Press release

Emendo Biotherapeutics presented the results of its next generation CRISPR-based gene editing approaches for several indications in an oral presentation and three posters at the 25th Annual Meeting of the American Society of Gene & Cell Therapy (ASGCT) held May 16-19, 2022, in Washington, D.C. Emendo presented pre-clinical data for the treatment of ELANE-related Severe Congenital Neutropenia using an allele-specific editing approach, demonstrating the power of Emendo’s dual technology platforms that enable the development of a highly specific editing composition that demonstrates no off-targets and complete allele specificity. Significantly, the lack of off-target achieved by Emendo’s engineered and optimized OMNI nuclease also eliminated any translocations. Edited patient derived CD34+ cells differentiated normally into neutrophils both in-vitro and in-vivo, showing full engraftment and reconstitution of all blood lineages, as required for the desired therapeutic effect. “ELANE-based

Piper Sandler Advises PETRONAS Chemicals Group Berhad on Acquisition of Perstorp17.5.2022 20:59:00 EEST | Press release

Piper Sandler & Co. chemicals investment banking announced today that it has advised PETRONAS Chemicals Group Berhad (PCG) on its acquisition of Perstorp Holding AB. The transaction Enterprise Value is €2,300 million and base purchase price, less adjusted net debt, is €1,538 million. It is expected to close in Q3 2022 subject to customary closing conditions. PCG is the leading integrated chemicals producer in Malaysia and one of the largest in Southeast Asia. It operates a number of world-class production sites, which are fully vertically integrated from feedstock to downstream end-products. With a total combined production capacity of 12.8 million metric tons per annum (mtpa), it is involved primarily in manufacturing, marketing, and selling a diversified range of chemical products, including olefins, polymers, fertilizers, methanol and other basic chemicals and derivative products. Listed on Bursa Malaysia in 2010 and with more than three decades of experience in the chemicals indust

Morinaga Milk Obtains the Registration of "New Food Ingredient" in China for Use of Its Probiotic Bifidobacterium longum BB536 in Infant and Toddler Foods17.5.2022 20:53:00 EEST | Press release

Morinaga Milk Industry Co., Ltd. (TOKYO:2264), a leading Japanese dairy product company, today announced its proprietary probiotic Bifidobacterium longum BB536 was approved by the National Health Commission (NHC) of the People’s Republic of China as a new food ingredient for use in infant and toddler foods (under the age of three) on 11th May 2022. This press release features multimedia. View the full release here: Morinaga Milk obtains the registration of "New Food Ingredient" in China for use of its probiotic Bifidobacterium longum BB536 in infant and toddler foods on 11th May 2022. (Graphic: Business Wire) Following a complex and lengthy registration process, the probiotic strain B. longum BB536 meets the highest standards of safety and regulatory compliance and has now completed the approval process for use as an ingredient in infant and toddler milk and food products for children under three years old in China. “We are extr

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom