Business Wire

GALDERMA

25.1.2024 07:01:33 CET | Business Wire | Press release

Share
IMCAS 2024: Galderma to Present Latest Updates From Its Unparalleled Aesthetics Portfolio Reinforcing Its Leadership Position

Galderma will be sharing the latest updates from across its broad and unparalleled portfolio at the International Master Course on Aging Science (IMCAS) World Congress 2024 from February 1-3, 2024, in Paris. The updates reinforce Galderma’s leadership in aesthetic injectables and dermatological skincare. In addition to presenting 10 research posters highlighting data from across the portfolio —including on our investigational neuromodulator RelabotulinumtoxinA — Galderma will host a number of events dedicated to addressing the real needs of physicians. This will include three symposia and several ‘Meet the Expert’ and interactive booth sessions.

 

“The breadth of our data and activities at IMCAS truly embodies our commitment to responding directly to the needs of healthcare professionals and patients. We’re looking forward to another opportunity to listen and learn from the aesthetics community to help us further advance our groundbreaking innovations.”

 

BALDO SCASSELLATI SFORZOLINI, M.D., Ph.D.

GLOBAL HEAD OF R&D

GALDERMA

Data from our leading neuromodulator portfolio

RelabotulinumtoxinA was developed over the past 15 years as part of our ambition to expand our leadership in neuromodulation and to create an ideal neuromodulator for aesthetic use. Results from the phase III READY-1 and READY-2 studies will be presented, showing that RelabotulinumtoxinA was highly effective and well-tolerated when treating moderate to severe glabellar lines (frown lines) and lateral canthal lines (crow’s feet). Results demonstrated rapid onset as early as day one, sustained results through six months, and high patient satisfaction.1 39% and 34% of people with glabellar lines and lateral canthal lines, respectively, reported onset within one day. The median time to return to baseline line was >24 weeks (end of study) for glabellar lines and 24.7 weeks for lateral canthal lines on both investigator- and patient-assessed scales.1 Both studies had low rates of treatment-related adverse events with RelabotulinumtoxinA compared to placebo.1

The READY (RElabotulinumtoxin Aesthetic Development StudY) clinical trial program is composed of four phase III trials, which enrolled more than 1,900 participants.4-7

The data will be presented as an e-poster, displayed throughout the whole conference period at the Open Stage Library.

Showcasing our latest clinical and educational efforts

Three symposia will highlight Galderma’s innovations and science as well as educational efforts to support the aesthetics community.

Through lectures and live demonstrations, the first symposium, Our Aesthetic Lives – Pushing the Boundaries in Aesthetics, will delve into the aesthetic lives of patients and the aesthetics practitioners who treat them. It will focus on looking beyond lines and wrinkles to consider how to approach surgical cases with injectables. The event is taking place in the Amphitheatre Bleu, Level 2 on Friday, February 2, from 10:30 AM to 12:30 PM CET.

Our second symposium, Skin Science by Galderma Medical Affairs, will focus on diversity in skin health and beauty and uncover the science behind our injectables (Restylane® SKINBOOSTERS™ and Sculptra). The event is taking place in Room 351 - Level 3 on Friday, February 2, from 2:00 to 3:30 PM CET.

Finally, the AART™ of Sculptra symposium will explore how Sculptra’s applications have expanded over the last 25 years, enabling us today to understand the right patients’ profile, with the support of a holistic facial assessment tool. The event is taking place in Room 252 - Level 2 on Friday, February 2, from 4:00 to 5:00 PM CET.

We will also host a number of ‘Meet the Expert’ sessions, which will provide education on our Holistic Individualized Treatment (HIT™) approach. We will explore a range of our treatment protocols that combine different solutions from our Galderma portfolio, such as Kiss & Smile™, SHAPE UP™ and CTMP™: Cleanse, Treat, Moisturize, Protect, as well as products including ALASTIN Skincare®, Restylane® and Sculptra.

Celebrating 25 years of innovation with Sculptra

We are proud to have reached the 25th anniversary landmark for Sculptra, the first and original injectable biostimulator containing microparticles of unique PLLA-SCA™.8-11 Sculptra addresses the root causes of skin aging, stimulating the body's own collagen production to help gradually restore structural support and firmness, improving skin quality and radiance for 2 years.8-11

Building on the extensive body of evidence on Sculptra’s mode of action and proven efficacy and safety profile, we will be presenting multiple posters on Sculptra at IMCAS including positive results in non-facial areas.9-14 More details on Galderma’s scientific presentations at IMCAS can be found here.

About RelabotulinumtoxinA (QM1114)

Developed by Galderma, RelabotulinumtoxinA is a highly-active, innovative, complex-free, and ready-to-use liquid botulinum toxin A with a proprietary strain and manufactured using a unique state-of-the-art process. It is designed as a liquid, avoiding the traditional requirement to reconstitute from powder and eliminating variability, errors and risks associated with reconstitution, which would be expected to improve the consistency of results. RelabotulinumtoxinA is currently being investigated globally by Galderma, to expand its neuromodulator portfolio as part of the broadest Injectable Aesthetics portfolio on the market.

About Sculptra®

Sculptra is the first and original injectable biostimulator containing microparticles of PLLA-SCA™, which helps gradually restore the skin’s structural support and firmness, improving overall skin quality for natural-looking results for more than 2 years.8-11§ Sculptra was first approved for aesthetic use in 1999 in Europe and is currently available in more than 40 countries globally.

§Clinical study ended at 96 weeks (2 years)

About Galderma

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market though Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body’s largest organ – the skin – meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin we are in shapes our lives, we are advancing dermatology for every skin story. For more information: www.galderma.com.

References:

  1. Gold, M, et al. Ph III efficacy and safety data on relabotulinumtoxinA, an investigational liquid botulinum toxin for treatment of glabellar or lateral canthal lines. Abstract presented at IMCAS 2024.
  2. Solish, N, et al. Treatment of Moderate-to-Severe Glabellar Lines with RelabotulinumtoxinA, an Investigational Liquid Botulinum Toxin: Clinical Efficacy and Safety Results from the READY-1 Phase III trial. Abstract presented at TOXINS 2024.
  3. Ablon, G, et al. Treatment of Lateral Canthal Lines with RelabotulinumtoxinA, an Investigational Liquid Botulinum Toxin: Clinical Efficacy and Safety Results from the READY-2 Phase III Trial. Abstract presented at TOXINS 2024.
  4. ClinicalTrials.Gov. Treatment of Moderate to Severe Glabellar Lines (READY-1). Available online: https://clinicaltrials.gov/study/NCT04249583. Last accessed January 2024.
  5. ClinicalTrials.Gov. Treatment of Moderate to Severe Lateral Canthal Lines (READY-2). Available online: https://clinicaltrials.gov/study/NCT04249687. Last accessed January 2024.
  6. ClinicalTrials.Gov. Treatment of Moderate to Severe Lateral Canthal Lines and Glabellar Lines Alone or in Combination (READY-3). Available online: https://clinicaltrials.gov/study/NCT04247074. Last Accessed January 2024.
  7. ClinicalTrials.Gov. Long-term Treatment of Moderate to Severe Glabellar Lines and Lateral Canthal Lines (READY-4). Available online: https://clinicaltrials.gov/study/NCT04225260. Last accessed January 2024.
  8. Sculptra. Instructions for Use. Galderma Laboratories. 2023.
  9. Data on file. 43USSA1812EXT clinical study report. Fort Worth, TX: Galderma Laborato-ries, L.P. 2022.
  10. Goldberg, D, et al. Single-arm study for the characterization of human tissue response to injectable poly-L-lactic acid. EDermatol Surg. 2013;39(6):915-922. doi: 10.1111/dsu.12164.
  11. Fitzgerald, R, et al. Physiochemical Characteristics of Poly-L-Lactic Acid (PLLA). Aesthet Surg J. 2018;38(suppl_1):S13-S17. doi: 10.1093/asj/sjy012.
  12. Bohnert K. et al. Randomized, Controlled, Multicentered, Double-Blind Investigation of Injectable Poly-L-Lactic Acid for Improving Skin Quality Dermatol Surg. 2019;45:718–724. doi: 10.1097/DSS.0000000000001772.
  13. Durairaj, K, et al. A multi-center, retrospective, chart review to evaluate the safety of poly-L-lactic acid injectable implant when used in non-facial areas. Abstract presented at IMCAS 2024.
  14. Humphrey, S, et al. Safety and Effectiveness of Poly-L-lactic acid (PLLA-SCA) for the Improvement in Appearance of Cellulite – A Pilot Study. Abstract presented at IMCAS 2024.

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

View source version on businesswire.com: https://www.businesswire.com/news/home/20240124001879/en/

About Business Wire

Business Wire
Business Wire
101 California Street, 20th Floor
CA 94111 San Francisco

http://businesswire.com
DK

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

Visa Direct and UnionPay International Will Extend Global Money Movement Network to Billions of Cards in Chinese Mainland3.2.2026 13:00:00 CET | Press release

By connecting Visa Direct’s card network to UnionPay International’s (UPI) MoneyExpress platform, Visa Direct will unlock real‑time1 cross‑border money movement in one of the world’s largest remittance corridors At Web Summit Qatar, Visa (NYSE:V) and UnionPay International (UPI) announced an agreement to enable cross-border money movement into Chinese Mainland through Visa Direct. Once fully rolled out, clients will be able to send cross-border remittances and business-to-consumer payouts to more than 95 percent of UnionPay International debit cardholders in Chinese Mainland, through a single connection. By connecting Visa Direct’s global money movement network to UPI’s MoneyExpress platform, Visa will provide a more seamless, secure, and transparent way for consumers and businesses worldwide to send money into Chinese Mainland, one of the world’s largest remittance destinations. This milestone showcases Visa’s commitment to opening global corridors and extending reliable money movemen

China NMPA Approves Promega MSI Detection Kit as Companion Diagnostic for KEYTRUDA®3.2.2026 13:00:00 CET | Press release

The National Medical Products Administration (NMPA) has approved the OncoMate® Microsatellite Instability (MSI) Detection Kit as a Class III in vitro diagnostic medical device in China. It is intended for use as a companion diagnostic to identify MSI-High (MSI-H) solid tumor patients for treatment with KEYTRUDA® (pembrolizumab), Merck & Co., Inc., Rahway, NJ, USA’s anti-PD-1 therapy. This is the first Promega companion diagnostic to receive NMPA approval. “This approval represents a step toward more personalized and effective cancer treatment in China,” says Alok Sharma, Global Clinical Market Director at Promega. “We are proud to collaborate with pharmaceutical companies to deliver global solutions that expand access to innovative technologies and life-saving, effective therapies.” China continues to face one of the world’s highest cancer burdens, with solid tumors representing the vast majority of diagnoses nationwide. Despite advances in oncology care, most patients with advanced so

Rising Global Bullion Market Risks Are Forcing European Investors to Rethink Physical Gold Access3.2.2026 10:35:00 CET | Press release

As volatility reshapes global financial markets, European institutional investors are turning to safe-haven assets. While physical gold remains one of the world's most resilient and attractive store-of-value assets, secure and verifiable access to bullion has become increasingly difficult. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260203826775/en/ Illustrative image of physical gold bullion bars. (Photo: AETOSWire) Recent industry developments have placed structural pressure on the gold market. Elevated price levels have heightened concerns around counterfeit bars, fragmented supply chains, and the complexity of cross-border custody. For European institutions operating under strict regulatory oversight, the challenge is no longer whether to allocate to gold — but how to do so safely, transparently, and within established compliance frameworks. To this end, Golden Ark Reserve, operated by Golden Ark General Trading (FZC)

Hyper-Personalization at Scale: Why Brands Must Shift to an Agentic AI Strategy3.2.2026 10:00:00 CET | Press release

As Infobip celebrates 20 years of customer communication innovation, the AI-first company envisions the future of agentic AI Global AI-first cloud communications platform Infobip, celebrating two decades of innovation, predicts an imminent and seismic shift in brand-consumer engagement. Moving away from the current application-to-person (A2P) messaging, Infobip forecasts a widespread shift to an agent-to-person model, eventually leading to a fully autonomous agent-to-agent future by 2030. The Evolution of Engagement Swift AI adoption is driving enterprises toward agentic AI communication models, which drive autonomous customer communications across all touchpoints. This technology enables hyper-personalization across multiple channels, creating highly engaging content tailored to individual needs. Silvio Kutić, Infobip CEO, comments: “How we communicate with brands is constantly evolving. In this new agentic AI world, brands must seize the opportunity to take a holistic approach to com

Corona Cero Unveils Global Roster of Athlete Ambassadors to Champion TIME CERO at Milano Cortina 20263.2.2026 09:00:00 CET | Press release

A First-of-Its-Kind Initiative, In Partnership with International Olympics Committee (IOC), TIME CERO Empowers Athletes to Unwind, Recharge, and Celebrate the Moment Corona Cero Invites Fans to Celebrate Together in Italy with Corona Hotel, Casa Corona, and Other Immersive Activities Corona Cero today unveiled its global roster of brand ambassadors who will champion TIME CERO, the brand’s new initiative created in partnership with the IOC and Athlete365, throughout the Olympic Winter Games. Together, Team Corona Cero will bring the brand’s “For Every Golden Moment” global platform to life, reminding people that meaningful golden moments can happen anytime, anywhere, or in any season. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260203205858/en/ Team Corona Cero Central to Corona Cero’s commitment as a Worldwide Olympic Partner, TIME CERO is designed to celebrate Olympians and help them relax, stay present, and embrace bala

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
World GlobeA line styled icon from Orion Icon Library.HiddenA line styled icon from Orion Icon Library.Eye