GALDERMA
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:
- 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.
- 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.
- 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.
- ClinicalTrials.Gov. Treatment of Moderate to Severe Glabellar Lines (READY-1). Available online: https://clinicaltrials.gov/study/NCT04249583. Last accessed January 2024.
- ClinicalTrials.Gov. Treatment of Moderate to Severe Lateral Canthal Lines (READY-2). Available online: https://clinicaltrials.gov/study/NCT04249687. Last accessed January 2024.
- 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.
- 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.
- Sculptra. Instructions for Use. Galderma Laboratories. 2023.
- Data on file. 43USSA1812EXT clinical study report. Fort Worth, TX: Galderma Laborato-ries, L.P. 2022.
- 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.
- 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.
- 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.
- 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.
- 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
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
IFF to Release Fourth Quarter & Full Year 2025 Results on Feb. 11, 2026; IFF to Present at 2026 CAGNY Conference on Feb. 19, 202621.1.2026 22:15:00 CET | Press release
IFF (NYSE:IFF) today announced that it will release its fourth quarter and full year 2025 earnings results following the market close on Wednesday, Feb. 11, 2026. The management team will host a live webcast on Thursday, Feb. 12, 2026, at 9:00 a.m. ET to discuss results and outlook with the investor community. IFF also announced today that the Company’s management will speak at the Consumer Analyst Group of New York (CAGNY) conference on Thursday, Feb. 19, 2026 at 1:00 PM ET. Investors may access the live webcast and accompanying slide presentation on the Company's website at ir.iff.com. For those unable to listen to the live webcast, a recorded version will be made available for replay. Welcome to IFF At IFF (NYSE: IFF), we make joy through science, creativity and heart. As the global leader in flavors, fragrances, food ingredients, health and biosciences, we deliver groundbreaking, sustainable innovations that elevate everyday products—advancing wellness, delighting the senses and en
UAE Research Program for Rain Enhancement Science Announces Awardees of 6th Cycle Grants21.1.2026 21:17:00 CET | Press release
The UAE Research Program for Rain Enhancement Science (UAEREP), managed by the National Center of Meteorology (NCM), announced the awardees of its Sixth Cycle research grants. Each recipient will receive up to US$1.5 million over three years, with a maximum annual allocation of US$550,000. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260121231610/en/ UAE Research Program for Rain Enhancement Science Announces Awardees of 6th Cycle Grants (Photo: AETOSWire) The Sixth Cycle awardees are Dr. Dixon Michael, Principal Radar Meteorologist and Software Engineer at Echo Science Works, USA, for “Advancing Cloud Seeding Science with Dual-Polarization Radar Signatures and AI”; Prof. Linda Zou, Adjunct Professor at Victoria University, Australia, for “AI-assisted Development and Optimization of Glaciogenic Cloud Seeding Materials”; and Dr. Oliver Branch, Senior Scientist at the University of Hohenheim, Germany, for “Rainfall Enhanceme
Logical Intelligence Introduces First Energy-Based Reasoning AI Model, Signals Early Steps Toward AGI, Adds Yann LeCun and Patrick Hillmann to Leadership21.1.2026 19:21:00 CET | Press release
Logical Intelligence, an artificial intelligence company developing energy-based (EBM) reasoning systems, today announced that Kona 1.0, its pioneering EBM for reasoning, will enter pilot programs with select partners in the energy, advanced manufacturing, and semiconductor industries later this quarter. Logical Intelligence also released a live demonstration of Kona 1.0 on its website, beginning with head-to-head sudoku challenges against leading large language models. Additional demonstrations, including chess and Go, are planned. The company said the goal is to give researchers and the public a clear view into how energy-based reasoning differs from probabilistic systems. “Kona learns by recognizing and correcting its own mistakes, rather than guessing the most likely answer,” said Eve Bodnia, founder and CEO of Logical Intelligence. “If general intelligence means the ability to reason across domains, learn from error, and improve without being retrained for each task, then we are s
Galderma Provides Update on Arbitration Case Regarding Neuromodulator Research and Development Partnership21.1.2026 17:35:00 CET | Press release
Galderma (SIX:GALD), the pure-play dermatology category leader, today announced that an International Chamber of Commerce arbitral tribunal issued an award confirming the termination of a 2014 neuromodulator research & development partnership with Ipsen. The partnership was limited to the rights and obligations relating to the companies’ early-stage neuromodulator pipeline for aesthetic indications. Galderma welcomes the clarity provided by the arbitral tribunal. This decision has no impact on the commercialization of Galderma’s neuromodulator portfolio. Galderma will continue to commercialize and supply Dysport®/Azzalure®, Alluzience®, and RelfydessTM in all territories where it has regulatory approval and in accordance with our existing agreements with our partner Ipsen. Progressing on our path towards becoming the undisputed dermatology powerhouse Galderma remains focused on its ambition to become the world’s undisputed dermatology powerhouse across the full spectrum of a fast-growi
ThetaRay Appoints Financial Markets Technology Leader Brad Levy as Chief Executive Officer21.1.2026 17:00:00 CET | Press release
Former Symphony CEO to lead ThetaRay’s next phase of AI-driven category leadership in transaction monitoring and due diligence ThetaRay, a global leader in Cognitive AI financial crime compliance, today announced the appointment of Brad Levy as Chief Executive Officer. Levy, a leading financial markets infrastructure executive and former CEO of Symphony, will lead ThetaRay’s next phase of growth as the company continues to scale its Cognitive AI platform, now emerging as the leading AI strategy and technology for transaction monitoring and transaction due diligence, across banks and fintechs worldwide. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260121002476/en/ ThetaRay Appoints Brad Levy as CEO Levy brings decades of experience building and leading mission-critical financial infrastructure at scale. Most recently, he served as CEO of Symphony, the financial markets infrastructure and technology platform established by a
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
