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

BeOne Medicines’ BEQALZI™ (sonrotoclax) Approved by U.S. FDA as First and Only BCL2 Inhibitor for R/R Mantle Cell Lymphoma13.5.2026 19:27:00 CEST | Press release

BEQALZI is a foundational BCL2 inhibitor designed for greater potency and selectivity, with potential to improve efficacy, tolerability, and convenience versus others in the classApproval of BEQALZI marks the first new BCL2 inhibitor approved in a decade in the U.S. and the only BCL2 inhibitor approved in MCL, aiming to set a new standard of innovation BeOne Medicines Ltd. (“BeOne”) (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced that the U.S. Food and Drug Administration (FDA) has granted accelerated approval to BEQALZI™(bee-KAHL-zee; sonrotoclax), a foundational, next-generation BCL2 inhibitor, for the treatment of adult patients with relapsed or refractory (R/R) mantle cell lymphoma (MCL), after at least two lines of systemic therapy, including a Bruton’s tyrosine kinase (BTK) inhibitor. BEQALZI was designed to enhance BCL2 inhibition—with greater potency, selectivity, and a pharmacologic profile with potential to improve efficacy, tolerability, a

Boomi Unveils Innovations That Power the Agentic Enterprise13.5.2026 16:30:00 CEST | Press release

Orchestration capabilities simplify workflows, while advanced agent connectivity and an enhanced context layer activate data and scale AI Boomi, the data activation company for AI, today announced a major expansion of the Boomi Enterprise Platform at Boomi World 2026, introducing new capabilities across orchestrated agentic workflows, agentic engineering, governed agent connectivity, grounded agent context, and localized agent infrastructure. Together, these innovations are designed to power the agentic enterprise — where agents and humans work together to drive action and operationalize AI at scale. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260513996223/en/ Boomi Unveils Innovations That Power the Agentic Enterprise The enterprise has reached a defining moment as AI becomes the primary interface for work and MCP emerges as the new standard. While the shift toward a headless, agentic enterprise is inevitable, this visio

Boomi and Red Hat Collaborate on Production-Ready Agentic AI13.5.2026 16:30:00 CEST | Press release

Companies team to deliver a unified, enterprise-scale agentic stack to help organizations with managing data sovereignty and optimizing AI costs Boomi, the data activation company for AI, and Red Hat, the world’s leading provider of open source solutions, today announced a strategic collaboration to deliver a single, integrated stack for deploying agentic AI at scale. For many organizations, building production AI today means assembling numerous disconnected vendor choices spanning agent builders, orchestration tools, governance platforms, model providers, integration middleware, and security infrastructure, which can lead to data leaks and unpredictable costs. Boomi and Red Hat are working together to simplify AI innovation for customers by bringing together Boomi’s Agentstudio with the enterprise-grade power of Red Hat AI. This makes it easier for organizations to build agents that solve real business problems while supporting corporate standards for sovereignty, infrastructure flexi

Boomi and Couchbase Partner to Power Enterprise AI Agents with Trusted Recollection, Connectivity, and Governance13.5.2026 16:30:00 CEST | Press release

Partnership enables customers to accelerate AI agents from pilot to production with accuracy, performance, and control by combining Boomi's connectivity, agent runtime, and governance with Couchbase's operational data platform Boomi, the data activation company for AI, and Couchbase, Inc., the operational data platform for AI, today announced a partnership through which the two companies are collaborating closely to accelerate AI pilots to production. The companies will co-engineer solutions that give customers a production-ready foundation for agentic AI, combining Boomi's connectivity, runtime, and governance for AI agents with Couchbase's scalable recollection and vector capabilities. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260513350337/en/ Enterprises deploying AI agents today face a common challenge: while agents perform well in pilots, they struggle to scale due to inconsistent access to trusted context, recolle

Lenovo Named a Leader and Star Performer in Mid-Market Digital Workplace Solutions Assessment by Everest Group13.5.2026 15:00:00 CEST | Press release

One of only two Star Performers, Lenovo was recognized for helping mid-market CIOs with cost reduction, faster onboarding, productivity gains Lenovo’s ability to help mid‑market organizations reduce IT support costs, accelerate time-to-value, and improve workforce productivity at scale has earned recognition as a Leader and Star Performer in Everest Group’s 2026 Digital Workplace Services PEAK Matrix® Assessment for Mid‑Market Enterprises. Lenovo’s Digital Workplace Solutions (DWS) enable customers to improve speed, cut costs, and elevate employee experiences, helping new employees reach productivity up to 50% faster, increasing employee satisfaction by 30%, lowering end-user support costs by up to 30%, and proactively resolving up to 40% of issues to minimize downtime and business disruption1. Lenovo delivers these results by uniquely integrating device, services, and intelligence into a single, scalable delivery model built for the mid‑market. Through lifecycle services delivered at

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