Business Wire

GALDERMA Showcases Its Continued Commitment to Innovation in Dermatology With New Data to Be Presented at 2022 EADV Congress

Share

Galderma has announced it will be showcasing its latest scientific updates at the 31st European Academy of Dermatology and Venereology (EADV) congress in Milan, September 7-10, 2022. These include on-site clinical data presentations, a symposia series and booth activities, all focusing on serving patients by providing options across the Therapeutic Dermatology, Dermo-cosmetics and Injectable Aesthetics categories. As the pure-play dermatology leader, Galderma’s significant presence at EADV reaffirms its commitment to delivering a truly innovative, science-based portfolio of premium cutting-edge brands and services.

The latest science presented by Galderma at EADV reflects the company’s significant investments in research and development with large trials across multiple indications for severe conditions such as prurigo nodularis, atopic dermatitis, acne, rosacea, non-melanoma skin cancer and onychomycosis. For over 40 years, Galderma has solely focused on dermatology and has proven to be one of the few players capable of providing not only best-in-class product solutions but also first-in-class solutions with new innovative modes of action. Today, Galderma is a leading scientific voice in these disease areas and remains committed to delivering further advances for patients with these and other severe skin concerns.

One of the most awaited updates from the company this year will be a focus on IL-31, a neuroimmune cytokine that has been demonstrated to be a central mediator in prurigo nodularis and atopic dermatitis. The cytokine acts as a bridge between the immune and nervous systems and plays a crucial role in igniting and fueling the pathophysiological aspects, including itch and inflammation1,2. Two symposia and eight scientific posters will examine the disease burden, the role of IL-31 in these inflammatory skin conditions and treatments under development.

Another area of focus for Galderma will be on sensitive skin, which affects a major portion of the population with over 70% of women reporting suffering from its effects3. With its strong consumer skin range dedicated to sensitive skin including Cetaphil and the recent acquisition of Alastin Skincare, Galderma understands the need for specifically designed treatments and personalized skincare regimes. At the EADV this year, Galderma, along with key opinion leaders, will be challenging the existing paradigms on sensitive skin and challenging the community on whether it should be considered as a standalone skin condition.

Other skin conditions that drive patients to their dermatologist are acne, rosacea, actinic keratosis and non-melanoma skin cancer, conditions that affect a significant cross-section of society. Galderma has been researching these conditions and bringing innovative products to patients and consumers for decades. At EADV, the company will present new data and host scientific meetings and discussions to look at novel patient-centered, holistic approaches in each of these areas to support the identification of the best personalized treatment regimens for each patient.

Galderma’s significant presence at EADV this year reflects its expertise across these common and often severe skin conditions and is testament to its commitment to advancing dermatology for every skin story.

 

“We look forward to engaging with the dermatology community at the
EADV congress to exchange information, share insights and
showcase our recent developments and data spanning the full
spectrum of dermatology. This reinforces our enduring commitment to
understanding the needs of patients and consumers and developing
truly innovative dermatological solutions.”

 

BALDO SCASSELLATI SFORZOLINI, M.D.
GLOBAL HEAD OF RESEARCH & DEVELOPMENT, GALDERMA

 

Below is a full list of activities taking place.

Prurigo nodularis and atopic dermatitis

  • Thinking differently about atopic dermatitis: It’s time for a new perspective – September 9, 1:00 PM - 2:00 PM CEST (Room: AMBER 3 and 4). Chaired by Professor Diamant Thaçi (Germany) and featuring Professor Marjolein de Bruin-Weller (Netherlands) and Professor Andreas Wollenberg (Germany)
  • Navigating new data in prurigo nodularis: restoring hope for patients – September 10, 1:00 PM - 2:00 PM CEST (Room: CORAL 6). Chaired by Professor Sonja Ständer (Germany) and Professor Giampiero Girolomoni (Italy), and featuring Professor Doctor Shawn Kwatra (U.S.) and Professor Doctor Bernhard Homey (Germany)

Sensitive skin

  • Simplifying sensitive skin: can we define it as a standalone skin condition? September 7, 1:00 PM - 2:00 PM CEST (Room: CORAL 6). Chaired by Professor Giovanni Pellacani (Italy) and featuring Professor Adam Friedman (U.S.) and Doctor Krzysztof Piotrowski (Switzerland)

Acne

  • A novel patient-centered approach for acne management – September 8, 1:00 PM - 2:00 PM CEST (Room: CORAL 6). Co-chaired by Professor Alison Layton (UK) and Professor Doctor Jerry Tan (Canada), and featuring Doctor Vincenzo Bettoli (Italy)
  • Opportunities for a holistic approach to acne vulgaris management – September 9, 9:15 AM -10:00 AM CEST (Room: HUB 2.05). Featuring Professor Brigitte Dreno (France), Professor Gabriella Fabbrocini and Doctor Magda Belmontesi (Italy)
  • Acne update: Recent advances on skin microbiome, strain co-residence of C. acnes and treatment best practices – September 9, 4:00 PM - 4:45 PM CEST (Room: HUB 2.08). Featuring Professor Brigitte Dreno (France) and Professor Tami Lieberman (U.S.)

Rosacea

  • Clinical challenges in rosacea: overcoming obstacles on the road to treatment optimization – September 8, 6:00 PM - 7:30 PM CEST (Room: CORAL 6). Featuring Professor Doctor Giuseppe Micali (Italy), Professor Doctor Martin Schaller (Germany) and Professor Doctor Jerry Tan (Canada)

Actinic keratosis / non-melanoma skin cancer

  • An integrated approach for actinic keratosis and non-melanoma skin cancer management – September 8, 2:30 PM - 3:15 PM CEST (Room: HUB 2.03). Chaired by Professor Merete Haedersdal (Denmark) and featuring Professor Claas Ulrich (Germany) and Doctor Magda Belmontesi (Italy)
  • Beyond the lesion: Expert recommendations for longitudinal, patient-centered actinic keratosis management – September 9, 6:00 PM - 7:30 PM CEST (Room: AMBER 3 and 4). Co-chaired by Professor Rolf-Markus Szeimies (Germany) and Professor Colin Morton (UK) and featuring Professor Piergiacomo Calzavara-Pinton (Italy)
  • Personalizing Actinic Keratosis Treatment (PAKT): Expert recommendations to support patient-centered management of actinic keratosis (oral presentation) – September 10, 10:15 AM CEST (Room: BROWN 2, FC05: Free comms in cutaneous oncology and genetics). Featuring Professor Rolf-Markus Szeimies (Germany)

Onychomycosis

  • Onychomycosis update: Quantified penetration profile of topical amorolfine in infected human nails – September 8, 9:15 AM - 10:00 AM CEST (Room: HUB 2.01). Featuring Professor Martin Schaller (Germany)

A broad range of new scientific data posters has been accepted for EADV this year and can be provided upon request.

About Galderma
Galderma is the 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 through Injectable Aesthetics, Dermo-Cosmetics 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’re in shapes our lives, we are advancing dermatology for every skin story. Galderma’s portfolio of flagship brands includes Restylane, Dysport, Azzalure, Alluzience and Sculptra in Injectable Aesthetics; Soolantra, Epiduo, Differin, Aklief, Epsolay, Twyneo, Oracea, Metvix, Benzac and Loceryl in Therapeutic Dermatology; and Cetaphil and Alastin in Dermo-cosmetics. For more information: www.galderma.com.

References

1.Williams KA, Roh YS, Brown I, et al. Pathophysiology, diagnosis, and pharmacological treatment of prurigo nodularis. Expert Rev Clin Pharmakoi.2021;14(1):67-77. doi:10.1080/17512433.2021.1852080
2. Nemmer JM, Kuchner M, Datsi A, et al. Interleukin-31 signaling bridges the gap between immune cells, the nervous system and epithelial tissues. Front Med (Lausanne). 2021;8: 639097. doi:10.3389/fmed.2021.639097
3. Farage, Miranda A. “The Prevalence of Sensitive Skin.” US National Library of Medicine National Institutes of Health, www.ncbi.nlm.nih.gov/pmc/articles/PMC6533878.

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

Contact information

Christian Marcoux, M.Sc.
Chief Communications Officer
christian.marcoux@galderma.com
+41 76 315 26 50

Rachel Mooney
Global Franchise Communications
rachel.mooney@galderma.com
+41 76 261 64 41

Tracy Krumme
Global Head of Investor Relations
investors@galderma.com
+1-817-961-5530

Sébastien Cros
Corporate Communications Director
Sebastian.cros@galderma.com
+41 79 529 59 85

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

Kinaxis Positioned Highest on Ability to Execute in the Gartner® Magic Quadrant™ for Supply Chain Planning Solutions26.4.2024 19:03:00 EEST | Press release

Kinaxis® Inc. (TSX:KXS), a global leader in end-to-end supply chain orchestration, today announced it has been named a Leader in the 2024 Gartner® Magic Quadrant™ for Supply Chain Planning Solutions. Of the 20 vendors evaluated, Gartner positioned Kinaxis highest on Ability to Execute, marking the company’s 10th consecutive Leaders Quadrant within the report, a complimentary copy of which can be downloaded here. Kinaxis attributes its position to its patented concurrency approach and a proven track record of delivering innovative solutions against the foundation of its leading vision through the use of advanced technology such as AI, ML, and an intuitive user experience. Bolstered by a rich ecosystem of third-party implementation partners, Kinaxis continues to demonstrate that regardless of a customer’s industry, size, or maturity level, the company can be counted on to seamlessly orchestrate supply chain networks end-to-end from strategic planning to last-mile delivery. The recognitio

Vertex Announces European Commission Approval for KALYDECO® to Treat Infants With Cystic Fibrosis Ages 1 Month and Older26.4.2024 18:43:00 EEST | Press release

Vertex Pharmaceuticals (Nasdaq: VRTX) today announced that the European Commission has granted approval for the label expansion of KALYDECO® (ivacaftor) for the treatment of infants down to 1 month of age with cystic fibrosis (CF) who have one of the following mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: R117H, G551D, G1244E, G1349D, G178R, G551S, S1251N, S1255P, S549N or S549R. “Today’s approval is an important milestone for the cystic fibrosis community. Treating CF early in life can potentially slow the progression of the disease, which is why it is so important to start treatment from a very young age,” said Carmen Bozic, M.D., Executive Vice President, Global Medicines Development and Medical Affairs, and Chief Medical Officer, Vertex. As a result of existing access agreements in Austria, Czech Republic, Denmark, Ireland, Norway, Sweden, and The Netherlands, eligible patients will have access to the expanded indication of KALYDECO® (ivacaftor)

Suzano 2023 annual report on Form 20-F26.4.2024 18:22:00 EEST | Press release

Suzano S.A. (B3: SUZB3 | NYSE: SUZ) informs that its 2023 Annual Report on Form 20-F was filed today with the U.S. Securities and Exchange Commission. Holders of the Company’s equity securities can receive hard copies of the Annual Report, including its audited financial statements, without charge by request directed to: ri@suzano.com.br. This document is also available on Suzano’s website (http://ir.suzano.com.br/). For further information, please contact our Investor Relations Department: Phone: (+55 11) 3503-9330 E-mail: ri@suzano.com.br View source version on businesswire.com: https://www.businesswire.com/news/home/20240426289818/en/ Contact information Hawthorn Advisors suzano@hawthornadvisors.com

Takeda Receives Positive CHMP Opinion for Fruquintinib in Previously Treated Metastatic Colorectal Cancer26.4.2024 15:30:00 EEST | Press release

Takeda (TSE:4502/NYSE:TAK) today announced that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended the approval of fruquintinib, a selective inhibitor of vascular endothelial growth factor receptors (VEGFR) -1, -2 and -3 for the treatment of adult patients with previously treated metastatic colorectal cancer (mCRC). The European Commission (EC) will consider the CHMP positive opinion when determining the potential marketing authorization for fruquintinib for mCRC throughout the European Union (EU), Norway, Liechtenstein and Iceland. If approved, fruquintinib will be the first and only selective inhibitor of all three VEGF receptors approved in the EU for previously treated mCRC.1,2 “People living with metastatic colorectal cancer in the European Union currently have limited treatment options, which can lead to poor outcomes. With this positive opinion for fruquintinib, we are one step closer to potentially offering patients a new

MEDIA ALERT: Wolters Kluwer expert comments on European Parliament vote to pass amendment implementing Basel III reforms26.4.2024 15:00:00 EEST | Press release

The European financial landscape saw a milestone event this week, as the EU Parliament passed the Amendment to Regulation (EU) No 575/2013, implementing the Basel III finalization within Europe. This monumental step forward comes with the adoption of the Capital Requirements Regulation (CRR3) amendments, which are part of a broader legislative package, including amendments to Directive 2013/36/EU, known as the Capital Requirements Directive or CRD. Jeroen Van Doorsselaere, Vice President of Global Product & Platform Management, Wolters Kluwer FRR, said: “The adoption of the Capital Requirements Regulation (CRR3) amendments represents a landmark change for the banking industry, designed to strengthen the framework for risk-based capital requirements and address ESG risks. “This is a major overhaul of the capital requirements framework, impacting various aspects, including credit risk, operational risk, market risk, and the capital floor. Whereas other significant jurisdictions, includin

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
HiddenA line styled icon from Orion Icon Library.Eye