AAD 2026: Galderma Showcases Latest Evidence Supporting Its Full-Spectrum, Science-Driven Solutions for Diverse Skin Needs

Author of the article:You can save this article by registering for free here. Or sign-in if you have an account.Subscribe now to read the latest news in your city and across Canada.Subscribe now to read the latest news in your city and across Canada.Create an account or sign in to continue with your reading experience.Create an account or sign in to continue with your reading experience.ZUG, Switzerland — Galderma (SIX: GALD), the pure-play dermatology category leader, will present the latest updates on its innovations across its broad portfolio at the 2026 American Academy of Dermatology (AAD) Annual Meeting, taking place from March 27-31 in Denver, Colorado. Twenty-two abstracts will be presented, including late-breaking data and three oral presentations spanning Therapeutic Dermatology, Injectable Aesthetics, and Dermatological Skincare.Get the latest headlines, breaking news and columns.By signing up you consent to receive the above newsletter from Postmedia Network Inc.A welcome email is on its way. If you don't see it, please check your junk folder.The next issue of Top Stories will soon be in your inbox.We encountered an issue signing you up. Please try againInterested in more newsletters? Browse here.“Galderma is on a path towards becoming the undisputed dermatology powerhouse and, as such, aims to set the bar for scientific excellence in the field. The range of data we are presenting at AAD shows the strength of our commitment to this across every part of our portfolio. Patients deserve sophisticated, effective solutions that meet their diverse and evolving needs, and our science is built to deliver exactly that.”BALDO SCASSELLATI SFORZOLINI, M.D., PH.D.GLOBAL HEAD OF R&D AND CORPORATE DEVELOPMENTGALDERMAFour presentations on Nemluvio (nemolizumab), the first approved monoclonal antibody that specifically targets and inhibits the signaling of IL-31, will explore its efficacy and safety in different patient populations with moderate-to-severe atopic dermatitis.1-4,15-17 This includes a late-breaking presentation assessing the pharmacokinetics, safety and efficacy of nemolizumab in pediatric patients (aged 2 to 11 years) on Saturday, March 28 at 10:24-10:36 AM MDT / 5:24-5:36 PM CET in Bellco Theatre 3.1 Additionally, an oral presentation of post hoc data from the ARCADIA long-term extension trial, taking place on Saturday, March 28 at 2:10-2:15 PM MDT / 9:10-9:15 PM CET in Lobby C, Poster Center 2, will look at the long-term maintenance of itch and skin responses with Nemluvio up to 104 weeks.2 Two other posters will display data on Nemluvio’s long-term efficacy and safety up to two years in adolescents, and in patients with partial and minimal skin response at 16 weeks.3,4 Our product theater on Sunday, March 29 at 10:30-11:15 AM MDT / 6:30-7:15 PM CET in Theatre 1 will delve into the critical role of neuroimmune interactions in atopic dermatitis and prurigo nodularis, focusing on how targeted IL-31 treatment can improve patient outcomes.Galderma will also present four e-posters on AKLIEF (trifarotene) cream, showcasing decades of innovation behind four generations of retinoids, including fourth-generation trifarotene, its role in acne and skin health, and its molecular design.7,8 Real-world data will further evaluate its impact on acne outcomes and skin quality through personalized regimens and assess its efficacy and safety for facial and truncal acne in Indian patients.5,6Dermatological Skincare: Nine presentations spanning sensitive skin, acne, eczema-prone and mature skin Two oral presentations will be delivered at the congress: one exploring how high-risk factors for sensitive skin can be identified through artificial intelligence (Saturday March 28 at 1:05-1:10 PM MDT / 8:05-8:10 PM CET in Lobby C, Poster Center 2), and another to share results from a survey of dermatology practitioners on post-isotretinoin acne management (Sunday March 29 at 3:10-3:15 PM MDT / 11:10-11:15 PM CET in Lobby C, Poster Center 1).9,18 Five e-posters will investigate the properties of Galderma’s Cetaphil portfolio in different skin types, including the time to itch relief with Cetaphil Restoraderm Eczema Soothing Moisturizer and Restoraderm Eczema Rapid Relief Cream for patients with eczema-prone skin, its efficacy in mature and aging skin, its blendability with Sun Protection Factor across a range of skin tones, and the mildness of Cetaphil Gentle Skin Cleanser.19-21 Ahead of AAD, Galderma will host the Cetaphil Innovation Forum 2026 in collaboration with Galderma’s Global Sensitive Skincare Faculty bringing together healthcare professionals from around the globe to share how innovative biology-driven solutions, including AM/PM Serums and Skin Activator Hydrating & Firming Line, can improve skin health by mitigating two key biological drivers of skin aging: oxidative stress and cellular senescence. Together, these strategies support a broader vision of skin longevity and resilience over time.Five e-posters will share the latest development updates from Galderma’s injectable aesthetics portfolio, including data:More details on Galderma’s scientific presentations at AAD can be found here.Galderma (SIX: GALD) 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, 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.Indication: AKLIEF® (trifarotene) cream, 0.005% is a retinoid indicated for the topical treatment of acne vulgaris in patients 9 years of age and older. Adverse Events: The most common adverse reactions (incidence ≥ 1%) in patients treated with AKLIEF cream were application site irritation, application site pruritus (itching), and sunburn.Warnings/Precautions: Patients using AKLIEF Cream may experience erythema, scaling, dryness, and stinging/burning. Use a moisturizer from the initiation of treatment, and, if appropriate, depending upon the severity of these adverse reactions, reduce the frequency of application of AKLIEF Cream, suspend or discontinue use. Avoid application of AKLIEF Cream to cuts, abrasions or eczematous or sunburned skin. Use of “waxing” as a depilatory method should be avoided on skin treated with AKLIEF Cream. Minimize exposure to sunlight and sunlamps. Use sunscreen and protective clothing over treated areas when exposure cannot be avoided.You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088.Indications: NEMLUVIO® (nemolizumab-ilto) is an interleukin-31 receptor alpha antagonist indicated for: • the treatment of adults and pediatric patients 12 years of age and older with moderate-to-severe atopic dermatitis in combination with topical corticosteroids and/or calcineurin inhibitors when the disease is not adequately controlled with topical prescription therapies. • the treatment of adults with prurigo nodularis. Contraindication: Known hypersensitivity to nemolizumab-ilto or to any of the excipients in NEMLUVIO. Warnings/Precautions: Hypersensitivity reactions have been reported with NEMLUVIO use. If a clinically significant hypersensitivity reaction occurs, immediately institute appropriate therapy, and discontinue NEMLUVIO. Avoid use of live vaccines during treatment with NEMLUVIO. Adverse Events: Most common adverse reactions (incidence ≥1%) are: • Atopic Dermatitis: headache (including migraine), arthralgia, urticaria, and myalgia. • Prurigo Nodularis: headache, dermatitis atopic, eczema, and eczema nummular. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. Please see full Prescribing Information including Patient Information. https://www.businesswire.com/news/home/20260323553707/en/ContactsChristian Marcoux, M.Sc.

Chief Communications Officer christian.marcoux@galderma.com +41 76 315 26 50Richard Harbinson Corporate Communications Director richard.harbinson@galderma.com +41 76 210 60 62Céline Buguet Franchises and R&D Communications Director celine.buguet@galderma.com +41 76 249 90 87Emil Ivanov Head of Strategy, Investor Relations, and ESG emil.ivanov@galderma.com +41 21 642 78 12Jessica Cohen Investor Relations and Strategy Director jessica.cohen@galderma.com +41 21 642 76 43#distroPostmedia is committed to maintaining a lively but civil forum for discussion. Please keep comments relevant and respectful. Comments may take up to an hour to appear on the site. You will receive an email if there is a reply to your comment, an update to a thread you follow or if a user you follow comments. Visit our Community Guidelines for more information.