Business Wire

Galderma Delivers Strong FY 2022 Growth Driven by Innovation and Commercial Performance

13.3.2023 09:00:00 EET | Business Wire | Press release

Share

Galderma:

Galderma delivered strong performance

  • Galderma delivered at the top end of its 2022 revenue guidance with 13.9% year-on-year net sales growth on a constant currency basis at 3,760 M USD and delivered above its 2022 profitability guidance with 14.5% Core EBITDA year-on-year growth on a constant currency basis at 791 M USD
    • Sustained growth momentum fueled by continued strong performance in Injectable Aesthetics and Dermatological Skincare with year-on-year net sales growth of 22.3% and 30.7% respectively, on a constant currency basis, primarily driven by volume growth
    • Topline growth and margin expansion demonstrate continued strong operating and commercial performance despite a challenging external environment

Significant progress in advancing the R&D pipeline with notable milestones for differentiated biologic entries expected to fuel significant long-term sustainable growth

  • Galderma completed three phase III clinical trials studying nemolizumab, a first-in-class investigational monoclonal antibody directed against the IL-31 receptor alpha with a central role in pruritus (itch) and skin inflammation, in the treatment of prurigo nodularis and atopic dermatitis
  • Galderma presented positive data from two phase III studies on RelabotulinumtoxinA (QM-1114), a novel liquid formulation botulinumtoxinA for the treatment of glabellar lines (frown) and lateral canthal lines (crow’s feet). As already announced, both studies met their primary endpoints and the results showed both rapid onset of action and long duration of action through to six months

Net sales growth and significant Core EBITDA margin expansion expected in 2023

  • In 2023, Galderma expects to deliver 6-9% net sales growth on a constant currency basis, and 200-300 bps Core EBITDA margin expansion (vs 2022). The 2023 Core EBITDA margin expansion guidance includes significant nemolizumab costs

 

“This has been a year of strong performance for Galderma. We have delivered against our full-year guidance and continued our upward growth trajectory against a backdrop of turbulent macro-economic conditions. We are delivering on our ambition of category leadership in dermatology, through our focus on commercial execution, portfolio and geographic expansion, our innovation pipeline and new product launches. I am pleased with our positive pipeline developments including RelabotulinumtoxinA, our novel liquid formulation botulinum toxin A, and nemolizumab, for the treatment of prurigo nodularis and atopic dermatitis. We look forward to continuing to deliver leading products to address the unmet needs of customers across the globe.

 

FLEMMING ØRNSKOV, M.D., MPH

CHIEF EXECUTIVE OFFICER

 

Financial and commercial update

With its premiumization strategy, Galderma is well positioned to capitalize on growing demand in its attractive, high growth consumer-driven markets. The growing and resilient nature of the dermatology market is underpinned by positive long-term trends and has shown to be recession-proof during periods of macro-economic and geopolitical turbulence.

In 2022, growth was driven by Injectable Aesthetics and Dermatological Skincare, with both product categories outperforming the market with double-digit growth, primarily driven by volume. This demonstrates the continued consumer demand for science-based, premium products in dermatology.

  • Injectable Aesthetics outperformed the market with double digit net sales growth and market share gains across the portfolio. Galderma’s net sales in Injectable Aesthetics grew by 22.3% year-on-year on a constant currency basis, driven by strong demand for neuromodulators and the launch of next generation neuromodulator Alluzience in Europe
  • Dermatological Skincare strongly outperformed the market, with net sales growth of 30.7% year-on-year on a constant currency basis (year-on-year growth on a constant currency basis of Dermatological Skincare excluding Alastin, consolidated as of FY 2022: +21.3%), fueled by increased consumer demand, new launches, channel expansion and particularly robust e-commerce performance
  • Therapeutic Dermatology, Galderma’s smallest product category by net sales, experienced a year-on-year net sales decline as Galderma navigated the anticipated annualization of Epiduo Forte and Soolantra loss of exclusivity in the U.S., increased patient access rebates, and greater competition, with the profit impact partially offset by royalties from authorized generics. This product category continued growing in Asia and Latin America

From a geographical perspective, Galderma’s larger region, International1, grew 20.2% year-on-year on a constant currency basis, with particularly strong performance in fast growing markets, such as in China, India, Brazil, Mexico, and the Philippines, with robust growth across all product categories. U.S. grew 6.8% year-on-year on a constant currency basis (+15.2% excluding the impact of loss of exclusivity in Therapeutic Dermatology) primarily driven by volume growth in Injectable Aesthetics and Dermatological Skincare.

Galderma delivered at the top end of its 2022 revenue guidance with 13.9% net sales year-on-year growth on a constant currency basis and exceeded its 2022 profitability guidance, delivering 14.5% Core EBITDA year-on-year growth on a constant currency basis, driven by sales growth, savings from the end-to-end transformation program and cost discipline despite the challenging inflationary environment. Galderma’s ongoing transformation program is delivering a leaner, fit-for-purpose and efficient corporate platform through optimized processes, upgraded systems and tools. In January 2023, Galderma announced the opening of a new Global Capability Center in Spain to centralize its commercial and certain support functions in a cost-efficient manner, which aims to create c.50 jobs in Barcelona in 2023.

Galderma is expanding its manufacturing footprint in response to growing global demand of its products. In October 2022, the Company announced its intention to expand its manufacturing and innovation footprint in the Asia-Pacific region, with support from the Singapore Economic Development Board. In addition, Galderma announced expansion with a new production site in Uppsala, Sweden to meet increasing global demand for its Injectable Aesthetic products.

ESG remains a core focus for Galderma, and it made further significant progress on developing its ESG profile during 2022, with its leadership in ESG emphasized by a reputable external ESG assessment, ranking it among the leading companies in its category.

Continued pipeline momentum and product launches

Throughout 2022, Galderma has continued its investment in scientific innovation. Galderma continues to demonstrate its best-in-class innovation capabilities: inventing, developing and bringing to market innovative dermatological solutions for consumers, patients, and healthcare professionals.

Therapeutic Dermatology

In Therapeutic Dermatology, Galderma celebrated many important achievements – most notably, the completion of three out of four phase III clinical trials studying nemolizumab in the treatment of prurigo nodularis and atopic dermatitis. The results of Galderma’s phase III nemolizumab programs show that nemolizumab, a first-in-class investigational monoclonal antibody directed against the IL-31 receptor alpha with a central role in pruritus (itch) and skin inflammation, has the potential to respond to significant unmet needs of patients with prurigo nodularis and atopic dermatitis.

Prurigo nodularis update

In June 2022, Galderma announced positive data from OLYMPIA 2, the first of two phase III trials, confirming the potential of nemolizumab as monotherapy in prurigo nodularis which was reconfirmed as Breakthrough Therapy by the U.S. Food and Drug Administration (FDA). Patients treated with nemolizumab monotherapy (without background topical corticosteroids or topical calcineurin inhibitors) showed clinically and statistically significant improvement in both primary endpoints of skin lesions and pruritus compared to placebo after 16 weeks of treatment. The trial also met all key secondary endpoints and confirmed early onset of action on itch, skin lesions and sleep disturbance. Nemolizumab demonstrated a favorable benefit-risk balance in this trial.

Galderma is on track to receive the results from its second clinical trial in prurigo nodularis, OLYMPIA 1 and plans to launch in the U.S. in H2 2024.

Atopic dermatitis update

Galderma also recently completed its ARCADIA program, which included two identical, pivotal phase III clinical trials and more than 1,700 patients. The trials evaluated the efficacy and safety of nemolizumab administered subcutaneously every four weeks, compared to placebo, in adolescent and adult patients with moderate to severe atopic dermatitis.

The two-phase III ARCADIA trials met all co-primary endpoints and key secondary endpoints, confirming nemolizumab, in combination with background topical therapy, improved skin lesions, pruritus and sleep disturbance.

Galderma is planning to present the results from these two trials to the scientific community at a congress later in 2023 and is on track to launch in the U.S. in H2 2024.

Acne and rosacea update

In the U.S., Galderma launched Twyneo®, the first and only tretinoin and benzoyl peroxide combination proven to treat moderate-to-severe acne and Epsolay®, the first and only microencapsulated benzoyl peroxide topical treatment proven to relieve the bumps and blemishes of rosacea.

The effectiveness of Galderma’s acne treatments is further demonstrated by sales data from IQVIA. The data, which is based on OTC and prescription treatment sales across 75 countries around the world, confirmed that Galderma’s range of anti-acne products is the number one choice globally. Galderma’s portfolio includes Differin®, Epiduo® Forte, Aklief®, Twyneo®, Actinica® and Benzac®.

Injectable Aesthetics

Data from the READY-1 and READY-2 phase III studies of RelabotulinumtoxinA (QM-1114) for the treatment of glabellar lines (frown) and lateral canthal lines (crow's feet) demonstrated high patient satisfaction and psychological well-being, in addition to previously reported safety and efficacy. Both studies met their primary endpoints, with significantly higher response than placebo after one month for both frown lines and crow's feet.

  • Results showed rapid onset of action, with 39% patients seeing results on Day 1 for frown lines and 34% on Day 1 for crow's feet
  • Results also demonstrated long duration of action through to six months
  • Treatment was well tolerated, with all treatment-related adverse events mild-to-moderate and non-serious

In October, Galderma announced a new pivotal study with data demonstrating the safety and effectiveness of Sculptra®, the only U.S. FDA-approved PLLA biostimulator, in the correction of cheek wrinkles, an investigational indication.

  • The data from its phase III randomized, controlled pivotal study showed long-lasting efficacy out to month 12, with a Galderma Cheek Wrinkle Scales (GCWS at rest) responder rate of 71.6% and improved skin radiance, tightness, and jawline contour (≥ 86%)
  • The treatment was considered safe and well tolerated in the study, with mostly mild and transient related adverse events resolving within two weeks

As highlighted at its H1 results in August 2022, Galderma also saw the launch of the neuromodulator, Alluzience®, in certain European countries as the first ready-to-use liquid form of botulinum toxin type A. In addition, Galderma presented phase IV data confirming the effectiveness and natural-looking effects with the Restylane® range of hyaluronic acid fillers, with all patients achieving the aim of their treatment, whether projection or contouring/volumization, with results that were natural-looking with high subject satisfaction.2

Dermatological Skincare

In 2022, Galderma demonstrated renewed commitment to innovation for consumers with sensitive skin. Galderma’s leading dermatologist-recommended brand, Cetaphil®, marked its 75th anniversary in 2022. Galderma’s latest initiatives, including its We Do Skin. You Do You campaign, aims to establish a new standard in clinical skincare testing to shift the dynamic of the industry, ensuring it is more representative of diverse skin tones. In addition, Galderma completed the rollout of the Cetaphil® Optimal Hydration range in Asia, comprising three new products powered by hyaluronic acid and exclusive HydroSensitivComplex to hydrate and improve sensitive skin.

Following the successful acquisition of Alastin Skincare in January 2022, Galderma has launched further products including most recently, A-LUMINATE BRIGHTENING SERUM®, designed to help reduce the appearance of surface hyperpigmentation without any harsh, irritating ingredients. ALASTIN’s proprietary PATH-3 Technology helps to minimize the recurrence of surface pigmentation and protect against future damage with continued use.

Galderma formed a global Sensitive Skincare Faculty in partnership with the Department of Dermatology at the George Washington University School of Medicine and Health Sciences. The faculty comprises 13 experts from across the world, representing diverse geographies. So far, two grants have been awarded to help people with sensitive skin live better lives.

Notes and references:

1.

Galderma reports revenue by two geographies: U.S. and International

2.

Nikolis A et al. Oral Presentation #114864 to be presented at IMCAS 2022.

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 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. 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 Dermatological Skincare. For more information: www.galderma.com.

Forward-looking statements

Certain statements in this announcement are forward-looking statements, including 2023 financial targets. Forward looking statements are statements that are not historical facts and may be identified by words such as "plans", "targets", "aims", " believes", "expects", "anticipates", "intends", "estimates", "will", "may", "continues", "should" and similar expressions. These forward-looking statements reflect, at the time, Galderma's beliefs, intentions and current targets/aims concerning, among other things, Galderma's results of operations, financial condition, industry, liquidity, prospects, growth and strategies and are subject to change. The estimated financial information is based on management's current expectations and is subject to change. By their nature, forward-looking statements involve a number of risks, uncertainties and assumptions that could cause actual results or events to differ materially from those expressed or implied by the forward-looking statements. These risks, uncertainties and assumptions could adversely affect the outcome and financial consequences of the plans and events described herein. Actual results may differ from those set forth in the forward-looking statements as a result of various factors (including, but not limited to, future global economic conditions, changed market conditions, intense competition in the markets in which Galderma operates, costs of compliance with applicable laws, regulations and standards, diverse political, legal, economic and other conditions affecting the Galderma's markets, and other factors beyond the control of Galderma). Neither Galderma nor its shareholders, directors, officers, employees, advisors, or any other person is under any obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise. You should not place undue reliance on forward-looking statements, which speak of the date of this announcement. Statements contained in this announcement regarding past trends or events should not be taken as a representation that such trends or events will continue in the future. Some of the information presented herein is based on statements by third parties, and no representation or warranty, express or implied, is made as to, and no reliance should be placed on, the fairness, reasonableness, accuracy, completeness or correctness of this information or any other information or opinions contained herein, for any purpose whatsoever.

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

Contact information

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

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

Emil Ivanov
Head of Strategy, Investor Relations, and ESG
emil.ivanov@galderma.com
+41 21 642 78 12

Jessica Cohen
Investor Relations and Strategy Director
jessica.cohen@galderma.com
+41 21 642 76 43

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

Agenus Announces Oversubscribed Private Placement of Up to $340 Million to Advance Registrational ROBBIN Trial of Neoadjuvant BOT+BAL in MSS Colon Cancer13.7.2026 13:00:00 EEST | Press release

Agenus Inc. (Nasdaq: AGEN), a leader in immuno-oncology innovation, today announced that it has entered into a securities purchase agreement for a private placement of approximately $85 million in upfront gross proceeds, before the deduction of private placement expenses, and up to an additional $255 million upon the full exercise of purchase warrants. The financing was led by Commodore Capital, with participation from RA Capital Management, TCGX, Invus, and Ligand Pharmaceuticals. The net proceeds of this financing are expected to support Agenus’ strategic prioritization of botensilimab and balstilimab (BOT+BAL) for the neoadjuvant treatment of microsatellite-stable (MSS) colon cancer, including advancement of ROBBIN1, the Company’s planned registrational Phase 3 neoadjuvant trial in microsatellite-stable (MSS) colon cancer. High-risk Stage II and Stage III MSS colon cancer affect an estimated 38,000 patients annually in the US and more than 200,000 patients worldwide,2 representing a

Zayed Sustainability Prize Closes 2027 Submissions with Strong Global Participation13.7.2026 12:48:00 EEST | Press release

The Zayed Sustainability Prize, the UAE’s pioneering award for innovative solutions to global challenges, has officially closed submissions for its 2027 awards cycle, receiving an unprecedented 10,233 entries from 177 countries across its six categories of Health, Food, Energy, Water, Climate Action and Global High Schools. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260713519403/en/ Zayed Sustainability Prize Closes 2027 Submissions with Strong Global Participation (Photo: AETOSWire) Now in its 18th year, the Prize continues to attract a diverse and growing pool of small and medium-sized enterprises, nonprofit organisations and high schools developing solutions that improve lives, particularly in vulnerable and underserved communities. This year’s submissions point to a growing emphasis on resilience, adaptability and systems-level impact. Across regions, applicants are addressing complex global challenges through practi

Ant Group Open-Sources SingGuard-NSFA to Establish New Security Paradigms for Autonomous AI Agents13.7.2026 12:01:00 EEST | Press release

Ant Group’s AI Security Lab today announced the open-source release of SingGuard-NSFA, a specialized security guardrail framework designed specifically for autonomous AI agents. The framework secures agentic AI systems against operational threats like prompt injection, addressing critical vulnerabilities as AI transitions from passive content generation to active, autonomous execution. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20260712722454/en/ As AI agents rapidly move from research labs to business scenarios, the security landscape has fundamentally shifted. The explosive global adoption of open-source agent frameworks like OpenClaw, celebrated for their "one-click deployment" and "full-stack autonomy", has simultaneously exposed significant operational risks, including permission escalation and prompt injection. Industry frameworks, including the OWASP (Open Web Application Security Project) Top 10 for Agentic Applica

Incyte Presents Phase 1/2 Multidose Data for VGA039 (Latarcibart) at ISTH 2026, Showing Substantial Bleed Reductions in Patients with all Von Willebrand Disease Types13.7.2026 11:00:00 EEST | Press release

Incyte (Nasdaq: INCY) today announced complete safety and efficacy data from all patients (n=16) enrolled in the Phase 1/2 multidose study of VGA039 (latarcibart), a novel, Protein S-targeting, investigational monoclonal antibody for patients with von Willebrand disease (VWD). The data are being shared in an oral presentation today at the 34th Congress of the International Society on Thrombosis and Haemostasis (ISTH 2026 Congress) in Paris. Latarcibart modulates Protein S to improve hemostasis, potentially enhancing the body’s ability to prevent or reduce the frequency of bleeding episodes. Latarcibart is in pivotal Phase 3 development for patients with VWD, the most common inherited bleeding disorder. If approved, latarcibart has the potential to be the first, once monthly subcutaneous prophylactic therapy for patients with VWD, offering an important alternative to the frequent intravenous infusions of replacement factor concentrates commonly used in the prophylactic setting today. Gi

Europe’s Demand for Tech Services Accelerates in Q2, As Spending on AI and Managed Services Rises: ISG Index™13.7.2026 11:00:00 EEST | Press release

Demand for technology services in Europe continued to accelerate in the second quarter, as the region increasingly turns to managed services to reduce costs and cloud services to meet AI objectives, according to the latest state-of-the-industry report from Information Services Group (ISG) (Nasdaq: III), a global AI-centered technology research and advisory firm. The EMEA ISG Index™, which measures commercial outsourcing contracts with annual contract value (ACV) of US $5 million or more, shows second-quarter ACV for the combined market (both managed services and cloud-based as-a-service) soared 46 percent—its largest growth in eight years—to US $13.0 billion. The latest quarter adds to a string of three straight quarters in which growth has averaged 33 percent. “Europe has become the fastest-growing region for technology services, fueled not only by an increasing demand for AI, but for managed services, which acts as a cost-savings lever to help fund AI ambitions and continued digital

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