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Articles published by Galderma

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Galderma Announces Appointment of New Chief Financial Officer
From Galderma
Via Business Wire
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We Are All Sculptra: First-of-its-Kind Galderma Initiative to Demonstrate How Everyone Can Benefit from Sculptra’s Regenerative Properties
From Galderma
Via Business Wire
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Galderma Expands Restylane® Portfolio in Japan With Launch of OBT™ Hyaluronic Acid Injectables Restylane Defyne™ and Refyne™
From Galderma
Via Business Wire
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Galderma Announces U.S. FDA Acceptance of RelabotulinumtoxinA Biologics License Application Resubmission
From Galderma
Via Business Wire
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Galderma Tackles Menopause-related Skin Changes With Global Survey and Clinical Trial Inclusivity
From Galderma
Via Business Wire
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Galderma Unveils ‘Wake Up To Restylane’, Underscoring Restylane as the Ideal Hyaluronic Acid Treatment for Always-On Natural Beauty
From Galderma
Via Business Wire
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IMCAS 2026: Galderma Showcases the Latest Scientific Advances Behind the Industry’s Broadest Injectable Aesthetics Portfolio
From Galderma
Via Business Wire
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Galderma Provides Update on Arbitration Case Regarding Neuromodulator Research and Development Partnership
From Galderma
Via Business Wire
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TOXINS 2026: Clinical Updates on Galderma’s Leading Neuromodulator Portfolio Further Reinforce Its Leadership in Injectable Aesthetics
From Galderma
Via Business Wire
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New Published Data Confirms Nemluvio® (Nemolizumab) Can Rapidly Relieve Itch and Improve Sleep in as Early as Two Days in Both Atopic Dermatitis and Prurigo Nodularis
From Galderma
Via Business Wire
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Galderma Announces First Patient Enrollment in Study to Assess Nemolizumab in Adults With Chronic Pruritus of Unknown Origin
From Galderma
Via Business Wire
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Galderma Opens up New Chapter for Sculptra® with MDR Certification and New Expanded Indication for Body
From Galderma
Via Business Wire
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Galderma Secures ‘BBB’ Credit Rating With Positive Outlook from S&P Global Ratings
From Galderma
Via Business Wire
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ASDS 2025: Compelling New Data on Restylane, Sculptra and Relfydess Highlight Galderma’s Innovative Injectable Aesthetics Portfolio and Pipeline
From Galderma
Via Business Wire
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AMWC Dubai: Galderma Demonstrates Injectable Aesthetics Leadership Through Updates on Its Scientific Innovations and Community Education
From Galderma
Via Business Wire
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Galderma Launches Transformative Skincare Segment With Cetaphil’s New Skin Activator Hydrating & Firming Line, in Partnership With Actor and Filmmaker Mariska Hargitay
From Galderma
Via Business Wire
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EADV 2025: Galderma Reinforces Leadership in Dermatology With Latest Advances in Sensitive Skin and Itch
From Galderma
Via Business Wire
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Galderma Launches Alastin® in China, Supporting the Skin’s Natural Regenerative Abilities in a Rapidly Expanding Market
From Galderma
Via Business Wire
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Galderma Delivers Record First Half 2025 Net Sales of 2.448 Billion USD and 12.2% Year-on-Year Growth at Constant Currency, Raises Full-Year Top-Line Guidance
From Galderma
Via Business Wire
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Galderma Initiates Two New Clinical Trials Investigating Nemolizumab in Patients With Systemic Sclerosis and Chronic Pruritus of Unknown Origin
From Galderma
Via Business Wire
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ICD 2025: New data demonstrate Nemluvio®’s (nemolizumab) favorable safety profile and sustained and clinically meaningful improvements in symptoms of prurigo nodularis up to two years
From Galderma
Via Business Wire
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RAD 2025: Long-Term Data on Nemluvio® (nemolizumab) Demonstrate its Favorable Safety Profile and Sustained and Increased Improvements in Itch and Skin Lesions in Patients With Atopic Dermatitis up to Two Years
From Galderma
Via Business Wire
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Galderma Buys Back Shares Worth CHF 233 Million in the Context of Accelerated Bookbuild Offering
From Galderma
Via Business Wire
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Galderma Launches Sculptra® in China, Further Fueling Its Growth Into One of the Fastest Growing Aesthetics Markets
From Galderma
Via Business Wire
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Galderma’s Nemluvio® (Nemolizumab) Granted Marketing Authorization in the United Kingdom and Switzerland for Moderate-to-Severe Atopic Dermatitis and Prurigo Nodularis
From Galderma
Via Business Wire
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Galderma’s Nemluvio® (Nemolizumab) Approved in the European Union for Moderate-to-Severe Atopic Dermatitis and Prurigo Nodularis
From Galderma
Via Business Wire
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IMCAS 2025: New Galderma Phase IIIb Data Reinforce Rapid Onset and Long-lasting Aesthetic Improvement with RelabotulinumtoxinA (Relfydess™)
From Galderma
Via Business Wire
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Galderma Demonstrates Injectable Aesthetics Leadership in Medication-Driven Weight Loss With New Research and First International Consensus-Based Guidelines
From Galderma
Via Business Wire
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IMCAS 2025: Galderma’s Broad Presence and New Data on Recently Launched Products Restylane® SHAYPE™ and Relfydess® Reaffirm Its Category Leadership
From Galderma
Via Business Wire
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Galderma Premieres Positive Interim Results Demonstrating the Efficacy of Its Injectable Aesthetics Portfolio in Addressing Facial Volume Loss as a Result of Medication-driven Weight Loss
From Galderma
Via Business Wire
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