Galderma Launches New Alastin Regenerating Skin Nectar with TriHex+™, Powered by Its Next-Generation TriHex Technology® Regenerative Platform
16.4.2026 07:00:00 CEST | Business Wire | Press release
Regenerating Skin Nectar has long played a central role in the peri-procedural skin journey as part of Alastin’s dedicated procedure support portfolio, enhancing the body’s natural processes for removing damaged collagen and elastin while creating an optimal environment for new, healthy collagen and elastin production — visibly improving how the skin prepares for, responds to, and recovers from procedures. With the addition of our proprietary Octapeptide‑45, Regenerating Skin Nectar with TriHex+™ introduces an advanced formulation that builds on the original Tri-Hex Technology® foundation, while further supporting the skin’s natural production of new collagen, elastin, and high‑molecular‑weight hyaluronic acid (HA).1 The new formulation also helps reinforce skin structure, restore skin barrier, and support long-term skin longevity. This innovation underscores Galderma’s commitment to advancing peri-procedural skincare and empowering providers with science-based solutions designed to deliver exceptional aesthetic and procedural outcomes.
Galderma (SIX: GALD), the pure-play dermatology category leader, today announced the launch of Regenerating Skin Nectar with TriHex+™, the newest innovation from Alastin, a leader in peptide-based regenerative skincare.
As a pioneer in peri‑procedural skincare, Alastin helped establish the category with the original Regenerating Skin Nectar — one of the first products specifically developed to prepare the skin before cosmetic procedures, complement procedural outcomes, and visibly support a smoother, accelerated recovery.
For more than a decade, it has served as a foundational peri-procedural product used by aesthetic providers to improve skin readiness and enhance treatment response. Today, among physicians who offer the brand, Alastin is their preferred peri-procedural skincare choice, and it remains the only product in this category with published clinical data demonstrating the benefits of preconditioning the skin prior to a procedure.
The new and enhanced Regenerating Skin Nectar with TriHex+™ builds on this foundation with an advanced formulation designed to help visibly improve how the skin prepares for, responds to, and recovers from procedures. It complements a broad range of aesthetic and surgical procedures such as facelifts, microneedling, laser resurfacing, chemical peels, and radiofrequency ablation, among others.
Regenerating Skin Nectar with TriHex+™ is the second product to feature the next-generation TriHex+™ platform, following the successful launch of Restorative Skin Complex with TriHex+™. TriHex Technology® uniquely combines proprietary peptide components that help clear aged, damaged collagen and elastin while simultaneously supporting the production of new, healthy collagen and elastin — a dual mechanism that underpins its regenerative approach. TriHex+™ is the next evolution of this technology. The addition of proprietary Octapeptide‑45 advances this activity by supporting the skin’s natural production of high‑molecular‑weight HA, a critical component of skin structure and resilience, and working synergistically with TriHex Technology® to further enhance production of collagen, elastin, and HA. This reinforces the skin’s underlying structural integrity, including the dermal-epidermal junction (DEJ), and supports the skin’s response to procedural stress in ways that contribute to more consistent outcomes and long-term skin longevity.
“Galderma continues to deepen the understanding of extracellular matrix remodeling, which is now recognized as a key driver of skin aging and longevity. Our new TriHex+™ formulation represents the evolution of our regenerative platform, focusing on key proteins and membranes that influence how the skin responds to procedural stress at a structural level. This innovation reflects our continued commitment to developing science-driven solutions that not only aid in procedural outcomes, but also support a more resilient skin recovery.”
ALAN D. WIDGEROW, MBBCH, MMED, FCS, FACS CHIEF SCIENTIFIC OFFICER, GALDERMA HEAD, SKIN SCIENCE CENTER FOR INNOVATION
|
Peer-reviewed clinical studies support the use of Regenerating Skin Nectar with TriHex+™ as a foundational peri‑procedural product. In a randomized, double‑blind facelift pre‑conditioning study, 100% of patients showed visible improvements in key extracellular matrix (ECM) markers—including collagen, elastin, and high‑molecular‑weight HA—alongside reductions in solar elastosis and a stronger, more defined DEJ.2 The improvement in DEJ definition is clinically meaningful, as DEJ integrity helps skin better withstand mechanical and thermal stress during procedures.3,4 Additional evaluations demonstrated statistically significant improvements in skin barrier function as early as 30 minutes post-application, with continued improvement through day 14, alongside increased skin hydration observed from day 3.² Clinical grading and photography showed visibly improved healing responses, including reduced appearance of erythema (redness), edema (swelling), and crusting. Split‑face microneedling evaluations also demonstrated improved tolerability compared with exosome-based products.5 These findings reinforce the role of peri-procedural skincare in optimizing overall treatment outcomes.
The formulation is water-free, preservative-free, and bacteriostatic, allowing for use immediately following procedures. This enables early integration into post-procedure care when the skin is most vulnerable and requires products that will not irritate or disrupt healing.
“In my practice, patients are looking for treatments that deliver strong results while minimizing downtime. Alastin Regenerating Skin Nectar has helped support that balance by preparing the skin ahead of procedures, visibly improving how it responds during treatment, and promoting a more efficient recovery afterward. With TriHex+™, the clinical data demonstrates it supports advanced improvements in hydration, barrier function, and recovery response — factors I prioritize to help deliver more consistent, high-quality outcomes for my patients.”
NAZANIN SAEDI, MD BOARD-CERTIFIED DERMATOLOGIST DERMATOLOGY ASSOCIATES OF PLYMOUTH MEETING
|
Galderma will launch Regenerating Skin Nectar with TriHex+™ in the United States this month. For an extended initial period, the product will be available exclusively through authorized Alastin skincare providers and dispensed directly through medical aesthetic practices, including dermatology and plastic surgery offices, and medical spas. Galderma is working to expand availability to additional international markets where Alastin is present.
About Alastin
Alastin by Galderma is the leader in peri-procedural regenerative skincare, offering innovative, scientifically proven, and clinically tested products. The Alastin Skincare portfolio provides a comprehensive collection of cutting-edge formulas designed specifically for peri-procedural use, as well as daily skincare regimens, all powered by proprietary peptides and innovative, clinically meaningful, science-backed ingredients designed to amplify the skin’s own natural regenerative abilities. With more than 60 international dermatological publications and 20 patents granted, Alastin is one of the most clinically studied professional-grade skincare brands.
About Galderma
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.
References
- Widgerow AD, et al. J Drugs Dermatol. 2024 May 1;23(5):347-352.
- Jalian HR, et al. J Cosmet Dermatol. 2025;24(12):e70556.
- Roig-Rosello E, Rousselle P. Biomolecules. 2020;10:1607.
- Fisher G, Rittié L. J Cell Commun Signal. 2018;12:401–411.
- Widgerow AD, Ziegler ME, Shafiq F, et al. J Dermat Cosmetol. 2024;8(3):87–92.
View source version on businesswire.com: https://www.businesswire.com/news/home/20260415545576/en/
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
Fourthline Trust Services Granted Status as Qualified Trust Service Provider in the EU24.8.2026 15:13:00 CEST | Press release
QTSP status allows for full control over the digital trust value chain from identity verification to qualified electronic signature (QES) issuance Fourthline Trust Services AB, a subsidiary of Fourthline, has been granted qualified status under the EU's eIDAS Regulation (910/2014)¹ and is now listed on the EU Trusted List as a Qualified Trust Service Provider (QTSP). Supervised by the Swedish Post and Telecom Authority (Post- och telestyrelsen, PTS), Fourthline Trust Services AB issues qualified certificates for electronic signatures. Fourthline, is the leading European provider of AI-powered identity verification (IDV) and compliance solutions. This milestone allows Fourthline full control over the entire digital trust value chain from identity verification to qualified electronic signature (QES) issuance. Ralph Post, Fourthline Trust Services AB Board Member: "By building our QTSP infrastructure similar to our sovereign AI-powered platform that drives our industry-leading identity ve
SLB Launches ExaCT Electrical Downhole CT Control System24.8.2026 13:02:00 CEST | Press release
New platform brings real-time electrical control to coiled tubing intervention, enabling greater precision, visibility and efficiency across intervention operations SLB (NYSE: SLB) today launched the ExaCT™ electrical downhole coiled tubing (CT) control system, an advanced intervention platform that introduces real-time electrical control to coiled tubing operations. By replacing pressure-dependent hydraulic actuation with electrical communication, power delivery and telemetry, the ExaCT system gives operators greater visibility, precision and control, helping improve intervention execution and reservoir access. The ExaCT system combines electrical power, telemetry and downhole measurements to enable communication with, actuation of and verification of downhole tools throughout an intervention. Continuous communication across the toolstring enables on-demand tool actuation across a wide range of intervention applications, including extended-reach and multilateral wells. The increased p
Wolters Kluwer Transforms Trusted Legal Content Into Structured, AI-Ready Intelligence That Powers the Next Wave of Legal AI24.8.2026 13:01:00 CEST | Press release
By transforming authoritative legal content into structured legal intelligence, Wolters Kluwer gives AI the context and relationships needed to deliver deeper research and higher-quality results Wolters KluwerLegal & Regulatory today announced the next evolution of Libra by Wolters Kluwer, its all-in-one Legal AI Workspace. By transforming authoritative legal sources, expert commentaries, and practical guidance into structured legal intelligence, Wolters Kluwer is making the relationships across the full breadth of its expert legal sources more explicit. This will enable deeper contextual research, more comprehensible answers, and workflow-ready results across legal work. Following the integration of Wolters Kluwer content into the Libra AI workspace in the first half of 2026, laws, rulings, expert commentaries, and practical guidance will now be linked to one another and to the matter at hand, creating a connected knowledge graph of expert-curated and authoredlegal knowledge that AI c
Daiichi Sankyo Appoints Markus Kosch to Lead Europe Business as Part of New Commercialization Organization24.8.2026 10:00:00 CEST | Press release
Daiichi Sankyo (TSE: 4568) today announced the appointment of Markus Kosch, MD, as Head of Europe Business, effective April 1, 2027. In this role, he will lead the company's European business within the new globally integrated Commercialization Unit and serve as General Manager of Daiichi Sankyo Europe GmbH, with legal responsibility for the company in Europe. The appointment reflects the next phase of growth of Daiichi Sankyo under its Five-Year Business Plan and the establishment of a new Commercialization Unit. Within this new structure, Markus Kosch will bring together the Oncology and Specialty businesses in Europe under one integrated leadership model to help bring innovative medicines to more patients across the region. For the past five years, Markus Kosch has led the Daiichi Sankyo Oncology Business Division in Europe and Canada, overseeing a period of significant growth and preparing the organization for an increasingly expanding oncology portfolio. Prior to joining Daiichi S
European Commission Approves DAYBU® (trofinetide) as the First and Only Treatment for Neurobehavioral Symptoms of Rett Syndrome in the European Union24.8.2026 09:01:00 CEST | Press release
Acadia Pharmaceuticals Inc. (Nasdaq: ACAD) today announced that the European Commission (EC) has granted marketing authorization for DAYBU (trofinetide) for the treatment of neurobehavioral symptoms of Rett syndrome in adults and pediatric patients aged five years and older, making it the first and only treatment approved for Rett syndrome in the European Union (EU). “The approval of DAYBU marks a significant milestone for the Rett syndrome community in the EU and advances our mission to bring this innovative treatment to patients and families who have long faced a profound unmet medical need,” said Catherine Owen Adams, Acadia’s Chief Executive Officer. “For people living with Rett syndrome, a devastating rare neurodevelopmental disorder, there have been no approved treatment options in the EU. We are proud to make DAYBU available and look forward to supporting patients, caregivers, and healthcare providers gain access to treatment." The DAYBU marketing authorization in the EU is prim
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