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Niagen Bioscience (NASDAQ: NAGE) has published groundbreaking clinical study results in Aging Cell, demonstrating the efficacy of their patented nicotinamide riboside (NR) ingredient, Niagen®, in treating Werner syndrome (WS), a rare genetic aging disorder. The 52-week randomized, double-blind, placebo-controlled crossover trial showed that daily 1,000mg Niagen supplementation increased NAD+ levels by approximately 140% and improved cardiovascular and skin health markers.

Key findings include improved arterial stiffness, beneficial changes in HDL particles, and reduced skin ulcer size. The study involved nine individuals with WS, with no moderate or severe adverse events reported. This research expands Niagen's rare disease portfolio, which includes promising results in Ataxia Telangiectasia (AT), where the FDA has granted both Orphan Drug Designation and Rare Pediatric Disease Designation.

Niagen Bioscience (NASDAQ: NAGE) ha pubblicato risultati innovativi di uno studio clinico su Aging Cell, dimostrando l'efficacia del loro ingrediente brevettato nicotinamide riboside (NR), Niagen®, nel trattamento della sindrome di Werner (WS), una rara malattia genetica legata all'invecchiamento. Il trial randomizzato, in doppio cieco, controllato con placebo e crossover della durata di 52 settimane ha mostrato che l'assunzione quotidiana di 1.000 mg di Niagen ha aumentato i livelli di NAD+ di circa il 140% e migliorato i parametri di salute cardiovascolare e cutanea.

I risultati principali includono un miglioramento della rigidità arteriosa, cambiamenti positivi nelle particelle HDL e una riduzione delle dimensioni delle ulcere cutanee. Lo studio ha coinvolto nove persone con WS, senza riportare eventi avversi moderati o gravi. Questa ricerca amplia il portafoglio di malattie rare di Niagen, che include risultati promettenti nell'Atassia Telangiectasia (AT), per la quale la FDA ha concesso sia la Designazione di Farmaco Orfano che quella di Malattia Pediatrica Rara.

Niagen Bioscience (NASDAQ: NAGE) ha publicado resultados revolucionarios de un estudio clínico en Aging Cell, demostrando la eficacia de su ingrediente patentado nicotinamida ribósido (NR), Niagen®, en el tratamiento del síndrome de Werner (WS), un raro trastorno genético relacionado con el envejecimiento. El ensayo aleatorizado, doble ciego, controlado con placebo y cruzado de 52 semanas mostró que la suplementación diaria con 1,000 mg de Niagen incrementó los niveles de NAD+ aproximadamente en un 140% y mejoró los marcadores de salud cardiovascular y cutánea.

Los hallazgos clave incluyen una mejora en la rigidez arterial, cambios beneficiosos en las partículas HDL y una reducción en el tamaño de las úlceras cutáneas. El estudio incluyó a nueve personas con WS, sin reportar eventos adversos moderados o graves. Esta investigación amplía el portafolio de enfermedades raras de Niagen, que incluye resultados prometedores en Ataxia Telangiectasia (AT), para la cual la FDA ha otorgado tanto la Designación de Medicamento Huérfano como la de Enfermedad Pediátrica Rara.

Niagen Bioscience (NASDAQ: NAGE)� Aging Cell� 획기적인 임상 연구 결과� 발표하며, 특허받은 니코틴아마이� 리보사이�(NR) 성분� Niagen®� 희귀 유전� 노화 질환� 베르� 증후�(WS) 치료� 효과적임� 입증했습니다. 52주간 진행� 무작� 배정, 이중맹검, 위약 대� 교차 시험에서 매일 1,000mg� Niagen 보충� NAD+ 수치� � 140% 증가시키� 심혈관 � 피부 건강 지표를 개선하는 것으� 나타났습니다.

주요 결과로는 동맥 경직� 개선, HDL 입자� 유익� 변�, 피부 궤양 크기 감소가 포함되며, WS 환자 9명이 참여했으� 중등� 또는 중증 부작용은 보고되지 않았습니�. � 연구� Niagen� 희귀 질환 포트폴리오를 확장하며, FDA가 희귀 소아 질환 지정과 희귀 의약� 지정을 부여한 운동실조� 모세혈관 확장�(AT)에서� 유망� 결과� 포함하고 있습니다.

Niagen Bioscience (NASDAQ : NAGE) a publié des résultats cliniques révolutionnaires dans Aging Cell, démontrant l'efficacité de leur ingrédient breveté nicotinamide riboside (NR), Niagen®, dans le traitement du syndrome de Werner (WS), une maladie génétique rare liée au vieillissement. L'essai randomisé, en double aveugle, contrôlé par placebo en crossover sur 52 semaines a montré qu'une supplémentation quotidienne de 1 000 mg de Niagen augmentait les niveaux de NAD+ d'environ 140% et améliorait les marqueurs de santé cardiovasculaire et cutanée.

Les résultats clés incluent une amélioration de la rigidité artérielle, des modifications bénéfiques des particules HDL et une réduction de la taille des ulcères cutanés. L'étude a impliqué neuf personnes atteintes de WS, sans événements indésirables modérés ou graves signalés. Cette recherche élargit le portefeuille de maladies rares de Niagen, qui comprend des résultats prometteurs dans l'ataxie télangiectasie (AT), pour laquelle la FDA a accordé à la fois la désignation de médicament orphelin et celle de maladie pédiatrique rare.

Niagen Bioscience (NASDAQ: NAGE) hat bahnbrechende klinische Studienergebnisse in Aging Cell veröffentlicht, die die Wirksamkeit ihres patentierten Nicotinamid-Ribosid (NR)-Bestandteils Niagen® bei der Behandlung des Werner-Syndroms (WS), einer seltenen genetischen Alterskrankheit, demonstrieren. Die 52-wöchige randomisierte, doppelblinde, placebokontrollierte Crossover-Studie zeigte, dass die tägliche Einnahme von 1.000 mg Niagen die NAD+-Spiegel um etwa 140% steigerte und die kardiovaskulären sowie Hautgesundheitsmarker verbesserte.

Wesentliche Ergebnisse umfassen eine verbesserte arterielle Steifigkeit, positive Veränderungen der HDL-Partikel und eine Verringerung der Hautgeschwürgröße. An der Studie nahmen neun Personen mit WS teil, ohne dass moderate oder schwere Nebenwirkungen auftraten. Diese Forschung erweitert das Portfolio seltener Erkrankungen von Niagen, zu dem auch vielversprechende Ergebnisse bei Ataxia Telangiectasia (AT) gehören, für die die FDA sowohl die Orphan-Drug- als auch die Rare Pediatric Disease-Designation vergeben hat.

Positive
  • Clinical trial demonstrated ~140% increase in plasma NAD+ levels vs. placebo
  • Significant improvements in cardiovascular markers and skin health
  • FDA granted Orphan Drug and Rare Pediatric Disease Designations for Ataxia Telangiectasia
  • Strong safety profile with fewer adverse events in treatment group vs. placebo
  • Successful expansion into rare disease therapeutic applications
Negative
  • Small trial size with only 9 participants limits statistical significance
  • Mild liver enzyme elevations noted in some participants

Results demonstrated that nicotinamide riboside (NR) significantly elevated NAD+ levels and improved multiple clinical markers in people with Werner Syndrome

Niagen Bioscience expands rare disease research portfolio, supporting further investigation of NAD+ augmentation with NR as a therapeutic strategy in rare progeroid diseases

LOS ANGELES--(BUSINESS WIRE)-- (NASDAQ: NAGE) (formerly ChromaDex Corp.), the global authority on NAD+ (nicotinamide adenine dinucleotide) with a focus on the science of healthy aging, shares positive results from a clinical study published in the peer-reviewed journal Aging Cell, by a team led by Masaya Koshizaka, M.D., Ph.D., Associate Professor, and Koutaro Yokote, M.D., Ph.D., MBA, President of Chiba University, both of the Center for Preventive Medical Sciences, Chiba University, and the Department of Diabetes, Metabolism and Endocrinology, Chiba University Hospital, Japan. This is the first study to demonstrate the safety and efficacy of Niagen Bioscience’s patented nicotinamide riboside (NR) ingredient, Niagen®, in individuals with Werner syndrome (WS), a rare genetic disorder marked by rapid aging and premature mortality.

The newly published double-blind, placebo-controlled study found that daily supplementation with Niagen significantly elevated blood NAD+ levels by approximately 140% and improved multiple clinical markers of cardiovascular and skin health in individuals with WS. Affecting approximately 1 in 380,000 to 1 in 1,000,000 people globally (), Werner syndrome is caused by mutations that impair DNA repair, leading to cellular aging decades ahead of normal progression.

Dr. Koshizaka noted, “We hope our work will accelerate studies on not only WS but also other premature aging disorders and common age-related diseases—ultimately helping to extend health span and improve quality of life in both patients and the broader population.�

Developing NAD+ Therapies for Rare, Age-Related Diseases

This study builds on the growing body of clinical research demonstrating Niagen’s potential in rare, age-related diseases (see Table 1 below). In Ataxia Telangiectasia (AT), Niagen has shown improvements in neurological function, coordination, and immune markers, including in pediatric populations.

Rob Fried, CEO of Niagen Bioscience, stated, “Rare disease research is a priority for Niagen Bioscience, particularly those indications associated with accelerated aging, mitochondrial dysfunction, or NAD+ deficiency.�

The U.S. Food and Drug Administration (FDA) granted Orphan Drug Designation (ODD) and Rare Pediatric Disease (RPD) Designation to NR for the treatment of AT. These designations underscore the urgent unmet need and potential therapeutic value of Niagen in rare disease populations.

Why NAD+ Matters in Rare Disease
Scientific research has shown that declining NAD+ levels can contribute to age-related decline, mitochondrial dysfunction, and impaired DNA repair. In both Werner syndrome and AT, NAD+ deficiency appears to play a central role in disease progression (). By restoring NAD+ levels, Niagen may help activate protective enzymes like SIRT1 and PARP1, reduce oxidative stress, and improve tissue function (Fang et al., 2016; Veenhuis et al., 2021; Presterud et al., 2023; Shoji et al., 2025; ).

Vilhelm Bohr, M.D., Ph.D., D.Sc., former National Institute on Aging (NIA) Chief of the Laboratory of Molecular Genetics, and current Affiliate Professor in Genome Instability and Neurodegeneration at the University of Copenhagen and Scientific Advisor to Niagen Bioscience and coauthor on the study, commented, “Werner syndrome is a rare genetic disorder that has long served as a valuable model for understanding the mechanisms of human aging. This study marks the first clinical trial using Niagen in those with Werner syndrome, and the findings—particularly improvements in cardiovascular markers—are promising. As Werner syndrome is a well-established model for normal aging, these results also suggest that NAD+ supplementation may support healthier aging in the broader population.�

Study Highlights

This 52-week randomized, double-blind, placebo-controlled crossover trial evaluated the safety and efficacy of oral Niagen supplementation in individuals with WS. The study randomized nine individuals (mean age: 47) who received 1,000 mg/day of Niagen or placebo for 26 weeks before crossing over to the alternate treatment for an additional 26 weeks.

Key findings include:

  • Robust increase in NAD+ levels: Niagen supplementation led to a ~140% increase in plasma NAD+ levels, compared to a ~4% decrease in the placebo group.
  • Improved arterial stiffness: Niagen significantly improved cardio-ankle vascular index (CAVI), a measure of arterial stiffness.
  • Cardioprotective lipid shift: Niagen increased the number of large HDL particles, indicating potential cardiovascular benefits.
  • Wound healing support: Niagen reduced skin ulcer size and heel pad thinning, while ulcers worsened in the placebo group.
  • Clinical safety profile: No moderate or severe adverse events were reported. Mild adverse events were fewer in individuals who received Niagen (7) compared to those who received placebo (12).
  • Tolerability in complex individuals: Although mild liver enzyme elevations were noted, they were deemed manageable and consistent with underlying liver sensitivities common in Werner syndrome.

​​This study represents the first clinical evaluation of Niagen in WS and supports further investigation of NAD+ augmentation as a therapeutic strategy in rare progeroid diseases.

For additional information on the science supporting Niagen®, visit .

Table 1
The table below provides an overview of the clinical research published to date on Niagen in rare age-related conditions.

Publication

Dose

Duration

Health Area

Study Design

Key Outcomes

Shoji et al., 2025

1000 mg

52 weeks

Werner syndrome

Randomized, double-blind, placebo-controlled crossover study in 11 individuals with Werner syndrome

~140% increase in plasma NAD+ levels; improved arterial stiffness and reduced skin ulcer size.

No moderate or severe adverse events reported.

Presterud et al., 2023

500 mg

2 years

Ataxia Telangiectasia (AT)

Open-label, single-arm observational study in 10 AT individuals

Significant improvements in motor coordination and eye movements. No serious adverse events. Longest NR supplementation trial to date.

Veenhuis et al., 2021

25 mg/kg

4 months

Ataxia Telangiectasia (AT)

Open-label proof-of-concept study in 24 AT individuals

Improved ataxia scores (SARA, ICARS); effects reversed after withdrawal. Increased IgG levels in immunodeficient individuals.

Tinnevelt et al., 2020

25 mg/kg

4 months

Ataxia Telangiectasia (AT)

Comparative study in 14 individuals with AT

NR-related pathways and metabolites significantly increased following NR supplementation.

About Niagen Bioscience:

(NASDAQ: NAGE), formerly ChromaDex Corp., is the global leader in NAD+ (nicotinamide adenine dinucleotide) science and healthy-aging research. As a trusted pioneer of NAD+ discoveries, Niagen Bioscience� is dedicated to advancing healthspan through precision science and innovative NAD+-boosting solutions.

The Niagen Bioscience team, composed of world-renowned scientists, works with independent investigators from esteemed universities and research institutions around the globe to uncover the full potential of NAD+. A vital coenzyme found in every cell of the human body, NAD+ declines with age and exposure to everyday lifestyle stressors. NAD+ depletion is a key contributor to age-related changes in health and vitality.

Distinguished by state-of-the-art laboratories, rigorous scientific and quality protocols, and collaborations with leading research institutions worldwide, Niagen Bioscience sets the gold standard for research, quality, and innovation. There’s a better way to age.

At the heart of its clinically proven product portfolio is Niagen® (patented nicotinamide riboside, or NR), the most efficient, well-researched, high-quality, and legal NAD+ booster available.

Niagen Bioscience’s robust patent portfolio protects NR and other NAD+ precursors. Niagen Bioscience maintains a website at , where copies of press releases, news, and financial information are regularly published.

Forward Looking Statements:

This release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities and Exchange Act of 1934, as amended, including statements related to infringement or non-infringement of intellectual property rights. Statements that are not a description of historical facts constitute forward-looking statements and may often, but not always, be identified by the use of such words as "expects," "anticipates," "intends," "estimates," "plans," "potential," "possible," "probable," "believes," "seeks," "may," "will," "should," "could" or the negative of such terms or other similar expressions. Risks that contribute to the uncertain nature of these forward-looking statements include the impact of the COVID-19 pandemic on our business and the global economy; our history of operating losses and need to obtain additional financing; the growth and profitability of our product sales; our ability to maintain sales, marketing and distribution capabilities; changing consumer perceptions of our products; our reliance on a single or limited number of third-party suppliers; and the risks and uncertainties associated with our business and financial condition. Xx Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and actual results may differ materially from those suggested by these forward-looking statements. All forward-looking statements are qualified in their entirety by this cautionary statement and Niagen Bioscience undertakes no obligation to revise or update this release to reflect events or circumstances after the date hereof.

Niagen Bioscience Media Contact:

Kendall Knysch, Senior Director of Media Relations & Partnerships

310.405.5227

[email protected]

Niagen Bioscience Investor Relations Contact:

ICR, LLC

Reed Anderson

(646) 277-1260

Stephanie Carrington

(646) 277-1282

[email protected]

Source: Niagen Bioscience, Inc

FAQ

What were the key results of Niagen's Werner Syndrome clinical trial?

The trial showed a 140% increase in NAD+ levels, improved arterial stiffness, beneficial changes in HDL particles, and reduced skin ulcer size. The treatment demonstrated a strong safety profile with no moderate or severe adverse events.

How many patients participated in NAGE's Werner Syndrome study?

The study included 9 participants with Werner Syndrome, with a mean age of 47, in a 52-week randomized, double-blind, placebo-controlled crossover trial.

What FDA designations has Niagen Bioscience received for rare diseases?

Niagen has received Orphan Drug Designation (ODD) and Rare Pediatric Disease (RPD) Designation from the FDA for the treatment of Ataxia Telangiectasia.

What is the dosage of Niagen used in the Werner Syndrome clinical trial?

Participants received 1,000 mg/day of Niagen or placebo for 26 weeks before crossing over to the alternate treatment for an additional 26 weeks.

What is Werner Syndrome and how rare is it?

Werner Syndrome is a rare genetic disorder causing rapid aging and premature mortality, affecting approximately 1 in 380,000 to 1 in 1,000,000 people globally. It is caused by mutations that impair DNA repair.
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