Niagen Bioscience Secures New U.S. Patent Covering Intravenous and Injection Formulations and Methods of Use for Nicotinamide Riboside (NR), Niagen®
MWN-AI** Summary
Niagen Bioscience, Inc. (NASDAQ: NAGE), a leader in NAD+ science and healthy aging, has secured U.S. Patent No. 12,558,367, enhancing its intellectual property portfolio. This patent protects methods of using nicotinamide riboside (NR), a key NAD+ precursor, in intravenous (IV) and injectable formulations, extending the company's exclusivity in this growing segment through 2044. CEO Rob Fried emphasized that this strategic extension allows Niagen to offer superior IV and injectable products that provide faster delivery and improved patient comfort across its expanding clinic network.
Under its Niagen Plus product line, the company has developed a new intravenous formulation designed for optimal cellular health and longevity. This formulation not only elevates NAD+ levels more effectively than traditional options but also reduces severe side effects commonly associated with NAD+ injections, thus reinforcing the commercial viability of the newly granted patent.
Niagen Bioscience boasts a robust portfolio of over 100 patents, underscoring its innovation in the healthy aging market. The new patent broadens protections for NR, encompassing aqueous formulations, various administration routes, and combinations with other NAD+ precursors, which supports additional commercial pathways and partnerships.
Niagen’s products are now available in over 1,200 healthcare and wellness clinics across the United States, and the company continues to research next-generation NAD+ precursors to stay ahead in the rapidly expanding sector. This patent not only solidifies Niagen Bioscience's position within the market but also acts as a significant deterrent against potential infringement, securing the future of its leading NR ingredient in both consumer and clinical applications. For more information on Niagen and its offerings, visit their websites.
MWN-AI** Analysis
Niagen Bioscience, Inc. (NASDAQ: NAGE) has recently secured U.S. Patent No. 12,558,367, which enhances its intellectual property portfolio related to nicotinamide riboside (NR), particularly in intravenous and injectable formulations. This strategic development is pivotal as it fortifies the company's competitive position in the fast-growing NAD+ (nicotinamide adenine dinucleotide) supplement market.
The new patent offers robust protection through 2044, enabling Niagen to capitalize on the expanding market for NAD+ boosters, especially in clinical settings. Given that the patent encompasses various administration methods and formulations, it opens avenues for further commercial partnerships and product variations. The IV format of Niagen’s products, specifically designed to support healthy aging, permits rapid delivery of the active compound, potentially attracting a diverse clientele at over 1,200 clinics across the U.S.
From a trading perspective, this patent could positively influence NAGE's stock performance. Investors should monitor the company’s upcoming quarterly earnings and any updates on product uptake or new clinic partnerships, which may strengthen its revenue streams. The growing emphasis on longevity and health in the consumer wellness sector also suggests an uptick in demand for such innovative health solutions.
However, potential investors should remain aware of market risks, including reliance on a limited number of suppliers and competitive pressures from other firms producing similar products. Niagen's continuous emphasis on research and innovation will be crucial in maintaining its leading position. Overall, this patent significantly enhances Niagen’s market viability and presents a compelling opportunity for growth, making it a stock worth considering for those interested in biotechnology and health sciences.
**MWN-AI Summary and Analysis is based on asking OpenAI to summarize and analyze this news release.
Patent strengthens Niagen Bioscience’s intellectual property moat in fast-growing NAD+-boosting IV and injectable delivery formats, supporting commercial expansion and deterring infringers
Niagen Bioscience, Inc. (NASDAQ: NAGE), the global authority on NAD+ (nicotinamide adenine dinucleotide) with a focus on the science of healthy aging, today announced the broadening of its NAD+ precursor intellectual property (IP) portfolio with the newly granted U.S. Patent No. 12,558,367 , which covers the methods of use of nicotinamide riboside (NR) and derivatives in intravenous and injectable formulations.
Rob Fried, CEO of Niagen Bioscience, commented, “This patent expands our intellectual property for our patented NR ingredient, Niagen ® , into IV and injectable delivery formats. With expected protection through 2044, it supports Niagen’s exclusivity in delivering a superior IV and injectable product with significantly faster delivery and improved comfort for patients across our expanding U.S. clinic footprint.”
Under its Niagen Plus product portfolio, Niagen Bioscience developed a next-generation intravenous formulation of pharmaceutical-grade Niagen designed to support healthy aging and longevity at the cellular level. Compared to traditional NAD+ IV, the aqueous-based intravenous Niagen formulation supports faster infusions and elevates NAD+ levels higher without the severe side effects of NAD+ IV, reinforcing the commercial relevance of this newly issued patent ( Reyna et al., 2026 ; Hawkins et al., 2024 ).
Niagen Bioscience continuously evaluates and investigates next-generation NAD+ precursors at the forefront of the burgeoning healthy aging category. The company owns and licenses a robust, secure portfolio of over 100 patents covering its flagship Niagen ingredient, the most efficient and high-quality NAD+ precursor on the market, as well as other NAD+ precursors.
Further reinforcing its leadership in the space, the newly issued U.S. Patent No. 12,558,367 adds meaningful protection for NR in IV and injectable delivery formats, with claims spanning aqueous formulations, multiple administration routes, defined administration parameters, select NR salt forms, and combination use with other NAD+ precursors. By extending the Company’s defensible IP footprint in this growing segment, the patent supports additional commercial pathways and partnerships and reinforces the durability of Niagen Bioscience’s Niagen product portfolio.
Niagen IV is available at over 1,200 healthcare, wellness, and longevity clinics across the U.S. Use the clinic locator at www.niagenplus.com to find a provider near you. For additional information on Niagen, visit www.niagenbioscience.com .
About Niagen Bioscience:
Niagen Bioscience, Inc. (NASDAQ: NAGE) 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, and high-quality NAD+ booster available. Niagen powers the Company’s consumer supplement, Tru Niagen ® , the number one NAD+ boosting oral supplement in the United States † (available at www.truniagen.com ), and Niagen Plus ™ , featuring pharmaceutical-grade intravenous (IV) and injectable Niagen products ( www.niagenplus.com ). Pharmaceutical-grade Niagen IV and injections are compounded and distributed by U.S. FDA-registered 503B outsourcing facilities and are available exclusively at clinics with a prescription.
Niagen Bioscience’s robust patent portfolio protects NR and other NAD+ precursors. Niagen Bioscience maintains a website at www.niagenbioscience.com , where copies of press releases, news, and financial information are regularly published.
† Based on the top-selling dietary supplement brands by revenue per the largest U.S. e-commerce marketplace (as of 1/1/2024 - 12/31/2024).
Forward Looking Statements:
This release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, and Section 21E of the Securities Exchange Act of 1934. 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,” “predicts,” “projects,” “continue,” “would” or the negative of such terms or other similar expressions.
Forward-looking statements are based on current expectations and assumptions and are subject to risks and uncertainties that could cause actual results to differ materially from those described. These risks and uncertainties include, but are not limited to, inflationary conditions and adverse economic conditions; our history of operating losses; the growth and profitability of our product sales; our ability to maintain and grow sales, marketing and distribution capabilities; changing consumer perceptions of our products; our reliance on a single or limited number of third-party suppliers; risks of conducting business in China; including unanticipated developments in and risks related to the Company’s ability to secure adequate quantities of pharmaceutical-grade Niagen in a timely manner; the Company’s ability to obtain appropriate contracts and arrangements with U.S. FDA-registered 503B outsourcing facilities required to compound and distribute pharmaceutical-grade Niagen to clinics; the Company’s ability to remain on the U.S. FDA Bulk Drug Substances Nominated for Use in Compounding Under Section 503B of the Federal Food, Drug, and Cosmetic Act Category 1 list; the Company’s ability to maintain and enforce the Company’s existing intellectual property and obtain new patents; whether the potential benefits of NRC can be further supported; further research and development and the results of clinical trials possibly being unsuccessful or insufficient to meet applicable regulatory standards or warrant continued development; the ability to enroll sufficient numbers of subjects in clinical trials; determinations made by the FDA and other governmental authorities, including with respect to products seeking to compete in our market; mislabeling or other misleading marketing practices by competitors; economic and market instability, including as a result of tariffs or trade conflicts; and the risks and uncertainties associated with our business and financial condition in general, described in our filings with the Securities and Exchange Commission (SEC), including, without limitation, our most recent Annual Report on Form 10-K and Quarterly Report on Form 10-Q as filed with the SEC.
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.
View source version on businesswire.com: https://www.businesswire.com/news/home/20260225271097/en/
Niagen Bioscience Media Contact:
Kendall Knysch, Senior Director of Media Relations & Partnerships
310.405.5227
kendall.knysch@niagenbio.com
Niagen Bioscience Investor Relations Contact:
Valter Pinto, Managing Director
KCSA Strategic Communications
212.896.1254
Niagen@kcsa.com
FAQ**
How does the recently granted U.S. Patent No. 12,558,367 enhance Niagen Bioscience Inc. (NAGE)'s competitive advantage in the NAD+ market, particularly concerning IV and injectable formulations?
What impact is the expansion of Niagen Bioscience Inc. (NAGE)’s IP portfolio expected to have on its commercial partnerships and pathways within the growing healthy aging segment?
Can you provide insights into how Niagen Bioscience Inc. (NAGE) plans to leverage its patent portfolio to deter potential infringers while promoting the adoption of its NAD+ boosting products?
Given the potential for future research, what additional developments should investors of Niagen Bioscience Inc. (NAGE) anticipate regarding new NAD+ applications derived from the recently issued patent?
**MWN-AI FAQ is based on asking OpenAI questions about Niagen Bioscience Inc. (NASDAQ: NAGE).
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