Niagen Bioscience, Inc. (NASDAQ: NAGE) 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.
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.
NAGE shares docked a penny to $5.10.
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