NMN is precluded in supplements, says pharma company to FDA

Josh Long, Associate editorial director, Natural Products Insider

January 3, 2024

3 Min Read

A clinical-stage pharmaceutical company that has been investigating the use of nicotinamide mononucleotide (NMN) to treat medical conditions, including Alzheimer’s, has requested the Food and Drug Administration uphold its determination that the ingredient is excluded from the definition of a dietary supplement product and cannot be marketed in such products.

Metro International Biotech LLC (Metro) in November wrote a 12-page letter to FDA, in response to a citizen petition filed in 2023 by the Alliance for Natural Health USA (ANH) and Natural Products Association (NPA). The citizen petition requested FDA reverse its position that a popular anti-aging ingredient, NMN, is excluded from the definition of a dietary supplement.

The pharma company agreed with FDA that NMN is properly barred from being marketed as a dietary supplement under the so-called drug exclusion clause of the Federal Food, Drug & Cosmetic Act (FDCA).

“The FDA should not permit NMN products to be sold as a dietary supplement, which would be in violation of the drug exclusion clause and without sufficient demonstration of safety, adequate directions for use, or compliance with good manufacturing practices,” Metro concluded in the Nov. 20 letter.

Metro is researching NMN as a new drug and said it has commenced substantial clinical investigations under an investigational new drug application (IND) to treat certain medical conditions, including Alzheimer’s, Friedreich ataxia and kidney disease.

Related:FDA sticking to its guns on NMN in dietary supplements

FDA has concluded NMN was authorized for investigation as a new drug and is the subject of substantial clinical investigations that have been instituted and made public, prior to being lawfully marketed as a dietary supplement product.

FDA has not yet substantively responded to the petition filed by ANH and NPA. In late August, the agency sent an interim response to the groups, saying it could not reach a decision on the petition within 180 days as a result of “competing agency priorities.”

FDA sent a similar interim response letter in November to the Council for Responsible Nutrition (CRN), in response to a petition it filed concerning FDA’s interpretation of the drug exclusion clause.

Dan Fabricant, president and CEO of NPA, said Metro’s comments make “it clear” there must “be a fix” to the drug exclusion clause in the FDCA “through one of the three branches of government.”

If Metro’s interpretations of the law are implemented by FDA, “there is no space or protection for dietary supplements or foods looking to play a role in health and wellness, only drugs going forward,” Fabricant told Natural Products Insider. “The very act of submitting an IND for a trial on a supplement or food, which many universities and their IRBs [institutional review boards] require, even for structure/function or kinetic endpoints, would exclude one from the market indefinitely as a supplement or food. I know it’s winter, but that’s an ice age on innovation, not a chill. We look forward to continued collaboration with ANH on a path forward.”

ANH Executive and Scientific Director Rob Verkerk said his organization concurred with NPA's assessment.

"There needs to be a fix for the drug preclusion clause that works against wider, low-cost access to highly effective dietary supplements like NMN," he said in an email. "We can't let pharmaceutical companies keep gaining monopolies on vital, natural ingredients Americans need to improve their health."

About the Author(s)

Josh Long

Associate editorial director, Natural Products Insider, Informa Markets Health and Nutrition

Josh Long directs the online news, feature and op-ed coverage at Natural Products Insider, which targets the health and wellness industry. He has been reporting on developments in the dietary supplement industry for over a decade, with a focus on regulatory issues, including at the Food and Drug Administration.

He has moderated and/or presented at industry trade shows, including SupplySide East, SupplySide West, Natural Products Expo West, NBJ Summit and the annual Dietary Supplement Regulatory Summit.

Connect with Josh on LinkedIn and ping him with story ideas at [email protected]

Education and previous experience

Josh majored in journalism and graduated from Arizona State University the same year "Jake the Snake" Plummer led the Sun Devils to the Rose Bowl against the Ohio State Buckeyes. He also holds a J.D. from the University of Wyoming College of Law, was admitted in 2008 to practice law in the state of Colorado and spent a year clerking for a state district court judge.

Over more than a quarter century, he’s written on various topics for newspapers and business-to-business publications – from the Yavapai in Arizona and a controversial plan for a nuclear-waste incinerator in Idaho to nuanced issues, including FDA enforcement of the Dietary Supplement Health and Education Act of 1994 (DSHEA).

Since the late 1990s, his articles have been published in a variety of media, including but not limited to, the Cape Cod Times (in Massachusetts), Sedona Red Rock News (in Arizona), Denver Post (in Colorado), Casper Star-Tribune (in Wyoming), now-defunct Jackson Hole Guide (in Wyoming), Colorado Lawyer (published by the Colorado Bar Association) and Nutrition Business Journal.

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