Criticism as Brian King Named Director of FDA Center for Tobacco Products

News
May.20.2022
Criticism as Brian King Named Director of FDA Center for Tobacco Products

Brian King, currently a higher-up at the Centers for Disease Control and Prevention (CDC) in Atlanta, will become the new director of the Food and Drug Administration’s Center for Tobacco Products (CTP), the FDA announced on May 20.

 

An epidemiologist, King has spent more than a decade at the CDC, most recently as the deputy director for research translation at the Office on Smoking and Health (OSH). He will assume his new role on July 3, 2022. His predecessor as permanent director, Mitch Zeller, retired in the spring after a contentious career; the CTP has since been headed by Michele Mital on an interim basis.

 

The news comes at a time when CTP still has to sort through many of the premarket tobacco product applications (PMTAs) from the largest vape manufacturers, and as the office has been under recent fire for poor public health communication about the relative risks of e-cigarettes and safer nicotine alternatives. The reaction among consumer advocates was mixed at best: Some expressed cautious optimism that an epidemiologist might understand the issues better than a lawyer like Zeller, while others feared this might be just a status-quo move—or worse.

 

Many observers have pointed to King’s botching, in his CDC role, of the lung illnesses—misleadingly dubbed “e-cigarette or vaping use-associated lung injury,” or EVALI—that cropped up in the summer of 2019. Three years later, the CDC has still failed to be explicit that the cases were only tied to vaping illicitly manufactured, adulterated THC cartridges—and not nicotine, as the agency originally implied.

 

“Brian King’s long history of obfuscation around the issue of tobacco harm reduction is hard to ignore.”

 

Criticism has also been levied at King’s past comments on e-cigarettes. He’s accused of having overemphasized the harms of vaping products among youth at the expense of their harm reduction role for adult smokers, and of fear-mongering—through claims that e-cigarettes could be modified to contain “heroin, methamphetamines, powdered cocaine, and bath salts.”

 

“While there is always value in optimism, Brian King’s long history of obfuscation around the issue of tobacco harm reduction is hard to ignore,” Greg Conley, the president of the American Vaping Association (AVA), told Filter. “In his role at the Office on Smoking and Health, King has ignored or downplayed CDC’s own surveys showing several million adult ex-smokers using vaping as a total alternative for smoking, while leaping at opportunities to make absurd claims about the impacts of youth vaping. We are hopeful the FDA’s hiring of an ideologue to act as a supposedly neutral regulator will lead to renewed interest in this issue by members of Congress.”

 

“Brian King is among the worst choices for CTP that exists,” an industry insider, who requested anonymity so as not to affect his company’s PMTAs, told Filter. “He has no understanding of tobacco harm reduction or the continuum of risk, and has demonstrated a fundamental misunderstanding of what an e-cigarette even is. I expect his reign to be plagued by litigation [and that he] never accomplishes any of his stated goals for the regulation of the industry.”

 

In a letter circulated to FDA staff, Robert Califf, the agency’s commissioner, lauded King on his expertise, writing that “he has an extensive and nuanced understanding of, and appreciation for the 2009 Family Smoking and Prevention Act, detailed knowledge of premarket review pathways, premarket tobacco product applications, substantial equivalence, and modified risk tobacco products, as well as experience in the interagency scientific review of regulatory documents related to tobacco product standards, testing and reporting of ingredients, and health information.”

 

King, for his part, is anxious to get started.

 

“There’s critical work to be done to further prevent people from starting to use tobacco products, encourage tobacco users to quit and reduce the harm caused by tobacco use,” King said in a press statement. “During my time at CDC, I’ve had the great privilege to work with the staff at the FDA’s Center for Tobacco Products on a number of important tobacco issues, and I’m excited to lead CTP to advance these efforts.”

 

Source:filtermag

Cyprus Bill to Regulate Nicotine Pouches Expected to Reach House Plenary in Early April
Cyprus Bill to Regulate Nicotine Pouches Expected to Reach House Plenary in Early April
A proposed law to regulate nicotine pouches in Cyprus is expected to reach the House plenary session in early April. The bill, submitted by Diko MP Chrysis Pantelidis, aims to establish a regulatory framework governing the marketing, composition and quality of nicotine pouches currently circulating on the market and to incorporate them into existing smoking control legislation.
Mar.13 by 2FIRSTS.ai
Aurora advances retail tobacco licensing ordinance to curb under-21 access to vapes and tobacco
Aurora advances retail tobacco licensing ordinance to curb under-21 access to vapes and tobacco
The Denver Post reported that Aurora’s City Council unanimously approved a retail tobacco licensure ordinance on first reading Monday night to reduce underage access to tobacco products, including e-cigarettes and vaping cartridges. The ordinance would stiffen fines for businesses that sell to people under 21 and tighten rules on where tobacco retailers can locate in the city.
Feb.26 by 2FIRSTS.ai
PMTA Manufacturing Panel Sees Small Firms Warn “Unknown Is Death” as FDA Defends Review Boundaries
PMTA Manufacturing Panel Sees Small Firms Warn “Unknown Is Death” as FDA Defends Review Boundaries
During FDA’s Feb 10 PMTA roundtable (manufacturing controls panel), small ENDS manufacturers warned that uncertainty in manufacturing expectations creates existential financial risk. FDA officials reiterated review flexibility is constrained by statutory and scientific boundaries. The panel debated testing standards, documentation requirements, open-system responsibility, supply chain changes, and software updates—highlighting unresolved PMTA challenges for small manufacturers.
Feb.11
Brazil’s MPF and Anvisa sign pact to intensify enforcement against vapes
Brazil’s MPF and Anvisa sign pact to intensify enforcement against vapes
Brazil’s Federal Public Prosecutor’s Office (MPF) and health regulator Anvisa signed a cooperation protocol to strengthen enforcement against electronic smoking devices (DEFs) and expand health-risk awareness campaigns.
Feb.03 by 2FIRSTS.ai
Product | Claiming a “first multi-beverage vaporizer” with refillable juice/cocktail water chamber, PEAKBAR launches new device in the U.S.
Product | Claiming a “first multi-beverage vaporizer” with refillable juice/cocktail water chamber, PEAKBAR launches new device in the U.S.
PEAKBAR’s new H2O 40K has begun selling through U.S. online retailers including Vape Sourcing. Marketed as the “world’s first multi-beverage vaporizer,” the device is promoted as allowing users to add liquids such as juice and cocktails into a water chamber for pairing. Publicly listed specifications include 20 ml of e-liquid, a rated 40,000 puffs, 0.5% nicotine, a 1,000 mAh rechargeable battery, and two power modes at 22W and 12W.
Jan.22 by 2FIRSTS.ai
TPB Q4 FY2025 Revenue Rises 29% to $121 Million; Modern Oral Business Up 266% Year Over Year
TPB Q4 FY2025 Revenue Rises 29% to $121 Million; Modern Oral Business Up 266% Year Over Year
Turning Point Brands, a U.S. nicotine and tobacco-related consumer products company, reported its fiscal 2025 fourth-quarter results: quarterly revenue was $121 million, up 29% year over year; adjusted EBITDA (Earnings Before Interest, Taxes, Depreciation and Amortization) was $30 million, up 14%. Net revenue from modern oral nicotine products was $41.3 million, up 266% year over year.
Mar.03 by 2FIRSTS.ai