Smokeless products face FDA test

Tobacco maker first in line for regulatory review

Tobacco companies want to market more smokeless tobacco and cigarette alternatives to make up for falling cigarette sales. Tobacco companies want to market more smokeless tobacco and cigarette alternatives to make up for falling cigarette sales. (Photos By Steve Helber/Associated Press)
By Michael Felberbaum
Associated Press / September 29, 2010

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RICHMOND — Tobacco maker Star Scientific Inc. hopes there’s fire where there’s no smoke.

The small Virginia company has made itself the test case for a big issue: whether the Food and Drug Administration will allow certain tobacco products — particularly the company’s tobacco lozenges — to be marketed as less harmful than cigarettes.

The application to market the product as safer also highlights a philosophical debate over how best to control tobacco. One camp says there’s no safe way to use tobacco and pushes for people to quit above all else. Others embrace the idea that lower-risk alternatives like smokeless tobacco or electronic cigarettes can improve public health, if they mean fewer people smoke.

How the FDA handles the products is being closely watched by both the public health community and bigger tobacco companies, which are looking for new products to sell as they face declining cigarette demand due to tax increases, health concerns, smoking bans, and social stigma.

A law enacted last year gives the FDA authority to evaluate tobacco products for their health risks and lets the agency approve ones that could be marketed as safer than what’s currently sold.

So far only Star Scientific has applied for approval to market what the agency calls “modified-risk’’ products. The company says the small tablets that dissolve in the user’s mouth contain “below detectable levels’’ of certain cancer-causing chemicals found in tobacco and its smoke. It wants to sell them to smokers as “a useful alternative — with greatly reduced toxin levels.’’

“Why shouldn’t tobacco users . . . have an opportunity to know this and make an informed decision? That’s why we took the risk, that’s why we spent the money,’’ Paul Perito, president of Star Scientific, said.

The company, formerly known as Star Tobacco and Pharmaceuticals, has sold varieties of the dissolvable tobacco under the Ariva and Stonewall brands since 2001. Its sales have grown about 47 percent since 2007.

The tablets contain tobacco’s most addictive component, nicotine. Star Scientific says its method of tobacco cultivation and preparation creates tobacco leaves with low levels of some carcinogens.

While the FDA’s Center for Tobacco Products has not yet ironed out its guidelines for approval of such products, draft guidelines suggest it could take nearly a year to review an application.

Tobacco companies want to market more smokeless tobacco and other cigarette alternatives to make up for falling cigarette sales. Some have introduced snus — small pouches like tea bags that users stick between the cheek and gum — and dissolving tobacco — finely milled tobacco shaped into orbs, sticks, and strips. But they can’t explicitly market them as less risky than cigarettes.

But a report from the Royal College of Physicians, a UK medical group, titled “Harm Reduction in Nicotine Addiction,’’ — along with other scientific studies — suggests that when compared with cigarettes, some smokeless tobacco products are about 90 percent less harmful.

Meanwhile, GlaxoSmithKline, which makes nicotine replacement therapy products like Nicorette gum and NicoDerm patch, has urged the FDA to take dissolvable tobacco off the market until companies can demonstrate that selling it is appropriate for the protection of public health.

The question remains whether smokers, which total about 46 million in the United States, are really willing to switch, even if it means saving their lives.

But tobacco company research shows that many smokers transition to smokeless products in about a year and a half once they begin to notice the benefits of going smoke-free, said David Sweanor, a Canadian law professor and tobacco specialist who consults with companies and others on industry issues.

Matthew Myers, president of the Campaign for Tobacco-Free Kids, said the FDA can now keep tobacco companies accountable for health claims and marketing, but also use scientific standards to assess health impacts.

“If there are tobacco products out there that can be marketed in such a way that can significantly reduce the risk of disease, I don’t know of anybody who opposes that,’’ Myers said.