FDA fostering generic competition for complex drugs

TRENTON, N.J. — The U.S. Food and Drug Administration is opening a new front in its efforts to reduce high drug prices by encouraging development of generic versions of hard-to-make medicines.

Complex drugs and drug-device combinations generally are very expensive, and some are widely used. Often, they don’t get generic competition right after their patent expires, as happens routinely with pills.

Difficulty in creating copies or near-copies of such drugs and getting them approved may deter generic companies from even trying, FDA Commissioner Dr. Scott Gottlieb wrote in a blog post.

That means patients don’t get access to cheaper versions of those drugs, and the brand-name medicine makers continue to rake in money — often billions of dollars a year per drug.

To get more generic versions of complex drugs on the market, the FDA will begin giving companies guidance on how to win approvals, including offering meetings with agency staff early on, to shorten the time for development and approval.

Examples of older complex drugs cited by Gottlieb that still lack generic competition include the Advair inhaler and the injected medicines Forteo for osteoporosis, Victoza for high blood sugar and Copaxone for multiple sclerosis.

Their monthly costs without insurance range from about $400 for Advair to up to $5,200 for Copaxone. A generic version of Copaxone was approved in 2015, but it’s not yet on sale because the maker hasn’t met FDA manufacturing standards.

“This is a shot across the bow” to the brand-name companies, said analyst Steve Brozak, president of WBB Securities.

Gottlieb’s close ties to drugmakers worried consumer groups when he was nominated. Now, Brozak said, he’s telling brand-name drugmakers to focus on developing new drugs, not wringing extra money out of blockbusters long on the market.

“Nothing in health care is instantaneous,” Brozak said, but Gottlieb “is starting to build a road map for how to prove” a generic is equivalent to a complex brand-name drug.

Longer-term plans include coming up with better tools to determine if a proposed copycatwill affect patients the same way.

The FDA has already made changes to increase competition, including reducing a backlog of generic pills that were awaiting approval.