Ironwood, Flush With Cash, Anticipates Big Year with Constipation Drug

Ask Ironwood Pharmaceuticals CEO Peter Hecht what he’s trying to accomplish in the next six to 12 months, and he doesn’t tiptoe around. “We’re trying to build the next great pharmaceutical company,” Hecht says. “I know that sounds ludicrous, but I thought I’d just start out with our ambition first.”

It’s an open question whether he will achieve that, but it’s clear that Ironwood is serious. It’s a private biotech company with 150 employees in Cambridge, MA, that changed its name from Microbia in April. The company has raised a total of $231 million in its 10-year history, including a $50 million private round announced on Oct. 1, led by Morgan Stanley, right when Lehman Brothers and much of Wall Street was crumbling around it. Other investors include notable names like Venrock Associates, Polaris Venture Partners, and Fidelity Biosciences.

The investors are mainly betting on Ironwood’s lead drug candidate, linaclotide. It’s a novel compound for chronic constipation and for constipation from irritable bowel syndrome. One week after the financing announcement crossed the wire, Ironwood and its partner, New York-based Forest Laboratories, said a study of 420 patients showed the drug significantly improved constipation symptoms and reduced abdominal pain. Researchers reported no serious side effects related to the drug, although 1 percent to 7 percent of patients on the medicine dropped out of the study because of diarrhea, according to a presentation at the American Society of Gastroenterology. These results were promising enough for Ironwood and Forest to start up a program of four final-stage clinical trials, encompassing a total of 2,500 patients, to amass enough evidence to potentially bring this drug to the marketplace.

To hear Hecht tell the story, Ironwood didn’t start down this path because it had narrow expertise in a specific disease like diabetes, or in a particular technology platform, like RNA interference drugs. “We don’t have any of that,” he says. “I know it sounds hokey and trite and incredibly naïve, but we have really talented people and enormous passion.”

The strategy at Ironwood, Hecht says, is to look for great areas of medical need and work to develop drugs for them. Constipation from irritable bowel syndrome was one such area. The numbers of patients diagnosed with this condition is fuzzy, but Novartis tegaserod maleate (Zelnorm) reached $561 million in peak sales for treating this condition in 2006, despite “modest efficacy,” Hecht says. The drug was pulled from the market in March 2007 after the FDA found it raised cardiovascular risks.

The Ironwood drug has been designed to work differently than the Novartis product.

Author: Luke Timmerman

Luke is an award-winning journalist specializing in life sciences. He has served as national biotechnology editor for Xconomy and national biotechnology reporter for Bloomberg News. Luke got started covering life sciences at The Seattle Times, where he was the lead reporter on an investigation of doctors who leaked confidential information about clinical trials to investors. The story won the Scripps Howard National Journalism Award and several other national prizes. Luke holds a bachelor’s degree in journalism from the University of Wisconsin-Madison, and during the 2005-2006 academic year, he was a Knight Science Journalism Fellow at MIT.