Forma Cuts $65M Deal With Boehringer Ingelheim to Discover Cancer Drugs

Another six months have gone by, so it must be time for another deal for Forma Therapeutics.

Sure enough, Watertown, MA-based Forma is announcing today it has struck a partnership to discover new cancer drugs with Germany-based Boehringer Ingelheim. The deal provides $65 million to Forma in a combination of upfront cash and four years’ worth of steady R&D financing. Forma could end up getting as much as $750 million in milestone payments as the drug candidates advance through development in the Boehringer Ingelheim’s pipeline. Further financial details aren’t being disclosed.

The new arrangement with Boehringer Ingelheim means that Forma has diversified with a roster of seven different deep-pocketed organizations that are putting their resources into Forma and its 100-person drug discovery crew. Forma last made news in June when it agreed to collaborate with Genentech on an experimental drug program to interfere with cancer cell metabolism. This new partnership will seek to build on Forma’s efforts to make drugs against molecular targets that have long been considered “undruggable” because they focus on protein/protein interactions. These are complex 3-D structures that are often known to play critical roles in disease processes, but they don’t usually have an obvious binding pocket that a small-molecule chemical compound can latch onto.

The wager is that Forma, through its team of biologists, chemists, and computational modelers, has found some promising new angles of attack against some of the classic cancer targets and some new ones that have promise, says Forma CEO Steven Tregay.

Still sounding like the organic chemist he was trained to be, Tregay is quick to admit that this isn’t totally obvious or some kind of easy thing to do.

Steven Tregay

“Protein/protein interactions are tough, you really need a partner that will go in with you and commit for four years and give it the good old-fashioned college try,” Tregay says. “We found a terrific partner in BI.”

Forma, founded in 2007 with a core group of scientists from the Broad Institute of MIT and Harvard, has been able to pull together a drug discovery team at precisely the moment when most biotech companies are looking to save money by cutting back on early-stage R&D and concentrate on later-stage clinical development of drug candidates that were discovered years ago. Forma has only raised $33 million in venture capital, but found a way to float a sizable R&D operation by relying on support from a network of partners like Novartis, Cubist Pharmaceuticals, the Leukemia & Lymphoma Society, Eisai Pharmaceuticals, and Experimental Therapeutics Center of Singapore, as well as Genentech and now Boehringer Ingelheim.

By stitching together that support network, Forma has now got a drug discovery engine with the capability of running 30 different campaigns a year for high-throughput screening of new small-molecule drug candidates against targets of interest, Tregay says. That’s “about on par” with what many Big Pharma companies have for in-house capability of screening cancer drugs, he says.

While Forma has invested heavily in the early drug discovery efforts, that hasn’t left a whole lot of room for later-stage development capability. Although Forma plans to develop at least some of its own drug candidates in the future, it primarily operates

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.