Biogen and Fellow Boston-Area Biotechs Ready for Biogenerics

Boston-area biotech companies have kept a close eye on how U.S. regulators decide to govern the approval of copycat versions of biotech drugs. Now I’m seeing more signs that some of these companies could actually become major players in the business of making biogenerics (which are also called biosimilars, follow-on biologics, and other names, depending who you’re taking to.)

Cambridge, MA-based Biogen Idec (NASDAQ:[[ticker:BIIB]]), for starters, has very quietly established a subsidiary called Eidetica Biopharma to develop and manufacture what Biogen calls biosimilars, according to unnamed sources with knowledge of the subsidiary. There’s scant information available on Zug, Switzerland-based Eidetica, but it’s clear that this firm is a sign that Biogen is looking to get a piece of the biogenerics pie.

Biogen is just one of several examples, though, of life sciences companies that are taking an interest in biogenerics as a potential revenue stream. Many already have the infrastructures and the internal brainpower to produce original biotech or biologic drugs. And a barrier to entering the business of making biogenerics is the huge investment required to build biotech drug plants, which must also be approved by regulators before the facilities can market products manufactured there. There are also businesses, such as Merck & Co.’s GlycoFi, of Lebanon, NH, where innovative technology has overcome some of the technical challenges of making copies of biotech drugs.

Scientia Advisors, a life sciences consulting firm in Cambridge, MA, has fielded a lot of inquiries lately from companies in the Boston area and elsewhere about the viability of the biogenerics market, Amit Agarwal, a partner at Scientia, tells me. He says the interested parties include all companies with the facilities to produce biologics. “What we’re seeing is that they are at least considering this market,” Agarwal says. “It’s out there and it’s not just coming from the usual suspects.”

The future of the biogenerics market, at least in the U.S., is very much up in the air at the moment. Biogenerics have been near the top of the biotech industry’s policy agenda for years, but the issue has heated up recently as U.S. lawmakers look to overhaul the healthcare system. There are biotech companies that fear an invasion of biogeneric drugs into the marketplace could hurt their sales, as well as their ability to fund the development of novel biotech drugs. But some lawmakers see the approval of these copycat treatments as important to controlling the rising cost of drugs. And at the center of the current biogeneric debate is how to formulate a regulatory pathway to approve these drugs.

Some of the key issues in the biogenerics debate are related to the inherent differences between biologics and small-molecule, chemical drugs. Biologics, typically made in processes that involve living cells and bioreactors, are often protein-based drugs with complex structures that cannot be duplicated like their small-molecule brethren. This means that biogeneric drugs aren’t exact copies of the originals, creating all manner of questions about whether the knockoffs should be required to undergo additional clinical trials to prove their safety and effectiveness. As I mentioned, there are local firms that have entered this market because they believe than can overcome some of the technical obstacles.

GlycoFi, for instance, has recombinant yeast technology that enables it to have greater control over the molecular form of protein-based drugs than is otherwise possible. Merck, which purchased GlycoFi for $400 million in 2006, is using this science as the technical backbone of its recently launched biogenerics business unit, Merck Bioventures. Here’s our recent story about the leading role that GlycoFi is playing in the biogenerics unit. In fact, Merck has even begun to call its copycat biotech drugs “bio-betters,” because it believes it can engineer the proteins to be better than the originals. (Henri Termeer, the chairman and CEO of Cambridge, MA-based biotech powerhouse Genzyme (NASDAQ:[[ticker:GENZ]]), poked fun at the bio-betters moniker during a recent interview, an audio recording of which is embedded in this post from last week.)

Indeed, Cambridge-based Momenta Pharmaceuticals’ (NASDAQ:[[ticker:MNTA]])

Author: Ryan McBride

Ryan is an award-winning business journalist who contributes to our life sciences and technology coverage. He was previously a staff writer for Mass High Tech, a Boston business and technology newspaper, where he and his colleagues won a national business journalism award from the Society of American Business Editors and Writers in 2008. In recent years, he has made regular TV appearances on New England Cable News. Prior to MHT, Ryan covered the life sciences, technology, and energy sectors for Providence Business News. He graduated with honors from the University of Rhode Island in 2001 with a bachelor’s degree in communications. When he’s not chasing down news, Ryan enjoys mountain biking and skiing in his home state of Vermont.