Archive for the ‘Biotechnology’ Category

Unlikely Biotech Buddies

Thursday, July 7th, 2011

Recent news in the world of drug development reveals that there’s a somewhat unexpected category of corporate business looking to enter the multibillion-dollar biotech market.  Just two weeks ago,  Reuters examined an interesting group of multinational companies including Hanwha Chemicals, Samsung, and Fujifilm, which are entering into new deals on biosimilars in order to grab the market currently held by the dozens of biologics that will lose patent protection over the next ten years.

Certainly, tech manufacturers and camera companies aren’t known for their expertise in drug development, yet they have the cash to make great deep-pocket partners for large pharma companies like Merck who are looking to ride their share of the biosimilar gravy train. For all of these businesses, Reuters notes, biosimilars offer a huge new revenue source, potentially registering in the billions. And because making these “follow-on” versions of biologic drugs will be a far more complex process than developing traditional small molecule generics, as described in my previous blog post on this topic, it will a venture dominated by large companies that most likely won’t be operating solo. (more…)

Interview: MSLGROUP Chats with Wendy Diller, Elsevier Business Intelligence

Thursday, December 23rd, 2010

Read on for a PR moment with Wendy Diller, Business Bureau Chief, Biopharma Group, Elsevier Business Intelligence – publisher of such publications as The Pink Sheet and INVIVO. Carol Perlman, MSLGROUP chats with Wendy.

CP: As a bureau chief in the Biopharma Group at Elsevier Business Intelligence (formerly FDC-Windhover), you specialize in analyzing and writing about corporate strategy, business development, and commercial issues in the biopharma industry.  Can you provide some insight as to your role, your team and your publications?
WD: I’m an executive editor at Elsevier Business Intelligence. I’m in charge of business coverage for our biopharma publications, The Pink Sheet and The Pink Sheet DAILY, and a writer/editor for our magazine IN VIVO. We’ve got a group of about nine people who write on business issues related to the biopharma industry for our publications.

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The CEO Roundtable: Season of Opportunity or Season of Turmoil? (Part 2 of 2)

Tuesday, November 9th, 2010

Today, our MSL Conversations Blog features the final part of Matt Gardner’s CEO Roundtable in which he chats with Rachel King, CEO of GlycoMimetics, Martin Babler, CEO of Talima Therapeutics and Omar Haffar, CEO of Presidio Pharmaceuticals about current industry trends. Find Part 1 here.

Gardner:  The overall atmosphere has been tough.  Recalls, FDA rejections, reform, finance, policy uncertainty.  Do you see our industry actively leading the charge in economic recovery?

Rachel: I think biotech will be a modest contributor to economic growth overall in the short term.  Longer term, I think the industry will be a major factor in growth and innovation.

Omar: I don’t see our industry playing a leading role in the economic recovery.  The biotech industry over the past 30 years has been somewhat peripheral from a direct impact perspective on the macroeconomic picture.  Our industry is immediately and severely impacted by economic downturns, even transient ones, while the slope for a sustained recovery is usually shallow and long.  This is due in part to the time and capital requirements needed to transition to a revenue generating organization, which also makes the prospect of being acquired as the main value driver.

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The Follow-On Biologics Debate

Monday, November 1st, 2010

The Biologics Price Competition and Innovation (BPCI) Act, which was included in the health care reform bill signed into law by President Obama on March 23rd, 2010, mandated the creation of an abbreviated approval process for follow-on biologic agents, similar to the pathway that currently exists for small-molecule drugs.

During the last few years, there had been tremendous pressure on the FDA to create such a pathway, given ever-rising healthcare costs and demands for greater access to biotechnology drugs. In June of 2009, in fact, President Obama (urged on by Representative Henry Waxman, chair of the Energy and Commerce committee), gave a speech to the AMA, asking the FDA and the industry “to introduce generic biologic drugs into the marketplace.”

He went on to say: “These are drugs used to treat illnesses like anemia, but right now, there is no pathway at the FDA for approving generic versions of these drugs. Creating such a pathway will save us billions of dollars.”

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