In Their Own Words: A Few Pharma CEOs Chat
5 CommentsBy Ed Silverman // October 31st, 2008 // 8:23 am
As part of a package of stories about big pharma, BusinessWeek grabbed the ceo at four drugmakers - Pfizer’s Jeff Kindler; Bristol-Myers Squibb’s Jim Cornelius; Lilly’s John Lechleiter and Roche’s Severin Schwan - to discuss the varied and vexing problems the industry faces. Here are a few of their comments…

BW: What’s the solution to the lack of productivity in drug research?
Cornelius: It’s troubling in that the Food & Drug Administration is approving 18 to 20 [new drugs a year], but we’re spending about $60 billion on research. That equation doesn’t work. Something has to give. We’ll have to be selective in the R&D bets we make. We’re going to see companies working together more to address that R&D productivity issue.
BW: Is it better for a drug company to diversify into other endeavors, such as devices or consumer health, or is staying focused on prescription drugs the way to go?
Lechleiter: There was a time when many of us couldn’t shed our non-core assets fast enough. Lilly built up in medical devices in the late 1970s, but ultimately split off that business, Guidant. Now we’re pretty much a pure-play drug company with the exception of our animal health business, Elanco. I think some diversification is necessary and prudent. Now, we look at Elanco and ask: How can we build it up? Being in biotech is a form of diversification, too. But our diversification strategy is going to be very thoughtful. We don’t intend to build a devices business or anything like it again.
BW: What’s the solution to the lack of productivity in drug research?
Schwan: Our philosophy is that people need enough freedom to make decisions in a decentralized manner. One thing we have done in the last 18 months is to further decentralize our management model in pharma by creating five “disease biology areas.” DBAs set priorities and make portfolio decisions for their specific diseases. An interesting thing happened when we implemented this new structure: We saw them streamlining certain projects. Previously the portfolio decisions were made high up in the organization, so everyone was fighting for their own portfolios—they wanted to get as many of their projects financed as possible. Now these decisions are made a level down in the organization. That means decisions are made by people who are closer to the projects, so they are willing to invest more in what they believe in, and remove money from those less likely to succeed.
BW: The public has a poor image of drug companies. What can be done to improve that trust?
Kindler: What you have seen from many companies is a willingness to make changes in response to some of the criticism the industry has. We’ve made commitments about posting our clinical trials, we have supported some legislation that Senator {Charles] Grassley [R-Iowa] has proposed regarding disclosure of certain payments [to doctors]. This is not about words, it’s about actions. I like to tell people our business is asking people to put our products in their body. The people we ask to do that are entitled to demand that they [can] trust us. Every day we need to earn that trust.
Outside the Box
Pieces like this from BW are very frustrating. On the one hand you have a group of the most senior industry executives answering pertinent questions that relate to the entire industry. On the other hand their answers are at best non-specific and at worst vacuous. I truly hope (for the sake of all the employees at these companies) that the real thinking that these gentlemen bring to the table is being cleverly concealed behind the answers given to BW. If these answers really represent the depth and breadth of their thought then we need to be looking elsewhere for industry leadership, because there doesn’t seem to be an original thought between them.
SP
Thank God they didn’t interview Fred Hassan, aka Fred Hasbeen!
Jim
The problem is the FDA is only approving 18 to 20 drugs a year!!!!
This self absorbed, self important group cannot see beyond their noses. Pfizer’s CEO’s statement that we have to earn the trust of the public is pure crap; if they wanted to earn the publics trust EVERY trial report for their drugs would be published.
If they were ethical there would be no need for the legislation introduced by Senator Grassley.
Someone
Hey Jim at BMS,
We hope you continue to work closely with patient groups who can help you make sure that the drugs you back to bring to the market get approved, or fast-tracked through the FDA.
We are particularly thinking about BMS 214622.
We understand BMS and you have made it your personal responsibility to bring this drug to market and potentially cure CML.
This was just what we needed to hear to restore our faith in this industry. Especially at this difficult financially stressful times. Just when patients in North America ar increasingly finding it hard to pay for their drugs. The prospect that they will have some relief (cure?)is quite encouraging.
We ARE counting on you, and we know if anyone knows how to do it, it would be you!
Doc
Let’s hope BMS R&D does better than Vanlev and Pargluva. Apixiban looks weak too.