This year has been a good one for development-services providers, especially those that support late development (i.e., Phase
II–III). CMOs and CDMOs report strong demand for late-stage clinical-trial materials and clinical-development services, and
our PharmSource surveys indicate that the industry could experience growth of 5–10% this year.
The buoyant conditions for late-development services may not last much longer, however, as there is growing evidence that
discovery and early development activity may be declining. CROs offering preclinical-development services, such as animal
toxicology testing, have reported soft market conditions and weak revenues throughout the year. CMOs specializing in process
development for small-molecule APIs note that demand for process development and early-stage clinical supplies remains weak
even as late-development demand has been strong. This situation is a big concern for late-development services, of course,
because a weak early-development pipeline means fewer Phase II and Phase III candidates in coming years.
Much of the blame for this state of affairs can be placed on the highly uncertain and volatile global financial environment.
Investors remain risk-averse and are less likely to embrace investments that require long gestation periods and have a low
probability of positive outcomes. Late-stage development candidates have a greater probability of success than candidates
in discovery or early development and are closer to a payoff in the form of licensing or outright sale to a global bio/pharmaceutical
This state of affairs is reflected in venture capital activity in the bio/pharmaceutical industry. According to US data provided
by the National Venture Capital Association, the number of venture-capital investments in the bio/pharmaceutical sector is
down 15% through the first nine months of 2011 compared with venture-capital investments in 2010. The actual dollar value
of investments is up, but that is because of some large deals that supported companies with strong late-development prospects,
such as the $300 million raised by Reata Pharmaceuticals from a single investor. Venture-capital support is crucial to early-stage
companies, and the decline in funding is a clear warning sign for the industry.
EUROPEAN UNION ECONOMIC CRISIS
The EU financial crisis is another cloud on the bio/pharmaceutical R&D horizon. As part of austerity measures required to
get their sovereign debt situation under control, many European governments are slashing expenditures on drugs. In countries
such as Greece and Spain, governments have cut the prices they will pay for drugs by as much as 25% or more and are forcing
a conversion to generic drugs from branded drugs. (The southern-tier countries that have the greatest debt problems have lower
generic-drug penetration than northern European countries).
According to a report by the investment firm Jefferies and Company, the top-line squeeze is likely to force small and mid-size
companies in Europe to cut their R&D expenditures as part of overall cost-cutting measures. A recent article in the Wall Street
Journal cites Spain's Almirall and Greece's Alapis as mid-size companies that are facing R&D cuts as revenues fall (1).
If European revenues are severely affected, even the global bio/pharmaceutical companies could end up reducing their R&D spending
in Europe. Although those companies try to maintain global R&D networks to tap into the broadest array of opportunities, their
R&D activities have typically been matched to the regions with the greatest revenue and profit potential. Over the past 10-plus
years, the locus has been in North America, where the high prices and margins in the US market have funded most of the R&D
budgets at global bio/pharmaceutical companies. More recently, the focus has been shifting to the high-growth emerging markets.
Even though some of the largest global bio/pharmaceutical companies are headquartered in Europe, continuing sales and profit
pressures could force them to move more R&D activity to other locales.