Comptroller Kevin Lembo Archive > NewsCOMPTROLLER LEMBO REPORT TO FEDERAL DELEGATION: "
INVESTIGATE AND REVERSE RUNAWAY PHARMACEUTICAL DRUG PRICES"
Comptroller Kevin Lembo today, in a report to
Connecticut's federal delegation, detailed the consequences of a runaway
pharmaceutical drug marketplace that threatens to obstruct patient care and
overcome health care budgets across the public and private sectors.
Lembo, who administers health benefits on behalf of more than 200,000 state and municipal employees, retirees and their dependents, is calling for an immediate federal investigation and swift action to reverse the root causes of these alarming pharmaceutical drug price increases.
Recent reports highlighted an extreme example of a price spike for the drug Daraprim after the rights to the drug were acquired by Turing Pharmaceuticals.
The headline rightfully grabbed significant attention- but the issues raised
are not isolated or unique¨ Lembo said. "They signal a more pervasive and
intensifying trend in the pharmaceutical marketplace.
The sharp rise in pharmacy costs comes at a time when we are seeing great success in limiting medical spending by promoting preventive care and chronic disease management through the state's Health Enhancement Program (HEP). The drastic increases in pharmacy costs are undermining our medical cost savings.
The factors behind rising pharmacy costs include market consolidation, new pricing models and outright profiteering. Projections indicate no future relief as pharmacy costs are expected to continue to rise at an exorbitant rate in the coming years. Meanwhile, pharmaceutical companies are recording historic profits.
We applaud the profit motive in our free market society as a mechanism to efficiently distribute resources and drive innovation, but excessive profits can cause significant harm when applied unbridled to essential and lifesaving medicines in an uncompetitive marketplace. High costs are pushing certain treatments out of reach for some and, on a macro level, our society has fewer resources to expend on other important priorities.¨
Lembo said the issues plaguing the pharmaceutical market are twofold- and each will likely require distinct remedies. The issues are:
significant price increases in certain traditional brand and generic medications, and;
significant additional costs associated with the introduction and expanded utilization of new specialty drugs.
Generic and Brand Price Hikes
The state plan has experienced significant cost increases for non-specialty drugs- an unsustainable 16.9 percent- as a result of substantial price hikes in traditional brand and generic medications, Lembo said.
"The increased costs come at a time when we are seeing very little change in overall utilization for brand and generics- and the changes we are seeing should result in lower, not higher, costs" Lembo said.
For example, last fiscal year the state experienced a slight reduction in the
utilization of brand drugs and a slight increase in the generic dispensing rate.
Despite these encouraging utilization patterns, Lembo said the state still
incurred significant additional costs driven by price hikes of long available
traditional brand and generic medications.
As the extreme case involving the drug Daraprim demonstrated, companies have been buying up the rights to generic and brand drugs and then increasing prices.
Industry consolidation has eroded competition in the market, which in turn
allows pharmaceutical companies to demand higher prices," Lembo said. "Even
worse, a significant backlog of applications to manufacture generic medications
at the U.S. Food and Drug Administration (FDA) is contributing to the lack of
competition and high prices."
Lembo urged the federal delegation to quickly:
Strengthen anti-trust laws to limit consolidation in the pharmaceutical industry and ensure that adequate competition remains to drive competitive pricing in all drug classes; and
Reduce the FDA backlog of generic drug approvals, and sharply reduce the review time of such applications, in order to swiftly introduce competition to consolidated markets.
"Additionally, the promise of lower cost generics only occurs when generics come to market after patent protection for a brand name drug expires," Lembo said. "Pharmaceutical company stall tactics have delayed the introduction of generic competition for some blockbuster brand drugs."
In Fiscal Year 2015, the state employee plan incurred significant costs for the brand drug Nexium as a result of a significant delay in the release of a generic version of the drug. The delay resulted in substantial costs for the state employee plan, which expended more than $8 million that year for the brand name version when an available generic would have significantly reduced the costs to the plan.
"The combination of delayed approvals at the FDA and significant market consolidation has increased prices for generic and brand drugs as a result of reduced competition," Lembo said.
"The specialty drug market poses its own
significant challenges that are separate and distinct from those related to
traditional brand and generic drugs," Lembo said. "The added costs resulting
from specialty drugs, in large part, are for new innovative treatments that are
often more effective than those previously available. As such, specialty drug
manufacturers are adding real value to the medical system. Still, specialty
medications are launching at much higher price points than similar specialty
drugs released just three or four years ago - creating a significant cost burden
for health plans and consumers."
Lembo detailed the effect of specialty drug cost increases on the state plan:
Specialty drug costs for the state employee plan are increasing at an astronomical 54.7 percent.
Specialty drugs accounted for just 1.2 percent of total prescriptions in Fiscal Year 2015, but 25.6 percent of total costs - and the percentage is rising fast.
At the current cost trend, specialty drug costs will increase to more than half of the state's total drug spend in just a few short years.
"All indications are that the trend will continue as the majority of new FDA approvals anticipated in the next four years are specialty drugs," Lembo said. "Many of these medications will bring much needed relief to individuals, but the runaway prices are unsustainable and must be addressed."Significant investments have been made in the development of these new treatments, and better treatments like the new class of Hepatitis C drugs are saving lives and reducing long-term medical costs, Lembo said. However, not all specialty drugs have such clear medical cost savings, and yet the high prices are not limited to the Hepatitis C drugs. They can be found across the spectrum of specialty drugs.
Lembo said at least two current proposals should be thoroughly examined:
- Reducing the data exclusivity period from 12 years to 7 years for
biologics (the exclusivity period refers to the time during which data used
to obtain FDA approval is protected from use by generic manufacturers); and
- Allowing Medicare to use its market power to negotiate lower drug prices.
"Both should be thoroughly examined -- however, provisions should also ensure that negotiated Medicare prices serve as a reference price for the privately insured market," Lembo said. "Otherwise the benefits of lower prices for Medicare may result in higher costs for the privately insured, an outcome that, while successfully reducing federal expenditures, would not solve the sustainability issues associated with the rising costs of pharmaceuticals.
"The State of Connecticut and health plans across the country are seeing unsustainable growth in pharmacy drug spending. Swift action is necessary to infuse competition into the marketplace and institute strategies to control costs where competition is inadequate or impossible.
"I urge congress to fully evaluate the options available to put pharmacy spending back on a sustainable path."