COMMENTARY

From the Pandemic, a Roadmap for Lowering the Costs of Medicine

Michael Kinch and Lori Weiman

Disclosures

March 26, 2021

Editor's note: Find the latest COVID-19 news and guidance in Medscape's Coronavirus Resource Center.

Just under A decade ago, health care analysts at a pair of U.K.-based financial firms identified a trend they playfully referred to as "Eroom's Law." The name was an inversion of "Moore's Law," the observation that computers and transistors tend to become exponentially faster and cheaper over time. Unlike its better-known counterpart, Eroom's Law observed that since at least the mid-20th century, the inflation-adjusted cost to bring a new drug to market in the U.S. has been doubling roughly every nine years. Some pharmaceutical companies now report that development costs for a new medicine routinely exceed a billion dollars. Undoubtedly, these rising costs have contributed to surging prescription drug prices, a problem that has escalated to crisis proportions in recent years.

Through our research at the intersection of drug development and policy, we've unearthed inefficiencies in the development, regulation, and distribution of prescription drugs — all of which likely contribute to Eroom's Law. But over the past year, we've also seen what drug development can look like when it's freed from those inefficiencies. As the public and private sectors have galvanized to deploy new treatments for Covid-19, they've not only shown us that Eroom's Law can be broken; they've shown us how to break it.

The decades-long trend of rising drug prices described by Eroom's Law is in part a result of regulatory inefficiencies. Like the federal tax code, the U.S. Food and Drug Administration's review process for new medicines has grown increasingly onerous over time, with drug makers being asked to perform an ever-growing number of procedures and clinical measurements to win approval. Arguably, the agency has overreacted to high profile safety lapses such as that of the arthritis medication Vioxx, which was pulled from the market when research linked the drug to an increased risk of heart attack and stroke. In the wake of the Vioxx debacle, the FDA began requiring extensive cardiac monitoring during clinical trials, as well as extensive monitoring of drugs following approval. Such regulatory reactions are well-meaning, but reminiscent of the old adage that military planners are always fighting the last war, not the one to come. The mounting testing and paperwork burdens led one Eli Lilly executive to quip that were the required documentation for a drug approval application to be printed out and stacked, it would reach taller than the Empire State Building. In recognition of this over-reaction, the FDA has begun revising some of the regulations, as evidenced by updated guidance conveyed in March 2020.

Last year, however, as Covid-19 spawned a global crisis, the FDA embraced a more nimble and innovative regulatory posture — and a more open exchange of information with the companies and institutions working to discover, develop, and deploy new treatments for the disease. Early on, the agency pledged not only to expedite reviews of the final data packages submitted at the end of each three-phase clinical trial, but also to rapidly review preliminary data provided before and during a trial's first phase. The improved communication and coordination set the tone for a collaborative approach between the public and private sectors, and it helped pave the way for a Covid-19 vaccine to be developed in a fraction of the time required to develop previous vaccines.

Moving forward, it should be possible to streamline this process even further. One important step will be to assess which of the vast data and testing requirements for drug approval are critical for ensuring safety and efficacy, and which are merely box-checking exercises. In recent decades, for example, the FDA — scarred by episodes like the Vioxx debacle and buoyed by scientists' increased understanding of the body — has pressed drug makers to demonstrate increasingly rigorous understanding of the mechanisms by which their medicines work. Yet, one might argue that these guidelines reflect either hubris or naivete: The vast majority of safe and effective drugs were approved despite uncertainty about their mechanisms of action. Even today, scientists do not completely understand how acetaminophen works, yet the world is a far healthier place for having this drug.

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