Skip to content
Sign up to receive our free weekday morning edition, and you'll never miss a scoop.

THE FUTURE OF

Medicine

Presented by

In this edition, we’ll highlight some of the key players within Congress, the federal government and the lobbying world.

Medicine

The Players

The future of medicine depends on a complicated relationship among several entities working to influence the direction of health care policy. In this edition, we’ll highlight some of these key players.

They’re policymakers working on legislation that will shape the industry for a long time; government agencies writing rules and overseeing the sector; and industry and advocacy groups pushing for policy that works in their favor.

These players have to contend with the chaotic first few months of the second Trump administration, which has sent both promising and concerning signals to the sprawling health care industry:

 Congress is working to cut billions of dollars from Medicaid through the reconciliation process.

 The White House and Department of Government Efficiency have frozen billions of dollars more in funding for drug development, research and clinical trials.

Health and Human Services Secretary Robert F. Kennedy Jr. is upending the federal government’s approach to vaccines, health and safety protocols, pesticides and more.

One policy. Far-reaching consequences. 

Price control proposals like the Most Favored Nation (MFN) model threaten America’s leadership in medical innovation. By tying U.S. drug prices to those set by foreign governments, MFN would discourage the private investment that drives the development of new treatments. This short-sighted approach risks stalling research, harming startups, and delaying patient access to lifesaving therapies across the board. The U.S. leads the world in drug innovation because we reward risk-taking and scientific progress.  

 

MFN doesn’t just borrow from other countries — it imports their worst ideas.
Learn more at incubatecoalition.org.

Many of the sector’s advocates are focused on threats to federal funding for health care research. 

“We have a huge emphasis and priority on federal research funding given, right now, that there’s a lot of movement to cut federal funding throughout the government,” said Mark Fleury, a policy principal at the American Cancer Society Cancer Action Network. 

“We’re in an era where our biological understanding of cancer has really allowed us to take off with drug development, and that’s really been thanks to long-standing commitment to federal research,” Fleury added. 

It’s unclear what that commitment will look like through the rest of the Trump administration. 

In the meantime, advocates are pushing the government to embrace innovations in artificial intelligence and ease barriers for health care-focused startups and novel drug developments.

Here are some of the key players:

Congress

Sen. Bill Cassidy (R-La.)

Sen. Bill Cassidy (R-La.)

Chair of the Senate Health, Education, Labor and Pensions Committee

Sen. Patty Murray (D-Wash.)

Sen. Patty Murray (D-Wash.)

Ranking member on the Senate Appropriations Committee

Rep. Brett Guthrie (R-Ky.)

Rep. Brett Guthrie (R-Ky.)

Chair of the House Energy and Commerce Committee

Rep. Frank Pallone (D-N.J.)

Rep. Frank Pallone (D-N.J.)

Ranking member on the House Energy and Commerce Committee

Sen. Bill Cassidy (R-La.) 

The chair of the Senate Health, Education, Labor and Pensions Committee, whom we recently interviewed, plays a crucial role in crafting the health agenda for Senate Republicans.

With key Trump nominations out of the way, Cassidy has turned to longstanding priorities like reforming the National Institutes of Health, including the release of a white paper in May calling for a top-down review of the agency’s functions and transparency. 

Sen. Patty Murray (D-Wash.)

The longtime Washington Democrat has positioned herself as a critical backstop against the Trump administration’s crackdown on research funding. As the top Democrat on the Senate Appropriations Committee, Murray blasted the White House for taking a “wrecking ball to our biomedical research enterprise” during an April hearing. 

Murray has also worked alongside Appropriations Committee Chair Susan Collins (R-Maine) to decry the White House’s proposed cuts to medical research.

Rep. Brett Guthrie (R-Ky.) 

As chair of the House Energy and Commerce Committee, Guthrie played a key role in negotiations around the GOP’s hunt for federal savings during the reconciliation process. That culminated in changes to Medicaid that the Congressional Budget Office estimates will cost 8.6 million Americans their insurance coverage. 

Guthrie has plenty of policy priorities, too, having expressed concern over “significant consolidation” among pharmacy benefit managers. 

The Kentucky Republican has also pushed for increased transparency at the NIH and is among several lawmakers seeking changes to the Inflation Reduction Act that would extend the time period “small molecule” drugs can be on the market before they’re eligible for Medicare price negotiations.

Rep. Frank Pallone (D-N.J.) 

The top Democrat on the House Energy and Commerce Committee has had his hands full responding to the Republican effort to cut Medicaid funding in reconciliation. 

Pallone guided Democrats through a 26-hour markup protesting the changes in mid-May. As the former chair of the panel, Pallone led efforts in 2022 to modernize and strengthen the FDA’s approval process for drugs on an accelerated review timetable. 

The New Jersey Democrat also helped create the Advanced Research Projects Agency for Health (ARPA-H) to help fund medical breakthroughs.

How can one legislative fix catalyze medical innovation? The bipartisan Ensuring Pathways to Innovative Cures (EPIC) Act aims to eliminate the “pill penalty,” aligning small molecule drug policies with those of biologics. This change would restore incentives for developing vital treatments and ensure continued progress in patient care.  

Government

Center for Biologics Evaluation and Research 

This branch of the Food and Drug Administration specializes in approving and regulating gene therapies, mRNA vaccines and other diagnostic tools with biological origins. CBER has been at the heart of some of the Trump administration’s most tumultuous shifts in healthcare policy. Under the new administration, the center in May announced a new framework for vaccinations against Covid-19. 

The first Trump administration began efforts to “streamline” certain CBER approval processes, and that will likely continue now.

Center for Drug Evaluation and Research 

The CDER, another wing of the FDA, is the primary office responsible for drug approvals in the United States. The bureau has been working to streamline its approval and review processes for years now. Those efforts include creating a new office in late 2024 to better coordinate scientific reviews, outreach and regulatory initiatives. 

CDER has also embarked on an initiative to study the use of artificial intelligence in drug development. The unit established an AI Council in 2024.

The Advanced Research Projects Agency for Health

Created in 2022 and designed to model the Defense Advanced Research Projects Agency (DARPA), ARPA-H funds high-risk, high-reward medical research. In the years since, the independent organization has pursued interventions in osteoarthritis, precision cancer surgery and various forms of immunotherapy. ARPA-H has been held up as a model of cutting regulatory red tape.

Centers for Medicare & Medicaid Services

The heart of the federal government’s administrative approach to Medicare and Medicaid coverage isn’t the most nimble federal office. But since 2023, CMS has been testing new ways to accelerate novel approaches to coverage and reimbursement, including pilot programs to test “value-based” primary care in rural areas. 

The CMS has also taken on newfound economic clout with its ability to negotiate drug prices.  

Influence

PhRMA 

The Pharmaceutical Research and Manufacturers of America is the predominant trade group for drugmakers. PhRMA invokes innovation constantly in its public messaging and policy work. That includes opposition to Medicare price negotiations, which PhRMA argues “fundamentally alters the incentives for medicine development.” The group has also defended the FDA’s accelerated approval program. 

American Cancer Society

The ACS, combined with its advocacy arm, is a major force in Washington on cancer research and prevention. The organization partnered with the Biden administration for the launch of the Cancer Moonshot initiative in 2022. Advocates say they haven’t lost their focus on equitable access to treatment under the Trump administration. 

“It’s just presenting that in a way that folks understand is not after a particular political agenda – that it’s really just trying to solve a problem,” Fleury said. 

National Venture Capital Association 

The nation’s venture capitalists have a real stake in health care policy, particularly for drug development. Ashlyn Roberts, vice president of government affairs at the NVCA, said the sector is positioned to help innovations survive the transition from lab work to the real world.

“There’s this big chunk of time when the discovery gets spun out and iterated on for years and years, anywhere from between five to 11 or 12 years,” Roberts told us. “A lot of our folks really provide the highest risk capital in that long time horizon to develop these innovations and make them into products.”

– Brendan Pedersen

Listen on the platform of your choice

How can one idea protect millions of lives? 
The U.S. patent system drives life sciences innovation, giving researchers the time and certainty to develop new treatments. 
Policy proposals that chip away at IP rights jeopardize the very ecosystem that makes medical breakthroughs possible.