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Wednesday, October 2, 2024

Charted: The cost of weight-loss drugs in the US vs. other countries


According to a new report from 
KFF, the United States pays significantly more for weight-loss drugs, including Ozempic and Wegovy, than peer nations, with U.S. prices sometimes being 10 times higher. 

This should be no surprise, just about all drugs are more expensive in the USA.


The weight management medication market is facing a crucial turning point. Learn about the five game-changing moments that will affect the use of GLP-1s for weight loss — from expanded indications to Medicare coverage — and find out what stakeholders should do now to prepare for the future. 

Catalyst 1: FDA approval of new weight management drugs
Weight-management drug competition is ramping up. Though currently only one GLP-1 has been approved for weight management (Novo Nordisk’s semaglutide—also known as Wegovy), early reports from Eli Lilly’s tirzepatide show that the drug may outperform semaglutide in recipients’ percentage of weight loss and percentage of lean muscle mass retained. Furthermore, additional anti-obesity drugs are likely to hit the market in coming years that appeal even more to patients. If the FDA approves these drugs, they will likely have a positive impact on the perception of GLP-1s overall and ease some of the access and price concerns held today.

Ripple effects

Supply chain issues will lessen as more treatment options increase supply
Steeper rebates for health plans as pharmacy benefit managers gain the upper hand in negotiations with manufacturers
Net costs are likely to decrease, but patients may face cost-sharing barriers from persistently high list prices
Catalyst 2: SELECT trial results
Novo Nordisk’s SELECT trial for semaglutide seeks to demonstrate the drug’s efficacy in reducing major cardiovascular events for individuals with established cardiovascular disease. Researchers and clinicians seem confident that results will be positive, making it likely that the FDA will update the drug’s indicated use to include cardiovascular risk reduction in addition to chronic weight management for those above a designated BMI threshold.

Ripple effects

Increased pressure on commercial health plans and employers to cover semaglutide (and future competitors) given the demonstrated relation to cardiovascular health
A new mechanism for Medicare to provide coverage for semaglutide for patients with established cardiovascular disease
Force competitors with drugs in the pipeline to expand their trials to also focus on cardiovascular disease and/or other related health outcomes
Catalyst 3: New data on prescribing and utilization rates
Today, we have little real-world data on how GLP-1s are prescribed and used, limiting the ability of decision-makers to form long-term strategies. In the coming years as more data becomes available, payers and providers will be able to make more informed moves, influencing how these drugs are prescribed, managed, and reimbursed.

Ripple effects

Providers will have a better sense of the overall patient population and more insight into how to manage follow-up care to improve outcomes
Payers will develop more informed coverage policies to limit low-value use of the drugs
Patient medication use and adherence patterns will reveal the scale and clinical impact of drug-related weight cycling (patients take the medication, lose weight, go off the treatment and regain weight, and then get on the medication again)  
Catalyst 4: Patient outcomes from wrap-around services for weight management drugs
Some payers are responding to the demand for GLP-1s and weight loss services by directing members to obesity centers of excellence to ensure the right patients are receiving weight management medications as part of holistic obesity care. At the same time, wellness companies like WeightWatchers and Noom are expanding into prescribing with new telehealth offerings that increase subscriber access to GLP-1s in combination with behavioral interventions. The success (or failure) of these wrap-around service models will likely shape how patients access these drugs and obesity management services in the future.

Ripple effects

If wrap-around service models improve patient outcomes and experience long-term, more payers and wellness companies are likely to employ these models, solidifying this as a new model for obesity care that will come with its own risks and rewards
If these early wrap-around models aren’t successful, healthcare leaders will likely experiment with different ways to facilitate the use of weight management medications as part of holistic obesity care to improve long-term outcomes. Whether via wrap-around services or some alternative model, weight management drugs are unlikely to have a positive impact unless healthcare leaders find a way to integrate them into holistic obesity care  
Catalyst 5: Medicare weight loss coverage reversal
Right now, Medicare cannot legally cover weight-management medications. Advocates have been lobbying to reverse this restriction for years and lawmakers are likely to reintroduce a bill that would do so later this year. The bill had bipartisan support in the past; however, its passage is uncertain given Medicare cost implications. If lobbyists are successful, the change will increase access to these medications—not to mention costs to Medicare and patients, increasing fears about the financial impact of GLP-1s.  

Ripple effects

A large group of patients would gain access to medications covered by their Medicare Part D plans, reducing access disparities
Increase in Medicare Part D plan premiums to accommodate for high cost and projected high utilization of weight management drugs
11 years after FDA approves each weight-management drug, Medicare could negotiate its price as long as generics are not developed
So what should stakeholders be doing now as we wait to see how these catalytic moments transpire?
Providers, especially those unused to providing obesity care, can brush up on clinical guidelines and ensure that patients seeking out weight management drugs receive holistic care. Purchasers can start collecting claims data on prescribing and utilization practices, and surveying members and employees about how likely they are to seek access to these medications.



Charted: The cost of weight-loss drugs in the US vs. other countries

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A new anti-aging treatment for antiaging, using viral vectors.


As people age, their cells gradually become less effective at carrying out their daily functions and repairing damage. This micro-cellular decline can then lead to life-threatening macro-effects such as organ failure and disease. Traditionally, medicine focuses on treating the symptoms of this damage - such as cognitive decline or high cholesterol. However, ambitious biotechnology company BioViva is instead centering its attention on fixing the root cause of it all: cellular aging.


BioViva is implementing personalized, regenerative gene therapies to slow down and reverse biological aging. The firm has a patent on a gene delivery process known as adeno-associated virus (AAV). AAV, which uses the natural ability of a virus to deliver genetic material into cells, and therefore, can be used as a vehicle to carry therapeutic genes into human cells.


In addition to this, the biotechnology company has a patent pending on CMV, a gene delivery method with the capacity to support larger genetic loads due to its greater genome size and unique ability to incorporate multiple genes. CMV thus minimizes the number of treatments needed because more genetic information can be delivered at once. In initial animal studies, CMV treatment was seen to extend lifespan by over 41%. It has been proven to be a potent delivery vector and is being utilized as a part of multiple immunotherapies, including treatments for cancer, AIDS, and malaria.

Through this innovative form of gene therapy, BioViva is setting out to extend humans' health spans - which is the amount of time spent in good health - rather than focusing purely on improving lifespans. This is an issue that grows more critical as the global elderly population expands, particularly due to their increased susceptibility to COVID-19 and susceptibility to aging-associated diseases. Although life expectancy has increased by around three months per year in recent decades, UK data highlights that men are expected to spend around 16 years in ill health while women are expected to spend 19 years in poor health at the end of their lives. As a result, armed with its new gene therapy, BioViva is striving to narrow the gap between our health spans and our lifespans.

The older population's vulnerability is largely due to their immune system being in cellular senescence, where cells no longer divide and repair themselves; this comes as a result of the shortening of telomeres - which can be likened to shoelace-caps located at the ends of our DNA strands - that inevitably comes with biological aging. This damage is associated with diseases such as osteoporosis, heart disease, dementia, Alzheimer's, and cancers.

"Today, we are living longer than ever - which is great. But the caveat is that this means we are also in ill health longer than ever," says Liz Parrish, the CEO of BioViva. "Biological aging is the biggest killer on the planet. Not only does it impact the individual, but the effects of aging-related diseases ripple through to family members who have to see their loved ones struggle with these illnesses - illnesses that we believe will one day be preventable. This is what continues to inspire the entire team at BioViva to find solutions to aging-related decline and to reduce the detrimental impact of disease." Parrish has undergone gene therapy twice with positive results, underlining her conviction in the effectiveness of these treatments.

BioViva's gene therapy presents an opportunity to stop a disease in its tracks before it has been given a chance to spread; the company hopes this could offer cures to conditions that we now consider incurable. The company is now working with five gene candidates and expanding its gene candidates yearly.



 As of my last knowledge update in October 2023, Bioviva's gene therapy products had not received FDA approval. Bioviva has been involved in various gene therapy projects, but specific approvals can change over time. For the most current information, it's best to check the FDA's official website or Bioviva's announcements.






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