COVID-19 allowed governments to critically examine the biopharma space to increase access to vaccines, but there's still a way to go, according to Monique Mansoura, PhD, MBA, executive director of global health security and biotechnology at the MITRE Corporation, at the International Generic and Biosimilar Medicines Association’s annual meeting.
Monique Mansoura, PhD, MBA, executive director of global health security and biotechnology at the MITRE Corporation, explained the intricacies of how geopolitical issues, like the COVID-19 pandemic and inflation, impact pharmaceuticals and contribute to ongoing drug supply shortages.
The annual meeting of the International Generic and Biosimilar Medicines Association (IGBA) was held in Orlando, Florida, from February 15 to February 16.
How has the COVID-19 pandemic contributed to supply chain issues within the pharmaceutical industry, including biologics and biosimilars?
Mansoura: From my perspective, the most dramatic evidence of this intersection of COVID-19 and supply chains with medical pharmaceuticals, is the recognition of the criticality of these assets for national and economic security.
In large part, it's because of the access to diagnostics, therapeutics, and of course, vaccines that allowed in large part the restoration to some sort of new normal, if you will, of how we go about our daily lives—school, work, play. And it was, again, in large part access.
So, the intersection of national security with the biopharma medical supply ecosystem, industrial-based supply chain has been core to the work we've been doing at MITRE and the work that I've been doing in various capacities over the last 20-plus years.
Beside the COVID-19 pandemic, how have other geopolitical issues factored into drug supply shortages and government entities abilities to address them?
Mansoura: This heightened awareness of how important access to medicines, drugs, and again, what we would call national security assets, COVID-19 vaccines, has really been heightened by not only COVID-19, of course, but I think through the CHIPS [the Creating Helpful Incentives to Produce Semiconductors] and Science Act, the broader discussions that are going on in the US and around the world about access to key technologies, whether it's semiconductors or AI [artificial intelligence] or autonomous vehicles, electric batteries, or Russian oil.
I think an awareness of the resiliency, the surety, and security of access to key assets like that, that really are critical to our national and economic security. I think many of us—as consumers but also as professionals in this space—have responsibilities to ensure sort of the surety and security of access to critical assets. There is clearly a shift in in attention to this through legislation, through policy, through executive orders, and through everyday public discourse. So, clearly heightened sensitivity.
Treatment Persistence, Safety After Switching to Infliximab Biosimilars in Canadians With IBD
October 5th 2024A retrospective study of a mandatory nonmedical switch in Canada found no significant differences in rates of treatment persistence, loss of response, or adverse events in patients with inflammatory bowel disease (IBD) on maintenance therapy 1 year post-switch.
Eye on Pharma: EC Approved Ustekinumab; Zymfentra Expansion; Biosimilar Policy Briefing
September 26th 2024The European Commission (EC) approved Celltrion's ustekinumab biosimilar for chronic inflammatory diseases, Celltrion expanded access to Zymfentra (subcutaneous infliximab-dyyb) through partnerships with Cigna and Express Scripts, and the Association for Accessible Medicines held a policy briefing addressing barriers to biosimilar adoption.
Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
AAM Report: Despite Massive Savings, Patient OOP Costs on Biosimilars, Generics Remain High, Part 2
September 24th 2024Part 2 of our series diving into the Association for Accessible Medicines' (AAM) latest report discusses that while generics and biosimilars saved $445 billion in 2023, their potential is hindered by high patient costs, drug shortages, and ineffective policies, underscoring the need for reforms to fully realize their benefits.
French Study Finds High Patient Satisfaction With Adalimumab Biosimilar Treatment for IBD
September 21st 2024An observational study assessing patient satisfaction with adalimumab for inflammatory bowel disease (IBD) reported a high level of satisfaction with all adalimumab product, including biosimilars.