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Seth Ginsberg: What Biosimilar Developers Should Know About the Rheumatic Disease Community
Seth Ginsberg, co-founder and president of the Global Healthy Living Foundation, explains what biosimilar developers should know about patients with rheumatic diseases.
Transcript:
What do you want biosimilar developers to know about patients with inflammatory diseases?
There remains an unmet need for safe and effective treatments for inflammatory diseases. We support the research, development, and marketing of biosimilars to our community and related patient communities.
There are no words that can accurately summarize what biologics have meant to our community of patients. They have changed our lives. I remember when we created CreakyJoints back in 1999, from my dorm room bunk bed in the first year of college. We began by holding community-based patient events in libraries and community centers all around the country. One thing that sticks out in my mind is the instruction we’d give the meeting planners for those events—they’d set up 100 chairs for the event, but right before it started, pull the front right quadrant of 25 chairs so we’d make room for people with mobility assistance devices like wheelchairs or walkers.
Today, when we hold a patient event, if there is 1 wheelchair, it’s the outlier. This is directly the result of the innovation that has occurred with biologics, and biosimilars represent the continuation and proliferation of that innovation for our community.
As the next wave of therapies—in the form of biosimilars—comes to market, we must all work together to ensure that the cost savings that are realized by these versions of the treatments make their way to the patients’ purses and wallets.
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.
Q&A With Dr Chelsee Jensen: Navigating FDA Approvals, Challenges in the Biosimilar Landscape
January 14th 2024Chelsee Jensen, PharmD, BCPS, senior pharmacy specialist and pharmaceutical formulary manager at Mayo Clinic, reacts to the biggest FDA approvals of 2023 and how she sees the adalimumab, natalizumab, and tocilizumab spaces playing out.
Breaking Barriers in Osteoporosis Care: New Denosumab Biosimilars Wyost, Jubbonti Approved
June 16th 2024In this episode, The Center for Biosimilars® delves into the FDA approval of the first denosumab biosimilars, Wyost and Jubbonti (denosumab-bbdz), and discuss their potential to revolutionize osteoporosis treatment with expert insights from 2 rheumatologists.
IGBA 2023: Dr Monique Mansoura Highlights the Intersection of Geopolitical Issues, Biopharma
February 19th 2023COVID-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.
