Sandoz’ Edward Li on Using Filgrastim to Ease the Risk of Febrile Neutropenia
October 20th 2020Edward Li, PharmD, director of Health Economics and Outcomes Research for Sandoz, discussed how biosimilar filgrastim (Zarxio) used as primary prophylaxis saves money and helps reduce the risk of febrile neutropenia in patients with cancer.
Thomas Wakim On Neuclone’s Early Dive Into Developing PD-1 Inhibitor Biosimilars
October 15th 2020Thomas Wakim, strategic analyst for Neuclone, discussed the company’s decision to break into the world of PD-1 inhibitors, its partnership with the Serum Institute in India, and Neuclone’s biosimilar pipeline.
Part 2: Sean McGowan on Ensuring a Future Competitive Biosimilar Market
October 1st 2020Sean McGowan, senior director of Biosimilars at AmerisourceBergen, discusses the physician and practice issues with having multiple biosimilars for the same molecule on the market and what is needed to ensure more biosimilar competition in the future.
Part 1: Sean McGowan on the Challenges of Bringing a Biosimilar to Market
September 29th 2020Sean McGowan, senior director of Biosimilars at AmerisourceBergen, discussed the challenges of bringing a new biosimilar to market both generally and during the time of the coronavirus disease 2019 (COVID-19) pandemic.
Hillel Cohen, PhD, on How to Avoid Confusion in Biosimilar Promotions
September 22nd 2020Hillel Cohen, PhD, Education Committee co-chair for the Biosimilars Forum and executive director of Scientific Affairs for Sandoz, discussed whether disclosure statements are needed for biosimilar products and what they should contain, according to the biosimilar industry perspective.
Part 2: Wayne Winegarden, PhD, on What Canada Can Teach the United States About Biosimilars
September 17th 2020Wayne Winegarden, PhD, senior fellow in business and economics at the Pacific Research Institute (PRI) and director of PRI’s Center for Medical Economics and Innovation, discussed why importing drugs may not lower costs and what we can learn from Canada’s biosimilar programs.
Part 1: Wayne Winegarden, PhD, on How Employers Can Better Manage Their Formularies
September 15th 2020Wayne Winegarden, PhD, senior fellow in business and economics at the Pacific Research Institute (PRI) and director of PRI’s Center for Medical Economics and Innovation, discussed where the biosimilar market is heading and how employers can incentivize biosimilar utilization.
Part 2: Brian Gifford on How Treatment Adherence Can Help Employers Save
September 10th 2020Brian Gifford, research director of the Integrated Benefits Institute (IBI), discussed how employers can improve treatment adherence for their employees with rheumatic conditions in order to keep them productive and on the job.
Part 1: Brian Gifford on the Hidden Costs of Rheumatoid Arthritis
September 8th 2020Brian Gifford, research director of the Integrated Benefits Institute (IBI), discussed employer challenges with managing expenses associated with rheumatoid arthritis and how skillful management of rheumatoid arthritis can keep employees on the job and reduce expense.
Part 2: Surya Singh, MD, on Whether Biosimilars Will Lower Drug Costs
September 3rd 2020Surya Singh, MD, president and owner of Singh Healthcare Advisors LLC in Lexington, Massachusetts, discussed the future for the US adalimumab market and whether biosimilars can deliver on the promise of lower cost health care.
Part 1: Surya Singh, MD, on Biosimilar Rebates and Payer Decisions
September 2nd 2020Surya Singh, MD, president and owner of Singh Healthcare Advisors LLC in Lexington, Massachusetts, discussed how payers’ decisions regarding formulary lists affect patient out-of-pocket costs and access to biosimilars.
Part 2: Cheryl Larson on What Employers Can Do to Influence Health Plan Decisions
August 27th 2020Cheryl Larson, president and CEO of the Midwest Business Group on Health, based in Chicago, Illinois, discussed what employers can do to get biosimilars added to their formulary lists and ensure their pharmacy benefit managers (PBMs) aren’t taking advantage of them.
Part 1: Cheryl Larson on How Employers Are Taking on PBMs
August 25th 2020Cheryl Larson, president and CEO of Midwest Business Group on Health, based in Chicago, Illinois, discussed how some employers are taking on pharmacy benefit managers (PBMs) to get biosimilars added to their formularies and what it could mean for biosimilar savings going forward.
Part 2: Swaminathan P. Iyer, MD, Discusses Changing the Infrastructure of Drug Access
August 20th 2020Swaminathan P. Iyer, MD, a professor of medicine in the Department of Lymphoma and Myeloma at The University of Texas MD Anderson Cancer Center, discussed oncology biologics that are too costly for patients whether the Doha Declaration, which would enable governments to license the manufacture of these products, is a viable option.
Part 1: Swaminathan P. Iyer, MD, Discusses Need for Biosimilars in India, US
August 18th 2020Swaminathan Iyer, MD, a professor of medicine in the Department of Lymphoma and Myeloma at the University of Texas MD Anderson Cancer Center, discussed the importance of biosimilars in India and the United States and the main concerns originator companies have regarding biosimilar competition.