Roman Drai Discusses Geropharm's Biosimilar Pursuits
May 12th 2020Roman Drai, MD, PhD, deputy director and head of clinical operations at Geropharm, discussed Geropharm’s budding biosimilar pipeline and the company’s international pursuits during the World Biosimilar Congress USA 2020 at the Festival of Biologics USA in San Diego, California.
Part 1: Jim Koeller Talks Payer Influence on Biosimilars
May 11th 2020Jim Koeller, a professor of pharmacotherapy and member of the Center for Pharmacoeconomic Studies in the College of Pharmacy at the University of Texas at Austin, discusses how payers influence biosimilar prescriptions and the pressure to lower drug costs for patients.
Part 3: Axinn Attorneys Discuss Patent Exclusivity and the BPCIA
May 8th 2020Ted Mathias and Stacie Ropka, PhD, both patent attorneys and partners at Axinn, Veltrop and Harkrider LLP, discuss patent exclusivity for biological drugs and other important issues that need to be addressed whether or not the ACA and the Biologics Price Competition and Innovation Act (BPCIA) are ruled invalid.
Part 2: Axinn Patent Attorneys Discuss Fallout From Challenges to the ACA
May 6th 2020Ted Mathias and Stacie Ropka, PhD, patent attorneys and partners at Axinn, Veltrop, and Harkrider LLP, discuss past and future court decisions that leave the Affordable Care Act (ACA) in jeopardy and what could happen to the Biologics Price Competition and Innovation Act (BPCIA) as a result.
Molly Burich: How to Improve Biosimilar Uptake
May 5th 2020Molly Burich, MS, head of public policy at Boehringer Ingelheim, discusses several tactics that would help increase biosimilar uptake in the United States and get around current obstacles during the World Biosimilar Congress USA 2020 at the Festival of Biologics USA in San Diego, California.
Part 1: Axinn Patent Attorneys Talk ACA Pushback and the BPCIA
May 4th 2020Ted Mathias and Stacie Ropka, PhD, patent attorneys and partners at Axinn, Veltrop, and Harkrider LLP, discuss the overall pushback to the Affordable Care Act (ACA) and what that means for the Biologics Price Competition and Innovation Act (BPCIA).
IPD Analytics Experts Discuss Humira's Influence on Biosimilars
April 29th 2020Two IPD Analytics pharmacy experts discuss the ever-growing number of Humira (adalimumab) biosimilars, how developers are trying to stand out from the crowd, and the potential for the first-ever interchangeable biosimilar.
Molly Burich Discusses the FDA's Interchangeability Guidance Update
April 22nd 2020Molly Burich, MS, head of public policy at Boehringer Ingelheim (BI), discusses how the FDA's new guidance on interchangeability designation will improve confidence and acceptance for biosimilars during the World Biosimilar Congress USA 2020 at the Festival of Biologics USA in San Diego, California.
Molly Burich Discusses the Lack of Interchangeable Biosimilars
April 21st 2020Molly Burich, MS, head of public policy at Boehringer Ingelheim, discusses the why there currently are no biosimilars with an interchangeability designation during the World Biosimilar Congress USA 2020 at the Festival of Biologics USA in San Diego, California..
Ruby Singh Previews the AMCP eLearning Days Virtual Meeting
April 17th 2020Ruby Singh, vice president for Education and Training, Academy of Managed Care Pharmacy (AMCP), speaks with Mary Caffrey about the upcoming AMCP eLearning Days, a virtual meeting that will take place April 20 to 24. AMCP's annual meeting was canceled due to coronavirus disease 2019 (COVID-19). This transcript is edited slightly for clarity.
Surya Singh, MD, Explains How Biosimilar Education Has Reduced Provider Doubt
April 15th 2020Surya Singh, MD discusses how education efforts have reduced providers’ doubts surrounding the similarity between biosimilars and their reference products at the March 2020 FDA/Federal Trade Commission workshop on anticompetitive practices.
Sarfaraz K. Niazi, PhD, Discusses How COVID-19 May Help Biosimilar Uptake
April 13th 2020Sarfaraz Niazi, PhD, an adjunct professor of biopharmaceutical Sciences at the College of Pharmacy at the University of Illinois at Chicago, discusses how the COVID-19 (coronavirus) pandemic is affecting drug shortages, challenging the FDA, and creating an greater opportunity for biosimilars down the road.
Surya Singh, MD, Explains How Drug Procurement Affects Cost and Access
April 8th 2020Surya Singh, MD, discussed dynamics that affect biosimilar uptake on the medical benefits side and how that differs from the pharmacy benefits side at the recent FDA/Federal Trade Commission workshop on anticompetitive practices.
New Rule: Matt Harman Talks About Employer Interest in Biosimilar Promotion
March 26th 2020Matt Harman talks about employer interest in biosimilar promotion and how the FDA's new biologics pathway change will affect interest levels, during the World Biosimilar Congress USA 2020 at the Festival of Biologics USA in San Diego, California.
Wayne Winegarden, PhD, Explains the Impact of the BPCIA Regulatory Change
March 24th 2020Wayne Winegarden, PhD, talked about the issues and benefits of the FDA's switch to a biologics regulatory pathway for certain products, especially insulin, during the World Biosimilar Congress USA 2020 at the Festival of Biologics USA in San Diego, California.
Sheila Frame Discusses Biosimilar Policy Developments and Market Impact
March 17th 2020Sheila Frame, the vice president of marketing, market access, and patient services at Sandoz, discusses US biosimilar policies in development and the impact they will have on the market at the World Biosimilar Congress 2020 at the Festival of Biologics USA in San Diego, California.