The Association for Accessible Medicines, which represents generic and biosimilar manufacturers, chose a leader with a research, public relations, and strategic planning background.
Dan Leonard, former president and CEO of the National Pharmaceutical Council (NPC), has been named president and CEO of the generic and biosimilar industry trade group Association for Accessible Medicines (AAM), effect September.
He succeeds Chester “Chip” Davis Jr, who left AAM in February 2020. AAM represents manufacturers and distributors of generic pharmaceuticals, biosimilars, and bulk pharmaceutical chemicals. Its membership includes suppliers of other goods and services to the generic industry.
Within AAM is the Biosimilars Council, which works to improve biosimilar awareness and uptake with an emphasis on public and health expert education, government affairs, legal affairs, and regulatory policy.
At the NPC, Leonard helped with the group's mission to develop pharmaceutical and pharmaceutical innovation through research and sponsorship of research. Previously, Leonard was executive vice president of advocacy and professional services for America’s Health Insurance Plans, a trade association that represents US payers.
He is a regularly published columnist with Chain Drug Review. In a recent column, Leonard highlighted the challenges to ensuring access to health care for populations affected by coronavirus disease 2019 (COVID-19). He predicted increased Medicaid enrollment leading to challenges for states with limited budgets.
Members of AAM expressed confidence in Leonard’s abilities to lead group toward greater success. “Dan’s decades of leadership experience across the pharmaceutical ecosystem and his unparalleled background in policy and communications make him the perfect person to lead our industry’s efforts to advocate for policies to increase patient access to generic and biosimilar medicines through greater competition,” said Alok Sonig, chairman of the AAM Board of Directors and CEO, US Generics and Head, Global R&D and Biosimilars, Lupin.
Leonard’s background includes more than 20 years of experience in strategic communications, legislative management, politics, and broadcast journalism. During the search for Davis’ replacement, AAM was helmed by its senior vice president and general counsel, Jeff Francer.
Julie Reed: Why 2024 Is Important for Biosimilars
April 17th 2024Julie Reed, executive director of the Biosimilars Forum, showcases how the biosimilar industry is expected to develop throughout 2024, including major policy changes and hope for continued improvement in market share for adalimumab biosimilars.
Decoding the Patent Puzzle: Navigating the Legal Landscape of Biosimilars
March 17th 2024On this episode of Not So Different, Ha Kung Wong, JD, an intellectual patent attorney and partner at Venable LLP, details the confusing landscape that is the US patent system and how it can be improved to help companies overcome barriers to biosimilar competition.
Alvotech’s Stelara Biosimilar, Selarsdi, Receives FDA Approval
April 16th 2024Alvotech’s Selarsdi (ustekinumab-aekn), a biosimilar referencing Stelara (ustekinumab), gained FDA approval, making it the second ustekinumab biosimilar and second for the company to be given the green light for the American market.
Exploring the Biosimilar Horizon: Julie Reed's Predictions for 2024
February 18th 2024On this episode of Not So Different, Julie Reed, executive director of the Biosimilars Forum, returns to discuss her predictions for the biosimilar industry for 2024 and beyond as well as the impact that the Forum's 4 new members will have on the organization's mission.
BioRationality: Removing the Misconceptions Surrounding Interchangeability
April 15th 2024Sarfaraz K. Niazi, PhD, outlines the current state of interchangeable biosimilars in the US and policy changes needed to clear up misconceptions surrounding the meaning behind interchangeability designations.
Global Biosimilar Market Projected to Reach $1.3 Trillion by 2032
April 11th 2024The global biosimilar market is projected to surge from $25.1 billion in 2022 to approximately $1.3 trillion by 2032, with a compound annual growth rate of 17.6%, driven mainly by the increasing prevalence of cancer and the cost-effectiveness of biosimilars, as outlined in a report by Towards Healthcare.