Maggie L. Shaw


New Data Support Hulio as an Interchangeable Adalimumab Option

June 16, 2025

The new data were collected to fulfill the FDA's requirements to designate adalimumab-fkjp (Hulio) as interchangeable with Humira, enhancing access to affordable biologics for chronic plaque psoriasis treatment.

Eye on Pharma: Interchangeability Labels and Expanded Biosimilar Partnerships

May 29, 2025

The FDA designates 2 biosimilars as interchangeable, enhancing access to treatments for inflammatory diseases and multiple sclerosis, while 2 other companies expand their biosimilar partnership to include more products.

Dr Andre Harvin Answers How Oncologists Can Work to Expand Access to Biosimilars

May 07, 2023

Andre Harvin, PharmD, executive director of pharmacy and oncology services at Cone Health, explains how oncologists can work with other stakeholders to expand access to biosimilars and how patients can work with providers and biosimilar manufacturers to address financial challenges.

Dr Andre Harvin Explains His Excitement for Neulasta Onpro Biosimilars

April 23, 2023

Andre Harvin, PharmD, executive director of pharmacy and oncology services at Cone Health, expressed staunch belief that biosimilars referencing Neulasta Onpro, the on-body injector version of reference pegfilgrastim, are one of the most exciting things coming to the supportive cancer care space.

Updated EULAR RA Treatment Recommendations Address Patient Concerns, Recent Developments

February 09, 2020

Updated guidelines from the European League Against Rheumatism (EULAR), based on new evidence and a review of the literature from 2016 to 2018, address recommendations on the use of disease-modifying antirheumatic drugs and glucocorticoids to treat patients with rheumatoid arthritis (RA). Included is guidance on mono- and combination therapies, treatment strategies, and tapering treatment.