Henlius and Organon’s pertuzumab biosimilar met phase 3 goals; Meitheal expanded its US biosimilars; Celltrion’s subcutaneous infliximab (Zymfentra) showed monotherapy could be as effective as ...
The article by Sarfaraz K. Niazi, PhD, argues that the FDA’s classification of future copies of messenger RNA (mRNA) products could be reconsidered, suggesting they might be eligible for new drug ...
On this episode of Not So Different, we discuss the GRx+Biosims conference, which included discussions on data transparency, ...
Number 4: Regulatory experts and representatives from some of the top biosimilar manufacturers emphasized the importance of global harmonization and streamlining biosimilar development during a panel ...
Direct costs associated with IBD include ambulatory visits to gastroenterologists, emergency department visits, admissions ...
By expanding educational initiatives to clarify biosimilar safety, efficacy, and interchangeability, stakeholders can foster ...
In October, the GRx+Biosims conference included discussions on data transparency, artificial intelligence, and collaboration ...
An IQVIA report highlights challenges to the sustainability of infused biosimilars in the US, citing rebate walls and ...
Sophia Humphreys, PharmD, MHA, BCBBS, of Sutter Health notes that although initial adoption of adalimumab biosimilars remained low in 2023, competitive pricing pressures have already benefited ...
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