The Top 5 Biosimilars Articles for the Week of January 7
The Center for Biosimilars® recaps the top news for the week of January 7, 2019.
Transcript:
Hi, I’m Samantha DiGrande for The Center for Biosimilars®, your resource for clinical, regulatory, business, and policy news in the rapidly changing world of biosimilars.
Here are the top 5 biosimilars articles for the week of January 7.
Number 5: Samsung Bioepis has announced that it will partner with biopharmaceutical company 3SBio to develop and commercialize multiple biosimilars in mainland China.
Number 4: The United Kingdom-based Patients Association recently released results of a survey and focus group that sought to understand patient needs in switching to biosimilars from reference products.
Number 3: At the J.P. Morgan Healthcare Conference, Coherus presented an overview of the company’s “branded approach” to selling its newly launched biosimilar pegfilgrastim, Udenyca.
Number 2: The Community Oncology Alliance recently formed a standing Biosimilars Committee aimed at educating providers.
Number 1: During the J.P. Morgan Healthcare Conference, Pfizer and Teva gave a look at their strategies for 2019 and beyond.
Finally, last week, our e-newsletter asked if new US policies to promote biosimilar insulins will help.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
HHS Praises Biosimilars Savings but Opportunities to Reduce Part B Spending Remain
November 28th 2023Although biosimilars have already generated savings for Medicare Part B programs and beneficiaries, opportunities for substantial reductions in spending remain, according to a report from the HHS.
Biosimilar Business Roundup for October 2023—Podcast Edition
November 5th 2023On this episode, we discuss the biggest news to come out of October 2023, including 3 regulatory approvals, 2 complete response letters, and new data and industry insights that have the potential to impact the entire US biosimilar industry.
Biosimilars Regulatory Roundup for September 2023—Podcast Edition
October 1st 2023On this episode, we discuss several regulatory updates from around the globe, including some European and Japanese approvals, the FDA’s 2-day workshop on the present science behind clinical efficacy testing for biosimilars, and streamlining biosimilar development.
Part 3: Study Questions Usefulness of Clinical Efficacy Trials for Oncology Biosimilars in Europe
November 16th 2023In part 3 of a 3-part series for Global Biosimilars Week, The Center for Biosimilars® reviews an analysis investigating whether clinical efficacy studies have an impact on prescribing decisions for oncology biosimilars across Europe.
