- Bone Health
- Immunology
- Hematology
- Respiratory
- Dermatology
- Diabetes
- Gastroenterology
- Neurology
- Oncology
- Ophthalmology
- Rare Disease
- Rheumatology
The Top 5 Biosimilars Articles for the Week of August 28
The Center for Biosimilars recaps the top 5 stories in biosimilars news for the week of August 28, 2017.
Transcript:
Hi, I’m Kelly Davio 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 August 28.
Number 5: A recent study concluded that reference pricing can help drive down the cost of drugs for health plans, but can raise out-of-pocket costs for patients.
Number 4: Amgen and Sandoz have filed new briefs stating their positions on how the lower courts should address their claims after the Supreme Court’s recent ruling in Sandoz v Amgen.
Number 3: Ireland’s National Cancer Control Programme has issued new guidance on the use of biosimilar medicines in the treatment of cancer.
Number 2: Drug maker Biocon has announced that the FDA will delay a decision on its trastuzumab biosimilar by 3 months.
And Number 1: The FDA has approved Boehringer Ingelheim’s adalimumab biosimilar. Cyltezo is the second FDA-approved biosimilar of the blockbuster reference drug, Humira.
Finally, last week, our newsletter asked you to share your thoughts about whether drug pricing contracts between reference product developers and payers are bad news for biosimilars. To view results of the poll, follow The Center for Biosimilars® on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
Biosimilars Policy Roundup for September 2024—Podcast Edition
October 6th 2024On this episode of Not So Different, we discuss the FDA's approval of a new biosimilar for treating retinal conditions, which took place in September 2024 alongside other major industry developments, including ongoing legal disputes and broader trends in market dynamics and regulatory challenges.
Senators Introduce Bipartisan Legislation to Protect Skinny Labeling
January 2nd 2025To close out the year, 4 senators came together to introduce a new bipartisan bill to protect biosimilar and generic drug manufacturers from patent litigation when obtaining “skinny label” approvals for their products.
The Top 5 Most-Read Policy Articles of 2024
December 28th 2024The top biosimilar policy articles of 2024 highlight advancements that include FDA guidance to simplify biosimilar interchangeability and CMS drug price negotiations under the Inflation Reduction Act, alongside challenges posed by pharmacy benefit manager rebate practices and the need for more active stakeholder engagement.
How Vertical Integration Drives Innovation and Access in Biosimilars
December 27th 2024Elie Bahou, PharmD, highlights how vertical integration in the biosimilar industry streamlines costs, improves supply reliability, accelerates market adoption, and enhances patient access, while emphasizing the value of collaboration, quality control, and value-based contracts for sustainable health care delivery.
