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The Top 5 Biosimilars Articles for the Week of October 7
The Center for Biosimilars® recaps the top stories for the week of October 7, 2019.
Transcript
Hi, I’m Jaime Rosenberg 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 October 7, 2019.
Number 5: A new study reports that, for children who switch to biosimilars, factors like device type, citrates, and even color can be primary concerns.
Number 4: The Institute for Clinical and Economic Review says that brand-name adalimumab, rituximab, and pegfilgrastim, all of which have approved biosimilars, have seen substantial increases to price that have not been supported by new clinical data.
Number 3: Nevada’s Department of Health and Human Services sent letters to drug firms that did not provide required information about their costs, and it issued $17.4 million in penalties for noncompliance.
Number 2: The FDA has approved Pfenex’s follow-on teriparatide, referencing Forteo, for the treatment of osteoporosis.
Number 1: The FDA has issued a complete response letter for Tanvex’s proposed filgrastim biosimilar.
Finally, last week, our e-newsletter asked whether you think that the United States should allow external reference pricing to help reduce drug costs.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
Top 5 Most-Read Regulatory Articles of 2024
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Biosimilars in America: Overcoming Barriers and Maximizing Impact
July 21st 2024Join us as we explore the complexities of the US biosimilars market, discussing legislative influences, payer and provider adoption factors, and strategies to overcome industry challenges with expert insights from Kyle Noonan, PharmD, MS, value & access strategy manager at Cencora.
Eye on Pharma: Golimumab Biosimilar Update; Korea Approves Denosumab; Xbrane, Intas Collaboration
December 10th 2024Alvotech and Advanz Pharma have submitted a European marketing application for their golimumab biosimilar to treat inflammatory diseases, while Celltrion secured Korean approval for denosumab biosimilars, and Intas Pharmaceuticals partnered with Xbrane Biopharma on a nivolumab biosimilar.
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.
Denosumab Biosimilars Earn Positive CHMP Opinion for Bone Loss and Giant Cell Tumor of Bone
November 26th 2024The European Medicines Agency Committee for Medicinal Products for Human Use (CHMP) has issued a positive opinion for the denosumab biosimilars SB16 for all indications referencing Prolia and Xgeva.
The Rebate War: How Originator Companies Are Fighting Back Against Biosimilars
November 25th 2024Few biologics in the US have multiple biosimilar competitors, but originator biologics respond quickly to competition by increasing rebates and lowering net prices, despite short approval-to-launch timelines for biosimilars.
