The Center for Biosimilars® recaps the top news for the week of April 29, 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 April 29.
Number 5: The market for orphan drugs is set to grow over the next 4 years, a pharmaceutical report says.
Number 4: Researchers report that patients with psoriasis who switched between 2 different infliximab biosimilars did not have an increase in Psoriasis Area and Severity Index scores or increased adverse events.
Number 3: The European Medicines Agency’s Committee for Medicinal Products for Human Use has adopted a positive opinion for Juta Pharma’s pegfilgrastim biosimilar.
Number 2: Sandoz has entered into a partnership with Taiwan-based EirGenix for a proposed trastuzumab biosimilar referencing Herceptin.
Number 1: Last week, the FDA approved Samsung Bioepis’ etanercept biosimilar referencing Enbrel.
Finally, last week, our e-newsletter asked whether you think that Novartis’ novel eye drug could beat out future biosimilars of aflibercept.
To view results of the poll, visit us on LinkedIn.
To read all of these articles and more, visit centerforbiosimilars.com.
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.
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.
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.
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.
Boosting Health Care Sustainability: The Role of Biosimilars in Latin America
November 21st 2024Biosimilars could improve access to biologic treatments and health care sustainability in Latin America, but their adoption is hindered by misconceptions, regulatory gaps, and weak pharmacovigilance, requiring targeted education and stronger regulations.