A new deal between pharma giants AbbVie and Samsung Bioepis is designed to postpone competition against a biosimilar to Humira until 2023.
A new deal between pharma giants AbbVie and Samsung Bioepis is designed to postpone competition against Samsung a biosimilar to Humira until 2023.
Samsung Bioepis signed a licensing agreement with AbbVie, which settles all pending patent litigation between the 2 companies and clears the way for the worldwide commercialization of Samsung Bioepis’ SB5, a biosimilar referencing adalimumab (Humira), in all approved markets worldwide.
Related: Will new biosimilars hurt blockbuster autoimmune drug?
Humira, the blockbuster drug that treats rheumatoid arthritis, raked in more than $18 billion in sales last year and accounted for nearly two-thirds of AbbVie’s net revenue, according to Reuters.
Under the terms of the new deal, SB5 may be launched in Europe from October 16, 2018, onwards and, if approved, in the United States, from June 30, 2023, onwards. AbbVie previously announced a global resolution with Amgen allowing its biosimilar to Humira to enter the US market on January 31, 2023.
Related: Potential blockbuster arthritis drug delayed
SB5 has been granted marketing authorization by the European Commission (EC) as Imraldi, and will be commercialized in Europe by Biogen.
“The earliest impact of this agreement will likely be seen in Europe, where SB5 has already been approved and is expected to become our third TNF inhibitor available in the region,” said Jaywoo Kim, senior vice president and head of the commercial division at Samsung Bioepis, in a statement.
Read more: Patient group pushes FDA to improve biosimilar education
FDA Approves Neffy 1 mg Nasal Spray for Pediatric Patients
March 6th 2025Neffy 1 mg is now approved by the FDA to treat pediatric patients who weigh 33 to 65 lbs. Neffy was first FDA-approved as a 2 mg dose in August 2024 for the emergency treatment of anaphylaxis in children and adults weighing at least 66 lbs.
Read More
Trelegy and Breo Offer Incremental Improvement Over Generics
March 3rd 2025The Institute for Clinical and Economic Review has prepared a special report on Trelegy and Breo, two therapies that treat patients with chronic obstructive pulmonary disease that are part of CMS's drug price negotiation program.
Read More