Through a partnership with Merck, Samsung Bioepis adds to its portfolio of biosimilars available in Australia.
Samsung Bioepis, of Incheon, Republic of Korea, is reporting that its adalimumab biosimilar Hadlima has been launched in Australia. The agent references AbbVie’s Humira and is indicated for the treatment of rheumatoid arthritis, juvenile idiopathic arthritis, psoriatic arthritis, ankylosing spondylitis, adult and pediatric Crohn disease, ulcerative colitis, hidradenitis suppurativa, and plaque psoriasis.
“With the launch in Australia, Samsung Bioepis’ adalimumab is now available in 3 markets: Europe, Canada, and Australia,” the company said in a statement. Via a partnership with Biogen, Hadlima was originally launched in 2018 in Europe under the brand name Imraldi. It was made available in Canada in 2021 via a partnership with Merck, which is also assisting with the Australia launch.
Hadlima marks the third anti–tumor necrosis factor biosimilar Samsung Bioepis has launched in Australia. The others are etanercept (Brenzys) and infliximab (Renflexis) biosimilars, in 2016 and 2017, respectively.
Hadlima will be available on the Australian Pharmaceutical Benefits Scheme (PBS) starting April 1, 2021. The PBS subsidizes medicines for residents of Australia.
Biosimilars Gastroenterology Roundup for November 2024—Podcast Edition
December 1st 2024On this episode of Not So Different, we discuss market changes in the adalimumab space; calls for PBM transparency and biosimilar access reforms grew; new data for biosimilars in gastroenterology conditions; and all the takeaways from this year's Global Biosimilars Week.
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.
No Disease Activity Changes After Children With IBD Switched to Infliximab Biosimilar
January 25th 2025A real-world study in adolescent and young adult patients with inflammatory bowel disease (IBD) found no significant differences in lab markers or disease activity between those on Remicade and those switched to biosimilar CT-P13 (Inflectra).
A Banner Year for Biosimilars: The 19 FDA Approvals From 2024
January 21st 2025In 2024, the FDA approved 19 biosimilars across various therapeutic areas, including the first biosimilars for ustekinumab and denosumab, marking significant progress in expanding treatment options and market competition.